Wang Jinguo, Xie Sheng, Liu Jun, Li Tao, Wang Wanrong, Xie Ziping
Department of Andrology, Renmin Hospital, Hubei University of Medicine, No. 39 Chaoyang Middle Road, Maojian District, Shiyan, 442000, Hubei, People's Republic of China.
BMC Urol. 2021 Mar 19;21(1):40. doi: 10.1186/s12894-021-00810-x.
Emerging evidence suggests that microRNAs (miRNAs) play multiple roles in human cancers through regulating mRNAs and distinct pathways. This paper focused on the functions of miR-4429 in prostate cancer (PCa) progression and the molecules involved.
Expression of miR-4429 in PCa tissues and cells was determined. Upregulation of miR-4429 was introduced in PCa cells to examine its role in the malignant behaviors of cells. The putative target mRNA of miR-4429 involved in PCa progression was predicted from a bioinformatic system and validated through luciferase assays. Overexpression of distal-less homeobox 1 (DLX1) was further induced in cells to validate its implication in miR-4429-mediated events. The activity of Wnt/β-catenin pathway was determined.
miR-4429 was poorly expressed in PCa tissues and cells. Artificial upregulation of miR-4429 significantly reduced proliferation, growth, invasion, migration and resistance to death of cancer cells and inactivated the Wnt/β-catenin pathway. DLX1 mRNA was found as a target of miR-4429. Upregulation of DLX1 restored the malignant behaviors of PCa cells which were initially suppressed by miR-4429, and it activated the Wnt/β-catenin pathway.
Our study highlights that miR-4429 inhibits the growth of PCa cells by down-regulating DLX1 and inactivating the Wnt/β-catenin pathway. This finding may offer novel insights into PCa treatment.
新出现的证据表明,微小RNA(miRNA)通过调节mRNA和不同途径在人类癌症中发挥多种作用。本文聚焦于miR-4429在前列腺癌(PCa)进展中的功能及相关分子。
测定miR-4429在PCa组织和细胞中的表达。在PCa细胞中上调miR-4429以研究其在细胞恶性行为中的作用。通过生物信息学系统预测参与PCa进展的miR-4429的假定靶mRNA,并通过荧光素酶测定进行验证。在细胞中进一步诱导远端同源盒1(DLX1)的过表达,以验证其在miR-4429介导的事件中的作用。测定Wnt/β-连环蛋白通路的活性。
miR-4429在PCa组织和细胞中低表达。人工上调miR-4429可显著降低癌细胞的增殖、生长、侵袭、迁移和抗死亡能力,并使Wnt/β-连环蛋白通路失活。发现DLX1 mRNA是miR-4429的靶标。DLX1的上调恢复了最初被miR-4429抑制的PCa细胞的恶性行为,并激活了Wnt/β-连环蛋白通路。
我们的研究强调,miR-4429通过下调DLX1和使Wnt/β-连环蛋白通路失活来抑制PCa细胞的生长。这一发现可能为PCa治疗提供新的见解。