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MicroRNA-149 通过调节 C4-2 CRPC 细胞系中的 Akt1 抑制癌细胞恶性表型。

MicroRNA‑149 inhibits cancer cell malignant phenotype by regulating Akt1 in C4‑2 CRPC cell line.

机构信息

Department of Urology, Beijing Anzhen Hospital, Capital Medical University, Chaoyang, Beijing 100029, P.R. China.

出版信息

Oncol Rep. 2021 Dec;46(6). doi: 10.3892/or.2021.8209. Epub 2021 Oct 26.

DOI:10.3892/or.2021.8209
PMID:34698359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8561672/
Abstract

Prostate cancer (PCa) is an androgen‑dependent disease. Androgen receptor (AR) has a crucial role in the development and progression of PCa. Recently, several microRNAs (miRNAs/miRs) involved in AR regulation have been associated with castration‑resistant prostate cancer (CRPC), the terminal stage of PCa. Nevertheless, the precise mechanism remains unclear. The present study aimed to identify a novel miR‑149 regulatory network and potential therapeutic target for CRPC. It was found that ectopic expression of miR‑149 mimic could inhibit AR expression, repress epithelial‑mesenchymal transition, induce cell cycle arrest and apoptosis in CRPC cell line C4‑2, whereas the miR‑149 inhibitor exerted the opposite effects. Furthermore, it was also revealed that miR‑149 could reduce the functional activity of the PI3K/Akt1 signaling pathway by targeting Akt1 protein, the key regulatory factor of the PI3K/Akt1 signaling pathway. Knockdown of Akt1 by short hairpin RNA increased apoptosis, reduced proliferation, and restrained migration and invasion in CRPC cells, with the effect of AR inhibition. In conclusion, these results revealed that miR‑149 acts as a tumor suppressor in CRPC cell line C4‑2 and restrains its progression through the AR signaling pathway by targeting Akt1. The miR‑149/Akt1/AR regulatory pathway may represent a novel PCa therapeutic target.

摘要

前列腺癌(PCa)是一种雄激素依赖性疾病。雄激素受体(AR)在 PCa 的发生和发展中起关键作用。最近,几种参与 AR 调节的 microRNAs(miRNAs/miRs)与去势抵抗性前列腺癌(CRPC)有关,CRPC 是 PCa 的终末期。然而,确切的机制尚不清楚。本研究旨在确定一个新的 miR-149 调控网络和 CRPC 的潜在治疗靶点。结果发现,miR-149 模拟物的异位表达可抑制 AR 表达,抑制上皮-间充质转化,诱导 CRPC 细胞系 C4-2 中的细胞周期停滞和细胞凋亡,而 miR-149 抑制剂则产生相反的效果。此外,还发现 miR-149 可通过靶向 Akt1 蛋白抑制 PI3K/Akt1 信号通路的功能活性,Akt1 蛋白是 PI3K/Akt1 信号通路的关键调节因子。短发夹 RNA 敲低 Akt1 可增加 CRPC 细胞的凋亡,减少增殖,并抑制迁移和侵袭,同时抑制 AR。综上所述,这些结果表明,miR-149 在 CRPC 细胞系 C4-2 中作为肿瘤抑制因子发挥作用,通过靶向 Akt1 抑制其进展。miR-149/Akt1/AR 调控途径可能代表一种新的前列腺癌治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/f6b1a4dbdb9a/or-46-06-08209-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/afba79019586/or-46-06-08209-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/7a8f061ba5a6/or-46-06-08209-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/55dd8c3a0e3b/or-46-06-08209-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/6ee3b199264d/or-46-06-08209-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/954e13254603/or-46-06-08209-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/f6b1a4dbdb9a/or-46-06-08209-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/afba79019586/or-46-06-08209-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/7a8f061ba5a6/or-46-06-08209-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/55dd8c3a0e3b/or-46-06-08209-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/6ee3b199264d/or-46-06-08209-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/954e13254603/or-46-06-08209-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706c/8561672/f6b1a4dbdb9a/or-46-06-08209-g05.jpg

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