• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

MicroRNA-154-5p 通过沉默 Cullin2 和. 抑制宫颈癌的生长和转移。

MicroRNA-154-5p suppresses cervical carcinoma growth and metastasis by silencing Cullin2 and .

机构信息

Department of Obstetrics and Gynecology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi Province, China.

Department of Obstetrics and Gynecology, Peking University People's Hospital, Beijing, China.

出版信息

PeerJ. 2023 Jun 27;11:e15641. doi: 10.7717/peerj.15641. eCollection 2023.

DOI:10.7717/peerj.15641
PMID:37397007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10312157/
Abstract

BACKGROUND

MicroRNA-154-5p (miR-154-5p) plays a role in tumorigenesis in diverse human malignancies. Nevertheless, little is known about the mechanism by which miR-154-5p alters the growth and metastasis of cervical cancer. This research aimed to analyze the role of miR-154-5p in the pathology of cervical cancer and .

METHODS

The level of miR-154-5p in human papillomavirus 16 positive cervical cancer cells was examined by real-time quantitative polymerase chain reaction. Bioinformatics predicted the downstream targets and potential functions of miR-154-5p. Furthermore, lentiviral technology was used to construct SiHa cell lines with stable up- and down-expression levels of miR-154-5p. Its differential expression effects on the progress and metastasis of cervical cancer were analyzed using cell culture and animal models.

RESULTS

MiR-154-5p showed low expression in cervical cancer cells. Overexpression of miR-154-5p could markedly inhibit the proliferation, migration, and colony formation ability of SiHa cells, concomitantly leading to G1 arrest of the cell cycle, while silencing miR-154-5p triggered the opposite results. Meanwhile, overexpression of miR-154-5p restrained the growth and metastasis of cervical cancer by silencing CUL2 . Additionally, miR-154-5p reduced CUL2 level, and overexpression of CUL2 influenced the effect of miR-154-5p in cervical cancer. In conclusion, miR-154-5p restrained the growth and metastasis of cervical cancer by directly silencing CUL2.

摘要

背景

MicroRNA-154-5p(miR-154-5p)在多种人类恶性肿瘤的发生中起作用。然而,miR-154-5p 如何改变宫颈癌的生长和转移机制知之甚少。本研究旨在分析 miR-154-5p 在宫颈癌中的作用。

方法

采用实时定量聚合酶链反应检测人乳头瘤病毒 16 阳性宫颈癌细胞中 miR-154-5p 的水平。生物信息学预测了 miR-154-5p 的下游靶标和潜在功能。此外,采用慢病毒技术构建 miR-154-5p 稳定过表达和低表达的 SiHa 细胞系。利用细胞培养和动物模型分析其对宫颈癌进展和转移的差异表达效应。

结果

miR-154-5p 在宫颈癌细胞中表达较低。过表达 miR-154-5p 可显著抑制 SiHa 细胞的增殖、迁移和集落形成能力,同时导致细胞周期 G1 期阻滞,而沉默 miR-154-5p 则引发相反的结果。同时,过表达 miR-154-5p 通过沉默 CUL2 抑制宫颈癌的生长和转移。此外,miR-154-5p 降低了 CUL2 的水平,而过表达 CUL2 影响 miR-154-5p 在宫颈癌中的作用。综上所述,miR-154-5p 通过直接沉默 CUL2 抑制宫颈癌的生长和转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/bc563e5f6e28/peerj-11-15641-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/ef98d62c44f1/peerj-11-15641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/8fb83ce67466/peerj-11-15641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/73954614b0b9/peerj-11-15641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/0b624ea66711/peerj-11-15641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/c1890fef491e/peerj-11-15641-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/a1a600c53846/peerj-11-15641-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/372dee6f668d/peerj-11-15641-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/bc563e5f6e28/peerj-11-15641-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/ef98d62c44f1/peerj-11-15641-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/8fb83ce67466/peerj-11-15641-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/73954614b0b9/peerj-11-15641-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/0b624ea66711/peerj-11-15641-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/c1890fef491e/peerj-11-15641-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/a1a600c53846/peerj-11-15641-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/372dee6f668d/peerj-11-15641-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fbd/10312157/bc563e5f6e28/peerj-11-15641-g008.jpg

