LARS1 is a Prognostic Biomarker and Exhibits a Correlation with Immune Infiltrates in Hepatocellular Carcinoma
To study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC). The clinical characteristics together with LARS1 expression levels were obtained from the TCGA database. Immunohistochemistry confirmed LARS1 expression levels in paraneoplasti...
Saved in:
Published in: | International journal of general medicine Vol. 17; pp. 2203 - 2221 |
---|---|
Main Authors: | , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
New Zealand
Dove
01-01-2024
Dove Medical Press |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | To study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC).
The clinical characteristics together with LARS1 expression levels were obtained from the TCGA database. Immunohistochemistry confirmed LARS1 expression levels in paraneoplastic and tumor tissues. To investigate LARS1-related downstream molecules, a network of protein-protein interactions (PPIs) and the Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) were built. Furthermore, gene set enrichment analysis (GSEA) was used to analyze the pathways associated with LARS1 expression, whereas Single-sample GSEA (ssGSEA) was applied to perform an association study between immune infiltration and LARS1 gene expression. The TISCH Database and the TISIDB database were used to compare the difference of LARS1 expression in hepatocellular carcinoma and immunomodulators.
In comparison to that in normal tissues, the LARS1 expression level was elevated in tumor tissues. LARS1 expression exhibited substantial correlation with AFP, Histologic grade, pathologic stage, Residual tumor, and Vascular invasion in HCC. Higher LARS1 expression in HCC was linked to lower progression-free survival (PFS), disease-specific survival (DSS), and overall survival (OS). According to the GO/KEGG study, the important biological process (neutral lipid metabolic process), cellular component (triglyceride-rich plasma lipoprotein), molecular functions (lipase inhibitor activity), and KEGG pathway (cholesterol metabolism) could be a probable function mechanism in promoting HCC. Various pathways as per GSEA revealed that they were enriched in samples with elevated LARS1 expression. The expression level of LARS1 in malignant tumor cells after immunotherapy was significantly higher than that before immunotherapy. LARS1 was also remarkably linked to the infiltration level and the immunomodulators.
LARS1 can be used as a biomarker of HCC, which is associated to immune infiltration of HCC. |
---|---|
AbstractList | PurposeTo study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC).Patients and MethodsThe clinical characteristics together with LARS1 expression levels were obtained from the TCGA database. Immunohistochemistry confirmed LARS1 expression levels in paraneoplastic and tumor tissues. To investigate LARS1-related downstream molecules, a network of protein-protein interactions (PPIs) and the Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) were built. Furthermore, gene set enrichment analysis (GSEA) was used to analyze the pathways associated with LARS1 expression, whereas Single-sample GSEA (ssGSEA) was applied to perform an association study between immune infiltration and LARS1 gene expression. The TISCH Database and the TISIDB database were used to compare the difference of LARS1 expression in hepatocellular