Mouse models of thyroid cancer: Bridging pathogenesis and novel therapeutics

Cancer Lett. 2020 Jan 28:469:35-53. doi: 10.1016/j.canlet.2019.09.017. Epub 2019 Oct 4.

Abstract

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.

Keywords: Anti-cancer therapeutics; Mouse model; Preclinical testing; Thyroid cancer.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / antagonists & inhibitors
  • Biomarkers, Tumor / genetics*
  • CRISPR-Cas Systems / genetics
  • Disease Models, Animal
  • Disease Progression
  • Gene Expression Regulation
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Incidence
  • Mice
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Thyroid Gland / drug effects
  • Thyroid Gland / pathology
  • Thyroid Neoplasms / drug therapy*
  • Thyroid Neoplasms / epidemiology
  • Thyroid Neoplasms / etiology
  • Thyroid Neoplasms / pathology
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor