Literature DB >> 33857392

How can we turn the PI3K/AKT/mTOR pathway down? Insights into inhibition and treatment of cancer.

Said M Afify1,2, Aung Ko Ko Oo3, Ghmkin Hassan1,4, Akimasa Seno1, Masaharu Seno1.   

Abstract

Introduction: The phosphatidylinositol 3-kinase/protein kinase-B/mammalian target of rapamycin (PI3K/AKT/mTOR) pathway is a fundamental regulator of cell proliferation and survival. Dysregulation in this pathway leads to the development of cancer. Accumulating evidence indicates that dysregulation in this pathway is involved in cancer initiation, progression, and recurrence. However, the pathway consists of various signal transducing factors related with cellular events, such as transformation, tumorigenesis, cancer progression, and drug resistance. Therefore, it is very important to determine the targets in this pathway for cancer therapy. Although many drugs inhibiting this signaling pathway are in clinical trials or have been approved for treating solid tumors and hematologic malignancies, further understanding of the signaling mechanism is required to achieve better therapeutic efficacy.Areas covered: In this review, we have describe the PI3K/AKT/mTOR pathway in detail, along with its critical role in cancer stem cells, for identifying potential therapeutic targets. We also summarize the recent developments in different types of signaling inhibitors.Expert opinion: Downregulation of the PI3K/AKT/mTOR pathway is very important for treating all types of cancers. Thus, further studies are required to establish novel prognostic factors to support the current progress in cancer treatment with emphasis on this pathway.

Entities:  

Keywords:  4E-BP; AKT/PKB; HIF1-alpha; PI3K; Rhev; S6 kinase; Signaling pathway; TSC1/2; dual inhibitors; mTOR

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Year:  2021        PMID: 33857392     DOI: 10.1080/14737140.2021.1918001

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  6 in total

Review 1.  Novel Effects of Statins on Cancer via Autophagy.

Authors:  Daniela Mengual; Luz Elena Medrano; Wendy Villamizar-Villamizar; Estefanie Osorio-Llanes; Evelyn Mendoza-Torres; Samir Bolívar
Journal:  Pharmaceuticals (Basel)       Date:  2022-05-24

2.  The efficacy of PI3Kγ and EGFR inhibitors on the suppression of the characteristics of cancer stem cells.

Authors:  Yanning Xu; Said M Afify; Juan Du; Bingbing Liu; Ghmkin Hassan; Qing Wang; Hanbo Li; Yixin Liu; Xiaoying Fu; Zhengmao Zhu; Ling Chen; Masaharu Seno
Journal:  Sci Rep       Date:  2022-01-10       Impact factor: 4.379

3.  Network pharmacology and experimental investigation of Rhizoma polygonati extract targeted kinase with herbzyme activity for potent drug delivery.

Authors:  Yingqiu Xie; Chengling Mu; Bexultan Kazybay; Qinglei Sun; Aidana Kutzhanova; Guldan Nazarbek; Na Xu; Lazzat Nurtay; Qian Wang; Amr Amin; Xugang Li
Journal:  Drug Deliv       Date:  2021-12       Impact factor: 6.419

4.  ZDQ-0620, a Novel Phosphatidylinositol 3-Kinase Inhibitor, Inhibits Colorectal Carcinoma Cell Proliferation and Suppresses Angiogenesis by Attenuating PI3K/AKT/mTOR Pathway.

Authors:  Xiaochun Qin; Mingyue Liu; Chang Xu; Bo Xing; Xiangbo Xu; Yuting Wu; Huaiwei Ding; Qingchun Zhao
Journal:  Front Oncol       Date:  2022-03-02       Impact factor: 6.244

5.  Cancer stem cells induced by chronic stimulation with prostaglandin E2 exhibited constitutively activated PI3K axis.

Authors:  Hideki Minematsu; Said M Afify; Yuki Sugihara; Ghmkin Hassan; Maram H Zahra; Akimasa Seno; Masaki Adachi; Masaharu Seno
Journal:  Sci Rep       Date:  2022-09-17       Impact factor: 4.996

Review 6.  Clinical analysis and literature review of a case of ovarian clear cell carcinoma with PIK3CA gene mutation: A case report.

Authors:  Abdulkarim Mohamed Farah; Shiyu Gu; Yan Jia
Journal:  Medicine (Baltimore)       Date:  2022-09-16       Impact factor: 1.817

  6 in total

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