4.6 Review

PI3K/Akt/mTOR Signaling Pathway: Role in Esophageal Squamous Cell Carcinoma, Regulatory Mechanisms and Opportunities for Targeted Therapy

Journal

FRONTIERS IN ONCOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.852383

Keywords

PI3K; Akt; mTOR pathway; ESCC; inhibitor; drug resistance; mutation

Categories

Funding

  1. National Natural Science Foundation of China [82172996, 82073075]
  2. Science and technology project of Henan Province [182102310324, 202102310206]
  3. Training plan for young backbone teachers of Zhengzhou University [2018ZDGGJS037]
  4. Training plan for young backbone teachers of Henan Province [2020GGJS010]
  5. Basic research and Cultivation Fund for young teachers of Zhengzhou University [JC202035023]
  6. Science and technology innovation talents support plan of Henan Province [21HASTIT048]
  7. Innovation team support plan for outstanding young talents of Zhengzhou University

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Esophageal squamous cell carcinoma (ESCC) is the most common type of esophageal cancer worldwide, mainly occurring in specific regions of Asia. The PI3K/Akt/mTOR signaling pathway plays a crucial role in regulating cell growth, differentiation, migration, metabolism, and proliferation, and is closely associated with survival and prognosis in ESCC patients. Many molecules can regulate this pathway and lead to its aberrant activation. Several effective inhibitors of the PI3K/Akt/mTOR pathway have been developed.
Esophageal squamous cell carcinoma (ESCC), is the most common type of esophageal cancer worldwide, mainly occurring in the Asian esophageal cancer belt, including northern China, Iran, and parts of Africa. Phosphatidlinositol 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) signaling pathway is one of the most important cellular signaling pathways, which plays a crucial role in the regulation of cell growth, differentiation, migration, metabolism and proliferation. In addition, mutations in some molecules of PI3K/Akt/mTOR pathway are closely associated with survival and prognosis in ESCC patients. A large number of studies have found that there are many molecules in ESCC that can regulate the PI3K/Akt/mTOR pathway. Overexpression of these molecules often causes aberrant activation of PI3K/Akt/mTOR pathway. Currently, several effective PI3K/Akt/mTOR pathway inhibitors have been developed, which can play anticancer roles either alone or in combination with other inhibitors. This review mainly introduces the general situation of ESCC, the composition and function of PI3K/Akt/mTOR pathway, and regulatory factors that interact with PI3K/Akt/mTOR signaling pathway. Meanwhile, mutations and inhibitors of PI3K/Akt/mTOR pathway in ESCC are also elucidated.

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