Tumor MK2 transcript levels are associated with improved response to chemotherapy and patient survival in non-small cell lung cancer

Author:

Suresh Karthik1ORCID,Del Rosario Othello1,Kallem Medha1,Singh Gayatri1,Shah Anika1,Zheng Linda1,Yun Xin1,Philip Nicolas M.1,Putcha Nirupama1,McClure Marni B.1,Jiang Haiyang1,D’Alessio Franco1,Srivastava Meera2,Bera Alakesh2,Shimoda Larissa A.1ORCID,Merchant Michael3,Rane Madhavi J.3,Machamer Carolyn E.4,Mock Jason5ORCID,Hagan Robert5ORCID,Koch Abigail L.6,Punjabi Naresh M.6,Kolb Todd M.1ORCID,Damarla Mahendra1ORCID

Affiliation:

1. Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

2. Department of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States

3. Department of Medicine, University of Louisville School of Medicine, Louisville, Kentucky, United States

4. Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

5. Department of Medicine, University of North Carolina, School of Medicine, Chapel Hill, North Carolina, United States

6. Department of Medicine, School of Medicine, University of Miami, Miami, Florida, United States

Abstract

MK2, known to promote caspase-3 nuclear translocation in the execution of apoptosis, is reduced in non-small cell lung cancer cells. In adenocarcinomas of patients, higher MK2 expression is associated with early-stage disease, better clinical response following chemotherapy and independently associated with improved survival.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

Publisher

American Physiological Society

Subject

Genetics,Physiology

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