PI3K/Akt/mTOR Pathway as a Therapeutic Target for Colorectal Cancer: A Review of Preclinical and Clinical Evidence

被引:239
作者
Narayanankutty, Arunaksharan [1 ]
机构
[1] St Josephs Coll Autonomous, Post Grad & Res Dept Zool, Calicut 673008, Kerala, India
关键词
Anticancer activity; metastasis; PI3K pathway; natural products; colon cancer; synthetic inhibitors; COLON-CANCER; SIGNALING PATHWAY; ANTITUMOR-ACTIVITY; MTOR PATHWAY; DRUG-RESISTANCE; UP-REGULATION; TUMOR-GROWTH; CELL-GROWTH; INHIBITORS; APOPTOSIS;
D O I
10.2174/1389450120666190618123846
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Phosphoinositide 3-kinase (PI3Ks) is a member of intracellular lipid kinases and involved in the regulation of cellular proliferation, differentiation and survival. Overexpression of the PI3K/Akt/mTOR signalling has been reported in various forms of cancers, especially in colorectal cancers (CRC). Due to their significant roles in the initiation and progression events of colorectal cancer, they are recognized as a striking therapeutic target. Objective: The present review is aimed to provide a detailed outline on the role of PI3K/Akt/mTOR pathway in the initiation and progression events of colorectal cancers as well as its function in drug resistance. Further, the role of PI3K/Akt/mTOR inhibitors alone and in combination with other chemotherapeutic drugs, in alleviating colorectal cancer is also discussed. The review contains preclinical and clinical evidence as well as patent literature of the pathway inhibitors which are natural and synthetic in origin. Methods: The data were obtained from PubMed/Medline databases, Scopus and Google patent literature. Results: PI3K/Akt/mTOR signalling is an important event in colorectal carcinogenesis. In addition, it plays significant roles in acquiring drug resistance as well as metastatic initiation events of CRCs. Several small molecules of natural and synthetic origin have been found to be potent inhibitors of CRCs by effectively downregulating the pathway. Data from various clinical studies also support these pathway inhibitors and several among them are patented. Conclusion: Inhibitors of the PI3K/mTOR pathway have been successful for the treatment of primary and metastatic colorectal cancers, rendering the pathway as a promising clinical cancer therapeutic target.
引用
收藏
页码:1217 / 1226
页数:10
相关论文
共 109 条
[1]   Dual mTOR/PI3K inhibitor NVP-BEZ235 arrests colorectal cancer cell growth and displays differential inhibition of 4E-BP1 [J].
Alqurashi, Naif ;
Hashimi, Saeed M. ;
Alowaidi, Faisal ;
Ivanovski, Saso ;
Wei, Ming Q. .
ONCOLOGY REPORTS, 2018, 40 (02) :1083-1092
[2]   Crocin synergistically enhances the antiproliferative activity of 5-flurouracil through Wnt/PI3K pathway in a mouse model of colitis-associated colorectal cancer [J].
Amerizadeh, Forouzan ;
Rezaei, Nastaran ;
Rahmani, Farzad ;
Hassanian, Seyed Mahdi ;
Moradi-Marjaneh, Reyhaneh ;
Fiuji, Hamid ;
Boroumand, Nadia ;
Nosrati-Tirkani, Abolfazl ;
Ghayour-Mobarhan, Majid ;
Ferns, Gordon A. ;
Khazaei, Majid ;
Avan, Amir .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2018, 119 (12) :10250-10261
[3]  
[Anonymous], INTERDISCIP SCI
[4]  
[Anonymous], ACTA PHARM SIN
[5]  
[Anonymous], J EXP CLIN CANCER RE
[6]   Diclofenac induced apoptosis via altering PI3K/Akt/MAPK signaling axis in HCT 116 more efficiently compared to SW480 colon cancer cells [J].
Arisan, Elif Damla ;
Ergul, Zehragul ;
Bozdag, Gulnihal ;
Rencuzogullari, Ozge ;
Coker-Gurkan, Ajda ;
Obakan-Yerlikaya, Pinar ;
Coskun, Deniz ;
Palavan-Unsal, Narcin .
MOLECULAR BIOLOGY REPORTS, 2018, 45 (06) :2175-2184
[7]   Anti-colon cancer activity of Murraya koenigii leaves is due to constituent murrayazoline and O-methylmurrayamine A induced mTOR/AKT downregulation and mitochondrial apoptosis [J].
Arun, Ashutosh ;
Patel, Om P. S. ;
Saini, Deepika ;
Yadav, Prem P. ;
Konwar, Rituraj .
BIOMEDICINE & PHARMACOTHERAPY, 2017, 93 :510-521
[8]   Verbascoside: Identification, Quantification, and Potential Sensitization of Colorectal Cancer Cells to 5-FU by Targeting PI3K/AKT Pathway [J].
Attia, Yasmeen M. ;
El-Kersh, Dina M. ;
Wagdy, Hebatallah A. ;
Elmazar, Mohamed M. .
SCIENTIFIC REPORTS, 2018, 8
[9]   Targeting the phosphatidylinositol 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) pathway: An emerging treatment strategy for squamous cell lung carcinoma [J].
Beck, Joseph Thaddeus ;
Ismail, Amen ;
Tolomeo, Christina .
CANCER TREATMENT REVIEWS, 2014, 40 (08) :980-989
[10]   PI3K/AKT/mTOR pathway activation in primary and corresponding metastatic breast tumors after adjuvant endocrine therapy [J].
Beelen, Karin ;
Hoefnagel, Laurien D. C. ;
Opdam, Mark ;
Wesseling, Jelle ;
Sanders, J. ;
Vincent, Andrew D. ;
van Diest, Paul J. ;
Linn, Sabine C. .
INTERNATIONAL JOURNAL OF CANCER, 2014, 135 (05) :1257-1263