Loading…
Molecular mechanism study of HGF/c-MET pathway activation and immune regulation for a tumor diagnosis model
Hepatocyte growth factor (HGF) binds to the c-mesenchymal-epithelial transition (C-MET) receptor and activates downstream signaling pathways, playing an essential role in the development of various cancers. Given the role of this signaling pathway, the primary therapeutic direction focuses on identi...
Saved in:
Published in: | Cancer cell international 2021-07, Vol.21 (1), p.374-374, Article 374 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53 |
---|---|
cites | cdi_FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53 |
container_end_page | 374 |
container_issue | 1 |
container_start_page | 374 |
container_title | Cancer cell international |
container_volume | 21 |
creator | Shen, Zhibo Xue, Wenhua Zheng, Yuanyuan Geng, Qishun Wang, Le Fan, Zhirui Wang, Wenbin Yue, Ying Zhai, Yunkai Li, Lifeng Zhao, Jie |
description | Hepatocyte growth factor (HGF) binds to the c-mesenchymal-epithelial transition (C-MET) receptor and activates downstream signaling pathways, playing an essential role in the development of various cancers. Given the role of this signaling pathway, the primary therapeutic direction focuses on identifying and designing HGF inhibitors, antagonists and other molecules to block the binding of HGF to C-MET, thereby limiting the abnormal state of other downstream genes.
This study focuses on the analysis of immune-related genes and corresponding immune functions that are significantly associated with the HGF/c-MET pathway using transcriptome data from 11 solid tumors.
We systematically analyzed 11 different cancers, including expression correlation, immune infiltration, tumor diagnosis and survival prognosis from HGF/c-MET pathway and immune regulation, two biological mechanisms having received extensive attention in cancer analysis.
We found that the HGF/c-MET pathway affected the tumor microenvironment mainly by interfering with expression levels of other genes. Immune infiltration is another critical factor involved in changes to the tumor microenvironment. The downstream immune-related genes activated by the HGF/c-MET pathway regulate immune-related pathways, which in turn affect the degree of infiltration of immune cells. Immune infiltration is significantly associated with cancer development and prognosis. |
doi_str_mv | 10.1186/s12935-021-02051-2 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_2834207af6f54dbeb670542069b2bd9a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_2834207af6f54dbeb670542069b2bd9a</doaj_id><sourcerecordid>2552979054</sourcerecordid><originalsourceid>FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53</originalsourceid><addsrcrecordid>eNpdkk1v1DAQhi0EoqXwBzggS1y4hHqc-CMXJFT1S2rFpZytie3seknixU6K9t_j7paq5WCNNX7nGc_oJeQjsK8AWp5m4G0tKsahHCag4q_IMTRKVFxL9frZ_Yi8y3nDGCgt2VtyVDdcQiPVMfl1GwdvlwETHb1d4xTySPO8uB2NPb26vDi11e35Hd3ivP6DO4p2Dvc4hzhRnBwN47hMnia_Koh9to-JIp2XsUQXcDXFHDIdo_PDe_KmxyH7D4_xhPy8OL87u6puflxen32_qaxo1VzZutG1VQqc19A0giv0oKTTnWSt7NqaO-vL0MjBgpNWatDAGnCil-idqE_I9YHrIm7MNoUR085EDGafiGllMM3BDt5wXVbBFPayF43rfCcVEyUj2453rsXC-nZgbZdu9KXxNCccXkBfvkxhbVbx3miutGqgAL48AlL8vfg8mzFk64cBJx-XbLgQvFVt6Vqkn_-TbuKSprKqB1XNuRJMFhU_qGyKOSffP30GmHnwhTn4wpQVmb0vDC9Fn56P8VTyzwj1X_n0sz0</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2553227506</pqid></control><display><type>article</type><title>Molecular mechanism study of HGF/c-MET pathway activation and immune regulation for a tumor diagnosis model</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Shen, Zhibo ; Xue, Wenhua ; Zheng, Yuanyuan ; Geng, Qishun ; Wang, Le ; Fan, Zhirui ; Wang, Wenbin ; Yue, Ying ; Zhai, Yunkai ; Li, Lifeng ; Zhao, Jie</creator><creatorcontrib>Shen, Zhibo ; Xue, Wenhua ; Zheng, Yuanyuan ; Geng, Qishun ; Wang, Le ; Fan, Zhirui ; Wang, Wenbin ; Yue, Ying ; Zhai, Yunkai ; Li, Lifeng ; Zhao, Jie</creatorcontrib><description>Hepatocyte growth factor (HGF) binds to the c-mesenchymal-epithelial transition (C-MET) receptor and activates downstream signaling pathways, playing an essential role in the development of various cancers. Given the role of this signaling pathway, the primary therapeutic direction focuses on identifying and designing HGF inhibitors, antagonists and other molecules to block the binding of HGF to C-MET, thereby limiting the abnormal state of other downstream genes.
This study focuses on the analysis of immune-related genes and corresponding immune functions that are significantly associated with the HGF/c-MET pathway using transcriptome data from 11 solid tumors.
We systematically analyzed 11 different cancers, including expression correlation, immune infiltration, tumor diagnosis and survival prognosis from HGF/c-MET pathway and immune regulation, two biological mechanisms having received extensive attention in cancer analysis.
We found that the HGF/c-MET pathway affected the tumor microenvironment mainly by interfering with expression levels of other genes. Immune infiltration is another critical factor involved in changes to the tumor microenvironment. The downstream immune-related genes activated by the HGF/c-MET pathway regulate immune-related pathways, which in turn affect the degree of infiltration of immune cells. Immune infiltration is significantly associated with cancer development and prognosis.</description><identifier>ISSN: 1475-2867</identifier><identifier>EISSN: 1475-2867</identifier><identifier>DOI: 10.1186/s12935-021-02051-2</identifier><identifier>PMID: 34261467</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Antagonists ; Batch processing ; c-MET ; c-Met protein ; Cancer ; Clinical trials ; Diagnosis ; Gene expression ; Growth factors ; Hepatocyte growth factor ; HGF ; Immune cells ; Immune infiltration ; Immunoregulation ; Infiltration ; Kinases ; Lymphocytes ; Medical prognosis ; Mesenchyme ; Metastases ; Pathway score ; Primary Research ; Prognosis ; RNAseq ; Signal transduction ; Solid tumors ; Statistical analysis ; Transcriptomes ; Tumor microenvironment ; Tumors</subject><ispartof>Cancer cell international, 2021-07, Vol.21 (1), p.374-374, Article 374</ispartof><rights>2021. The Author(s).</rights><rights>2021. 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.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53</citedby><cites>FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53</cites><orcidid>0000-0003-1168-8384</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278741/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2553227506?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34261467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Zhibo</creatorcontrib><creatorcontrib>Xue, Wenhua</creatorcontrib><creatorcontrib>Zheng, Yuanyuan</creatorcontrib><creatorcontrib>Geng, Qishun</creatorcontrib><creatorcontrib>Wang, Le</creatorcontrib><creatorcontrib>Fan, Zhirui</creatorcontrib><creatorcontrib>Wang, Wenbin</creatorcontrib><creatorcontrib>Yue, Ying</creatorcontrib><creatorcontrib>Zhai, Yunkai</creatorcontrib><creatorcontrib>Li, Lifeng</creatorcontrib><creatorcontrib>Zhao, Jie</creatorcontrib><title>Molecular mechanism study of HGF/c-MET pathway activation and immune regulation for a tumor diagnosis model</title><title>Cancer cell international</title><addtitle>Cancer Cell Int</addtitle><description>Hepatocyte growth factor (HGF) binds to the c-mesenchymal-epithelial transition (C-MET) receptor and activates downstream signaling pathways, playing an essential role in the development of various cancers. Given the role of this signaling pathway, the primary therapeutic direction focuses on identifying and designing HGF inhibitors, antagonists and other molecules to block the binding of HGF to C-MET, thereby limiting the abnormal state of other downstream genes.
This study focuses on the analysis of immune-related genes and corresponding immune functions that are significantly associated with the HGF/c-MET pathway using transcriptome data from 11 solid tumors.
We systematically analyzed 11 different cancers, including expression correlation, immune infiltration, tumor diagnosis and survival prognosis from HGF/c-MET pathway and immune regulation, two biological mechanisms having received extensive attention in cancer analysis.
