Abstract 5013: A 3D culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer
We previously reported that single cells from a human colorectal cancer (CRC) cell line (HCA-7) formed either hollow single-layered polarized cysts or solid spiky masses when plated within type-I collagen in 3D. To begin in-depth analyses into whether clonal cysts and spiky masses possessed divergen...
Saved in:
Published in: | Cancer research (Chicago, Ill.) Vol. 77; no. 13_Supplement; p. 5013 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-07-2017
|
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | We previously reported that single cells from a human colorectal cancer (CRC) cell line (HCA-7) formed either hollow single-layered polarized cysts or solid spiky masses when plated within type-I collagen in 3D. To begin in-depth analyses into whether clonal cysts and spiky masses possessed divergent malignant properties, individual colonies of each morphology were isolated and expanded. The lines thus derived faithfully retained the parental cystic and spiky morphologies and were termed CC (cystic) and SC (spiky), respectively. Although both CC and SC expressed EGF receptor (EGFR), cetuximab strongly inhibited growth of CC, whereas SC was resistant to growth inhibition and this was coupled to increased tyrosine phosphorylation of MET and RON. Addition of the dual MET/RON tyrosine kinase inhibitor, crizotinib, to cetuximab in SC restored cetuximab sensitivity. To characterize genome-wide divergence between CC and SC, we performed comprehensive genomic and transcriptomic analysis of CC and SC in 3D. One of the most upregulated genes in CC was the tumor suppressor 15-PGDH/HPGD and the most upregulated gene in SC was versican (VCAN) in 3D and xenografts. Analysis of a human CRC tissue microarray showed that epithelial, but not stromal, VCAN staining strongly correlated with reduced survival, and combined epithelial VCAN and absent HPGD staining portended a poorer prognosis. Thus, with this 3D system, we have identified a new mode of cetuximab resistance and a potential prognostic marker in CRC. As such, this represents a potentially powerful system to identify additional therapeutic sensitivities and disease-relevant genes for CRC.
Citation Format: Bhuminder Singh, Cunxi Li, Ramona Graves-Deal, Haiting Ma, Alina Starchenko, William H. Fry, Yuanyuan Lu, Yang Wang, Galina Bogatcheva, Mohseen P. Khan, Ginger L. Milne, Shilin Zhao, Gregory D. Ayers, Nenggan Li, Mary K. Washington, Timothy J. Yeatman, Oliver G. McDonald, Qi Liu, Robert J. Coffey. A 3D culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 5013. doi:10.1158/1538-7445.AM2017-5013 |
---|---|
AbstractList | We previously reported that single cells from a human colorectal cancer (CRC) cell line (HCA-7) formed either hollow single-layered polarized cysts or solid spiky masses when plated within type-I collagen in 3D. To begin in-depth analyses into whether clonal cysts and spiky masses possessed divergent malignant properties, individual colonies of each morphology were isolated and expanded. The lines thus derived faithfully retained the parental cystic and spiky morphologies and were termed CC (cystic) and SC (spiky), respectively. Although both CC and SC expressed EGF receptor (EGFR), cetuximab strongly inhibited growth of CC, whereas SC was resistant to growth inhibition and this was coupled to increased tyrosine phosphorylation of MET and RON. Addition of the dual MET/RON tyrosine kinase inhibitor, crizotinib, to cetuximab in SC restored cetuximab sensitivity. To characterize genome-wide divergence between CC and SC, we performed comprehensive genomic and transcriptomic analysis of CC and SC in 3D. One of the most upregulated genes in CC was the tumor suppressor 15-PGDH/HPGD and the most upregulated gene in SC was versican (VCAN) in 3D and xenografts. Analysis of a human CRC tissue microarray showed that epithelial, but not stromal, VCAN staining strongly correlated with reduced survival, and combined epithelial VCAN and absent HPGD staining portended a poorer prognosis. Thus, with this 3D system, we have identified a new mode of cetuximab resistance and a potential prognostic marker in CRC. As such, this represents a potentially powerful system to identify additional therapeutic sensitivities and disease-relevant genes for CRC.