carcinoma and immunomodulators.ResultsIn comparison to that in normal tissues, the LARS1 expression level was elevated in tumor tissues. LARS1 expression exhibited substantial correlation with AFP, Histologic grade, pathologic stage, Residual tumor, and Vascular invasion in HCC. Higher LARS1 expression in HCC was linked to lower progression-free survival (PFS), disease-specific survival (DSS), and overall survival (OS). According to the GO/KEGG study, the important biological process (neutral lipid metabolic process), cellular component (triglyceride-rich plasma lipoprotein), molecular functions (lipase inhibitor activity), and KEGG pathway (cholesterol metabolism) could be a probable function mechanism in promoting HCC. Various pathways as per GSEA revealed that they were enriched in samples with elevated LARS1 expression. The expression level of LARS1 in malignant tumor cells after immunotherapy was significantly higher than that before immunotherapy. LARS1 was also remarkably linked to the infiltration level and the immunomodulators.ConclusionLARS1 can be used as a biomarker of HCC, which is associated to immune infiltration of HCC. To study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC). The clinical characteristics together with LARS1 expression levels were obtained from the TCGA database. Immunohistochemistry confirmed LARS1 expression levels in paraneoplastic and tumor tissues. To investigate LARS1-related downstream molecules, a network of protein-protein interactions (PPIs) and the Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) were built. Furthermore, gene set enrichment analysis (GSEA) was used to analyze the pathways associated with LARS1 expression, whereas Single-sample GSEA (ssGSEA) was applied to perform an association study between immune infiltration and LARS1 gene expression. The TISCH Database and the TISIDB database were used to compare the difference of LARS1 expression in hepatocellular carcinoma and immunomodulators. In comparison to that in normal tissues, the LARS1 expression level was elevated in tumor tissues. LARS1 expression exhibited substantial correlation with AFP, Histologic grade, pathologic stage, Residual tumor, and Vascular invasion in HCC. Higher LARS1 expression in HCC was linked to lower progression-free survival (PFS), disease-specific survival (DSS), and overall survival (OS). According to the GO/KEGG study, the important biological process (neutral lipid metabolic process), cellular component (triglyceride-rich plasma lipoprotein), molecular functions (lipase inhibitor activity), and KEGG pathway (cholesterol metabolism) could be a probable function mechanism in promoting HCC. Various pathways as per GSEA revealed that they were enriched in samples with elevated LARS1 expression. The expression level of LARS1 in malignant tumor cells after immunotherapy was significantly higher than that before immunotherapy. LARS1 was also remarkably linked to the infiltration level and the immunomodulators. LARS1 can be used as a biomarker of HCC, which is associated to immune infiltration of HCC. Longfei Fan,1 Zhongqiang Qin,1 Di Wu,1 Yunchuan Yang,2 Yigang Zhang,2 Bo Xie,1 Jingyu Qian,1 Jianzhu Wei,1 Zhaoying Wang,1 Peipei Yang,1 Zhen Qian,1 Mu Yuan,1 Ziyi Zhu,1 Yulin Tan,1 Yi Tan2 1Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People’s Republic of China; 2Department of Hepatobiliary