Mouse models of thyroid cancer: Bridging pathogenesis and novel therapeutics

PI3K/AKT/mTOR通路 甲状腺间变性癌 甲状腺癌 癌症 癌症研究 甲状腺 医学 生物信息学 发病机制 生物 内科学 信号转导 免疫学 遗传学
作者
Yuchen Jin,Min Liu,Ri Sa,Hao Fu,Lin Cheng,Libo Chen
出处
期刊:Cancer Letters [Elsevier BV]
卷期号:469: 35-53 被引量:19
标识
DOI:10.1016/j.canlet.2019.09.017
摘要

Due to a global increase in the incidence of thyroid cancer, numerous novel mouse models were established to reveal thyroid cancer pathogenesis and test promising therapeutic strategies, necessitating a comprehensive review of translational medicine that covers (i) the role of mouse models in the research of thyroid cancer pathogenesis, and (ii) preclinical testing of potential anti-thyroid cancer therapeutics. The present review article aims to: (i) describe the current approaches for mouse modeling of thyroid cancer, (ii) provide insight into the biology and genetics of thyroid cancers, and (iii) offer guidance on the use of mouse models for testing potential therapeutics in preclinical settings. Based on research with mouse models of thyroid cancer pathogenesis involving the RTK, RAS/RAF/MEK/ERK, PI3K/AKT/mTOR, SRC, and JAK-STAT signaling pathways, inhibitors of VEGFR, MEK, mTOR, SRC, and STAT3 have been developed as anti-thyroid cancer drugs for "bench-to-bedside" translation. In the future, mouse models of thyroid cancer will be designed to be ''humanized" and "patient-like," offering opportunities to: (i) investigate the pathogenesis of thyroid cancer through target screening based on the CRISPR/Cas system, (ii) test drugs based on new mouse models, and (iii) explore the underlying mechanisms based on multi-omics.
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