PI3K/Akt/mTOR Signaling Pathway in Blood Malignancies-New Therapeutic Possibilities.
Wojciech WieseJulia BarczukOlga RacinskaNatalia SiweckaWioletta Rozpedek-KaminskaArtur SlupianekRadoslaw SierpinskiIreneusz MajsterekPublished in: Cancers (2023)
Blood malignancies remain a therapeutic challenge despite the development of numerous treatment strategies. The phosphatidylinositol-3 kinase (PI3K)/protein kinase B/mammalian target of rapamycin (PI3K/Akt/mTOR) signaling pathway plays a central role in regulating many cellular functions, including cell cycle, proliferation, quiescence, and longevity. Therefore, dysregulation of this pathway is a characteristic feature of carcinogenesis. Increased activation of PI3K/Akt/mTOR signaling enhances proliferation, growth, and resistance to chemo- and immunotherapy in cancer cells. Overactivation of the pathway has been found in various types of cancer, including acute and chronic leukemia. Inhibitors of the PI3K/Akt/mTOR pathway have been used in leukemia treatment since 2014, and some of them have improved treatment outcomes in clinical trials. Recently, new inhibitors of PI3K/Akt/mTOR signaling have been developed and tested both in preclinical and clinical models. In this review, we outline the role of the PI3K/Akt/mTOR signaling pathway in blood malignancies' cells and gather information on the inhibitors of this pathway that might provide a novel therapeutic opportunity against leukemia.
Keyphrases
- signaling pathway
- induced apoptosis
- cell cycle
- protein kinase
- pi k akt
- clinical trial
- acute myeloid leukemia
- epithelial mesenchymal transition
- bone marrow
- cell proliferation
- cell cycle arrest
- liver failure
- photodynamic therapy
- squamous cell carcinoma
- stem cells
- healthcare
- radiation therapy
- cancer therapy
- hepatitis b virus
- squamous cell
- study protocol
- drug delivery
- smoking cessation
- tyrosine kinase
- social media
- health information
- aortic dissection
- phase iii
- replacement therapy