Loading…

Emerging role of tumor cell plasticity in modifying therapeutic response

Resistance to cancer therapy is a major barrier to cancer management. Conventional views have proposed that acquisition of resistance may result from genetic mutations. However, accumulating evidence implicates a key role of non-mutational resistance mechanisms underlying drug tolerance, the latter...

Full description

Saved in:
Bibliographic Details
Published in:Signal transduction and targeted therapy 2020-10, Vol.5 (1), p.228-228, Article 228
Main Authors: Qin, Siyuan, Jiang, Jingwen, Lu, Yi, Nice, Edouard C., Huang, Canhua, Zhang, Jian, He, Weifeng
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-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73
cites cdi_FETCH-LOGICAL-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73
container_end_page 228
container_issue 1
container_start_page 228
container_title Signal transduction and targeted therapy
container_volume 5
creator Qin, Siyuan
Jiang, Jingwen
Lu, Yi
Nice, Edouard C.
Huang, Canhua
Zhang, Jian
He, Weifeng
description Resistance to cancer therapy is a major barrier to cancer management. Conventional views have proposed that acquisition of resistance may result from genetic mutations. However, accumulating evidence implicates a key role of non-mutational resistance mechanisms underlying drug tolerance, the latter of which is the focus that will be discussed here. Such non-mutational processes are largely driven by tumor cell plasticity, which renders tumor cells insusceptible to the drug-targeted pathway, thereby facilitating the tumor cell survival and growth. The concept of tumor cell plasticity highlights the significance of re-activation of developmental programs that are closely correlated with epithelial–mesenchymal transition, acquisition properties of cancer stem cells, and trans-differentiation potential during drug exposure. From observations in various cancers, this concept provides an opportunity for investigating the nature of anticancer drug resistance. Over the years, our understanding of the emerging role of phenotype switching in modifying therapeutic response has considerably increased. This expanded knowledge of tumor cell plasticity contributes to developing novel therapeutic strategies or combination therapy regimens using available anticancer drugs, which are likely to improve patient outcomes in clinical practice.
doi_str_mv 10.1038/s41392-020-00313-5
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7541492</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2449261028</sourcerecordid><originalsourceid>FETCH-LOGICAL-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73</originalsourceid><addsrcrecordid>eNp9kU9LxDAQxYMorqhfwIP06KU6Sdo0vQgi_oMFL3oO2WS6RtqmJq2w396sq8t68ZIE5jdvMu8RckbhkgKXV7GgvGY5MMgBOOV5uUeOGJR1zgUv93feM3Ia4zsAUMGrqiwOyYxzYFKCPCKPdx2GpeuXWfAtZr7JxqnzITPYttnQ6jg648ZV5vqs89Y1qzU6vmHQA06plgWMg-8jnpCDRrcRT3_uY_J6f_dy-5jPnx-ebm_muSkKMeYVIuUVCGqllVCbhZC14XZRWimwWkjRSMvAaqEtGm1kY7AEmQ5WCyxMxY_J9UZ3mBYdWoP9GHSrhuA6HVbKa6f-Vnr3ppb-U6XNaVGzJHDxIxD8x4RxVJ2L63V1j36KihWJEjQZlFC2QU3wMQZstmMoqHUKapOCSimo7xRUmZrOdz-4bfn1PAF8A8RU6pcY1LufQp9M-0_2C4c9lPc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2449261028</pqid></control><display><type>article</type><title>Emerging role of tumor cell plasticity in modifying therapeutic response</title><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Qin, Siyuan ; Jiang, Jingwen ; Lu, Yi ; Nice, Edouard C. ; Huang, Canhua ; Zhang, Jian ; He, Weifeng</creator><creatorcontrib>Qin, Siyuan ; Jiang, Jingwen ; Lu, Yi ; Nice, Edouard C. ; Huang, Canhua ; Zhang, Jian ; He, Weifeng</creatorcontrib><description>Resistance to cancer therapy is a major barrier to cancer management. Conventional views have proposed that acquisition of resistance may result from genetic mutations. However, accumulating evidence implicates a key role of non-mutational resistance mechanisms underlying drug tolerance, the latter of which is the focus that will be discussed here. Such non-mutational processes are largely driven by tumor cell plasticity, which renders tumor cells insusceptible to the drug-targeted pathway, thereby facilitating the tumor cell survival and growth. The concept of tumor cell plasticity highlights the significance of re-activation of developmental programs that are closely correlated with epithelial–mesenchymal transition, acquisition properties of cancer stem cells, and trans-differentiation potential during drug exposure. From observations in various cancers, this concept provides an opportunity for investigating the nature of anticancer drug resistance. Over the years, our understanding of the emerging role of phenotype switching in modifying therapeutic response has considerably increased. This expanded knowledge of tumor cell plasticity contributes to developing novel therapeutic strategies or combination therapy regimens using available anticancer drugs, which are likely to improve patient outcomes in clinical practice.