Targeting of 3D oral cancer spheroids by αVβ6 integrin using near-infrared peptide-conjugated IRDye 680

In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infra...

Full description

Saved in:
Bibliographic Details
Published in:Cancer cell international Vol. 24; no. 1; pp. 228 - 17
Main Authors: Dirheimer, L, Pons, T, François, A, Lamy, L, Cortese, S, Marchal, F, Bezdetnaya, L
Format: Journal Article
Language:English
Published: England BioMed Central 29-06-2024
BMC
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells. αVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population. αVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts. The present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers.
AbstractList In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells.BACKGROUNDIn the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells.αVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population.METHODSαVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population.αVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts.RESULTSαVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts.The present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers.CONCLUSIONSThe present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers.
BackgroundIn the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells.MethodsαVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population.ResultsαVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts.ConclusionsThe present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers.
In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells. αVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population. αVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts. The present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers.
Abstract Background In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells. Methods αVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population. Results αVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts. Conclusions The present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers. Graphical Abstract
Background: In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local recurrence and lower survival rates. Therefore, the universal goal of oral surgical oncology is to achieve microscopically clear margins. Near-infrared fluorescence guided surgery (FGS) could improve surgical resection using fluorescent probes. αVβ6 integrin has shown great potential for cancer targeting due to its overexpression in oral cancers. Red fluorescent contrast agent IRDye 680 coupled with anti-αVβ6 peptide (IRDye-A20) represents an asset to improve FGS of oral cancer. This study investigates the potential of IRDye-A20 as a selective imaging agent in 3D three-dimensional tongue cancer cells. Methods αVβ6 integrin expression was evaluated by RT-qPCR and Western Blotting in 2D HSC-3 human tongue cancer cells and MRC-5 human fibroblasts. Targeting ability of IRDye-A20 was studied in both cell lines by flow cytometry technique. 3D tumor spheroid models, homotypic (HSC-3) and stroma-enriched heterotypic (HSC-3/MRC-5) spheroids were produced by liquid overlay procedure and further characterized using (immuno)histological and fluorescence-based techniques. IRDye-A20 selectivity was evaluated in each type of spheroids and each cell population.Results: αVβ6 integrin was overexpressed in 2D HSC-3 cancer cells but not in MRC-5 fibroblasts and consistently, only HSC-3 were labelled with IRDye-A20. Round shaped spheroids with an average diameter of 400 μm were produced with a final ratio of 55%/45% between HSC-3 and MRC-5 cells, respectively. Immunofluorescence experiments demonstrated an uniform expression of αVβ6 integrin in homotypic spheroid, while its expression was restricted to cancer cells only in heterotypic spheroid. In stroma-enriched 3D model, Cytokeratin 19 and E-cadherin were expressed only by cancer cells while vimentin and fibronectin were expressed by fibroblasts. Using flow cytometry, we demonstrated that IRDye-A20 labeled the whole homotypic spheroid, while in the heterotypic model all cancer cells were highly fluorescent, with a negligible fluorescence in fibroblasts.Conclusions: The present study demonstrated an efficient selective targeting of A20FMDV2-conjugated IRDye 680 in 3D tongue cancer cells stroma-enriched spheroids. Thus, IRDye-A20 could be a promising candidate for the future development of the fluorescence-guided surgery of oral cancers.