We found that the HGF/c-MET pathway affected the tumor microenvironment mainly by interfering with expression levels of other genes. Immune infiltration is another critical factor involved in changes to the tumor microenvironment. The downstream immune-related genes activated by the HGF/c-MET pathway regulate immune-related pathways, which in turn affect the degree of infiltration of immune cells. Immune infiltration is significantly associated with cancer development and prognosis.</description><subject>Antagonists</subject><subject>Batch processing</subject><subject>c-MET</subject><subject>c-Met protein</subject><subject>Cancer</subject><subject>Clinical trials</subject><subject>Diagnosis</subject><subject>Gene expression</subject><subject>Growth factors</subject><subject>Hepatocyte growth factor</subject><subject>HGF</subject><subject>Immune cells</subject><subject>Immune infiltration</subject><subject>Immunoregulation</subject><subject>Infiltration</subject><subject>Kinases</subject><subject>Lymphocytes</subject><subject>Medical prognosis</subject><subject>Mesenchyme</subject><subject>Metastases</subject><subject>Pathway score</subject><subject>Primary Research</subject><subject>Prognosis</subject><subject>RNAseq</subject><subject>Signal transduction</subject><subject>Solid tumors</subject><subject>Statistical analysis</subject><subject>Transcriptomes</subject><subject>Tumor microenvironment</subject><subject>Tumors</subject><issn>1475-2867</issn><issn>1475-2867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1v1DAQhi0EoqXwBzggS1y4hHqc-CMXJFT1S2rFpZytie3seknixU6K9t_j7paq5WCNNX7nGc_oJeQjsK8AWp5m4G0tKsahHCag4q_IMTRKVFxL9frZ_Yi8y3nDGCgt2VtyVDdcQiPVMfl1GwdvlwETHb1d4xTySPO8uB2NPb26vDi11e35Hd3ivP6DO4p2Dvc4hzhRnBwN47hMnia_Koh9to-JIp2XsUQXcDXFHDIdo_PDe_KmxyH7D4_xhPy8OL87u6puflxen32_qaxo1VzZutG1VQqc19A0giv0oKTTnWSt7NqaO-vL0MjBgpNWatDAGnCil-idqE_I9YHrIm7MNoUR085EDGafiGllMM3BDt5wXVbBFPayF43rfCcVEyUj2453rsXC-nZgbZdu9KXxNCccXkBfvkxhbVbx3miutGqgAL48AlL8vfg8mzFk64cBJx-XbLgQvFVt6Vqkn_-TbuKSprKqB1XNuRJMFhU_qGyKOSffP30GmHnwhTn4wpQVmb0vDC9Fn56P8VTyzwj1X_n0sz0</recordid><startdate>20210714</startdate><enddate>20210714</enddate><creator>Shen, Zhibo</creator><creator>Xue, Wenhua</creator><creator>Zheng, Yuanyuan</creator><creator>Geng, Qishun</creator><creator>Wang, Le</creator><creator>Fan, Zhirui</creator><creator>Wang, Wenbin</creator><creator>Yue, Ying</creator><creator>Zhai, Yunkai</creator><creator>Li, Lifeng</creator><creator>Zhao, Jie</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1168-8384</orcidid></search><sort><creationdate>20210714</creationdate><title>Molecular mechanism study of HGF/c-MET pathway activation and immune regulation for a tumor diagnosis model</title><author>Shen, Zhibo ; Xue, Wenhua ; Zheng, Yuanyuan ; Geng, Qishun ; Wang, Le ; Fan, Zhirui ; Wang, Wenbin ; Yue, Ying ; Zhai, Yunkai ; Li, Lifeng ; Zhao, Jie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antagonists</topic><topic>Batch processing</topic><topic>c-MET</topic><topic>c-Met protein</topic><topic>Cancer</topic><topic>Clinical trials</topic><topic>Diagnosis</topic><topic>Gene expression</topic><topic>Growth factors</topic><topic>Hepatocyte growth factor</topic><topic>HGF</topic><topic>Immune cells</topic><topic>Immune infiltration</topic><topic>Immunoregulation</topic><topic>Infiltration</topic><topic>Kinases</topic><topic>Lymphocytes</topic><topic>Medical prognosis</topic><topic>Mesenchyme</topic><topic>Metastases</topic><topic>Pathway score</topic><topic>Primary Research</topic><topic>Prognosis</topic><topic>RNAseq</topic><topic>Signal transduction</topic><topic>Solid tumors</topic><topic>Statistical analysis</topic><topic>Transcriptomes</topic><topic>Tumor microenvironment</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Zhibo</creatorcontrib><creatorcontrib>Xue, Wenhua</creatorcontrib><creatorcontrib>Zheng, Yuanyuan</creatorcontrib><creatorcontrib>Geng, Qishun</creatorcontrib><creatorcontrib>Wang, Le</creatorcontrib><creatorcontrib>Fan, Zhirui</creatorcontrib><creatorcontrib>Wang, Wenbin</creatorcontrib><creatorcontrib>Yue, Ying</creatorcontrib><creatorcontrib>Zhai, Yunkai</creatorcontrib><creatorcontrib>Li, Lifeng</creatorcontrib><creatorcontrib>Zhao, Jie</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cancer