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Loss of function STK11 alterations and poor outcomes in non–small-cell lung cancer: Literature and case series of US Veterans

  • Hafsa Farooq
  • , Harold Bien
  • , Victor Chang
  • , Daniel Becker
  • , Yeun Hee Park
  • , Susan E. Bates
  • Northport V.A. Medical Center
  • Stony Brook University
  • VA Medical Center
  • Rutgers - The State University of New Jersey, New Brunswick
  • New York Harbor Healthcare System
  • New York University
  • Columbia University

Research output: Contribution to journalReview articlepeer-review

8 Scopus citations

Abstract

Emerging evidence suggests that STK11 alterations, frequently found in non–small-cell lung cancers, may be prognostic and/or predictive of response to therapy, particularly immunotherapy. STK11 affects multiple important cellular pathways, and mutations lead to tumor growth by creating an immunosuppressive and altered metabolic environment through changes in AMPK, STING, and vascular endothelial growth factor pathways. We illustrate the questions surrounding STK11 genomic alteration in NSCLC with a case series comprising six United States Veterans from a single institution. We discuss the history of STK11, review studies on its clinical impact, and describe putative mechanisms of how loss of STK11 might engender resistance to immunotherapy or other therapies. While the exact impact of STK11 alteration in non–small-cell lung cancer remain to be fully elucidated, future research and ongoing clinical trials will help us better understand its role in cancer development and devise more effective treatment strategies.

Original languageEnglish
Pages (from-to)319-325
Number of pages7
JournalSeminars in Oncology
Volume49
Issue number3-4
DOIs
StatePublished - Jun 2022

Keywords

  • Adenocarcinoma
  • Adenosine monophosphate-activated protein kinase (AMPK)
  • Epidemiology
  • Immunotherapy
  • KRAS mutation
  • mTOR
  • Non–small-cell lung cancer
  • Prognosis
  • STING pathway
  • STK11
  • TP53

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