Loading…

Overcoming multiple myeloma drug resistance in the era of cancer 'omics'

Multiple myeloma (MM) is among the most compelling examples of cancer in which research has markedly improved the length and quality of lives of those afflicted. Research efforts have led to 18 newly approved treatments over the last 12 years, including seven in 2015. However, despite significant im...

Full description

Saved in:
Bibliographic Details
Published in:Leukemia & lymphoma 2018-03, Vol.59 (3), p.542-561
Main Authors: Guang, Matthew Ho Zhi, McCann, Amanda, Bianchi, Giada, Zhang, Li, Dowling, Paul, Bazou, Despina, O'Gorman, Peter, Anderson, Kenneth C.
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-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23
cites cdi_FETCH-LOGICAL-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23
container_end_page 561
container_issue 3
container_start_page 542
container_title Leukemia & lymphoma
container_volume 59
creator Guang, Matthew Ho Zhi
McCann, Amanda
Bianchi, Giada
Zhang, Li
Dowling, Paul
Bazou, Despina
O'Gorman, Peter
Anderson, Kenneth C.
description Multiple myeloma (MM) is among the most compelling examples of cancer in which research has markedly improved the length and quality of lives of those afflicted. Research efforts have led to 18 newly approved treatments over the last 12 years, including seven in 2015. However, despite significant improvement in overall survival, MM remains incurable as most patients inevitably, yet unpredictably, develop refractory disease. Recent advances in high-throughput 'omics' techniques afford us an unprecedented opportunity to (1) understand drug resistance at the genomic, transcriptomic, and proteomic level; (2) discover novel diagnostic, prognostic, and therapeutic biomarkers; (3) develop novel therapeutic targets and rational drug combinations; and (4) optimize risk-adapted strategies to circumvent drug resistance, thus bringing us closer to a cure for MM. In this review, we provide an overview of 'omics' technologies in MM biomarker and drug discovery, highlighting recent insights into MM drug resistance gleaned from the use of 'omics' techniques. Moving from the bench to bedside, we also highlight future trends in MM, with a focus on the potential use of 'omics' technologies as diagnostic, prognostic, or response/relapse monitoring tools to guide therapeutic decisions anchored upon highly individualized, targeted, durable, and rationally informed combination therapies with curative potential.
doi_str_mv 10.1080/10428194.2017.1337115
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_28610537</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1909745129</sourcerecordid><originalsourceid>FETCH-LOGICAL-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23</originalsourceid><addsrcrecordid>eNp9kU1P3DAQhq2qqHy0P6GVb_SSxeOv2BdUhFpAQuICZ8t17MWVEy92Atp_30S7oPbCaazx874zmhehr0BWQBQ5A8KpAs1XlEC7AsZaAPEBHQGhuqGcsI_Lm9NmgQ7Rca1_CCFCS_oJHVIlgQjWHqHru2dfXO7jsMb9lMa4SR73W59yb3FXpjUuvsY62sF5HAc8Pnrsi8U5YLf0Cj6dxa6efkYHwabqv-zrCXr49fP-8rq5vbu6uby4bRyXamxsF7RUAgILwnEVAvGeslYyHTjpeHBSaBvaEKRUvGNOKqlVEJ0EDUpZyk7Q-c53M_3ufef8MBabzKbE3patyTaa_3-G-GjW-dlIEFS17WzwfW9Q8tPk62j6WJ1PyQ4-T9WAJrrlAqieUbFDXcm1Fh_exgAxSwrmNQWzpGD2Kcy6b__u-KZ6PfsM_NgBcQi59PYll9SZ0W5TLqHMd43VsPdn_AX-kpcs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1909745129</pqid></control><display><type>article</type><title>Overcoming multiple myeloma drug resistance in the era of cancer 'omics'</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)</source><creator>Guang, Matthew Ho Zhi ; McCann, Amanda ; Bianchi, Giada ; Zhang, Li ; Dowling, Paul ; Bazou, Despina ; O'Gorman, Peter ; Anderson, Kenneth C.