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环状 RNA SET 结构域蛋白 3 通过调节 microRNA-147a 的表达促进鼻咽癌增殖、顺铂耐药和蛋白激酶 B/哺乳动物雷帕霉素靶蛋白通路的激活。

Circular RNA SET domain protein 3 promotes nasopharyngeal carcinoma proliferation, cisplatin resistance, and protein kinase B / mammalian target of rapamycin pathway activation by modulating microRNA-147a expression.

机构信息

Department of Otorhinolaryngology, Wuhan No. 1 Hospital of Hubei Province, Wuhan City, HuBei Province, China.

Department of Otorhinolaryngology, People's Hospital of Qinghai Province, Xining City, QingHai Province, China.

出版信息

Bioengineered. 2022 Mar;13(3):5843-5854. doi: 10.1080/21655979.2022.2036907.

Abstract

Circular RNA (circRNA) plays a crucial role in the establishment and progression of nasopharyngeal carcinoma (NPC). Understanding the role of circRNA in NPC is helpful to find new therapeutic targets for NPC. The purpose of this study was to explore the effects of circRNA SET domain protein 3 (circSETD3) on protein kinase B (Akt)/ mammalian target of rapamycin (mTOR) signaling pathway and cisplatin (DDP) resistance to NPC and explore its downstream mechanism. The results showed that circSETD3 was upregulated in NPC tissues and was related to DDP resistance to NPC. Functional experiments revealed that circSETD3 knockdown inhibited NPC proliferation and increased DDP sensitivity and apoptosis rate. The promotion effect of circSETD3 overexpression on NPC proliferation and DDP resistance and inhibition effect on apoptosis was reversed by elevated miR-147a. CircSETD3 knockdown or miR-147a overexpression prevented Akt/mTOR pathway's activation. In terms of the mechanism, circSETD3 acted as a sponge for miR-147a. Xenotransplantation experiments showed that knockdown circSETD3 or DDP treatment could restrain tumor growth, and the effect of DDP was enhanced by knockdown of circSETD3. In conclusion, the results of this study confirm that circSETD3 promotes NPC proliferation and DDP resistance by regulating miR-147a, and circSETD3/miR-147a axis may serve as a potential therapeutic target for NPC in the future.

摘要

环状 RNA(circRNA)在鼻咽癌(NPC)的发生和发展中起着至关重要的作用。了解 circRNA 在 NPC 中的作用有助于为 NPC 找到新的治疗靶点。本研究旨在探讨环状 RNA SET 结构域蛋白 3(circSETD3)对蛋白激酶 B(Akt)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路和顺铂(DDP)耐药性对 NPC 的影响,并探讨其下游机制。结果表明,circSETD3 在 NPC 组织中上调,与 NPC 对 DDP 的耐药性有关。功能实验表明,circSETD3 敲低抑制 NPC 增殖,增加 DDP 敏感性和细胞凋亡率。circSETD3 过表达对 NPC 增殖和 DDP 耐药性的促进作用以及对细胞凋亡的抑制作用,可被上调的 miR-147a 逆转。circSETD3 敲低或 miR-147a 过表达可阻止 Akt/mTOR 通路的激活。就机制而言,circSETD3 可作为 miR-147a 的海绵。异种移植实验表明,circSETD3 敲低或 DDP 处理可抑制肿瘤生长,circSETD3 敲低可增强 DDP 的作用。总之,本研究结果证实,circSETD3 通过调节 miR-147a 促进 NPC 增殖和 DDP 耐药性,circSETD3/miR-147a 轴可能成为未来 NPC 的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6204/8973767/c9cf99ced7f8/KBIE_A_2036907_UF0001_OC.jpg

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