ArticleNumber 228
Author François, A
Lamy, L
Marchal, F
Pons, T
Dirheimer, L
Cortese, S
Bezdetnaya, L
Author_xml – sequence: 1
  givenname: L
  surname: Dirheimer
  fullname: Dirheimer, L
  organization: Centre de Recherche en Automatique de Nancy, Centre National de la Recherche Scientifique, UMR 7039, Université de Lorraine, Vandoeuvre-lès-Nancy, France
– sequence: 2
  givenname: T
  surname: Pons
  fullname: Pons, T
  organization: ESPCI Paris, LPEM UMR 8213, PSL University, CNRS, Sorbonne University, Paris, France
– sequence: 3
  givenname: A
  surname: François
  fullname: François, A
  organization: Research Department, Institut de Cancérologie de Lorraine, 6 avenue de Bourgogne, Vandoeuvre-lès-Nancy, 54519, France
– sequence: 4
  givenname: L
  surname: Lamy
  fullname: Lamy, L
  organization: Research Department, Institut de Cancérologie de Lorraine, 6 avenue de Bourgogne, Vandoeuvre-lès-Nancy, 54519, France
– sequence: 5
  givenname: S
  surname: Cortese
  fullname: Cortese, S
  organization: Surgical Department, Institut de Cancérologie de Lorraine, 6 avenue de Bourgogne, Vandoeuvre-lès-Nancy, 54519, France
– sequence: 6
  givenname: F
  surname: Marchal
  fullname: Marchal, F
  organization: Surgical Department, Institut de Cancérologie de Lorraine, 6 avenue de Bourgogne, Vandoeuvre-lès-Nancy, 54519, France
– sequence: 7
  givenname: L
  surname: Bezdetnaya
  fullname: Bezdetnaya, L
  email: L.bolotine@nancy.unicancer.fr, L.bolotine@nancy.unicancer.fr
  organization: Research Department, Institut de Cancérologie de Lorraine, 6 avenue de Bourgogne, Vandoeuvre-lès-Nancy, 54519, France. L.bolotine@nancy.unicancer.fr
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38951897$$D View this record in MEDLINE/PubMed
https://hal.science/hal-04636463$$DView record in HAL
BookMark eNpdUltrFDEYHaRiL_oHfJCAL_VhNJeZXJ6ktGoXFgSpvoZM8s1slm2yJjOF_Vn6Q_qbzHRrafsQEk7OOd-Fc1wdhBigqt4S_JEQyT9lQhVra0ybGrOGiHr3ojoijWhrKrk4ePQ-rI5zXmNMhOT4VXXIpGqJVOKo8lcmDTD6MKDYI3aBYjIbZE2wkFDeriBF7zLqduj2z6_bvxz5MMKQfEBTnkUBTKp96JNJ4NAWtqN3UNsY1tNgxgItflzsAHGJX1cve7PJ8Ob-Pql-fv1ydX5ZL79_W5yfLWvLuBzrrlWEC-OEhKYDw5RlhvG2d8YRUVDVE9EqYI1kzgnLBVPgWsdtR5wyvWUn1WLv66JZ623y1ybtdDRe3wExDdqk0dsNaGwUxlL20hpa9me7tie21MKSGQe8LV6f917bqbsGZyGMZT1PTJ_-BL_SQ7zRhFAiKabF4cPeYfVMd3m21DOGG854OTekcE_vq6X4e4I86mufLWw2JkCcsmZYNIKKpp0be_-Muo5TCmWvM0tRKriYDemeZVPMOUH_0AHBeo6Q3kdIlwjpuwjpXRG9ezzzg-R_Ztg_uVnEyA
Cites_doi 10.3390/biomedicines11041058
10.1158/1078-0432.CCR-14-3284
10.1111/php.13550
10.1016/j.tranon.2020.100919
10.1016/j.neo.2022.01.001
10.1007/s11307-019-01469-5
10.1002/path.2745
10.2967/jnumed.114.150680
10.3389/fphar.2020.579068
10.1016/j.bcp.2023.115586
10.3389/fcell.2022.920303
10.1016/j.cbpa.2003.08.007
10.1016/j.ccr.2016.06.007
10.1042/BSR20180243
10.1016/j.jamcollsurg.2019.09.007
10.2174/1389201018666171004150050
10.1158/0008-5472.CAN-08-4410
10.3389/fonc.2022.1052163
10.21037/atm.2020.04.07
10.1002/smll.201701582
10.1016/j.amsu.2020.10.029
10.5535/arm.2015.39.2.210
10.1111/jop.12044
10.2147/IJN.S427350
10.1242/bio.037051
10.1080/17460441.2021.1878143
10.1158/0008-5472.CAN-18-0878
10.1002/path.2830
10.1088/2050-6120/ac1dbb
10.1016/j.pdpdt.2020.101838
10.1016/j.trecan.2018.05.009
10.3390/cancers9060056
10.1088/0022-3727/38/15/004
10.1016/S1470-2045(19)30317-1
10.4103/1735-3327.250974
10.1016/j.oraloncology.2013.11.001
10.3390/cancers12061474
10.1038/s41598-021-03134-w
10.1007/s00441-005-0148-2
10.2147/IJN.S146927
10.5732/cjc.012.10219
10.1007/s00441-016-2474-y
10.1038/srep39805
10.1186/s12957-020-01874-z
10.1038/srep10169
10.3390/jpm13111575
10.1016/j.neo.2017.05.002
10.1097/01.PRS.0000131872.90767.50
10.1016/j.jbc.2021.100657
10.1111/j.1600-0714.2005.00374.x
10.1002/jcb.26642
10.1002/hed.21166
10.1158/0008-5472.CAN-07-1026
10.1083/jcb.201102147
10.1006/bbrc.2001.5813
10.1021/acsnano.8b03900
10.1038/s41392-022-00904-4
10.1117/1.JBO.26.5.050901
ContentType Journal Article
Copyright 2024. The Author(s).
2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Distributed under a Creative Commons Attribution 4.0 International License
The Author(s) 2024
Copyright_xml – notice: 2024. The Author(s).