</description><identifier>ISSN: 2059-3635</identifier><identifier>ISSN: 2095-9907</identifier><identifier>EISSN: 2059-3635</identifier><identifier>DOI: 10.1038/s41392-020-00313-5</identifier><identifier>PMID: 33028808</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1059 ; 692/4028/67/1059 ; Animals ; Antineoplastic Agents - therapeutic use ; Cancer Research ; Cell Biology ; Cell Survival - drug effects ; Drug Delivery Systems ; Drug Resistance, Neoplasm - drug effects ; Epithelial-Mesenchymal Transition - drug effects ; Humans ; Internal Medicine ; Medicine ; Medicine &amp; Public Health ; Neoplasms - drug therapy ; Neoplasms - metabolism ; Neoplasms - pathology ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Oncology ; Pathology ; Review ; Review Article</subject><ispartof>Signal transduction and targeted therapy, 2020-10, Vol.5 (1), p.228-228, Article 228</ispartof><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73</citedby><cites>FETCH-LOGICAL-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73</cites><orcidid>0000-0002-1060-6925</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/PMC7541492/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541492/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33028808$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qin, Siyuan</creatorcontrib><creatorcontrib>Jiang, Jingwen</creatorcontrib><creatorcontrib>Lu, Yi</creatorcontrib><creatorcontrib>Nice, Edouard C.</creatorcontrib><creatorcontrib>Huang, Canhua</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>He, Weifeng</creatorcontrib><title>Emerging role of tumor cell plasticity in modifying therapeutic response</title><title>Signal transduction and targeted therapy</title><addtitle>Sig Transduct Target Ther</addtitle><addtitle>Signal Transduct Target Ther</addtitle><description>Resistance to cancer therapy is a major barrier to cancer management. Conventional views have proposed that acquisition of resistance may result from genetic mutations. However, accumulating evidence implicates a key role of non-mutational resistance mechanisms underlying drug tolerance, the latter of which is the focus that will be discussed here. Such non-mutational processes are largely driven by tumor cell plasticity, which renders tumor cells insusceptible to the drug-targeted pathway, thereby facilitating the tumor cell survival and growth. The concept of tumor cell plasticity highlights the significance of re-activation of developmental programs that are closely correlated with epithelial–mesenchymal transition, acquisition properties of cancer stem cells, and trans-differentiation potential during drug exposure. From observations in various cancers, this concept provides an opportunity for investigating the nature of anticancer drug resistance. Over the years, our understanding of the emerging role of phenotype switching in modifying therapeutic response has considerably increased. This expanded knowledge of tumor cell plasticity contributes to developing novel therapeutic strategies or combination therapy regimens using available anticancer drugs, which are likely to improve patient outcomes in clinical practice.</description><subject>631/67/1059</subject><subject>692/4028/67/1059</subject><subject>Animals</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Cancer Research</subject><subject>Cell Biology</subject><subject>Cell Survival - drug effects</subject><subject>Drug Delivery Systems</subject><subject>Drug Resistance, Neoplasm - drug effects</subject><subject>Epithelial-Mesenchymal Transition - drug effects</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Review</subject><subject>Review Article</subject><issn>2059-3635</issn><issn>2095-9907</issn><issn>2059-3635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kU9LxDAQxYMorqhfwIP06KU6Sdo0vQgi_oMFL3oO2WS6RtqmJq2w396sq8t68ZIE5jdvMu8RckbhkgKXV7GgvGY5MMgBOOV5uUeOGJR1zgUv93feM3Ia4zsAUMGrqiwOyYxzYFKCPCKPdx2GpeuXWfAtZr7JxqnzITPYttnQ6jg648ZV5vqs89Y1qzU6vmHQA06plgWMg-8jnpCDRrcRT3_uY_J6f_dy-5jPnx-ebm_muSkKMeYVIuUVCGqllVCbhZC14XZRWimwWkjRSMvAaqEtGm1kY7AEmQ5WCyxMxY_J9UZ3mBYdWoP9GHSrhuA6HVbKa6f-Vnr3ppb-U6XNaVGzJHDxIxD8x4RxVJ2L63V1j36KihWJEjQZlFC2QU3wMQZstmMoqHUKapOCSimo7xRUmZrOdz-4bfn1PAF8A8RU6pcY1LufQp9M-0_2C4c9lPc</recordid><startdate>20201007</startdate><enddate>20201007</enddate><creator>Qin, Siyuan</creator><creator>Jiang, Jingwen</creator><creator>Lu, Yi</creator><creator>Nice, Edouard C.