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The pan-cancer landscape of prognostic germline variants in 10,582 patients.

Ajay ChatrathRoza PrzanowskaShashi KiranZhangli SuShekhar SahaBriana WilsonTakaaki TsunematsuJi-Hye AhnKyung Yong LeeTeressa PaulsenEwelina SobierajskaManjari KiranXiwei TangTianxi LiPankaj KumarAakrosh RatanAnindya Dutta
Published in: Genome medicine (2020)
Germline variants are predictive of outcome in cancer patients and specific germline variants can improve patient outcome predictions beyond predictions made using clinical factors alone. The germline variants also implicate new means by which known oncogenes, tumor suppressor genes, and driver genes are perturbed in cancer and suggest roles in cancer for other genes that have not been extensively studied in oncology. Further studies in other cancer cohorts are necessary to confirm that germline variation is associated with outcome in cancer patients as this is a proof-of-principle study.
Keyphrases
  • papillary thyroid
  • dna repair
  • squamous cell
  • copy number
  • genome wide
  • newly diagnosed
  • lymph node metastasis
  • ejection fraction
  • multidrug resistant
  • gene expression
  • oxidative stress
  • young adults
  • dna damage