The Influence of Cancer Molecular Subtypes and Treatment on the Mutation Spectrum in Metastatic Breast Cancers.


Journal

Cancer research
ISSN: 1538-7445
Titre abrégé: Cancer Res
Pays: United States
ID NLM: 2984705R

Informations de publication

Date de publication:
01 08 2020
Historique:
received: 18 10 2019
revised: 21 01 2020
accepted: 31 03 2020
pubmed: 5 4 2020
medline: 5 1 2021
entrez: 5 4 2020
Statut: ppublish

Résumé

Next-generation sequencing has sparked the exploration of cancer genomes, with the aim of discovering the genetic etiology of the disease and proposing rationally designed therapeutic interventions. Driver gene alterations have been comprehensively charted, but the improvement of cancer patient management somewhat lags behind these basic breakthroughs. Recently, large-scale sequencing that focused on metastasis, the main cause of cancer-related deaths, has shed new light on the driving forces at work during disease progression, particularly in breast cancer. Despite a fairly stable pool of driver genetic alterations between early and late disease, a number of therapeutically targetable mutations have been found enriched in metastatic samples. The molecular processes fueling disease progression have been delineated in recent studies and the clonal composition of breast cancer samples can be examined in detail. Here we discuss how these findings may be combined to improve the diagnosis of breast cancer to better select patients at risk, and to identify targeted agents to treat advanced diseases and to design therapeutic strategies exploiting vulnerabilities of cancer cells rooted in their ability to evolve and drive disease progression.

Identifiants

pubmed: 32245795
pii: 0008-5472.CAN-19-3260
doi: 10.1158/0008-5472.CAN-19-3260
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3062-3069

Informations de copyright

©2020 American Association for Cancer Research.

Auteurs

Benjamin Verret (B)

Medical Oncology Department, Gustave Roussy Cancer Campus, Villejuif, France.

Tony Sourisseau (T)

Inserm, Gustave Roussy Cancer Campus, UMR981, Villejuif, France.

Bojana Stefanovska (B)

Inserm, Gustave Roussy Cancer Campus, UMR981, Villejuif, France.

Fernanda Mosele (F)

Inserm, Gustave Roussy Cancer Campus, UMR981, Villejuif, France.

Alicia Tran-Dien (A)

Inserm, Gustave Roussy Cancer Campus, UMR981, Villejuif, France.

Fabrice André (F)

Medical Oncology Department, Gustave Roussy Cancer Campus, Villejuif, France. fabrice.andre@gustaveroussy.fr.
Inserm, Gustave Roussy Cancer Campus, UMR981, Villejuif, France.

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Classifications MeSH