</creator><creator>Huang, Canhua</creator><creator>Zhang, Jian</creator><creator>He, Weifeng</creator><general>Nature Publishing Group UK</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1060-6925</orcidid></search><sort><creationdate>20201007</creationdate><title>Emerging role of tumor cell plasticity in modifying therapeutic response</title><author>Qin, Siyuan ; Jiang, Jingwen ; Lu, Yi ; Nice, Edouard C. ; Huang, Canhua ; Zhang, Jian ; He, Weifeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>631/67/1059</topic><topic>692/4028/67/1059</topic><topic>Animals</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Cancer Research</topic><topic>Cell Biology</topic><topic>Cell Survival - drug effects</topic><topic>Drug Delivery Systems</topic><topic>Drug Resistance, Neoplasm - drug effects</topic><topic>Epithelial-Mesenchymal Transition - drug effects</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Neoplastic Stem Cells - pathology</topic><topic>Oncology</topic><topic>Pathology</topic><topic>Review</topic><topic>Review Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qin, Siyuan</creatorcontrib><creatorcontrib>Jiang, Jingwen</creatorcontrib><creatorcontrib>Lu, Yi</creatorcontrib><creatorcontrib>Nice, Edouard C.</creatorcontrib><creatorcontrib>Huang, Canhua</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><creatorcontrib>He, Weifeng</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Signal transduction and targeted therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qin, Siyuan</au><au>Jiang, Jingwen</au><au>Lu, Yi</au><au>Nice, Edouard C.</au><au>Huang, Canhua</au><au>Zhang, Jian</au><au>He, Weifeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emerging role of tumor cell plasticity in modifying therapeutic response</atitle><jtitle>Signal transduction and targeted therapy</jtitle><stitle>Sig Transduct Target Ther</stitle><addtitle>Signal Transduct Target Ther</addtitle><date>2020-10-07</date><risdate>2020</risdate><volume>5</volume><issue>1</issue><spage>228</spage><epage>228</epage><pages>228-228</pages><artnum>228</artnum><issn>2059-3635</issn><issn>2095-9907</issn><eissn>2059-3635</eissn><abstract>Resistance to cancer therapy is a major barrier to cancer management. Conventional views have proposed that acquisition of resistance may result from genetic mutations. However, accumulating evidence implicates a key role of non-mutational resistance mechanisms underlying drug tolerance, the latter of which is the focus that will be discussed here. Such non-mutational processes are largely driven by tumor cell plasticity, which renders tumor cells insusceptible to the drug-targeted pathway, thereby facilitating the tumor cell survival and growth. The concept of tumor cell plasticity highlights the significance of re-activation of developmental programs that are closely correlated with epithelial–mesenchymal transition, acquisition properties of cancer stem cells, and trans-differentiation potential during drug exposure. From observations in various cancers, this concept provides an opportunity for investigating the nature of anticancer drug resistance. Over the years, our understanding of the emerging role of phenotype switching in modifying therapeutic response has considerably increased. This expanded knowledge of tumor cell plasticity contributes to developing novel therapeutic strategies or combination therapy regimens using available anticancer drugs, which are likely to improve patient outcomes in clinical practice.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33028808</pmid><doi>10.1038/s41392-020-00313-5</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-1060-6925</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2059-3635
ispartof Signal transduction and targeted therapy, 2020-10, Vol.5 (1), p.228-228, Article 228
issn 2059-3635
2095-9907
2059-3635
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7541492
source Publicly Available Content Database; PubMed Central; Springer Nature - nature.com Journals - Fully Open Access
subjects 631/67/1059
692/4028/67/1059
Animals
Antineoplastic Agents - therapeutic use
Cancer Research
Cell Biology
Cell Survival - drug effects
Drug Delivery Systems
Drug Resistance, Neoplasm - drug effects
Epithelial-Mesenchymal Transition - drug effects
Humans
Internal Medicine
Medicine
Medicine & Public Health
Neoplasms - drug therapy
Neoplasms - metabolism
Neoplasms - pathology
Neoplastic Stem Cells - metabolism
Neoplastic Stem Cells - pathology
Oncology
Pathology
Review
Review Article
title Emerging role of tumor cell plasticity in modifying therapeutic response
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T23%3A21%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Emerging%20role%20of%20tumor%20cell%20plasticity%20in%20modifying%20therapeutic%20response&rft.jtitle=Signal%20transduction%20and%20targeted%20therapy&rft.au=Qin,%20Siyuan&rft.date=2020-10-07&rft.volume=5&rft.issue=1&rft.spage=228&rft.epage=228&rft.pages=228-228&rft.artnum=228&rft.issn=2059-3635&rft.eissn=2059-3635&rft_id=info:doi/10.1038/s41392-020-00313-5&rft_dat=%3Cproquest_pubme%3E2449261028%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c446t-7ee137061d8d809cb689c3db5d86e7b86f8d20da6adecac8fce508ce5296e4c73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2449261028&rft_id=info:pmid/33028808&rfr_iscdi=true