Literature DB >> 26555006

PTEN and PI3K/AKT in non-small-cell lung cancer.

Cristina Pérez-Ramírez1,2, Marisa Cañadas-Garre1, Miguel Ángel Molina3, María José Faus-Dáder2, Miguel Ángel Calleja-Hernández1,4.   

Abstract

Non-small-cell lung cancer (NSCLC) is the leading cause of cancer deaths worldwide. In the last years, the identification of activating EGFR mutations, conferring increased sensitivity and disease response to tyrosine kinase inhibitors, has changed the prospect of NSCLC patients. The PTEN/PI3K/AKT pathway regulates multiple cellular functions, including cell growth, differentiation, proliferation, survival, motility, invasion and intracellular trafficking. Alterations in this pathway, mainly PTEN inactivation, have been associated with resistance to EGFR-tyrosine kinase inhibitor therapy and lower survival in NSCLC patients. In this review, we will briefly discuss the main PTEN/PI3K/AKT pathway alterations found in NSCLC, as well as the cell processes regulated by PTEN/PI3K/AKT leading to tumorigenesis.

Entities:  

Keywords:  EGFR; NSCLC; PI3K; PTEN; TKI; pharmacogenetics; resistance

Mesh:

Substances:

Year:  2015        PMID: 26555006     DOI: 10.2217/pgs.15.122

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  80 in total

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10.  Mcl-1 Interacts with Akt to Promote Lung Cancer Progression.

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