PI3K/Akt/mTOR Signaling Pathway as a Target for Colorectal Cancer Treatment

被引:77
作者
Leiphrakpam, Premila D. [1 ,2 ]
Are, Chandrakanth [1 ,2 ]
机构
[1] Univ Nebraska, Coll Med, Med Ctr, Grad Med Educ, Omaha, NE 68198 USA
[2] Univ Nebraska, Coll Med, Dept Surg, Div Surg Oncol,Med Ctr, Omaha, NE 68198 USA
关键词
colorectal cancer; PI3K; Akt; mTOR; cell survival; apoptosis; inhibitors; targeted therapy; ADVANCED SOLID TUMORS; I PI3K INHIBITOR; PHOSPHATIDYLINOSITOL 3-KINASE INHIBITOR; 1ST-IN-HUMAN PHASE-I; DOSE-ESCALATION; PI3K/MTOR INHIBITOR; PIK3CA MUTATIONS; DUAL INHIBITOR; BUPARLISIB BKM120; SAR245409; XL765;
D O I
10.3390/ijms25063178
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the last decade, pathway-specific targeted therapy has revolutionized colorectal cancer (CRC) treatment strategies. This type of therapy targets a tumor-vulnerable spot formed primarily due to an alteration in an oncogene and/or a tumor suppressor gene. However, tumor heterogeneity in CRC frequently results in treatment resistance, underscoring the need to understand the molecular mechanisms involved in CRC for the development of novel targeted therapies. The phosphatidylinositol 3-kinase/protein kinase B/mammalian target of the rapamycin (PI3K/Akt/mTOR) signaling pathway axis is a major pathway altered in CRC. The aberrant activation of this pathway is associated with CRC initiation, progression, and metastasis and is critical for the development of drug resistance in CRC. Several drugs target PI3K/Akt/mTOR in clinical trials, alone or in combination, for the treatment of CRC. This review aims to provide an overview of the role of the PI3K/Akt/mTOR signaling pathway axis in driving CRC, existing PI3K/Akt/mTOR-targeted agents against CRC, their limitations, and future trends.
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页数:20
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