Significance of miRNAs on the thyroid cancer progression and resistance to treatment with special attention to the role of cross-talk between signaling pathways

被引:51
|
作者
Doghish, Ahmed S. [1 ,2 ]
El-Mahdy, Hesham A. [2 ]
Ismail, Ahmed [2 ]
Hegazy, Maghawry [2 ]
Mokhtar, Mahmoud Mohamed [2 ]
Elkhawaga, Samy Y. [2 ]
Elkady, Mohamed A. [2 ]
Yehia, Amr Mohamed [2 ]
Elsakka, Elsayed G. E. [2 ]
机构
[1] Badr Univ Cairo BUC, Fac Pharm, Dept Biochem, Cairo 11829, Egypt
[2] Al Azhar Univ, Fac Pharm Boys, Biochem & Mol Biol Dept, Cairo 11231, Egypt
关键词
Thyroid cancer (TC); MiRNA; Oncogenic miRNA; Tumor suppressor miRNA; Pathogenesis; Drug resistance; EPITHELIAL-MESENCHYMAL TRANSITION; GROWTH-FACTOR RECEPTOR; RNA-BINDING PROTEIN; TGF-BETA; INHIBITS PROLIFERATION; MICRORNA REGULATION; CARCINOMA-CELLS; BIOLOGICAL BEHAVIORS; TUMOR ANGIOGENESIS; DOWN-REGULATION;
D O I
10.1016/j.prp.2023.154371
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Thyroid cancer (TC) is the most prevalent endocrine malignant tumor. It has many types, the Papillary thyroid cancer (PTC)(most common and follicular thyroid carcinoma (FTC). Several risk factors have been associated with TC radiation exposure, autoimmunity, and genetics. Microribonucleic acids (miRNAs) are the most important genetic determinants of TC. They are small chains of nucleic acids that are able to inhibit the expression of several target genes. They could target several genes involved in TC proliferation, angiogenesis, apoptosis, development, and even resistance to therapy. Besides, they could influence the stemness of TC. Moreover, they could regulate several signaling pathways such as WNT/beta-catenin, PI3K/AKT/mTOR axis, JAK/ STAT, TGF- beta, EGFR, and P53. Besides signaling pathways, miRNAs are also involved in the resistance of TC to major treatments such as surgery, thyroid hormone-inhibiting therapy, radioactive iodine, and adjuvant radiation. The stability and sensitivity of several miRNAs might be exploited as an approach for the usage of miRNAs as diagnostic and/or prognostic tools in TC.
引用
收藏
页数:17
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