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Oncotarget. 2017 Sep 11;8(45):78556-78572. doi: 10.18632/oncotarget.20833. eCollection 2017 Oct 03.

STK38L kinase ablation promotes loss of cell viability in a subset of KRAS-dependent pancreatic cancer cell lines.

Oncotarget

Trevor J Grant, Anita K Mehta, Anamika Gupta, Ahmad A D Sharif, Kshitij S Arora, Vikram Deshpande, David T Ting, Nabeel Bardeesy, Neil J Ganem, Alexander Hergovich, Anurag Singh

Affiliations

  1. Department of Pharmacology and Experimental Therapeutics, Center for Cancer Research, Boston University Graduate School of Medicine, Boston, MA, USA.
  2. University College London, Cancer Institute, London, United Kingdom.
  3. Massachusetts General Hospital Cancer Center, Harvard Medical School, Charlestown, MA, USA.

PMID: 29108249 PMCID: PMC5667982 DOI: 10.18632/oncotarget.20833

Abstract

Pancreatic ductal adenocarcinomas (PDACs) are highly aggressive malignancies, associated with poor clinical prognosis and limited therapeutic options. Oncogenic

Keywords: Hippo pathway; KRAS; kinase; oncogene dependency; pancreatic cancer

Conflict of interest statement

CONFLICTS OF INTEREST The authors declare that they do not have any conflicts of interest.

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