– notice: 2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: Distributed under a Creative Commons Attribution 4.0 International License
– notice: The Author(s) 2024
DBID NPM
AAYXX
CITATION
3V.
7TM
7TO
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
H94
K9.
M0S
PIMPY
PQEST
PQQKQ
PQUKI
PRINS
7X8
1XC
5PM
DOA
DOI 10.1186/s12935-024-03417-y
DatabaseName PubMed
CrossRef
ProQuest Central (Corporate)
Nucleic Acids Abstracts
Oncogenes and Growth Factors Abstracts
ProQuest Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
AUTh Library subscriptions: ProQuest Central
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni Edition)
Publicly Available Content Database (Proquest) (PQ_SDU_P3)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
Hyper Article en Ligne (HAL)
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle PubMed
CrossRef
Publicly Available Content Database
Oncogenes and Growth Factors Abstracts
ProQuest Central Essentials
ProQuest One Academic Eastern Edition
Nucleic Acids Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Central China
ProQuest Hospital Collection (Alumni)
ProQuest Central
ProQuest Health & Medical Complete
Health Research Premium Collection
ProQuest One Academic UKI Edition
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
AIDS and Cancer Research Abstracts
ProQuest One Academic
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
Publicly Available Content Database
PubMed


Database_xml – sequence: 1
  dbid: DOA
  name: Directory of Open Access Journals
  url: http://www.doaj.org/
  sourceTypes: Open Website
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 1475-2867
EndPage 17
ExternalDocumentID oai_doaj_org_article_0a90088f8ca2417cb5f1c65f083ade65
oai_HAL_hal_04636463v1
10_1186_s12935_024_03417_y
38951897
Genre Journal Article
GeographicLocations United Kingdom--UK
France
United States--US
Germany
GeographicLocations_xml – name: Germany
– name: United Kingdom--UK
– name: France
– name: United States--US
GroupedDBID ---
-56
-5G
-A0
-BR
0R~
29B
2WC
3V.
53G
5GY
5VS
6J9
7X7
8FI
8FJ
AAFWJ
AAJSJ
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACIWK
ACMJI
ACPRK
ACRMQ
ADBBV
ADINQ
ADRAZ
ADUKV
AEAQA
AENEX
AFKRA
AFPKN
AFRAH
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C24
C6C
CCPQU
CS3
DIK
DU5
E3Z
EBD
EBLON
EBS
ESX
F5P
FRP
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
ISR
ITC
KQ8
LGEZI
LOTEE
M~E
NADUK
NPM
NXXTH
O5R
O5S
OK1
P2P
PGMZT
PIMPY
PQQKQ
PROAC
RBZ
RNS
ROL
RPM
RSV
SBL
SOJ
TR2
TUS
UKHRP
W2D
WOQ
WOW
XSB
~8M
AAYXX
CITATION
7TM
7TO
7XB
8FK
AZQEC
DWQXO
H94
K9.
M48
PQEST
PQUKI
PRINS
7X8
1XC
5PM
ID FETCH-LOGICAL-c368t-b59167ad78e4bea39c3a365fdad17d789f1759e3483dd7c6739ed5d6cb1d9afc3
IEDL.DBID RPM
ISSN 1475-2867
IngestDate Tue Oct 22 15:12:12 EDT 2024
Tue Sep 17 21:28:30 EDT 2024
Tue Oct 15 14:56:05 EDT 2024
Sat Oct 26 04:49:56 EDT 2024
Thu Oct 10 22:53:16 EDT 2024
Fri Nov 22 03:09:30 EST 2024
Sat Nov 02 11:57:05 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Fluorescence imaging
Oral cancer
Near Infrared fluorescence (NIR)
αVβ6 integrin
Head and neck cancer
Tongue cancer
Spheroid
IRDye
Language English
License 2024. The Author(s).
Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c368t-b59167ad78e4bea39c3a365fdad17d789f1759e3483dd7c6739ed5d6cb1d9afc3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-2607-4652
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11218202/
PMID 38951897
PQID 3079227671
PQPubID 42567
PageCount 17
ParticipantIDs doaj_primary_oai_doaj_org_article_0a90088f8ca2417cb5f1c65f083ade65
pubmedcentral_primary_oai_pubmedcentral_nih_gov_11218202
hal_primary_oai_HAL_hal_04636463v1
proquest_miscellaneous_3074727455
proquest_journals_3079227671
crossref_primary_10_1186_s12935_024_03417_y
pubmed_primary_38951897
PublicationCentury 2000
PublicationDate 2024-06-29
PublicationDateYYYYMMDD 2024-06-29
PublicationDate_xml – month: 06
  year: 2024
  text: 2024-06-29
  day: 29
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle Cancer cell international
PublicationTitleAlternate Cancer Cell Int
PublicationYear 2024
Publisher BioMed Central
BMC
Publisher_xml – name: BioMed Central
– name: BMC
References 3417_CR42
EM Tosca (3417_CR32) 2023; 11
G Nicoletti (3417_CR7) 2004; 114
3417_CR45
3417_CR48
GJ Thomas (3417_CR21) 2006; 35
RZ Lin (3417_CR49) 2006; 324
A Francois (3417_CR34) 2023; 18
N Tajmirriahi (3417_CR2) 2019; 16
S Gupta (3417_CR3) 2021; 14
A Saha (3417_CR46) 2010; 222
SH Hausner (3417_CR63) 2015; 56
3417_CR33
VM Baart (3417_CR22) 2020; 12
AN Bashkatov (3417_CR57) 2005; 38
P Lu (3417_CR50) 2012; 196
D Marsh (3417_CR25) 2011; 223
3417_CR39
L Wang (3417_CR60) 2022; 7
H Xue (3417_CR23) 2001; 288
CW Barth (3417_CR53) 2020; 18
3417_CR37
3417_CR36
II Cardle (3417_CR27) 2021; 296
SH Hausner (3417_CR28) 2007; 67
JR Hsiao (3417_CR47) 2010; 32
L Bodner (3417_CR6) 2014; 50
RW Gao (3417_CR12) 2018; 78
C Lee (3417_CR38) 2014; 34
3417_CR9
M Xu (3417_CR43) 2018; 119
J Dardare (3417_CR44) 2022; 12
SH Hausner (3417_CR30) 2009; 69
JV Frangioni (3417_CR54) 2003; 7
3417_CR29
DS Chandrashekar (3417_CR41) 2022; 25
3417_CR26
Q Dai (3417_CR51) 2018; 12
S Hernot (3417_CR52) 2019; 20
M Millard (3417_CR59) 2017; 12
YR Son (3417_CR8) 2015; 39
Y Cui (3417_CR58) 2017; 18
DS Chandrashekar (3417_CR40) 2017; 19
3417_CR1
HX Li (3417_CR20) 2013; 42
HS Rehmani (3417_CR14) 2020; 8
Z Khan (3417_CR24) 2016; 365
3417_CR11
3417_CR55
S van Keulen (3417_CR13) 2019; 229
T Ganguly (3417_CR31) 2020; 22
SB Ravi (3417_CR61) 2014; 8
B Wang (3417_CR5) 2013; 32
3417_CR19
3417_CR18
3417_CR15
JM Dąbrowski (3417_CR56) 2016; 325
O Elaiwy (3417_CR4) 2020; 60
J Pan (3417_CR10) 2020; 18
I Arutyunyan (3417_CR35) 2023; 13
EL Rosenthal (3417_CR16) 2015; 21
L Finlayson (3417_CR62) 2022; 98
G Marsico (3417_CR17) 2018; 4
References_xml – volume: 11
  start-page: 1058
  issue: 4
  year: 2023
  ident: 3417_CR32
  publication-title: Biomedicines
  doi: 10.3390/biomedicines11041058
  contributor:
    fullname: EM Tosca
– volume: 21
  start-page: 3658
  year: 2015
  ident: 3417_CR16
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-14-3284
  contributor:
    fullname: EL Rosenthal
– volume: 98
  start-page: 974
  year: 2022
  ident: 3417_CR62
  publication-title: Photochem Photobiol
  doi: 10.1111/php.13550
  contributor:
    fullname: L Finlayson
– volume: 14
  start-page: 100919
  year: 2021
  ident: 3417_CR3
  publication-title: Transl Oncol
  doi: 10.1016/j.tranon.2020.100919
  contributor:
    fullname: S Gupta
– volume: 25
  start-page: 18
  year: 2022
  ident: 3417_CR41
  publication-title: Neoplasia
  doi: 10.1016/j.neo.2022.01.001
  contributor:
    fullname: DS Chandrashekar
– volume: 22
  start-page: 1170
  year: 2020
  ident: 3417_CR31
  publication-title: Mol Imaging Biol
  doi: 10.1007/s11307-019-01469-5
  contributor:
    fullname: T Ganguly
– volume: 222
  start-page: 52
  year: 2010
  ident: 3417_CR46
  publication-title: J Pathol
  doi: 10.1002/path.2745
  contributor:
    fullname: A Saha
– volume: 56