Surgery, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People’s Republic of ChinaCorrespondence: Yi Tan, Email doctortanyi2007@126.comPurpose: To study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC).Patients and Methods: The clinical characteristics together with LARS1 expression levels were obtained from the TCGA database. Immunohistochemistry confirmed LARS1 expression levels in paraneoplastic and tumor tissues. To investigate LARS1-related downstream molecules, a network of protein-protein interactions (PPIs) and the Gene Ontology (GO)/Kyoto Encyclopedia of Genes and Genomes (KEGG) were built. Furthermore, gene set enrichment analysis (GSEA) was used to analyze the pathways associated with LARS1 expression, whereas Single-sample GSEA (ssGSEA) was applied to perform an association study between immune infiltration and LARS1 gene expression. The TISCH Database and the TISIDB database were used to compare the difference of LARS1 expression in hepatocellular carcinoma and immunomodulators.Results: In comparison to that in normal tissues, the LARS1 expression level was elevated in tumor tissues. LARS1 expression exhibited substantial correlation with AFP, Histologic grade, pathologic stage, Residual tumor, and Vascular invasion in HCC. Higher LARS1 expression in HCC was linked to lower progression-free survival (PFS), disease-specific survival (DSS), and overall survival (OS). According to the GO/KEGG study, the important biological process (neutral lipid metabolic process), cellular component (triglyceride-rich plasma lipoprotein), molecular functions (lipase inhibitor activity), and KEGG pathway (cholesterol metabolism) could be a probable function mechanism in promoting HCC. Various pathways as per GSEA revealed that they were enriched in samples with elevated LARS1 expression. The expression level of LARS1 in malignant tumor cells after immunotherapy was significantly higher than that before immunotherapy. LARS1 was also remarkably linked to the infiltration level and the immunomodulators.Conclusion: LARS1 can be used as a biomarker of HCC, which is associated to immune infiltration of HCC.Keywords: hepatocellular carcinoma, leucyl-tRNA synthetase 1, bioinformatics analysis, biomarker, the cancer genome atlas |
Author | Qian, Zhen Yang, Yunchuan Xie, Bo Wei, Jianzhu Wang, Zhaoying Wu, Di Zhang, Yigang Yuan, Mu Tan, Yi Tan, Yulin Fan, Longfei Yang, Peipei Qian, Jingyu Qin, Zhongqiang Zhu, Ziyi |
Author_xml | – sequence: 1 givenname: Longfei surname: Fan fullname: Fan, Longfei organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 2 givenname: Zhongqiang surname: Qin fullname: Qin, Zhongqiang organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 3 givenname: Di surname: Wu fullname: Wu, Di organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 4 givenname: Yunchuan surname: Yang fullname: Yang, Yunchuan organization: Department of Hepatobiliary Surgery, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 5 givenname: Yigang surname: Zhang fullname: Zhang, Yigang organization: Department of Hepatobiliary Surgery, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 6 givenname: Bo surname: Xie fullname: Xie, Bo organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 7 givenname: Jingyu surname: Qian fullname: Qian, Jingyu organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 8 givenname: Jianzhu surname: Wei fullname: Wei, Jianzhu organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 9 givenname: Zhaoying surname: Wang fullname: Wang, Zhaoying organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 10 givenname: Peipei surname: Yang fullname: Yang, Peipei organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 11 givenname: Zhen surname: Qian fullname: Qian, Zhen organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 12 givenname: Mu surname: Yuan fullname: Yuan, Mu organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 13 givenname: Ziyi surname: Zhu fullname: Zhu, Ziyi organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 14 givenname: Yulin surname: Tan fullname: Tan, Yulin organization: Department of Interventional Radiology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China – sequence: 15 givenname: Yi orcidid: 0000-0003-0272-6633 surname: Tan fullname: Tan, Yi organization: Department of Hepatobiliary Surgery, The First Affiliated Hospital of Bengbu Medical University, Bengbu, 233000, People's Republic of China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38774724$$D View this record in MEDLINE/PubMed |
BookMark | eNpVkUtvEzEURi1URB-wY428ZEGKH2N7skIlKu2gIBCFtXXHvpO4zNipPeHx75mQULUrW_bR8f38nZKjmCIS8pKzc8Er87b5ePXp_KZSRhnzhJxwbuqZYaY6erA_Jqel3DKmtebyGTmWtTGVEdUJicuLrzechkKBfslpFVMZg6PvQxog_8BMIXp6-Xsd2jDumEXKGXsYQ4r0VxjXtBmGbUTaxC70Y4YRCw2RXuMGxuSw77c9ZLqA7EKclM_J0w76gi8O6xn5_uHy2-J6tvx81SwuljMnZT3OJDKHXDuumRdSu65rvdZKcaaFgkqA73zFDILxCkCLeWeMkMrUxnNVcynPSLP3-gS3dpPDlOaPTRDsv4OUVxbyFLRHK1GwTghoW4MVcJw7pxR0Thjv6877yfVu79ps2wG9wzjl7B9JH9_EsLar9NNyzpmZy_lkeH0w5HS3xTLaIZTd50DEtC1WMlVrWQtTTeibPepyKiVjd_8OZ3bXt931bQ99T_irh7Pdw_8Lln8BiVSpqg |
Cites_doi | 10.1002/hep.31288 10.4143/crt.2022.1527 10.1007/s00262-018-2150-z 10.1016/j.cell.2012.02.044 10.3390/biomedicines10051099 10.1093/jn/134.6.1558S 10.1038/s41392-022-01235-0 10.1126/science.1203486 10.1016/bs.ircmb.2022.09.001 10.3390/ijms22115801 10.1002/hep.31921 10.1126/science.aau2753 10.1158/0008-5472.Can-18-3962 10.3390/cancers15010159 10.1016/j.celrep.2021.109031 10.3858/emm.2008.40.2.229 10.1016/j.jhep.2023.01.011 10.1016/j.tranon.2022.101501 10.1053/j.gastro.2023.01.033 10.1158/2159-8290.Cd-20-1680 10.1016/j.celrep.2016.12.019 10.3390/diagnostics12122953 10.1038/s41467-022-30696-8 10.1186/s12967-022-03571-9 10.1038/s41556-022-00856-5 10.1159/000501501 10.3389/fimmu.2022.1058424 10.3389/fimmu.2023.1114717 10.1093/bioinformatics/btz210 |
ContentType | Journal Article |
Copyright | 2024 Fan et al. 2024 Fan et al. 2024 Fan et al. |
Copyright_xml | – notice: 2024 Fan et al. – notice: 2024 Fan et al. 2024 Fan et al. |
DBID | NPM AAYXX CITATION 7X8 5PM DOA |
DOI | 10.2147/IJGM.S457577 |
DatabaseName | PubMed CrossRef MEDLINE - Academic PubMed Central (Full Participant titles) Directory of Open Access Journals |
DatabaseTitle | PubMed CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic 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 | Medicine |
DocumentTitleAlternate | Fan et al |
EISSN | 1178-7074 |
EndPage | 2221 |
ExternalDocumentID | oai_doaj_org_article_3e20f22abb7e4a1e9cc55afc27dd8fdd 10_2147_IJGM_S457577 38774724 |
Genre | Journal Article |
GrantInformation_xml | – fundername: ; |
GroupedDBID | --- 0YH 29J 2WC 53G 5GY 5VS 7X7 8FI 8FJ 8G5 ABUWG ACGFO ADBBV ADRAZ AFKRA ALIPV ALMA_UNASSIGNED_HOLDINGS AOIJS AZQEC BAWUL BCNDV BENPR BPHCQ BVXVI C1A CCPQU DIK DWQXO E3Z EBD F5P FYUFA GNUQQ GROUPED_DOAJ GUQSH GX1 HMCUK HYE IAO IHR IHW IPNFZ ITC KQ8 M2O M48 MK0 M~E NPM O5R O5S OK1 P2P PGMZT PIMPY PQQKQ PROAC RIG RNS RPM TDBHL TR2 UKHRP VDV AAYXX CITATION 7X8 5PM |