相似文献

1
MicroRNA-154-5p suppresses cervical carcinoma growth and metastasis by silencing Cullin2 and .MicroRNA-154-5p 通过沉默 Cullin2 和. 抑制宫颈癌的生长和转移。
PeerJ. 2023 Jun 27;11:e15641. doi: 10.7717/peerj.15641. eCollection 2023.
2
MicroRNA-101-5p inhibits the growth and metastasis of cervical cancer cell by inhibiting CXCL6.微小 RNA-101-5p 通过抑制 CXCL6 抑制宫颈癌细胞的生长和转移。
Eur Rev Med Pharmacol Sci. 2019 Mar;23(5):1957-1968. doi: 10.26355/eurrev_201903_17234.
3
MicroRNA-125a-5p modulates human cervical carcinoma proliferation and migration by targeting ABL2.微小RNA-125a-5p通过靶向ABL2调节人宫颈癌的增殖和迁移。
Drug Des Devel Ther. 2015 Dec 24;10:71-9. doi: 10.2147/DDDT.S93104. eCollection 2016.
4
MicroRNA-140-5p targets insulin like growth factor 2 mRNA binding protein 1 (IGF2BP1) to suppress cervical cancer growth and metastasis.微小RNA-140-5p靶向胰岛素样生长因子2 mRNA结合蛋白1(IGF2BP1)以抑制宫颈癌的生长和转移。
Oncotarget. 2016 Oct 18;7(42):68397-68411. doi: 10.18632/oncotarget.11722.
5
MicroRNA-154-5p regulates the HPV16 E7-pRb pathway in Cervical Carcinogenesis by targeting CUL2.微小RNA-154-5p通过靶向CUL2调控宫颈癌发生中的HPV16 E7-pRb通路。
J Cancer. 2020 Jul 11;11(18):5379-5389. doi: 10.7150/jca.45871. eCollection 2020.
6
Transferrin receptor modulated by microRNA-497-5p suppresses cervical cancer cell malignant phenotypes.miRNA-497-5p 调控转铁蛋白受体抑制宫颈癌恶性表型。
Adv Clin Exp Med. 2024 Mar;33(3):273-282. doi: 10.17219/acem/168342.
7
miR-150-5p promotes the proliferation and epithelial-mesenchymal transition of cervical carcinoma cells via targeting SRCIN1.微小RNA-150-5p通过靶向SRCIN1促进宫颈癌细胞的增殖和上皮-间质转化。
Pathol Res Pract. 2019 Apr;215(4):738-747. doi: 10.1016/j.prp.2019.01.004. Epub 2019 Jan 7.
8
MicroRNA-96-5p Facilitates the Viability, Migration, and Invasion and Suppresses the Apoptosis of Cervical Cancer Cells byNegatively Modulating SFRP4.微小 RNA-96-5p 通过负向调控 SFRP4 促进宫颈癌细胞的活力、迁移和侵袭,抑制细胞凋亡。
Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820934132. doi: 10.1177/1533033820934132.
9
miR-199a-5p promotes proliferation and metastasis and epithelial-mesenchymal transition through targeting PIAS3 in cervical carcinoma.miR-199a-5p 通过靶向调控 PIAS3 促进宫颈癌的增殖、转移及上皮间质转化。
J Cell Biochem. 2019 Aug;120(8):13562-13572. doi: 10.1002/jcb.28631. Epub 2019 Apr 1.
10
Serum miR-486-5p as a diagnostic marker in cervical cancer: with investigation of potential mechanisms.血清 miR-486-5p 作为宫颈癌的诊断标志物:潜在机制的研究。
BMC Cancer. 2018 Jan 9;18(1):61. doi: 10.1186/s12885-017-3753-z.

