Investigating Cooperation Between KEAP1 and LKB1 Inactivation in Lung Adenocarcinoma

Abstract

Preliminary analysis in our laboratory reveals concurrent mutation of the LKB1 and KEAP1 tumor suppressors correlate with poor overall survival in lung adenocarcinoma (LA). Phenotypically, there is evidence to suggest that inactivation of KEAP1 may support adaptation to increased oxidative stress that results from LKB1 inactivation. We have found that inactivation of KEAP1 in the background of LKB1 inactivation results in increased growth and resistance to treatment. Further, we have evidence that cross-talk from the PERK kinase, may also further support adaptation to oxidative stress in combination with KEAP1 inactivation in LKB1-deficient LA. These findings suggest that KEAP1/LKB1 inactivation may represent a critical step in LA tumorigenesis and may have a role in therapeutic resistance.

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Document Details

Document Type
Technical Report
Publication Date
May 01, 2019
Accession Number
AD1087451

Entities

People

  • Landon J. Inge

Organizations

  • Dignity Health

Tags

DTIC Thesaurus Topics

  • Adenocarcinoma
  • Biomedical Research
  • Cancer
  • Cell Line
  • Cells
  • Culture Techniques
  • Diseases And Disorders
  • Infection
  • Lung Cancer
  • Mutations
  • Neoplasms
  • Oxidative Stress
  • Resistance
  • Small Molecules
  • Suppressors
  • Survival
  • Therapy

Fields of Study

  • Biology

Readers

  • Molecular and Cellular Biology
  • Molecular and genetic basis of cancer.
  • Oncology