4.7 Review

Targeting PI3K/AKT/mTOR-mediated autophagy for tumor therapy

Journal

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 104, Issue 2, Pages 575-587

Publisher

SPRINGER
DOI: 10.1007/s00253-019-10257-8

Keywords

PI3K/AKT/mTOR; Autophagy; Tumor; Tumor microenvironment; Drug resistance

Funding

  1. National Natural Science Foundation of China [81870105, 81770107]
  2. National Key Research and Development Program of China [2018YFA0107800]
  3. Key Project of Science and Technology of Hunan Provincial Health Commission [20201921]

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Autophagy is a highly conserved catabolic process and participates in a variety of cellular biological activities. The phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway, as a critical regulator of autophagy, is involved in the initiation and promotion of a series of pathological disorders including various tumors. Autophagy also participates in regulating the balance between the tumor and the tumor microenvironment. Natural products have been considered a treasure of new drug discoveries and are of great value to medicine. Mounting evidence has suggested that numerous natural products are targeting PI3K/AKT/mTOR-mediated autophagy, thereby suppressing tumor growth. Furthermore, autophagy plays a double-edged sword role in different tumors. Targeting PI3K/AKT/mTOR-mediated autophagy is an important therapeutic strategy for a variety of tumors, and plays important roles in enhancing the chemosensitivity of tumor cells and avoiding drug resistance. Therefore, we summarized the roles of PI3K/AKT/mTOR-mediated autophagy in tumorigenesis, progression, and drug resistance of tumors, which may be utilized to design preferably therapeutic strategies for various tumors.

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