PI3K/Akt/mTOR Signaling Pathway: Role in Esophageal Squamous Cell Carcinoma, Regulatory Mechanisms and Opportunities for Targeted Therapy

被引:54
作者
Luo, Qian [1 ,2 ]
Du, Ruijuan [1 ,2 ]
Liu, Wenting [1 ,2 ]
Huang, Guojing [1 ]
Dong, Zigang [1 ,2 ,3 ,4 ]
Li, Xiang [1 ,2 ,3 ,4 ]
机构
[1] Zhengzhou Univ, Sch Basic Med Sci, Dept Pathophysiol, Zhengzhou, Peoples R China
[2] China US Henan Hormel Canc Inst, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Henan Prov Cooperat Innovat Ctr Canc Chemoprevent, Zhengzhou, Peoples R China
[4] Zhengzhou Univ, State Key Lab Esophageal Canc Prevent & Treatment, Zhengzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
PI3K; Akt; mTOR pathway; ESCC; inhibitor; drug resistance; mutation; PHASE-II TRIAL; EPITHELIAL-MESENCHYMAL TRANSITION; GASTROESOPHAGEAL JUNCTION; MAMMALIAN TARGET; AKT INHIBITOR; ANTITUMOR-ACTIVITY; EVEROLIMUS RAD001; 2ND-LINE THERAPY; MTOR PATHWAY; IN-VITRO;
D O I
10.3389/fonc.2022.852383
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Esophageal squamous cell carcinoma (ESCC), is the most common type of esophageal cancer worldwide, mainly occurring in the Asian esophageal cancer belt, including northern China, Iran, and parts of Africa. Phosphatidlinositol 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) signaling pathway is one of the most important cellular signaling pathways, which plays a crucial role in the regulation of cell growth, differentiation, migration, metabolism and proliferation. In addition, mutations in some molecules of PI3K/Akt/mTOR pathway are closely associated with survival and prognosis in ESCC patients. A large number of studies have found that there are many molecules in ESCC that can regulate the PI3K/Akt/mTOR pathway. Overexpression of these molecules often causes aberrant activation of PI3K/Akt/mTOR pathway. Currently, several effective PI3K/Akt/mTOR pathway inhibitors have been developed, which can play anticancer roles either alone or in combination with other inhibitors. This review mainly introduces the general situation of ESCC, the composition and function of PI3K/Akt/mTOR pathway, and regulatory factors that interact with PI3K/Akt/mTOR signaling pathway. Meanwhile, mutations and inhibitors of PI3K/Akt/mTOR pathway in ESCC are also elucidated.
引用
收藏
页数:12
相关论文
共 99 条
[1]   A Phase II Trial of Bevacizumab plus Everolimus for Patients with Refractory Metastatic Colorectal Cancer [J].
Altomare, Ivy ;
Bendell, Johanna C. ;
Bullock, Karen E. ;
Uronis, Hope E. ;
Morse, Michael A. ;
Hsu, S. David ;
Zafar, S. Yousuf ;
Blobe, Gerard C. ;
Pang, Herbert ;
Honeycutt, Wanda ;
Sutton, Linda ;
Hurwitz, Herbert I. .
ONCOLOGIST, 2011, 16 (08) :1131-1137
[2]   Repression of AXL expression by AP-1/JNK blockage overcomes resistance to PI3Ka therapy [J].
Badarni, Mai ;
Prasad, Manu ;
Balaban, Noa ;
Zorea, Jonathan ;
Yegodayev, Ksenia M. ;
Ben-Zion, Joshua ;
Dinuri, Anat Bahat ;
Grenman, Reidar ;
Rotblatc, Barak ;
Cohen, Limor ;
Elkabets, Moshe .
JCI INSIGHT, 2019, 4 (08)
[3]   A phase II, randomised study of mFOLFOX6 with or without the Akt inhibitor ipatasertib in patients with locally advanced or metastatic gastric or gastroesophageal junction cancer [J].
Bang, Y-J ;
Kang, Y-K ;
Ng, M. ;
Chung, H. C. ;
Wainberg, Z. A. ;
Gendreau, S. ;
Chan, W. Y. ;
Xu, N. ;
Maslyar, D. ;
Meng, R. ;
Chau, I ;
Ajani, J. A. .
