The interplay of Klotho with signaling pathway and microRNAs in cancers

被引:14
作者
Abolghasemi, Maryam [1 ,2 ,3 ]
Yousefi, Tooba [1 ,2 ,3 ]
Maniati, Mahmood [4 ]
Qujeq, Durdi [1 ,2 ]
机构
[1] Babol Univ Med Sci, Cellular & Mol Biol Res Ctr, Hlth Res Inst, Babol Sar, Iran
[2] Babol Univ Med Sci, Sch Med, Dept Clin Biochem, Ganjafrooze Ave, Babol Sar 4717647745, Iran
[3] Babol Univ Med Sci, Student Res Comm, Babol Sar, Iran
[4] Ahvaz Jundishapur Univ Med Sci, English Dept, Ahvaz, Iran
关键词
cancer; Klotho; microRNAs; signaling pathways; tumor suppressor; FIBROBLAST GROWTH-FACTORS; TUMOR-SUPPRESSOR; CELL-PROLIFERATION; POOR-PROGNOSIS; OVARIAN-CANCER; UP-REGULATION; IGF SYSTEM; TGF-BETA; EXPRESSION; PROGRESSION;
D O I
10.1002/jcb.29022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Klotho (KL) gene has been accepted as an "aging suppressor" gene that encodes a single transmembrane protein in human known as Klotho which is commonly expressed in renal tubes. The interruption in the secretion of Klotho protein expedites aging whereas its high expression extends lifespan. The family of Klotho proteins has been reported to act as distinct receptors for endocrine fibroblast growth factors (FGFs), which manage multifarious metabolic processes. Further, the secreted Klotho is a hormonal factor that takes part in the ion channel organization. Numerous studies determined that this protein affects the function of a number of important signaling pathways, which may present an impact in tumorigenesis via the coordination of receptors located on them. This review article focuses on the effects of microRNAs on the performance of Klotho and how the interplay between Klotho and certain pathways like insulin-like growth factor, FGF, Wnt, and transforming growth factor beta contribute to the biogenesis of cancer. The present study is also pointed at defining the molecular mechanisms of these interactions.
引用
收藏
页码:14306 / 14317
页数:12
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