ID | FETCH-LOGICAL-c338t-3e0ce16c160d236cffbd665510625a42adfd407ea7d5aa629f77235787d158133 |
IEDL.DBID | RPM |
ISSN | 1178-7074 |
IngestDate | Tue Oct 22 15:08:45 EDT 2024 Tue Sep 17 21:28:46 EDT 2024 Sat Oct 26 05:16:56 EDT 2024 Fri Aug 23 02:24:11 EDT 2024 Sat Nov 02 12:26:01 EDT 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | leucyl-tRNA synthetase 1 the cancer genome atlas biomarker bioinformatics analysis hepatocellular carcinoma |
Language | English |
License | 2024 Fan et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c338t-3e0ce16c160d236cffbd665510625a42adfd407ea7d5aa629f77235787d158133 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ORCID | 0000-0003-0272-6633 |
OpenAccessLink | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11107939/ |
PMID | 38774724 |
PQID | 3058638274 |
PQPubID | 23479 |
PageCount | 19 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_3e20f22abb7e4a1e9cc55afc27dd8fdd pubmedcentral_primary_oai_pubmedcentral_nih_gov_11107939 proquest_miscellaneous_3058638274 crossref_primary_10_2147_IJGM_S457577 pubmed_primary_38774724 |
PublicationCentury | 2000 |
PublicationDate | 2024-01-01 |
PublicationDateYYYYMMDD | 2024-01-01 |
PublicationDate_xml | – month: 01 year: 2024 text: 2024-01-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | New Zealand |
PublicationPlace_xml | – name: New Zealand |
PublicationTitle | International journal of general medicine |
PublicationTitleAlternate | Int J Gen Med |
PublicationYear | 2024 |
Publisher | Dove Dove Medical Press |
Publisher_xml | – name: Dove – name: Dove Medical Press |
References | Kim (ref25) 2021; 35 Chen (ref15) 2022; 20 Liu (ref4) 2023; 78 Han (ref23) 2012; 149 Passarelli (ref16) 2022; 24 Fürst (ref21) 2004; 134 Toh (ref2) 2023; 164 Charoentong (ref9) 2017; 18 Liu (ref27) 2022; 12 Boissière-Michot (ref30) 2022; 13 Ru (ref18) 2019; 35 Gao (ref20) 2023; 14 Sharma (ref7) 2021; 11 Oura (ref26) 2021; 22 Kim (ref24) 2022; 13 Zhu (ref3) 2023; 8 Yoon (ref11) 2020; 367 Schreiber (ref5) 2011; 331 Finotello (ref17) 2018; 67 Hinshaw (ref6) 2019; 79 Zhang (ref10) 2023; 375 Shin (ref14) 2008; 40 McGlynn (ref1) 2021; 73 Cho (ref12) 2022; 15 Tian (ref22) 2023; 24 Yang (ref29) 2022; 24 Kudo (ref8) 2019; 8 Lee (ref13) 2023; 55 Yi (ref19) 2021; 74 Lee (ref28) 2022; 10 |
References_xml | – volume: 73 start-page: 4 year: 2021 ident: ref1 publication-title: Hepatology doi: 10.1002/hep.31288 contributor: fullname: McGlynn – volume: 55 start-page: 851 year: 2023 ident: ref13 publication-title: Cancer Res Treat doi: 10.4143/crt.2022.1527 contributor: fullname: Lee – volume: 67 start-page: 1031 year: 2018 ident: ref17 publication-title: Cancer Immunol Immunother doi: 10.1007/s00262-018-2150-z contributor: fullname: Finotello – volume: 149 start-page: 410 year: 2012 ident: ref23 publication-title: Cell doi: 10.1016/j.cell.2012.02.044 contributor: fullname: Han – volume: 10 year: 2022 ident: ref28 publication-title: Biomedicines doi: 10.3390/biomedicines10051099 contributor: fullname: Lee – volume: 134 start-page: 1558s year: 2004 ident: ref21 publication-title: J Nutr doi: 10.1093/jn/134.6.1558S contributor: fullname: Fürst – volume: 8 start-page: 58 year: 2023 ident: ref3 publication-title: Signal Transduct Target Ther doi: 10.1038/s41392-022-01235-0 