The Gene Expression Status of the PI3K/AKT/mTOR Pathway in Gastric Cancer Tissues and Cell Lines.

Pathol Oncol Res

Department of Pathology, Pontificia Universidad Católica de Chile, Marcoleta 377, 7th Floor, Postal Code, 8330024, Santiago, Chile.

Published: October 2016

AI Article Synopsis

  • The PI3K/AKT/mTOR pathway is essential for various cellular functions and its deregulation is linked to the development of gastric cancer (GC).
  • Researchers investigated gene expression related to this pathway in tumor and non-tumor gastric samples from advanced GC patients, as well as in three gastric cancer cell lines (AGS, MKN28, MKN45).
  • Results indicated an increase in expression of several key genes in the pathway, while the tumor suppressor gene PTEN was notably decreased, suggesting the pathway's activation plays a significant role in gastric cancer biology.

Article Abstract

The PI3K/AKT/mTOR pathway plays a crucial role in the regulation of multiple cellular functions including cell growth, proliferation, metabolism and angiogenesis. Emerging evidence has shown that deregulation of this pathway has a role promoting gastric cancer (GC). The aim was to assess the expression of genes involved in this pathway by qPCR in 23 tumor and 23 non-tumor gastric mucosa samples from advanced GC patients, and in AGS, MKN28 and MKN45 gastric cancer cell lines. Results showed a slight overexpression of PIK3CA, PIK3CB, AKT1, MTOR, RPS6KB1, EIF4EBP1 and EIF4E genes, and a slightly decreased PTEN and TSC1 expression. In AGS, MKN28 and MKN45 cells a significant gene overexpression of PIK3CA, PIK3CB, AKT1, MTOR, RPS6KB1 and EIF4E, and a significant repression of PTEN gene expression were observed. Immunoblotting showed that PI3K-β, AKT, p-AKT, PTEN, mTOR, p-mTOR, P70S6K1, p-P70S6K1, 4E-BP1, p-4E-BP1, eIF4E and p-eIF4E proteins were present in cell lines at different levels, confirming activation of this pathway in vitro. This is the first time this extensive panel of 9 genes within PI3K/AKT/mTOR pathway has been studied in GC to clarify the biological role of this pathway in GC and develop new strategies for this malignancy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890336PMC
http://dx.doi.org/10.1007/s12253-016-0066-5DOI Listing

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