Citation Format: Bhuminder Singh, Cunxi Li, Ramona Graves-Deal, Haiting Ma, Alina Starchenko, William H. Fry, Yuanyuan Lu, Yang Wang, Galina Bogatcheva, Mohseen P. Khan, Ginger L. Milne, Shilin Zhao, Gregory D. Ayers, Nenggan Li, Mary K. Washington, Timothy J. Yeatman, Oliver G. McDonald, Qi Liu, Robert J. Coffey. A 3D culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 5013. doi:10.1158/1538-7445.AM2017-5013 |
Author | Bogatcheva, Galina Washington, Mary K. Khan, Mohseen P. Coffey, Robert J. Milne, Ginger L. Yeatman, Timothy J. Singh, Bhuminder Fry, William H. Zhao, Shilin Liu, Qi Wang, Yang Lu, Yuanyuan Graves-Deal, Ramona Li, Nenggan Ayers, Gregory D. Starchenko, Alina Li, Cunxi McDonald, Oliver G. Ma, Haiting |
Author_xml | – sequence: 1 givenname: Bhuminder surname: Singh fullname: Singh, Bhuminder – sequence: 2 givenname: Cunxi surname: Li fullname: Li, Cunxi – sequence: 3 givenname: Ramona surname: Graves-Deal fullname: Graves-Deal, Ramona – sequence: 4 givenname: Haiting surname: Ma fullname: Ma, Haiting – sequence: 5 givenname: Alina surname: Starchenko fullname: Starchenko, Alina – sequence: 6 givenname: William H. surname: Fry fullname: Fry, William H. – sequence: 7 givenname: Yuanyuan surname: Lu fullname: Lu, Yuanyuan – sequence: 8 givenname: Yang surname: Wang fullname: Wang, Yang – sequence: 9 givenname: Galina surname: Bogatcheva fullname: Bogatcheva, Galina – sequence: 10 givenname: Mohseen P. surname: Khan fullname: Khan, Mohseen P. – sequence: 11 givenname: Ginger L. surname: Milne fullname: Milne, Ginger L. – sequence: 12 givenname: Shilin surname: Zhao fullname: Zhao, Shilin – sequence: 13 givenname: Gregory D. surname: Ayers fullname: Ayers, Gregory D. – sequence: 14 givenname: Nenggan surname: Li fullname: Li, Nenggan – sequence: 15 givenname: Mary K. surname: Washington fullname: Washington, Mary K. – sequence: 16 givenname: Timothy J. surname: Yeatman fullname: Yeatman, Timothy J. – sequence: 17 givenname: Oliver G. surname: McDonald fullname: McDonald, Oliver G. – sequence: 18 givenname: Qi surname: Liu fullname: Liu, Qi – sequence: 19 givenname: Robert J. surname: Coffey fullname: Coffey, Robert J. |
BookMark | eNo9kF9LwzAUxYNMcJt-BOF-gc6kaZrUtzL_wsSXvZc0uZFKl0qSqnvzo9sy8elwD-dcDr8VWfjBIyHXjG4YE-qGCa4yWRRiU7_klMlMUMbPyPLfX5AlpVRlopD5BVnF-D6dglGxJD91G1PQJsFcuoUa-B2YsU9jQIjHmPAAnUWfOtdhBA0ev-AwWITBgcE0fncH3ULA2MWkvUHQ3oLtIuqIWcAeP7VP8IZ-ancezNAPAU3SPZg5Hi7JudN9xKs_XZP9w_1--5TtXh-ft_UuMxXnWV4VbdnaSopcScc11SZX1HFZ0ZJTZ0uqy8lVvDSFtWhlaZVwPC8L4aSWmq-JOL01YYgxoGs-wrQ8HBtGm5liM9NqZlrNiWIzA-G_1DRnyg |
ContentType | Journal Article |
DBID | AAYXX CITATION |
DOI | 10.1158/1538-7445.AM2017-5013 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1538-7445 |
EndPage | 5013 |
ExternalDocumentID | 10_1158_1538_7445_AM2017_5013 |
GroupedDBID | --- -ET 18M 29B 2WC 34G 39C 476 53G 5GY 5RE 5VS 6J9 AAYXX ABOCM ACGFO ACIWK ACPRK ACSVP ADBBV ADCOW ADNWM AENEX AFHIN AFOSN AFRAH ALMA_UNASSIGNED_HOLDINGS BAWUL BTFSW CITATION CS3 DIK DU5 EBS EJD F5P FRP GX1 H13 IH2 KQ8 L7B LSO OK1 P0W P2P PQQKQ RCR RHF RHI RNS SJN TR2 W2D W8F WH7 WOQ YKV YZZ |