  start-page: 784
  year: 2015
  ident: 3417_CR63
  publication-title: J Nucl Med
  doi: 10.2967/jnumed.114.150680
  contributor:
    fullname: SH Hausner
– ident: 3417_CR19
  doi: 10.3389/fphar.2020.579068
– ident: 3417_CR33
  doi: 10.1016/j.bcp.2023.115586
– ident: 3417_CR45
  doi: 10.3389/fcell.2022.920303
– volume: 7
  start-page: 626
  year: 2003
  ident: 3417_CR54
  publication-title: Curr Opin Chem Biol Elsevier Ltd
  doi: 10.1016/j.cbpa.2003.08.007
  contributor:
    fullname: JV Frangioni
– volume: 325
  start-page: 67
  year: 2016
  ident: 3417_CR56
  publication-title: Coord Chem Rev Elsevier B V
  doi: 10.1016/j.ccr.2016.06.007
  contributor:
    fullname: JM Dąbrowski
– ident: 3417_CR42
  doi: 10.1042/BSR20180243
– volume: 229
  start-page: 560
  year: 2019
  ident: 3417_CR13
  publication-title: J Am Coll Surg
  doi: 10.1016/j.jamcollsurg.2019.09.007
  contributor:
    fullname: S van Keulen
– volume: 18
  start-page: 669
  year: 2017
  ident: 3417_CR58
  publication-title: Curr Pharm Biotechnol
  doi: 10.2174/1389201018666171004150050
  contributor:
    fullname: Y Cui
– volume: 69
  start-page: 5843
  year: 2009
  ident: 3417_CR30
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-08-4410
  contributor:
    fullname: SH Hausner
– volume: 34
  start-page: 6945
  year: 2014
  ident: 3417_CR38
  publication-title: Anticancer Res
  contributor:
    fullname: C Lee
– volume: 12
  start-page: 1052163
  year: 2022
  ident: 3417_CR44
  publication-title: Front Oncol
  doi: 10.3389/fonc.2022.1052163
  contributor:
    fullname: J Dardare
– volume: 8
  start-page: 813
  year: 2020
  ident: 3417_CR14
  publication-title: Ann Transl Med
  doi: 10.21037/atm.2020.04.07
  contributor:
    fullname: HS Rehmani
– ident: 3417_CR39
  doi: 10.1002/smll.201701582
– volume: 60
  start-page: 195
  year: 2020
  ident: 3417_CR4
  publication-title: Ann Med Surg (London)
  doi: 10.1016/j.amsu.2020.10.029
  contributor:
    fullname: O Elaiwy
– volume: 39
  start-page: 210
  year: 2015
  ident: 3417_CR8
  publication-title: Ann Rehabil Med
  doi: 10.5535/arm.2015.39.2.210
  contributor:
    fullname: YR Son
– volume: 42
  start-page: 547
  year: 2013
  ident: 3417_CR20
  publication-title: J Oral Pathol Med
  doi: 10.1111/jop.12044
  contributor:
    fullname: HX Li
– volume: 18
  start-page: 6545
  year: 2023
  ident: 3417_CR34
  publication-title: Int J Nanomed
  doi: 10.2147/IJN.S427350
  contributor:
    fullname: A Francois
– ident: 3417_CR48
  doi: 10.1242/bio.037051
– ident: 3417_CR29
  doi: 10.1080/17460441.2021.1878143
– volume: 78
  start-page: 5144
  year: 2018
  ident: 3417_CR12
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-18-0878
  contributor:
    fullname: RW Gao
– volume: 223
  start-page: 470
  year: 2011
  ident: 3417_CR25
  publication-title: J Pathol
  doi: 10.1002/path.2830
  contributor:
    fullname: D Marsh
– ident: 3417_CR55
  doi: 10.1088/2050-6120/ac1dbb
– ident: 3417_CR11
  doi: 10.1016/j.pdpdt.2020.101838
– volume: 4
  start-page: 537
  issue: 8
  year: 2018
  ident: 3417_CR17
  publication-title: Trends Cancer Cell Press
  doi: 10.1016/j.trecan.2018.05.009
  contributor:
    fullname: G Marsico
– ident: 3417_CR18
  doi: 10.3390/cancers9060056
– volume: 38
  start-page: 2543
  year: 2005
  ident: 3417_CR57
  publication-title: J Phys D Appl Phys
  doi: 10.1088/0022-3727/38/15/004
  contributor:
    fullname: AN Bashkatov
– volume: 20
  start-page: 354
  year: 2019
  ident: 3417_CR52
  publication-title: Lancet Oncol
  doi: 10.1016/S1470-2045(19)30317-1
  contributor:
    fullname: S Hernot
– volume: 16
  start-page: 117
  year: 2019
  ident: 3417_CR2
  publication-title: Dent Res J (Isfahan)
  doi: 10.4103/1735-3327.250974
  contributor:
    fullname: N Tajmirriahi
– volume: 50
  start-page: 84
  year: 2014
  ident: 3417_CR6