cell international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Zhibo</au><au>Xue, Wenhua</au><au>Zheng, Yuanyuan</au><au>Geng, Qishun</au><au>Wang, Le</au><au>Fan, Zhirui</au><au>Wang, Wenbin</au><au>Yue, Ying</au><au>Zhai, Yunkai</au><au>Li, Lifeng</au><au>Zhao, Jie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular mechanism study of HGF/c-MET pathway activation and immune regulation for a tumor diagnosis model</atitle><jtitle>Cancer cell international</jtitle><addtitle>Cancer Cell Int</addtitle><date>2021-07-14</date><risdate>2021</risdate><volume>21</volume><issue>1</issue><spage>374</spage><epage>374</epage><pages>374-374</pages><artnum>374</artnum><issn>1475-2867</issn><eissn>1475-2867</eissn><abstract>Hepatocyte growth factor (HGF) binds to the c-mesenchymal-epithelial transition (C-MET) receptor and activates downstream signaling pathways, playing an essential role in the development of various cancers. Given the role of this signaling pathway, the primary therapeutic direction focuses on identifying and designing HGF inhibitors, antagonists and other molecules to block the binding of HGF to C-MET, thereby limiting the abnormal state of other downstream genes.
This study focuses on the analysis of immune-related genes and corresponding immune functions that are significantly associated with the HGF/c-MET pathway using transcriptome data from 11 solid tumors.
We systematically analyzed 11 different cancers, including expression correlation, immune infiltration, tumor diagnosis and survival prognosis from HGF/c-MET pathway and immune regulation, two biological mechanisms having received extensive attention in cancer analysis.
We found that the HGF/c-MET pathway affected the tumor microenvironment mainly by interfering with expression levels of other genes. Immune infiltration is another critical factor involved in changes to the tumor microenvironment. The downstream immune-related genes activated by the HGF/c-MET pathway regulate immune-related pathways, which in turn affect the degree of infiltration of immune cells. Immune infiltration is significantly associated with cancer development and prognosis.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>34261467</pmid><doi>10.1186/s12935-021-02051-2</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1168-8384</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1475-2867 |
ispartof | Cancer cell international, 2021-07, Vol.21 (1), p.374-374, Article 374 |
issn | 1475-2867 1475-2867 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_2834207af6f54dbeb670542069b2bd9a |
source | Publicly Available Content Database; PubMed Central |
subjects | Antagonists Batch processing c-MET c-Met protein Cancer Clinical trials Diagnosis Gene expression Growth factors Hepatocyte growth factor HGF Immune cells Immune infiltration Immunoregulation Infiltration Kinases Lymphocytes Medical prognosis Mesenchyme Metastases Pathway score Primary Research Prognosis RNAseq Signal transduction Solid tumors Statistical analysis Transcriptomes Tumor microenvironment Tumors |
title | Molecular mechanism study of HGF/c-MET pathway activation and immune regulation for a tumor diagnosis model |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-14T03%3A34%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20mechanism%20study%20of%20HGF/c-MET%20pathway%20activation%20and%20immune%20regulation%20for%20a%20tumor%20diagnosis%20model&rft.jtitle=Cancer%20cell%20international&rft.au=Shen,%20Zhibo&rft.date=2021-07-14&rft.volume=21&rft.issue=1&rft.spage=374&rft.epage=374&rft.pages=374-374&rft.artnum=374&rft.issn=1475-2867&rft.eissn=1475-2867&rft_id=info:doi/10.1186/s12935-021-02051-2&rft_dat=%3Cproquest_doaj_%3E2552979054%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c597t-c3483c771de8144527ae176d8b6096b932dce021a21c1d6c68181041d5f6aed53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2553227506&rft_id=info:pmid/34261467&rfr_iscdi=true |