dc.contributor.author | Pasha, N | |
dc.contributor.author | Turner, NC | |
dc.date.accessioned | 2022-01-12T15:12:50Z | |
dc.date.available | 2022-01-12T15:12:50Z | |
dc.date.issued | 2021-07-19 | |
dc.identifier | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000675896600002&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=d4b848928d1c3e5c86d298abb68475f9 | |
dc.identifier.citation | NATURE CANCER, 2021, 2 (7), pp. 680 - 692 (13) | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/4956 | |
dc.identifier.eissn | 2662-1347 | |
dc.identifier.eissn | 2662-1347 | |
dc.identifier.doi | 10.1038/s43018-021-00229-1 | |
dc.identifier.doi | 10.1038/s43018-021-00229-1 | |
dc.description.abstract | Rational development of targeted therapies has revolutionized metastatic breast cancer outcomes, although resistance to treatment remains a major challenge. Advances in molecular profiling and imaging technologies have provided evidence for the impact of clonal diversity in cancer treatment resistance, through the outgrowth of resistant clones. In this Review, we focus on the genomic processes that drive tumoral heterogeneity and the mechanisms of resistance underlying metastatic breast cancer treatment and discuss implications for future treatment strategies. | |
dc.format.extent | 680 - 692 (13) | |
dc.language | English | |
dc.language.iso | eng | |
dc.publisher | NATURE PORTFOLIO | |
dc.rights.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
dc.subject | Science & Technology | |
dc.subject | Life Sciences & Biomedicine | |
dc.subject | Oncology | |
dc.subject | FIRST-LINE THERAPY | |
dc.subject | PHASE-III | |
dc.subject | TRASTUZUMAB EMTANSINE | |
dc.subject | POSTMENOPAUSAL WOMEN | |
dc.subject | CLONAL EVOLUTION | |
dc.subject | ESR1 MUTATIONS | |
dc.subject | DOUBLE-BLIND | |
dc.subject | INTRATUMOR HETEROGENEITY | |
dc.subject | ARTIFICIAL-INTELLIGENCE | |
dc.subject | MOLECULAR PORTRAITS | |
dc.title | Understanding and overcoming tumor heterogeneity in metastatic breast cancer treatment. | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2021-06-02 | |
rioxxterms.version | AM | |
rioxxterms.versionofrecord | 10.1038/s43018-021-00229-1 | |
rioxxterms.licenseref.startdate | 2021-07-19 | |
dc.relation.isPartOf | NATURE CANCER | |
pubs.issue | 7 | |
pubs.notes | Not known | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology | |
pubs.organisational-group | /ICR/Students | |
pubs.organisational-group | /ICR/Students/PhD and MPhil | |
pubs.organisational-group | /ICR/Students/PhD and MPhil/19/20 Starting Cohort | |
pubs.publication-status | Published | |
pubs.volume | 2 | |
pubs.embargo.terms | Not known | |
icr.researchteam | Molecular Oncology | |
dc.contributor.icrauthor | Pasha, Nida | |
dc.contributor.icrauthor | Turner, Nicholas | |