contributor: fullname: Zhu – volume: 331 start-page: 1565 year: 2011 ident: ref5 publication-title: Science doi: 10.1126/science.1203486 contributor: fullname: Schreiber – volume: 375 start-page: 1 year: 2023 ident: ref10 publication-title: Int Rev Cell Mol Biol doi: 10.1016/bs.ircmb.2022.09.001 contributor: fullname: Zhang – volume: 22 start-page: 11 year: 2021 ident: ref26 publication-title: Int J Mol Sci doi: 10.3390/ijms22115801 contributor: fullname: Oura – volume: 74 start-page: 2544 year: 2021 ident: ref19 publication-title: Hepatology doi: 10.1002/hep.31921 contributor: fullname: Yi – volume: 367 start-page: 6474):205 year: 2020 ident: ref11 publication-title: Science doi: 10.1126/science.aau2753 contributor: fullname: Yoon – volume: 79 start-page: 4557 year: 2019 ident: ref6 publication-title: Cancer Res doi: 10.1158/0008-5472.Can-18-3962 contributor: fullname: Hinshaw – volume: 15 year: 2022 ident: ref12 publication-title: Cancers doi: 10.3390/cancers15010159 contributor: fullname: Cho – volume: 35 start-page: 109031 year: 2021 ident: ref25 publication-title: Cell Rep doi: 10.1016/j.celrep.2021.109031 contributor: fullname: Kim – volume: 40 start-page: 229 year: 2008 ident: ref14 publication-title: Exp Mol Med doi: 10.3858/emm.2008.40.2.229 contributor: fullname: Shin – volume: 78 start-page: 770 year: 2023 ident: ref4 publication-title: J Hepatol doi: 10.1016/j.jhep.2023.01.011 contributor: fullname: Liu – volume: 24 start-page: 101501 year: 2022 ident: ref29 publication-title: Transl Oncol doi: 10.1016/j.tranon.2022.101501 contributor: fullname: Yang – volume: 164 start-page: 766 year: 2023 ident: ref2 publication-title: Gastroenterology doi: 10.1053/j.gastro.2023.01.033 contributor: fullname: Toh – volume: 11 start-page: 838 year: 2021 ident: ref7 publication-title: Cancer Discov doi: 10.1158/2159-8290.Cd-20-1680 contributor: fullname: Sharma – volume: 18 start-page: 248 year: 2017 ident: ref9 publication-title: Cell Rep doi: 10.1016/j.celrep.2016.12.019 contributor: fullname: Charoentong – volume: 12 year: 2022 ident: ref27 publication-title: Diagnostics doi: 10.3390/diagnostics12122953 contributor: fullname: Liu – volume: 13 start-page: 2904 year: 2022 ident: ref24 publication-title: Nat Commun doi: 10.1038/s41467-022-30696-8 contributor: fullname: Kim – volume: 20 start-page: 355 year: 2022 ident: ref15 publication-title: J Transl Med doi: 10.1186/s12967-022-03571-9 contributor: fullname: Chen – volume: 24 start-page: 307 year: 2022 ident: ref16 publication-title: Nat Cell Biol doi: 10.1038/s41556-022-00856-5 contributor: fullname: Passarelli – volume: 24 start-page: 3 year: 2023 ident: ref22 publication-title: Int J Mol Sci contributor: fullname: Tian – volume: 8 start-page: 221 year: 2019 ident: ref8 publication-title: Liver Cancer doi: 10.1159/000501501 contributor: fullname: Kudo – volume: 13 start-page: 1058424 year: 2022 ident: ref30 publication-title: Front Immunol doi: 10.3389/fimmu.2022.1058424 contributor: fullname: Boissière-Michot – volume: 14 start-page: 1114717 year: 2023 ident: ref20 publication-title: Front Immunol doi: 10.3389/fimmu.2023.1114717 contributor: fullname: Gao – volume: 35 start-page: 4200 year: 2019 ident: ref18 publication-title: Bioinformatics doi: 10.1093/bioinformatics/btz210 contributor: fullname: Ru |
SSID | ssj0066613 |
Score | 2.3395743 |
Snippet | To study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC).