</creator><creatorcontrib>Guang, Matthew Ho Zhi ; McCann, Amanda ; Bianchi, Giada ; Zhang, Li ; Dowling, Paul ; Bazou, Despina ; O'Gorman, Peter ; Anderson, Kenneth C.</creatorcontrib><description>Multiple myeloma (MM) is among the most compelling examples of cancer in which research has markedly improved the length and quality of lives of those afflicted. Research efforts have led to 18 newly approved treatments over the last 12 years, including seven in 2015. However, despite significant improvement in overall survival, MM remains incurable as most patients inevitably, yet unpredictably, develop refractory disease. Recent advances in high-throughput 'omics' techniques afford us an unprecedented opportunity to (1) understand drug resistance at the genomic, transcriptomic, and proteomic level; (2) discover novel diagnostic, prognostic, and therapeutic biomarkers; (3) develop novel therapeutic targets and rational drug combinations; and (4) optimize risk-adapted strategies to circumvent drug resistance, thus bringing us closer to a cure for MM. In this review, we provide an overview of 'omics' technologies in MM biomarker and drug discovery, highlighting recent insights into MM drug resistance gleaned from the use of 'omics' techniques. Moving from the bench to bedside, we also highlight future trends in MM, with a focus on the potential use of 'omics' technologies as diagnostic, prognostic, or response/relapse monitoring tools to guide therapeutic decisions anchored upon highly individualized, targeted, durable, and rationally informed combination therapies with curative potential.</description><identifier>ISSN: 1042-8194</identifier><identifier>EISSN: 1029-2403</identifier><identifier>DOI: 10.1080/10428194.2017.1337115</identifier><identifier>PMID: 28610537</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>bench to bedside ; Biomarkers - analysis ; drug resistance ; Drug Resistance, Neoplasm ; Genomics ; Humans ; immunomics ; immunotherapy ; Metabolomics ; Multiple myeloma ; Multiple Myeloma - drug therapy ; Neoplasm Recurrence, Local - diagnosis ; Neoplasm Recurrence, Local - prevention &amp; control ; omics ; Prognosis ; Proteomics ; Salvage Therapy ; transcriptomics ; translational medicine</subject><ispartof>Leukemia &amp; lymphoma, 2018-03, Vol.59 (3), p.542-561</ispartof><rights>2017 Informa UK Limited, trading as Taylor &amp; Francis Group 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23</citedby><cites>FETCH-LOGICAL-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28610537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guang, Matthew Ho Zhi</creatorcontrib><creatorcontrib>McCann, Amanda</creatorcontrib><creatorcontrib>Bianchi, Giada</creatorcontrib><creatorcontrib>Zhang, Li</creatorcontrib><creatorcontrib>Dowling, Paul</creatorcontrib><creatorcontrib>Bazou, Despina</creatorcontrib><creatorcontrib>O'Gorman, Peter</creatorcontrib><creatorcontrib>Anderson, Kenneth C.</creatorcontrib><title>Overcoming multiple myeloma drug resistance in the era of cancer 'omics'</title><title>Leukemia &amp; lymphoma</title><addtitle>Leuk Lymphoma</addtitle><description>Multiple myeloma (MM) is among the most compelling examples of cancer in which research has markedly improved the length and quality of lives of those afflicted. Research efforts have led to 18 newly approved treatments over the last 12 years, including seven in 2015. However, despite significant improvement in overall survival, MM remains incurable as most patients inevitably, yet unpredictably, develop refractory disease. Recent advances in high-throughput 'omics' techniques afford us an unprecedented opportunity to (1) understand drug resistance at the genomic, transcriptomic, and proteomic level; (2) discover novel diagnostic, prognostic, and