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本文引用的文献

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[miR-182 promotes cell proliferation of cervical cancer cells by targeting adenomatous polyposis coli (APC) gene].[微小RNA-182通过靶向腺瘤性息肉病基因(APC)促进宫颈癌细胞的增殖]
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MicroRNA-744 promotes prostate cancer progression through aberrantly activating Wnt/β-catenin signaling.微小RNA-744通过异常激活Wnt/β-连环蛋白信号通路促进前列腺癌进展。
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Aberrant activation of Wnt/β-catenin signaling drives proliferation of bone sarcoma cells.Wnt/β-连环蛋白信号通路的异常激活驱动骨肉瘤细胞增殖。
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Genetic variants in let-7/Lin28 modulate the risk of oral cavity cancer in a Chinese Han population.let-7/Lin28基因变异对中国汉族人群口腔癌风险的影响
Sci Rep. 2014 Dec 11;4:7434. doi: 10.1038/srep07434.
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Hsa-miRNA-765 as a key mediator for inhibiting growth, migration and invasion in fulvestrant-treated prostate cancer.Hsa-微RNA-765作为氟维司群治疗前列腺癌中抑制生长、迁移和侵袭的关键介质。
PLoS One. 2014 May 16;9(5):e98037. doi: 10.1371/journal.pone.0098037. eCollection 2014.
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Role of oncogenic K-Ras in cancer stem cell activation by aberrant Wnt/β-catenin signaling.致癌性 K-Ras 在异常 Wnt/β-连环蛋白信号通路激活肿瘤干细胞中的作用。
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Developing role of HPV in cervical cancer prevention.人乳头瘤病毒(HPV)在宫颈癌预防中的发展作用。
BMJ. 2013 Aug 7;347:f4781. doi: 10.1136/bmj.f4781.
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Analysing the impact of nucleo-cytoplasmic shuttling of β-catenin and its antagonists APC, Axin and GSK3 on Wnt/β-catenin signalling.分析β-连环蛋白及其拮抗剂 APC、Axin 和 GSK3 的核质穿梭对 Wnt/β-连环蛋白信号通路的影响。
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Prevalence of infection by different genotypes of human papillomavirus in women with cervical pathology.宫颈病变妇女中不同型别 HPV 感染的流行率。
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Aberrant activation of Wnt/β-catenin signaling pathway contributes to the sequential progression of DMBA-induced HBP carcinomas.Wnt/β-catenin 信号通路的异常激活促进了 DMBA 诱导的 HBP 癌的序贯进展。
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微小RNA-182通过激活Wnt/β-连环蛋白轴促进宫颈癌进展。

miR-182 promotes cervical cancer progression via activating the Wnt/β-catenin axis.

作者信息

Gao Fei, Yin Jilai, Wang Yongcun, Li Hao, Wang Daping

机构信息

The First Affiliated Hospital of Hainan Medical College Haikou, Hainan, China.

The Affiliated Hospital of Guangdong Medical University Zhanjiang, Guangdong, China.

出版信息

Am J Cancer Res. 2023 Aug 15;13(8):3591-3598. eCollection 2023.

PMID:37693162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10492123/
Abstract

Cervical cancer (CC) is among the leading causes of cancer-associated mortality in women worldwide; yet the molecular regulators involved in its progression are unclear. This study found that miR-182 was overexpressed in CC tissues when compared with adjacent normal tissues. Moreover, it found that miR-182 expression was significantly positively correlated with distant metastasis in patients with CC. Interestingly, experiments showed that overexpression and inhibition of miR-182 promoted and suppressed the growth of CC cells, respectively. The tumor-promoting effects of miR-182 on CC progression were achieved via the Wnt/β-catenin axis and its downstream genes. Thus, this study revealed the potential of miR-182/β-catenin as an effective new target for CC treatment.

摘要

宫颈癌(CC)是全球女性癌症相关死亡的主要原因之一;然而,其进展过程中涉及的分子调节因子尚不清楚。本研究发现,与相邻正常组织相比,miR-182在CC组织中过表达。此外,研究发现CC患者中miR-182表达与远处转移显著正相关。有趣的是,实验表明,miR-182的过表达和抑制分别促进和抑制了CC细胞的生长。miR-182对CC进展的促肿瘤作用是通过Wnt/β-连环蛋白轴及其下游基因实现的。因此,本研究揭示了miR-182/β-连环蛋白作为CC治疗有效新靶点的潜力。