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Role of KEAP1/NRF2 and TP53 Mutations in Lung Squamous Cell Carcinoma Development and Radiation Resistance.

Authors :
Jeong Y
Hoang NT
Lovejoy A
Stehr H
Newman AM
Gentles AJ
Kong W
Truong D
Martin S
Chaudhuri A
Heiser D
Zhou L
Say C
Carter JN
Hiniker SM
Loo BW Jr
West RB
Beachy P
Alizadeh AA
Diehn M
Source :
Cancer discovery [Cancer Discov] 2017 Jan; Vol. 7 (1), pp. 86-101. Date of Electronic Publication: 2016 Sep 23.
Publication Year :
2017

Abstract

Lung squamous cell carcinoma (LSCC) pathogenesis remains incompletely understood, and biomarkers predicting treatment response remain lacking. Here, we describe novel murine LSCC models driven by loss of Trp53 and Keap1, both of which are frequently mutated in human LSCCs. Homozygous inactivation of Keap1 or Trp53 promoted airway basal stem cell (ABSC) self-renewal, suggesting that mutations in these genes lead to expansion of mutant stem cell clones. Deletion of Trp53 and Keap1 in ABSCs, but not more differentiated tracheal cells, produced tumors recapitulating histologic and molecular features of human LSCCs, indicating that they represent the likely cell of origin in this model. Deletion of Keap1 promoted tumor aggressiveness, metastasis, and resistance to oxidative stress and radiotherapy (RT). KEAP1/NRF2 mutation status predicted risk of local recurrence after RT in patients with non-small lung cancer (NSCLC) and could be noninvasively identified in circulating tumor DNA. Thus, KEAP1/NRF2 mutations could serve as predictive biomarkers for personalization of therapeutic strategies for NSCLCs.<br />Significance: We developed an LSCC mouse model involving Trp53 and Keap1, which are frequently mutated in human LSCCs. In this model, ABSCs are the cell of origin of these tumors. KEAP1/NRF2 mutations increase radioresistance and predict local tumor recurrence in radiotherapy patients. Our findings are of potential clinical relevance and could lead to personalized treatment strategies for tumors with KEAP1/NRF2 mutations. Cancer Discov; 7(1); 86-101. ©2016 AACR.This article is highlighted in the In This Issue feature, p. 1.<br />Competing Interests: of potential conflicts of interest – A.M.N., A.A.A., and M.D. are co-inventors on patent applications related to CAPP-Seq. A.L. is currently an employee of Roche. A.M.N., A.A.A., and M.D. are consultants for Roche. Other authors disclose no conflicts of interest.<br /> (©2016 American Association for Cancer Research.)

Details

Language :
English
ISSN :
2159-8290
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
Cancer discovery
Publication Type :
Academic Journal
Accession number :
27663899
Full Text :
https://doi.org/10.1158/2159-8290.CD-16-0127