  publication-title: Oral Oncol
  doi: 10.1016/j.oraloncology.2013.11.001
  contributor:
    fullname: L Bodner
– volume: 12
  start-page: 1474
  year: 2020
  ident: 3417_CR22
  publication-title: Cancers (Basel)
  doi: 10.3390/cancers12061474
  contributor:
    fullname: VM Baart
– ident: 3417_CR36
  doi: 10.1038/s41598-021-03134-w
– volume: 324
  start-page: 411
  year: 2006
  ident: 3417_CR49
  publication-title: Cell Tissue Res
  doi: 10.1007/s00441-005-0148-2
  contributor:
    fullname: RZ Lin
– ident: 3417_CR37
– volume: 12
  start-page: 7993
  year: 2017
  ident: 3417_CR59
  publication-title: Int J Nanomed
  doi: 10.2147/IJN.S146927
  contributor:
    fullname: M Millard
– volume: 32
  start-page: 614
  year: 2013
  ident: 3417_CR5
  publication-title: Chin J Cancer
  doi: 10.5732/cjc.012.10219
  contributor:
    fullname: B Wang
– volume: 365
  start-page: 657
  year: 2016
  ident: 3417_CR24
  publication-title: Cell Tissue Res Springer Verlag
  doi: 10.1007/s00441-016-2474-y
  contributor:
    fullname: Z Khan
– ident: 3417_CR26
  doi: 10.1038/srep39805
– volume: 18
  start-page: 96
  year: 2020
  ident: 3417_CR10
  publication-title: World J Surg Oncol
  doi: 10.1186/s12957-020-01874-z
  contributor:
    fullname: J Pan
– ident: 3417_CR15
  doi: 10.1038/srep10169
– volume: 18
  start-page: 11222
  year: 2020
  ident: 3417_CR53
  publication-title: SPIE-Intl Soc Opt Eng
  contributor:
    fullname: CW Barth
– volume: 13
  start-page: 1575
  year: 2023
  ident: 3417_CR35
  publication-title: J Pers Med
  doi: 10.3390/jpm13111575
  contributor:
    fullname: I Arutyunyan
– ident: 3417_CR1
– volume: 19
  start-page: 649
  year: 2017
  ident: 3417_CR40
  publication-title: Neoplasia
  doi: 10.1016/j.neo.2017.05.002
  contributor:
    fullname: DS Chandrashekar
– volume: 8
  start-page: ZE01
  issue: 9
  year: 2014
  ident: 3417_CR61
  publication-title: J Clin Diagn
  contributor:
    fullname: SB Ravi
– volume: 114
  start-page: 329
  year: 2004
  ident: 3417_CR7
  publication-title: Plast Reconstr Surg
  doi: 10.1097/01.PRS.0000131872.90767.50
  contributor:
    fullname: G Nicoletti
– volume: 296
  start-page: 100657
  year: 2021
  ident: 3417_CR27
  publication-title: J Biol Chem
  doi: 10.1016/j.jbc.2021.100657
  contributor:
    fullname: II Cardle
– volume: 35
  start-page: 1
  year: 2006
  ident: 3417_CR21
  publication-title: J Oral Pathol Med
  doi: 10.1111/j.1600-0714.2005.00374.x
  contributor:
    fullname: GJ Thomas
– volume: 119
  start-page: 4193
  year: 2018
  ident: 3417_CR43
  publication-title: J Cell Biochem
  doi: 10.1002/jcb.26642
  contributor:
    fullname: M Xu
– volume: 32
  start-page: 160
  year: 2010
  ident: 3417_CR47
  publication-title: Head Neck
  doi: 10.1002/hed.21166
  contributor:
    fullname: JR Hsiao
– volume: 67
  start-page: 7833
  year: 2007
  ident: 3417_CR28
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-07-1026
  contributor:
    fullname: SH Hausner
– volume: 196
  start-page: 395
  issue: 4
  year: 2012
  ident: 3417_CR50
  publication-title: J Cell Biol
  doi: 10.1083/jcb.201102147
  contributor:
    fullname: P Lu
– volume: 288
  start-page: 610
  year: 2001
  ident: 3417_CR23
  publication-title: Biochem Biophys Res Commun
  doi: 10.1006/bbrc.2001.5813
  contributor:
    fullname: H Xue
– volume: 12
  start-page: 8423
  year: 2018
  ident: 3417_CR51
  publication-title: ACS Nano
  doi: 10.1021/acsnano.8b03900
  contributor:
    fullname: Q Dai
– volume: 7
  start-page: 48
  year: 2022
  ident: 3417_CR60
  publication-title: Signal Transduct Target Ther
  doi: 10.1038/s41392-022-00904-4
  contributor:
    fullname: L Wang
– ident: 3417_CR9
  doi: 10.1117/1.JBO.26.5.050901
SSID ssj0017860
Score 2.400018
Snippet In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher local...