The clinical characteristics... PurposeTo study the relationship between LARS1 expression and immune infiltration and prognosis in hepatocellular carcinoma (HCC).Patients and MethodsThe... Longfei Fan,1 Zhongqiang Qin,1 Di Wu,1 Yunchuan Yang,2 Yigang Zhang,2 Bo Xie,1 Jingyu Qian,1 Jianzhu Wei,1 Zhaoying Wang,1 Peipei Yang,1 Zhen Qian,1 Mu Yuan,1... |
SourceID | doaj pubmedcentral proquest crossref pubmed |
SourceType | Open Website Open Access Repository Aggregation Database Index Database |
StartPage | 2203 |
SubjectTerms | bioinformatics analysis biomarker hepatocellular carcinoma leucyl-trna synthetase 1 Original Research the cancer genome atlas |
SummonAdditionalLinks | – databaseName: Directory of Open Access Journals dbid: DOA link: http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3JbtswECXSHIJeimxtnQ0MkB5Vi5RFSsfYsWMHcRHULdCbQHFBBCRU4OX_MyPKRl0E6CVXkZCIGXHmPWr0hpCrjDOTJ3EZQbYuI8jQIiqNc5HhvRLCn9RJU004nskff7KbIcrkbFp9YU1YkAcOhusmlseOc1WW0vYUs7nWaaqc5tKYzBnTRN9YrMlUiMGAyVkSytyxD093cnc7_T7rATSRcisBNTr9b4HLf2sk_0o6o33yqUWL9Dqs8oDsWH9I9qbt9_Aj4u-vf84YrRZU0Yd5jUVzMJP2q_oZy27mVHlDh9gDu1rinAH24gjVbxRPYOkEfw-xdOJd9dTo1C5o5ekYctSyxjN9LFKlA-w35OGWx-T3aPhrMI7aDgqRBuq5jBIba8uEZiI2PBHaudIIASApBtqjelwZZ4DRWSVNqpTguQOwjfo30rA0A_r6mez62tuvhHJAKgCurNXAYThnKuWlg92cCstziAQd8m1t1uIlCGUUQDDQ_AWav2jN3yF9tPlmDspbNxfA6UXr9OJ_Tu-Qy7XHCtgOaA_lbb1aFBC-MggpwLU75Evw4OZRSQZYV3IYybZ8u7WW7RFfPTaS2wxpcp7kJ--x-lPykQM0Cgc5Z2R3OV_Zc_JhYVYXzVv8Cv5S-iU priority: 102 providerName: Directory of Open Access Journals |
Title | LARS1 is a Prognostic Biomarker and Exhibits a Correlation with Immune Infiltrates in Hepatocellular Carcinoma |
URI | https://www.ncbi.nlm.nih.gov/pubmed/38774724 https://www.proquest.com/docview/3058638274 https://pubmed.ncbi.nlm.nih.gov/PMC11107939 https://doaj.org/article/3e20f22abb7e4a1e9cc55afc27dd8fdd |
Volume | 17 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELbYHhAXxJtAqVwJjtmNncRJju12213EoooFiVvkZ4nUdap9_P_OOEnFVpy4Jk5ieeyZ73M-zxDyueTMVGmiYojWKoYILWJlnIsNzxS4v0KnQU04XxXff5cXM0yTI4azMEG0r1Uz9rfrsW_-BG3l3VpPBp3Y5Ho5ZUhaqrSajMgIwOHA0Tv_C3icpZ3EHWvwTBZfr5bjVQawpMCKe2kJgKfg2UEcCun6_4UxH0sl_4o9ly_I8x400rOucy_JE-tfkafL_rf4a-K_nf1YMdpsqaTXmxa1c9CSnjftGtU3Gyq9oTMshd3ssM0US3J0IjiKG7F0gadELF1419yGdLVb2ng6h1C1a3FrH7WqdIplhzy88g35dTn7OZ3HfSGFWAMD3cWpTbRlQjORGJ4K7ZwyQgBWSoD9yIxL4wwQOysLk0speOUAc2ManMKwvAQW-5Yc-dbb94RyACyAsazVQGU4ZzLnysGizoXlFTiEiHwZhrW-6_Jl1MAz0BI1WqLuLRGRcxzzhzaY5TpcaDc3dW_rOrU8cZxLpQqbSWYrrfNcOs0LY0pnTEROB4vVsCpwPKS37X5bgxcrwbMA5Y7Iu86CD58aZkBEygPbHvTl8A5MxJB5e5h4H_7_0Y_kGQdc1O3iHJOj3WZvP5HR1uxPwn7ASZjM9413-bg |
