Therapeutic implications of germline genetic findings in cancer.


Journal

Nature reviews. Clinical oncology
ISSN: 1759-4782
Titre abrégé: Nat Rev Clin Oncol
Pays: England
ID NLM: 101500077

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 21 2 2019
medline: 10 7 2019
entrez: 21 2 2019
Statut: ppublish

Résumé

Cancer is a genetic disease. To date, translational cancer genomics has focused largely on somatic alterations, driven by the desire to identify targets for personalized therapy. However, therapeutically relevant information is also latent within the germline genome. In addition to cancer susceptibility, alterations present in the germ line can determine responses to both targeted and more traditional anticancer therapies, as well as their toxicities. Despite the importance of these alterations, many algorithms designed to analyse somatic mutations conversely continue to subtract information on germline genetics during analysis. In the light of low actionable yields from somatic tumour testing, a need exists for diversification of the sources of potential therapeutic biomarkers. In this Review, we summarize the literature on the therapeutic potential of alterations in the germline genome. The therapeutic value of germline information will not only be manifest as improvements in treatment but will also drive greater levels of engagement and cooperation between traditional oncology services and familial risk management clinics.

Identifiants

pubmed: 30783251
doi: 10.1038/s41571-019-0179-3
pii: 10.1038/s41571-019-0179-3
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

386-396

Commentaires et corrections

Type : ErratumIn

Auteurs

Subotheni Thavaneswaran (S)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia.
The Kinghorn Cancer Centre, St Vincent's Hospital, Sydney, Australia.
St Vincent's Clinical School, University of New South Wales (Medicine), Sydney, Australia.

Emma Rath (E)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia.

Kathy Tucker (K)

Hereditary Cancer Clinic, Prince of Wales Hospital, Sydney, Australia.

Anthony M Joshua (AM)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia.
The Kinghorn Cancer Centre, St Vincent's Hospital, Sydney, Australia.
St Vincent's Clinical School, University of New South Wales (Medicine), Sydney, Australia.

Dominique Hess (D)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia.

Mark Pinese (M)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia.

Mandy L Ballinger (ML)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia. m.ballinger@garvan.org.au.

David M Thomas (DM)

Cancer Division, Garvan Institute of Medical Research, Sydney, Australia. d.thomas@garvan.org.au.
The Kinghorn Cancer Centre, St Vincent's Hospital, Sydney, Australia. d.thomas@garvan.org.au.
St Vincent's Clinical School, University of New South Wales (Medicine), Sydney, Australia. d.thomas@garvan.org.au.

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Classifications MeSH