BackgroundIn the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher...
Background: In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with higher...
Abstract Background In the treatment of oral cavity cancer, margin status is one of the most critical prognostic factors. Positive margins are associated with...
SourceID doaj
pubmedcentral
hal
proquest
crossref
pubmed
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 228
SubjectTerms Amino acids
Antibodies
Cancer
Cell culture
Cells
Contrast media
Cytokeratin
E-cadherin
Extracellular matrix
Fibroblasts
Fibronectin
Flow cytometry
Fluorescence
Fluorescence imaging
Fluorescent indicators
Head & neck cancer
Head and neck cancer
Heat
I.R. radiation
Immunofluorescence
Life Sciences
Microscopy
Nanoparticles
Oncology
Oral cancer
Oral carcinoma
Oral cavity
Peptides
Polymers
Spheroid
Spheroids
Squamous cell carcinoma
Stroma
Surgery
Tongue
Tongue cancer
Tumor cell lines
Tumors
Vimentin
Western blotting
αVβ6 integrin
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3LbtQwFLWgEhIbxJtAiwxih6wmcfxalk6rQUIsoCB2lp90WCTVpIOUz6If0m_qtZMZEViwYZGNHcXWvce-x871MUJvWFpVCB6IEyqSxntGVG0tKaMTUdkAESNtDSw_i4_f5OIkyeTsrvpKOWGjPPBouMPSKAhTMkpnINgIZ1msHGcRqIPxgY_qpaXYLqam_wdC8nJ7REbywz5FtXQSuSElTNuCDLMwlNX6Ibicp1zIv4nmn_mSvwWg0_vo3sQc8dHY4wfoVmgfojvjXZLDI7Q6yzndEIlwFzFd4HT0Hrvk1DXuk3hAt_I9tgO-_vX1-orjUShi1eKU-v4dtwB5AnBbp4x0fJGSXTzYtmt_bNJOm8fvPy2GgLksH6Mvpydnx0sy3aNAHOXyklgGHFAYL2RobDBUOWoomNAbXwkoVRE4hAq0kdR74bigKnjmubOVVyY6-gTttV0bniHotYzOAqWhNjSRK1Mb7kpXBsZkxVxdoLdbs-qLUS5D52WG5Hp0ggYn6OwEPRToXbL87s0kdZ0LAAB6AoD-FwAK9Br8NvvG8uiDTmVZDQ2en1WB9rdu1dMg7TVMb6quBRdQ_WpXDcMr_TMxbeg2-Z0GKF7DoJ2nIwp2TQHXY5VUokByho9ZX-Y17eo8S3gDy03K-fXz_2GBF-hunaHNSa320d7lehMO0O3eb17mUXEDBOUSUg
  priority: 102
  providerName: Directory of Open Access Journals
Title Targeting of 3D oral cancer spheroids by αVβ6 integrin using near-infrared peptide-conjugated IRDye 680
URI https://www.ncbi.nlm.nih.gov/pubmed/38951897
https://www.proquest.com/docview/3079227671
https://www.proquest.com/docview/3074727455
https://hal.science/hal-04636463
https://pubmed.ncbi.nlm.nih.gov/PMC11218202
https://doaj.org/article/0a90088f8ca2417cb5f1c65f083ade65
Volume 24
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3LbhMxFLVIJVA3iHcDJTKIHXIzL7-WpWmViocQFMTO8rMNojNR0iDNZ8GH9Ju49mSiBnYsZmN7Zizfa99j-_gYoVc0zio488RyGUjlHCWyMIZkwfIgjYeIEZcGpp_5h29ichxlclh_FiaR9q2ZHdQ_Lg_q2UXiVs4v7bjniY0_vj8CjBB1x4vxAA0AHPZz9PXeARcs64_HCDZexogWTyFXJIMhm5N2F92BME1zEZWebkSjJNoPMeYiUiL_xZt_0yZvxKGTe-juGkDiw66i99EtXz9At7srJduHaHaWqN0QkHATcDnB8QQ-ttG2C7yMGgLNzC2xafH1r6_Xvxnu9CJmNY4M-HNcg-cT8LpFJKbjeeS8OGjipv6-igtuDp9-mrQeM5E9Ql9Ojs-OpmR9nQKxJRNXxFCAglw7LnxlvC6lLXXJaHDa5RxSZQAoIX1ZidI5bhkvpXfUMWtyJ3Ww5WO0Uze130NQaxGsAWRTGl8FJnWhmc1s5ikVObXFEL3um1XNO9UMlWYbgqnOHgrsoZI9VDtEb2LLb0pGxeuU0CzO1druKtMS4IoIwmoAHdwaGnILtQcIqZ1ndIhegt22vjE9fKdiWhJFg-dnPkT7vVnVuq8uFYxysig445D9YpMNvSxunejaN6tUpgKkV1H4z5POCza_6n1piMSWf2zVZTsHHDspefeO_PT_X32Gdovk24wUch_tXC1W_jkaLN1qBDOE07ejtMowSl3kD4z4FP8