EUROPEAN JOURNAL OF CANCER, 2019, 108 :17-24
[4]   A phase Ib study of linsitinib (OSI-906), a dual inhibitor of IGF-1R and IR tyrosine kinase, in combination with everolimus as treatment for patients with refractory metastatic colorectal cancer [J].
Bendell, Johanna C. ;
Jones, Suzanne F. ;
Hart, Lowell ;
Spigel, David R. ;
Lane, Cassie M. ;
Earwood, Chris ;
Infante, Jeffrey R. ;
Barton, John ;
Burris, Howard A. .
INVESTIGATIONAL NEW DRUGS, 2015, 33 (01) :187-193
[5]   A multicenter phase 1 study of PX-866 and cetuximab in patients with metastatic colorectal carcinoma or recurrent/metastatic squamous cell carcinoma of the head and neck [J].
Bowles, Daniel W. ;
Senzer, Neil ;
Hausman, Diana ;
Peterson, Scott ;
Vo, Alex ;
Walker, Luke ;
Cohen, Roger B. ;
Jimeno, Antonio .
INVESTIGATIONAL NEW DRUGS, 2014, 32 (06) :1197-1203
[6]   Direct inhibition of the signaling functions of the mammalian target of rapamycin by the phosphoinositide 3-kinase inhibitors, wortmannin and LY294002 [J].
Brunn, GJ ;
Williams, J ;
Sabers, C ;
Wiederrecht, G ;
Lawrence, JC ;
Abraham, RT .
EMBO JOURNAL, 1996, 15 (19) :5256-5267
[7]   Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations [J].
Chang, Jiang ;
Tan, Wenle ;
Ling, Zhiqiang ;
Xi, Ruibin ;
Shao, Mingming ;
Chen, Mengjie ;
Luo, Yingying ;
Zhao, Yanjie ;
Liu, Yun ;
Huang, Xiancong ;
Xia, Yuchao ;
Hu, Jinlin ;
Parker, Joel S. ;
Marron, David ;
Cui, Qionghua ;
Peng, Linna ;
Chu, Jiahui ;
Li, Hongmin ;
Du, Zhongli ;
Han, Yaling ;
Tan, Wen ;
Liu, Zhihua ;
Zhan, Qimin ;
Li, Yun ;
Mao, Weimin ;
Wu, Chen ;
Lin, Dongxin .
NATURE COMMUNICATIONS, 2017, 8
[8]   Platelet-activating factor receptor-mediated PI3K/AKT activation contributes to the malignant development of esophageal squamous cell carcinoma [J].
Chen, J. ;
Lan, T. ;
Zhang, W. ;
Dong, L. ;
Kang, N. ;
Zhang, S. ;
Fu, M. ;
Liu, B. ;
Liu, K. ;
Zhang, C. ;
Hou, J. ;
Zhan, Q. .
ONCOGENE, 2015, 34 (40) :5114-5127
[9]   The diacylglycerol kinase α (DGKα)/Akt/NF-κB feedforward loop promotes esophageal squamous cell carcinoma (ESCC) progression via FAK-dependent and FAK-independent manner [J].
Chen, Jie ;
Zhang, Weimin ;
Wang, Yan ;
Zhao, Di ;
Wu, Mengjiao ;
Fan, Jiawen ;
Li, Jinting ;
Gong, Ying ;
Dan, Nana ;
Yang, Di ;
Liu, Rui ;
Zhan, Qimin .
ONCOGENE, 2019, 38 (14) :2533-2550
[10]   Isocitrate dehydrogenase 2 contributes to radiation resistance of oesophageal squamous cell carcinoma via regulating mitochondrial function and ROS/pAKT signalling [J].
Chen, Xuan ;
Zhuo, Shichao ;
Xu, Wenzhe ;
Chen, Xue ;
Huang, Di ;
Sun, Xiaozheng ;
Cheng, Yufeng .
BRITISH JOURNAL OF CANCER, 2020, 123 (01) :126-136