• 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

RAN 基因多态性与癌症风险关联的系统评价和荟萃分析。

A Systematic Review and Meta-Analysis for the Association of Gene Polymorphisms in RAN with Cancer Risk.

机构信息

Department of Anorectal Surgery, The First Hospital of China Medical University, Shenyang, Liaoning 110001, China.

出版信息

Dis Markers. 2020 Jan 16;2020:9026707. doi: 10.1155/2020/9026707. eCollection 2020.

DOI:10.1155/2020/9026707
PMID:32015773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6985935/
Abstract

As an important component of miRNA processing genes, RAN gene encodes the ras-related nuclear protein, which is a unique member of the Ras superfamily of GTPases. The mutations in RAN gene are very likely to play a critical role in pathology-related changes to miRNA transport and expression and thus participate in tumor genesis and development. Currently, accumulating studies have explored the association between RAN SNPs and cancer risk. However, the results are conflicting. In the present study, we performed a systematic review for the association of RAN SNPs with overall cancer risk. Meanwhile, a meta-analysis was conducted based on available data, aiming at clarifying the association between RAN SNPs and cancer susceptibility. After literature search and data extraction, 17 studies containing four RAN SNPs were involved in the systematic review. And 12 studies with two highly studied SNPs (RAN rs14035 C>T and rs3803012 A>G) were included in the final meta-analysis, consisting of 7662 cases and 9807 controls. The results showed that the rs14035 polymorphism was linked to a decreased cancer risk in overall subjects and hospital-based (HB) subgroup, while the rs3803012 polymorphism conferred to an increased cancer risk in overall subjects and population-based (PB) subgroup. Our findings suggested that the two SNPs had the potential to be predictive biomarkers for cancer risk. The study would provide novel clues for the identification of miRNA-related genetic biomarkers applied to predicting cancer susceptibility.

摘要

作为 miRNA 加工基因的重要组成部分,RAN 基因编码 Ras 相关核蛋白,它是 Ras 家族 GTP 酶的独特成员。RAN 基因的突变很可能在 miRNA 转运和表达的病理学相关变化中发挥关键作用,从而参与肿瘤的发生和发展。目前,越来越多的研究探讨了 RAN SNPs 与癌症风险之间的关联。然而,结果却存在矛盾。在本研究中,我们对 RAN SNPs 与总体癌症风险之间的关联进行了系统评价。同时,基于现有数据进行了荟萃分析,旨在阐明 RAN SNPs 与癌症易感性之间的关联。经过文献检索和数据提取,共有 17 项研究包含四个 RAN SNPs 纳入了系统评价。最终荟萃分析纳入了 12 项研究,其中包括两个高度研究的 SNPs(RAN rs14035 C>T 和 rs3803012 A>G),共包含 7662 例病例和 9807 例对照。结果表明,rs14035 多态性与总体和医院人群(HB)亚组的癌症风险降低相关,而 rs3803012 多态性与总体和人群(PB)亚组的癌症风险增加相关。我们的研究结果表明,这两个 SNP 可能是癌症风险的预测生物标志物。该研究为鉴定 miRNA 相关遗传生物标志物应用于预测癌症易感性提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7c/6985935/3ed1edf6d91c/DM2020-9026707.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7c/6985935/9fb6840b5503/DM2020-9026707.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7c/6985935/3ed1edf6d91c/DM2020-9026707.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7c/6985935/9fb6840b5503/DM2020-9026707.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7c/6985935/3ed1edf6d91c/DM2020-9026707.002.jpg

相似文献

1
A Systematic Review and Meta-Analysis for the Association of Gene Polymorphisms in RAN with Cancer Risk.RAN 基因多态性与癌症风险关联的系统评价和荟萃分析。
Dis Markers. 2020 Jan 16;2020:9026707. doi: 10.1155/2020/9026707. eCollection 2020.
2
3'-UTR Polymorphisms in the MiRNA Machinery Genes DROSHA, DICER1, RAN, and XPO5 Are Associated with Colorectal Cancer Risk in a Korean Population.微小RNA加工基因DROSHA、DICER1、RAN和XPO5的3'-非翻译区多态性与韩国人群的结直肠癌风险相关。
PLoS One. 2015 Jul 6;10(7):e0131125. doi: 10.1371/journal.pone.0131125. eCollection 2015.
3
Potentially functional genetic variants in microRNA processing genes and risk of HBV-related hepatocellular carcinoma.miRNA 加工基因中潜在功能的遗传变异与 HBV 相关肝细胞癌的风险。
Mol Carcinog. 2013 Nov;52 Suppl 1:E148-54. doi: 10.1002/mc.22062. Epub 2013 Jul 19.
4
Genetic variants in DICER1, DROSHA, RAN, and XPO5 genes and risk of pregnancy-induced hypertension.DICER1、DROSHA、RAN 和 XPO5 基因中的遗传变异与妊娠高血压的风险。
Pregnancy Hypertens. 2019 Apr;16:161-166. doi: 10.1016/j.preghy.2019.04.005. Epub 2019 Apr 16.
5
Investigation of the association of the (rs14035) and (rs11077) polymorphisms with venous thromboembolism.研究 (rs14035)和 (rs11077)多态性与静脉血栓栓塞的关系。
Rom J Intern Med. 2023 Jun 13;61(3):154-162. doi: 10.2478/rjim-2023-0014. Print 2023 Sep 1.
6
polymorphisms and neuroblastoma risk in Chinese children: a three-center case-control study.中国儿童的多态性与神经母细胞瘤风险:一项三中心病例对照研究
Aging (Albany NY). 2018 Apr 28;10(4):808-818. doi: 10.18632/aging.101429.
7
Association of microRNA biosynthesis genes XPO5 and RAN polymorphisms with cancer susceptibility: Bayesian hierarchical meta-analysis.微小RNA生物合成基因XPO5和RAN多态性与癌症易感性的关联:贝叶斯分层荟萃分析
J Cancer. 2020 Feb 3;11(8):2181-2191. doi: 10.7150/jca.37150. eCollection 2020.
8
Association of RAN and RANBP2 Gene Polymorphisms With Glioma Susceptibility in Chinese Children.RAN 和 RANBP2 基因多态性与中国儿童脑胶质瘤易感性的关联。
Cancer Rep (Hoboken). 2024 Jul;7(7):e2136. doi: 10.1002/cnr2.2136.
9
Variation in the Dicer and RAN Genes Are Associated with Survival in Patients with Hepatocellular Carcinoma.Dicer基因和RAN基因的变异与肝细胞癌患者的生存率相关。
PLoS One. 2016 Sep 9;11(9):e0162279. doi: 10.1371/journal.pone.0162279. eCollection 2016.
10
[The Association Between the Polymorphisms of miRNA Biogenesis Related Genes( and )and Unexplained Recurrent Spontaneous Abortion in Chinese Women].[微小RNA生物合成相关基因多态性与中国女性不明原因复发性自然流产的关联]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2017 Nov;48(6):880-885.

