piR-1919609 Is an Ideal Potential Target for Reversing Platinum Resistance in Ovarian Cancer.

IF 2.7 4区 医学 Q3 ONCOLOGY
Ying Yan, Dan Tian, Bingbing Zhao, Zhuang Li, Zhijiong Huang, Kuina Li, Xiaoqi Chen, Lu Zhou, Yanying Feng, Zhijun Yang
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引用次数: 0

Abstract

Purpose: PIWI-interacting RNAs (piRNAs) are a type of noncoding small RNA that can interact with PIWI-like RNA-mediated gene silencing (PIWIL) proteins to affect biological processes such as transposon silencing through epigenetic effects. Recent studies have found that piRNAs are widely dysregulated in tumors and associated with tumor progression and a poor prognosis. Therefore, this study aimed to investigate the effect of piR-1919609 on the proliferation, apoptosis, and drug resistance of ovarian cancer cells.

Methods: In this study, we used small RNA sequencing to screen and identify differentially expressed piRNAs in primary ovarian cancer, recurrent ovarian cancer, and normal ovaries. A large-scale verification study was performed to verify the expression of piR-1919609 in different types of ovarian tissue, including ovarian cancer tissue and normal ovaries, by RT-PCR and to analyze its association with the clinical prognosis of ovarian cancer. The expression of PIWILs in ovarian cancer was verified by RT-PCR, Western blotting and immunofluorescence. The effects of piR-1919609 on ovarian cancer cell proliferation, apoptosis and drug resistance were studied through in vitro and in vivo models.

Results: (1) piR-1919609 was highly expressed in platinum-resistant ovarian cancer tissues (p < 0.05), and this upregulation was significantly associated with a poor prognosis and a shorter recurrence time in ovarian cancer patients (p < 0.05). (2) PIWIL2 was strongly expressed in ovarian cancer tissues (p < 0.05). It was expressed both in the cytoplasm and nucleus of ovarian cancer cells. (3) Overexpression of piR-1919609 promoted ovarian cancer cell proliferation, inhibited apoptosis, and promoted tumor growth in nude mice. (4) Inhibition of piR-1919609 effectively reversed ovarian cancer drug resistance.

Conclusion: In summary, we showed that piR-1919609 is involved in the regulation of drug resistance in ovarian cancer cells and might be an ideal potential target for reversing platinum resistance in ovarian cancer.

piR-1919609 是逆转卵巢癌铂类抗性的理想潜在靶点
目的:PIWI-interacting RNAs(piRNAs)是一种非编码小 RNA,可与 PIWI-like RNA-mediated gene silencing(PIWIL)蛋白相互作用,通过表观遗传效应影响转座子沉默等生物过程。最近的研究发现,piRNA 在肿瘤中广泛失调,并与肿瘤进展和不良预后相关。因此,本研究旨在探讨 piR-1919609 对卵巢癌细胞增殖、凋亡和耐药性的影响:本研究利用小 RNA 测序技术筛选并鉴定了原发性卵巢癌、复发性卵巢癌和正常卵巢中差异表达的 piRNA。通过RT-PCR对piR-1919609在不同类型卵巢组织(包括卵巢癌组织和正常卵巢)中的表达进行了大规模验证研究,并分析了其与卵巢癌临床预后的相关性。通过RT-PCR、Western印迹和免疫荧光等方法验证了PIWILs在卵巢癌中的表达。通过体外和体内模型研究了 piR-1919609 对卵巢癌细胞增殖、凋亡和耐药性的影响:综上所述,我们发现 piR-1919609 参与了卵巢癌细胞耐药性的调控,可能是逆转卵巢癌铂类耐药性的理想潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
202
审稿时长
2 months
期刊介绍: Technology in Cancer Research & Treatment (TCRT) is a JCR-ranked, broad-spectrum, open access, peer-reviewed publication whose aim is to provide researchers and clinicians with a platform to share and discuss developments in the prevention, diagnosis, treatment, and monitoring of cancer.
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