link.rule.ids | 230,315,729,782,786,866,887,2106,27933,27934,53800,53802 |
linkProvider | National Library of Medicine |
linkToHtml | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB7RIgEX3oWUFowEx-wmTuIkx3a7ZRd2q4otErfI8QMidZ1qH_-_M3lUXcSp19hJLI89833J5xmALxkPdR4FpY_RuvQxQgu_1Nb6msclur9URY2acLJIL35nZ2NKkyP6szCNaF-V1cBdLweu-ttoK2-WatjrxIaX81FIpCWP8uEePMYNGwQ9S289MCLyMGpF7lSFZzj9_m0-WMQITFKquRdlCHlSHu9EoiZh__9Q5r9iyXvR5_zFQ8f9Ep53eJOdtO2v4JFxr-HJvPuj_gbc7OTnImTVmkl2uapJdoc92WlVL0m4s2LSaTamKtrVhvqMqJpHq59j9A2XTemAiWFTZ6vrJtPtmlWOTTDKbWr6K0AyVzaiikUOH_kWfp2Pr0YTv6vB4Cskrxs_MoEyoVChCDSPhLK21EIgzAqQOMmYS201ckIjU51IKXhuEa5TBp1Uh0mGBPgA9l3tzHtgHLEOwjNjFLIgzkOZ8NKiP0iE4Tn6Eg--9vYobtpUGwVSFDJhQSYsOhN6cErGuutDCbKbC_XqT9FNdxEZHljOZVmmJpahyZVKEmkVT7XOrNYefO5NXeCGovmQztTbdYEOMEOnhGzdg3et6e9e1S8dD7KdRbEzlt0WXAtN0u7e9ocPv_UTPJ1czWfFbHrx4wM84wiv2o9BR7C_WW3NMeyt9fZjsxduAQmADoo |
linkToPdf | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Zb9NAEB7RIlW8lBvcUlgkeHRsr---tWlCAk0VEZB4s9Z7gKVmHeX4_8z4qBrEE7za60M7uzPft_vtDMCHjAcqD_3SxWhduhihE7dUxriKRyW6v1SGjZpwskhvfmRXI0qTc96fhWlE-7KsBvZ2ObDVr0ZbuVpKr9eJefPZMCDSkoe5t1LGO4CHOGl93jP11gsjKg_CVuhOlXi86edPs8EiQnCSUt29MEPYk_JoLxo1Sfv_hjT_FEzei0Djx__z70_guMOd7KJt8xQeaPsMjmbdzvpzsNcXXxcBqzZMsPm6JvkdtmSXVb0kAc-aCavYiKppV1tqM6SqHq2OjtFaLpvSQRPNptZUt03G2w2rLJtgtNvWtDtAclc2pMpFFl_5Ar6PR9-GE7erxeBKJLFbN9S-1EEig8RXPEykMaVKEoRbPhIoEXGhjEJuqEWqYiESnhuE7ZRJJ1VBnCERfgmHtrb6NTCOmAdhmtYS2RDngYh5adAvxInmOfoUBz72NilWbcqNAqkKmbEgMxadGR24JIPdtaFE2c2Fev2z6Lq8CDX3DeeiLFMdiUDnUsaxMJKnSmVGKQfe9-YucGJRfwir692mQEeYoXNC1u7Aq9b8d5_qh48D2d7A2PuX_Ts4Hprk3b39T_790XdwNL8aF9fTmy-n8IgjymrXhN7A4Xa902dwsFG7t810-A2JgBEK |
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=LARS1+is+a+Prognostic+Biomarker+and+Exhibits+a+Correlation+with+Immune+Infiltrates+in+Hepatocellular+Carcinoma&rft.jtitle=International+journal+of+general+medicine&rft.au=Fan%2C+Longfei&rft.au=Qin%2C+Zhongqiang&rft.au=Wu%2C+Di&rft.au=Yang%2C+Yunchuan&rft.date=2024-01-01&rft.issn=1178-7074&rft.eissn=1178-7074&rft.volume=17&rft.spage=2203&rft.epage=2221&rft_id=info:doi/10.2147%2FIJGM.S457577&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1178-7074&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1178-7074&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1178-7074&client=summon |