ID | FETCH-LOGICAL-c933-294b6bd975287f3a0ac280f3790630fd60a63a0836c4dded76d85f32645f7a7a3 |
ISSN | 0008-5472 |
IngestDate | Thu Nov 21 23:23:21 EST 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 13_Supplement |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c933-294b6bd975287f3a0ac280f3790630fd60a63a0836c4dded76d85f32645f7a7a3 |
OpenAccessLink | https://doi.org/10.1158/1538-7445.am2017-5013 |
PageCount | 1 |
ParticipantIDs | crossref_primary_10_1158_1538_7445_AM2017_5013 |
PublicationCentury | 2000 |
PublicationDate | 2017-07-01 |
PublicationDateYYYYMMDD | 2017-07-01 |
PublicationDate_xml | – month: 07 year: 2017 text: 2017-07-01 day: 01 |
PublicationDecade | 2010 |
PublicationTitle | Cancer research (Chicago, Ill.) |
PublicationYear | 2017 |
SSID | ssj0005105 |
Score | 2.2765746 |
Snippet | We previously reported that single cells from a human colorectal cancer (CRC) cell line (HCA-7) formed either hollow single-layered polarized cysts or solid... |
SourceID | crossref |
SourceType | Aggregation Database |
StartPage | 5013 |
Title | Abstract 5013: A 3D culture system identifies a new mode of cetuximab resistance and disease-relevant genes in colorectal cancer |
Volume | 77 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Nb9NAEF2lRUJcUPkShRbNgZvl4Hhtr8MtbYKKIBxoDtystXetWmpd1DioR346M7trr1UQogcuVrKKJ47nZWZ2PfseY295pmIl1Qz_3zoLkwpruLmWcaiFiFRKBCvKSCeciy_f8uUqWU0mPQGzH_uvnsYx9DXtnL2HtwejOICv0ed4RK_j8Z_8vihp8aLqghTLLrvvnC8DS7ChHXFz0CjbJKS3gSRRcSOIYzrMdbe7ba5kGeA0nErLfkOBe5ATksYKFt8dSS-bXq6AaK8pbBLRCH38ZlzvnpqRwFEKXZhnxrb5wwSny8vpaCniHNOoWeU5udhdEY3j0Dj8ubH0n-1t4xuG5A-9DZfaKBYEX0k1aUgxa1MSn8mm6zOzW9iYiaEJ1gfrPEwTq-wz1T4-i8QyUPYB3OnAOKDywuih-sYhG5nppo-yfP_29wyS0q6I4Xumi7W5Nn_6mLH7TiYd-hvNzCrNCzJTkJnCminIzB57EGNUNPP_j598P5Lrt-1_tdtuhmbe_fFqRoXUqCLaHLDHbioDC4vBJ2yi26fs4do1azxjP3soAhl6DwvgS3BABAtE8EAECQhEICDCdQ0DEMEDERCIcBeIYIAITQseiGCB-JxtPqw2p2ehE_wIq7mRFEzKrFRzkeI0vuYyklWcRzUXcyKGq1UWyQxHc55VCWZlJTKVpzXOP5K0FlJI_oLtt9etfskAM4ueZSoSVaQSXqUy4lh511LmcV3GlTxk0_7mFd8trUvxV6e9uu8Jr9kjD-ojtt_d7PQx29uq3Rvj918YHZQK |
link.rule.ids | 315,782,786,27933,27934 |
linkProvider | Flying Publisher |
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=Abstract+5013%3A+A+3D+culture+system+identifies+a+new+mode+of+cetuximab+resistance+and+disease-relevant+genes+in+colorectal+cancer&rft.jtitle=Cancer+research+%28Chicago%2C+Ill.%29&rft.au=Singh%2C+Bhuminder&rft.au=Li%2C+Cunxi&rft.au=Graves-Deal%2C+Ramona&rft.au=Ma%2C+Haiting&rft.date=2017-07-01&rft.issn=0008-5472&rft.eissn=1538-7445&rft.volume=77&rft.issue=13_Supplement&rft.spage=5013&rft.epage=5013&rft_id=info:doi/10.1158%2F1538-7445.AM2017-5013&rft.externalDBID=n%2Fa&rft.externalDocID=10_1158_1538_7445_AM2017_5013 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0008-5472&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0008-5472&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0008-5472&client=summon |