Molecular Oncology (May 2021)

The direct miR‐874‐3p‐target FAM84A promotes tumor development in papillary thyroid cancer

  • Yu Ding,
  • Luyao Wu,
  • Xi Zhuang,
  • Jingsheng Cai,
  • Houchao Tong,
  • Yan Si,
  • Hao Zhang,
  • Xiaoting Wang,
  • Meiping Shen

DOI
https://doi.org/10.1002/1878-0261.12941
Journal volume & issue
Vol. 15, no. 5
pp. 1597 – 1614

Abstract

Read online

With the improvement in diagnostic technology, the incidence of thyroid cancer (TC) is on the rise. Papillary thyroid carcinoma (PTC) is the most common pathological type of thyroid cancer; therefore, it is important to explore some valuable molecular targets to improve the treatment and prognosis of PTC. Studies have shown that family with sequence similarity 84, member A (FAM84A) is involved in the development of various tumors. However, the role of FAM84A in PTC remains unknown. Herein, we explored the biological function and specific molecular mechanism of FAM84A in PTC. Results indicated that FAM84A was upregulated in PTC tissues and cells. In addition, patients with higher FAM84A expression tended to possess larger tumor size, higher lymph node metastasis rate, and advanced TNM stage. Further studies indicated that downregulation of FAM84A could inhibit the development of PTC in vitro and in vivo by repressing the epithelial–mesenchymal transition (EMT) and Wnt/β‐catenin signaling pathway. Moreover, FAM84A was confirmed to be negatively regulated by tumor suppressor miR‐874‐3p. In conclusion, our findings suggest that FAM84A may act as a potential diagnostic and therapeutic target for PTC.

Keywords