therapeutic biomarkers; (3) develop novel therapeutic targets and rational drug combinations; and (4) optimize risk-adapted strategies to circumvent drug resistance, thus bringing us closer to a cure for MM. In this review, we provide an overview of 'omics' technologies in MM biomarker and drug discovery, highlighting recent insights into MM drug resistance gleaned from the use of 'omics' techniques. Moving from the bench to bedside, we also highlight future trends in MM, with a focus on the potential use of 'omics' technologies as diagnostic, prognostic, or response/relapse monitoring tools to guide therapeutic decisions anchored upon highly individualized, targeted, durable, and rationally informed combination therapies with curative potential.</description><subject>bench to bedside</subject><subject>Biomarkers - analysis</subject><subject>drug resistance</subject><subject>Drug Resistance, Neoplasm</subject><subject>Genomics</subject><subject>Humans</subject><subject>immunomics</subject><subject>immunotherapy</subject><subject>Metabolomics</subject><subject>Multiple myeloma</subject><subject>Multiple Myeloma - drug therapy</subject><subject>Neoplasm Recurrence, Local - diagnosis</subject><subject>Neoplasm Recurrence, Local - prevention &amp; control</subject><subject>omics</subject><subject>Prognosis</subject><subject>Proteomics</subject><subject>Salvage Therapy</subject><subject>transcriptomics</subject><subject>translational medicine</subject><issn>1042-8194</issn><issn>1029-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kU1P3DAQhq2qqHy0P6GVb_SSxeOv2BdUhFpAQuICZ8t17MWVEy92Atp_30S7oPbCaazx874zmhehr0BWQBQ5A8KpAs1XlEC7AsZaAPEBHQGhuqGcsI_Lm9NmgQ7Rca1_CCFCS_oJHVIlgQjWHqHru2dfXO7jsMb9lMa4SR73W59yb3FXpjUuvsY62sF5HAc8Pnrsi8U5YLf0Cj6dxa6efkYHwabqv-zrCXr49fP-8rq5vbu6uby4bRyXamxsF7RUAgILwnEVAvGeslYyHTjpeHBSaBvaEKRUvGNOKqlVEJ0EDUpZyk7Q-c53M_3ufef8MBabzKbE3patyTaa_3-G-GjW-dlIEFS17WzwfW9Q8tPk62j6WJ1PyQ4-T9WAJrrlAqieUbFDXcm1Fh_exgAxSwrmNQWzpGD2Kcy6b__u-KZ6PfsM_NgBcQi59PYll9SZ0W5TLqHMd43VsPdn_AX-kpcs</recordid><startdate>20180304</startdate><enddate>20180304</enddate><creator>Guang, Matthew Ho Zhi</creator><creator>McCann, Amanda</creator><creator>Bianchi, Giada</creator><creator>Zhang, Li</creator><creator>Dowling, Paul</creator><creator>Bazou, Despina</creator><creator>O'Gorman, Peter</creator><creator>Anderson, Kenneth C.</creator><general>Taylor &amp; Francis</general><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></search><sort><creationdate>20180304</creationdate><title>Overcoming multiple myeloma drug resistance in the era of cancer 'omics'</title><author>Guang, Matthew Ho Zhi ; McCann, Amanda ; Bianchi, Giada ; Zhang, Li ; Dowling, Paul ; Bazou, Despina ; O'Gorman, Peter ; Anderson, Kenneth C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>bench to bedside</topic><topic>Biomarkers - analysis</topic><topic>drug resistance</topic><topic>Drug Resistance, Neoplasm</topic><topic>Genomics</topic><topic>Humans</topic><topic>immunomics</topic><topic>immunotherapy</topic><topic>Metabolomics</topic><topic>Multiple myeloma</topic><topic>Multiple Myeloma - drug therapy</topic><topic>Neoplasm Recurrence, Local - diagnosis</topic><topic>Neoplasm Recurrence, Local - prevention &amp; control</topic><topic>omics</topic><topic>Prognosis</topic><topic>Proteomics</topic><topic>Salvage Therapy</topic><topic>transcriptomics</topic><topic>translational medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guang, Matthew Ho Zhi</creatorcontrib><creatorcontrib>McCann, Amanda</creatorcontrib><creatorcontrib>Bianchi, Giada</creatorcontrib><creatorcontrib>Zhang, Li</creatorcontrib><creatorcontrib>Dowling, Paul</creatorcontrib><creatorcontrib>Bazou, Despina</creatorcontrib><creatorcontrib>O'Gorman, Peter</creatorcontrib><creatorcontrib>Anderson, Kenneth C.</creatorcontrib><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>Leukemia &amp; lymphoma</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guang, Matthew Ho Zhi</au><au>McCann, Amanda</au><au>Bianchi, Giada</au><au>Zhang, Li</au><au>Dowling, Paul</au><au>Bazou, Despina</au><au>O'Gorman, Peter</au><au>Anderson, Kenneth C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overcoming multiple myeloma drug resistance in the era of cancer 'omics'</atitle><jtitle>Leukemia &amp; lymphoma</jtitle><addtitle>Leuk Lymphoma</addtitle><date>2018-03-04</date><risdate>2018</risdate><volume>59</volume><issue>3</issue><spage>542</spage><epage>561</epage><pages>542-561</pages><issn>1042-8194</issn><eissn>1029-2403</eissn><abstract>Multiple myeloma (MM) is among the most compelling examples of cancer in which research has markedly improved the length and quality of lives of those afflicted. Research efforts have led to 18 newly approved treatments over the last 12 years, including seven in 2015. However, despite significant improvement in overall survival, MM remains incurable as most patients inevitably, yet unpredictably, develop refractory disease. Recent advances in high-throughput 'omics' techniques afford us an unprecedented opportunity to (1) understand drug resistance at the genomic, transcriptomic, and proteomic level; (2) discover novel diagnostic, prognostic, and therapeutic biomarkers; (3) develop novel therapeutic targets and rational drug combinations; and (4) optimize risk-adapted strategies to circumvent drug resistance, thus bringing us closer to a cure for MM. In this review, we provide an overview of 'omics' technologies in MM biomarker and drug discovery, highlighting recent insights into MM drug resistance gleaned from the use of 'omics' techniques. Moving from the bench to bedside, we also highlight future trends in MM, with a focus on the potential use of 'omics' technologies as diagnostic, prognostic, or response/relapse monitoring tools to guide therapeutic decisions anchored upon highly individualized, targeted, durable, and rationally informed combination therapies with curative potential.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>28610537</pmid><doi>10.1080/10428194.2017.1337115</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1042-8194
ispartof Leukemia & lymphoma, 2018-03, Vol.59 (3), p.542-561
issn 1042-8194
1029-2403
language eng
recordid cdi_pubmed_primary_28610537
source Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)
subjects bench to bedside
Biomarkers - analysis
drug resistance
Drug Resistance, Neoplasm
Genomics
Humans
immunomics
immunotherapy
Metabolomics
Multiple myeloma
Multiple Myeloma - drug therapy
Neoplasm Recurrence, Local - diagnosis
Neoplasm Recurrence, Local - prevention & control
omics
Prognosis
Proteomics
Salvage Therapy
transcriptomics
translational medicine
title Overcoming multiple myeloma drug resistance in the era of cancer 'omics'
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T18%3A54%3A27IST&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=Overcoming%20multiple%20myeloma%20drug%20resistance%20in%20the%20era%20of%20cancer%20'omics'&rft.jtitle=Leukemia%20&%20lymphoma&rft.au=Guang,%20Matthew%20Ho%20Zhi&rft.date=2018-03-04&rft.volume=59&rft.issue=3&rft.spage=542&rft.epage=561&rft.pages=542-561&rft.issn=1042-8194&rft.eissn=1029-2403&rft_id=info:doi/10.1080/10428194.2017.1337115&rft_dat=%3Cproquest_pubme%3E1909745129%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c468t-adf96851f3f5c48ff0ee237639f40d4fc659af7ff6684d3c68698f5d619188a23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1909745129&rft_id=info:pmid/28610537&rfr_iscdi=true