Abstract |
Abstract  Numerous studies have confirmed that abnormal activation of the phosphatidylinositol 3-kinase (PI3K)/ protein kinase B (AKT) signaling pathway is one of the most common induction mechanisms of T-ALL. In recent years, many literature report that multiple abnormally expressed microRNAs ( miRNAs) can participate in the development of T-ALL by regulating the PI3K/AKT signaling pathway. For example, overexpression of miR-19 and miR181a can activate the PI3K/AKT signaling pathway, which leads to the development of T-ALL and induction of chemotherapy drug resistance, as well as the low expression of miR-26b and miR-29a. Apart from the inhibitors and traditional Chinese medicines that target the PI3K/AKT signaling pathway, regulation of the expression of the corresponding miRNA may also be a potential treatment protocol for T-ALL. The mechanisms of PI3K/AKT signaling pathway involved in the development of T-ALL, the role of miRNAs in the PI3K/AKT signaling pathway and the targeted therapy based on this signaling pathway are summarized briefly in this review.
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Authors | Yong-Jun Li, Xiao-Fei Li, Er-Huan Yang, Min Shi |
Journal | Zhongguo shi yan xue ye xue za zhi
(Zhongguo Shi Yan Xue Ye Xue Za Zhi)
Vol. 27
Issue 4
Pg. 1344-1347
(Aug 2019)
ISSN: 1009-2137 [Print] China |
PMID | 31418405
(Publication Type: Journal Article, Review)
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Chemical References |
- MicroRNAs
- Phosphatidylinositol 3-Kinases
- Proto-Oncogene Proteins c-akt
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Topics |
- Humans
- Leukemia, T-Cell
- MicroRNAs
- Phosphatidylinositol 3-Kinases
- Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
- Proto-Oncogene Proteins c-akt
- Signal Transduction
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