Molecular target: pan-AKT in gastric cancer

Byung Woog Kang1, Ian Chau2

  • 1Department of Oncology/Hematology, Kyungpook National University Hospital, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.

ESMO Open
|September 19, 2020
PubMed

Insights

The phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway regulates cell functions and is often dysregulated in cancer. AKT inhibitors are being developed to treat various malignancies, including gastric cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • The PI3K/AKT/mTOR pathway is crucial for cellular processes like survival and proliferation.
  • This pathway is frequently dysregulated in solid tumors, contributing to cancer development.
  • AKT acts as a central regulator within this signaling cascade.

Purpose of the Study:

  • To review the role of AKT in gastric cancer pathogenesis.
  • To summarize recent advancements in AKT inhibitors for gastric cancer treatment.

Main Methods:

  • Literature review of scientific studies on AKT and its inhibitors in gastric cancer.
  • Analysis of the PI3K/AKT/mTOR pathway's significance in cancer biology.

Main Results:

  • Aberrant AKT activation is implicated in cancer pathogenesis.
  • AKT inhibitors represent a promising therapeutic strategy for various cancers.
  • Several AKT inhibitors are in clinical trials for gastric cancer.

Conclusions:

  • AKT is a significant therapeutic target for gastric cancer.
  • Further research into AKT inhibitors may improve treatment outcomes for gastric cancer patients.

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