引用本文的文献

1
Genetic Variation in MiRNA Processing Machinery Genes and Susceptibility to Colorectal Cancer in the Iranian Population.伊朗人群中微小RNA加工机制基因的遗传变异与结直肠癌易感性
Iran J Public Health. 2024 Dec;53(12):2812-2822.
2
Unleash Multifunctional Role of miRNA Biogenesis Gene Variants ( and ) with Susceptibility to Hepatocellular Carcinoma.释放微小RNA生物合成基因变异体(和)在肝细胞癌易感性中的多功能作用。
J Pers Med. 2023 Jun 6;13(6):959. doi: 10.3390/jpm13060959.
3
Ran GTPase: A Key Player in Tumor Progression and Metastasis.Ran GTP酶:肿瘤进展和转移中的关键因子

本文引用的文献

1
Comprehensive assessment and meta-analysis of the association between CTNNB1 polymorphisms and cancer risk.CTNNB1 多态性与癌症风险的综合评估和荟萃分析。
Biosci Rep. 2017 Nov 23;37(6). doi: 10.1042/BSR20171121. Print 2017 Dec 22.
2
A systematic review and meta-analysis of the association between long non-coding RNA polymorphisms and cancer risk.长非编码 RNA 多态性与癌症风险关联的系统评价和荟萃分析。
Mutat Res Rev Mutat Res. 2017 Jan-Mar;771:1-14. doi: 10.1016/j.mrrev.2016.10.002. Epub 2016 Nov 5.
3
Genetic variant in DICER gene is associated with prognosis of hepatocellular carcinoma in a Chinese cohort.
Front Cell Dev Biol. 2020 May 26;8:345. doi: 10.3389/fcell.2020.00345. eCollection 2020.
DICER基因的遗传变异与中国人群队列中肝细胞癌的预后相关。
Hepatol Res. 2017 Aug;47(9):845-853. doi: 10.1111/hepr.12824. Epub 2016 Nov 7.
4
Variation in the Dicer and RAN Genes Are Associated with Survival in Patients with Hepatocellular Carcinoma.Dicer基因和RAN基因的变异与肝细胞癌患者的生存率相关。
PLoS One. 2016 Sep 9;11(9):e0162279. doi: 10.1371/journal.pone.0162279. eCollection 2016.
5
Association of Polymorphic Variants of miRNA Processing Genes with Larynx Cancer Risk in a Polish Population.波兰人群中miRNA加工基因多态性变异与喉癌风险的关联
Biomed Res Int. 2015;2015:298378. doi: 10.1155/2015/298378. Epub 2015 Nov 25.
6
3'-UTR Polymorphisms in the MiRNA Machinery Genes DROSHA, DICER1, RAN, and XPO5 Are Associated with Colorectal Cancer Risk in a Korean Population.微小RNA加工基因DROSHA、DICER1、RAN和XPO5的3'-非翻译区多态性与韩国人群的结直肠癌风险相关。
PLoS One. 2015 Jul 6;10(7):e0131125. doi: 10.1371/journal.pone.0131125. eCollection 2015.
7
A 3'UTR polymorphism modulates mRNA stability of the oncogene and drug target Polo-like Kinase 1.一种3'非翻译区多态性调节癌基因及药物靶点Polo样激酶1的mRNA稳定性。
Mol Cancer. 2014 Apr 26;13:87. doi: 10.1186/1476-4598-13-87.
8
Genetic variants in RAN, DICER and HIWI of microRNA biogenesis genes and risk of cervical carcinoma in a Chinese population.中国人群中 miRNA 生物发生基因 RAN、DICER 和 HIWI 的遗传变异与宫颈癌风险。
Chin J Cancer Res. 2013 Oct;25(5):565-71. doi: 10.3978/j.issn.1000-9604.2013.10.03.
9
Potentially functional genetic variants in microRNA processing genes and risk of HBV-related hepatocellular carcinoma.miRNA 加工基因中潜在功能的遗传变异与 HBV 相关肝细胞癌的风险。
Mol Carcinog. 2013 Nov;52 Suppl 1:E148-54. doi: 10.1002/mc.22062. Epub 2013 Jul 19.
10
Evaluation of genetic variants in microRNA biosynthesis genes and risk of breast cancer in Chinese women.评估 miRNA 生物合成基因中的遗传变异与中国女性乳腺癌风险的关系。
Int J Cancer. 2013 Nov;133(9):2216-24. doi: 10.1002/ijc.28237. Epub 2013 Jul 11.