引用本文的文献

1
Exploring the Mechanism of Acupuncture in Improving Ovarian Function in Rats with Poor Ovarian Response Using High-Throughput Sequencing.运用高通量测序技术探究针刺改善卵巢反应不良大鼠卵巢功能的机制
Comb Chem High Throughput Screen. 2025;28(8):1443-1457. doi: 10.2174/0113862073365843241223093834.
2
Targeted regulation of miR-154-5p/Cullin2 pathway by hsa_circ_TRIM22 in promoting human papillomavirus 16 positive cervical cancer progression.hsa_circ_TRIM22对miR-154-5p/Cullin2通路的靶向调控在促进人乳头瘤病毒16型阳性宫颈癌进展中的作用
J Cancer. 2024 Feb 24;15(8):2137-2146. doi: 10.7150/jca.92631. eCollection 2024.
3

本文引用的文献

1
The hsa_circ_0000276-ceRNA regulatory network and immune infiltration in cervical cancer.环状 RNA hsa_circ_0000276 通过 ceRNA 调控网络调控宫颈癌的免疫浸润。
BMC Cancer. 2023 Mar 9;23(1):222. doi: 10.1186/s12885-023-10636-5.
2
Autophagy as a self-digestion signal in human cancers: Regulation by microRNAs in affecting carcinogenesis and therapy response.自噬作为人类癌症中的自我消化信号:microRNAs 对其的调控在影响癌症发生和治疗反应中的作用。
Pharmacol Res. 2023 Mar;189:106695. doi: 10.1016/j.phrs.2023.106695. Epub 2023 Feb 11.
3
MicroRNAs: Key modulators of inflammation-associated diseases.
MicroRNAs, long non-coding RNAs, and circular RNAs and gynecological cancers: focus on metastasis.
微小RNA、长链非编码RNA和环状RNA与妇科癌症:聚焦转移
Front Oncol. 2023 Oct 3;13:1215194. doi: 10.3389/fonc.2023.1215194. eCollection 2023.
微小RNA:炎症相关疾病的关键调节因子。
Semin Cell Dev Biol. 2024 Feb 15;154(Pt C):364-373. doi: 10.1016/j.semcdb.2023.01.009. Epub 2023 Jan 18.
4
MicroRNA let-7f-5p regulates PI3K/AKT/COX2 signaling pathway in bacteria-induced pulmonary fibrosis via targeting of in forest musk deer.微小 RNA let-7f-5p 通过靶向 调控细菌诱导的肺纤维化中 PI3K/AKT/COX2 信号通路。
PeerJ. 2022 Oct 5;10:e14097. doi: 10.7717/peerj.14097. eCollection 2022.
5
The potential of CircRNA1002 as a biomarker in hepatitis B virus-related hepatocellular carcinoma.环状 RNA1002 作为乙型肝炎病毒相关肝细胞癌生物标志物的潜力。
PeerJ. 2022 Jun 28;10:e13640. doi: 10.7717/peerj.13640. eCollection 2022.
6
The sphingosine kinase inhibitor SKI-V suppresses cervical cancer cell growth.鞘氨醇激酶抑制剂 SKI-V 抑制宫颈癌细胞生长。
Int J Biol Sci. 2022 Apr 18;18(7):2994-3005. doi: 10.7150/ijbs.71381. eCollection 2022.
7
A novel prognostic model for hepatocellular carcinoma based on 5 microRNAs related to vascular invasion.基于与血管侵犯相关的 5 个 microRNAs 的新型肝细胞癌预后模型。
BMC Med Genomics. 2022 Feb 24;15(1):34. doi: 10.1186/s12920-022-01162-7.
8
MiR-126-5p Promotes Tumor Cell Proliferation, Metastasis and Invasion by Targeting TDO2 in Hepatocellular Carcinoma.miR-126-5p 通过靶向 TD02 促进肝癌细胞增殖、转移和侵袭。
Molecules. 2022 Jan 10;27(2):443. doi: 10.3390/molecules27020443.
9
Molecular Markers to Predict Prognosis and Treatment Response in Uterine Cervical Cancer.预测子宫颈癌预后和治疗反应的分子标志物
Cancers (Basel). 2021 Nov 17;13(22):5748. doi: 10.3390/cancers13225748.
10
Time to infer miRNA sponge modules.推断 miRNA 海绵模块的时间。
Wiley Interdiscip Rev RNA. 2022 Mar;13(2):e1686. doi: 10.1002/wrna.1686. Epub 2021 Aug 3.