link.rule.ids 230,315,729,782,786,866,887,2107,27934,27935,53802,53804
linkProvider National Library of Medicine
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3LbhMxFLVoEdAN70eggEHskJt5-bUsTatUpBWCgNhZfrZBdCZKGqR8FnxIv4lrT6ZqYNfFbOx5eObe63vsOT5G6B2NowrOPLFcBlI5R4ksjCFZsDxI4yFjxKmB4Rd-_F0M9qNMDuvWwiTSvjWTnfrn2U49OU3cyumZ7Xc8sf6noz3ACFF3vOhvoJsQsFnRjdJXfw-4YFm3QEaw_jzmtLgOuSIZdNqcLLfQbUjUNBdR6-lKPkqy_ZBlTiMp8n_E-S9x8komOrh33Xe4j-6usCfebesfoBu-fohutbtRLh-hyTixwiGX4SbgcoDj4n1so1vM8DzKDzQTN8dmiS9-f7v4w3ArNTGpcSTPn-AagoaAw84ipx1PI13GgXWa-sciztU5fPh5sPSYiewx-nqwP94bktVODMSWTJwTQwFFcu248JXxupS21CWjwWmXcyiVAVCI9GUlSue4ZbyU3lHHrMmd1MGWT9Bm3dT-GYJWi2ANgKLS-CowqQvNbGYzT6nIqS166H1nDzVtBTdUGqgIplpDKjCkSoZUyx76EE12eWYUy04FzexErT63yrQEpCOCsBrwCreGhtxC6wF9aucZ7aG3YPC1ewx3RyqWJT01OH7lPbTd-YNahflcQQcpi4IzDtVvLqshQONfF137ZpHOqQAkVhSe87R1n8tHdU7YQ2LNsdbasl4D_pREwDv_eX79S1-jO8Px0UiNDo8_vkBbRQoQRgq5jTbPZwv_Em3M3eJViq2_s2UovQ
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3LbtQwFLVoEVU3vAsDBQxih9zJyy92pdNRK0pVQUHsLD_bQTQZzXSQ5rPgQ_pNXDuTUQd2sMjGdhIn917f4-T4GKHXNM4qOPPEchlI5RwlsjCGZMHyII2HjBE_DRx84sdfxWA_yuS87dbCJNK-NaOd-vvFTj06T9zK8YXtdzyx_smHPcAIUXe86I9d6K-hmxC0WdXN1Bd_ELhgWbdIRrD-NOa1uBa5IhkM3JzMN9EGJGuai6j3dC0nJel-yDTnkRj5N-r8kzx5LRsN7_zPc9xFtxcYFO-2be6hG76-j261u1LOH6DRaWKHQ07DTcDlAMdF_NhG95jgaZQhaEZuis0cX_38cvWL4VZyYlTjSKI_wzUEDwHHnURuOx5H2owDKzX1t1n8Zufw4cfB3GMmsofo83D_dO-ALHZkILZk4pIYCmiSa8eFr4zXpbSlLhkNTrucQ6kMgEakLytROsct46X0jjpmTe6kDrbcQut1U_vHCHotgjUAjkrjq8CkLjSzmc08pSKntuihN51N1LgV3lBpwiKYao2pwJgqGVPNe-hdNNuyZRTNTgXN5EwtXrnKtATEI4KwGnALt4aG3ELvAYVq5xntoVdg9JVrHOweqViWdNXg-JH30HbnE2oR7lMFA6UsCs44VL9cVkOgxr8vuvbNLLWpACxWFO7zqHWh5a06R-whseJcK31ZrQGfSmLgnQ89-fdTX6CNk8FQHR0ev3-KNosUI4wUchutX05m_hlam7rZ8xRevwH5rCs9
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Targeting+of+3D+oral+cancer+spheroids+by+%CE%B1V%CE%B26+integrin+using+near-infrared+peptide-conjugated+IRDye+680&rft.jtitle=Cancer+cell+international&rft.au=Dirheimer%2C+L&rft.au=Pons%2C+T&rft.au=Fran%C3%A7ois%2C+A&rft.au=Lamy%2C+L&rft.date=2024-06-29&rft.pub=BioMed+Central&rft.eissn=1475-2867&rft.volume=24&rft.spage=1&rft_id=info:doi/10.1186%2Fs12935-024-03417-y
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1475-2867&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1475-2867&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1475-2867&client=summon