PI3K/Akt/mTOR: A promising therapeutic target for non-medullary thyroid carcinoma

被引:177
作者
Petrulea, Mirela S. [1 ]
Plantinga, Theo S. [2 ,3 ]
Smit, Jan W. [2 ,3 ]
Georgescu, Carmen E. [1 ]
Netea-Maier, Romana T. [2 ,3 ]
机构
[1] Univ Med & Pharm Cluj Napoca Iuliu Hatieganu, Dept Endocrinol, Cluj Napoca, Romania
[2] Radboud Univ Nijmegen Med Ctr, Dept Internal Med, NL-6525 GA Nijmegen, Netherlands
[3] Radboud Univ Nijmegen Med Ctr, Div Endocrinol, NL-6525 GA Nijmegen, Netherlands
关键词
Thyroid carcinoma; Tumorigenesis; Therapy resistance; PI3K; Akt; mTOR; CANCER CELL-LINES; GENETIC ALTERATIONS; PHOSPHATIDYLINOSITOL; 3-KINASE/AKT; TUMOR-SUPPRESSOR; HIGH PREVALENCE; MOUSE MODEL; REDIFFERENTIATION THERAPY; PROLIFERATIVE SIGNALS; MOLECULAR PATHWAYS; MAMMALIAN TARGET;
D O I
10.1016/j.ctrv.2015.06.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Thyroid carcinoma (TC) is the most common endocrine malignancy. The pathogenesis of TC is complex and involves multiple genetic events that lead to activation of oncogenic pathways such as the MAP kinase (MAPK) pathway and the PI3K/Akt/mTOR pathway. The PI3K/Akt pathway has emerged as an important player in the pathogenesis of TC, particularly in follicular and advanced anaplastic or poorly differentiated TC. Because these patients have a poor prognosis, particularly when their tumors become resistant to the conventional treatment with radioactive iodine, efforts have been made to identify possible targets for therapy within these pathways. Orally available drugs targeting the PI3K/Akt/mTOR pathway are being used with success in treatment of several types of malignant tumors. There is an increasing amount of preclinical and clinical data supporting that this pathway may represent a promising target for systemic therapy in TC. The present review focuses on the most recent developments on the role of the PI3K/Akt pathway in the pathogenesis of non-medullary TC and will provide insight into how this pathway can be targeted either alone or in the context of multimodal therapeutic strategies for treatment of advanced TC. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:707 / 713
页数:7
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