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本文引用的文献

1
Advances in intravesical therapy for the treatment of non-muscle invasive bladder cancer (Review).非肌层浸润性膀胱癌膀胱内治疗的进展(综述)
Mol Clin Oncol. 2014 Sep;2(5):656-660. doi: 10.3892/mco.2014.314. Epub 2014 Jun 12.
2
Intervention on toll-like receptors in pancreatic cancer.胰腺癌中Toll样受体的干预措施
World J Gastroenterol. 2014 May 21;20(19):5808-17. doi: 10.3748/wjg.v20.i19.5808.
3
Toll-like receptors in esophageal cancer.食管癌中的Toll样受体
Front Immunol. 2014 May 7;5:200. doi: 10.3389/fimmu.2014.00200. eCollection 2014.
4
Platelet-derived growth factor receptor beta: a novel urinary biomarker for recurrence of non-muscle-invasive bladder cancer.血小板衍生生长因子受体β:一种用于非肌层浸润性膀胱癌复发的新型尿液生物标志物。
PLoS One. 2014 May 6;9(5):e96671. doi: 10.1371/journal.pone.0096671. eCollection 2014.
5
Toll-like receptors and skin cancer.Toll样受体与皮肤癌。
Front Immunol. 2014 Mar 31;5:135. doi: 10.3389/fimmu.2014.00135. eCollection 2014.
6
Perioperative chemotherapy for muscle-invasive bladder cancer: A population-based outcomes study.肌层浸润性膀胱癌的围手术期化疗:基于人群的结局研究。
Cancer. 2014 Jun 1;120(11):1630-8. doi: 10.1002/cncr.28510. Epub 2014 Apr 14.
7
Effect of TLR4 and B7-H1 on immune escape of urothelial bladder cancer and its clinical significance.TLR4和B7-H1对膀胱尿路上皮癌免疫逃逸的影响及其临床意义
Asian Pac J Cancer Prev. 2014;15(3):1321-6. doi: 10.7314/apjcp.2014.15.3.1321.
8
Association between microRNA polymorphisms and cancer risk based on the findings of 66 case-control studies.基于66项病例对照研究结果的微小RNA多态性与癌症风险之间的关联。
PLoS One. 2013 Nov 20;8(11):e79584. doi: 10.1371/journal.pone.0079584. eCollection 2013.
9
TLR9 signaling in the tumor microenvironment initiates cancer recurrence after radiotherapy.肿瘤微环境中的 TLR9 信号转导启动放疗后癌症复发。
Cancer Res. 2013 Dec 15;73(24):7211-21. doi: 10.1158/0008-5472.CAN-13-1314. Epub 2013 Oct 23.
10
Links between Toll-like receptor 4 and breast cancer.Toll样受体4与乳腺癌之间的联系。
Oncoimmunology. 2013 Feb 1;2(2):e22945. doi: 10.4161/onci.22945.

Toll样受体信号通路基因的微小RNA结合位点中的遗传变异与膀胱癌易感性之间的关联检测。

Association detection between genetic variants in the microRNA binding sites of toll-like receptors signaling pathway genes and bladder cancer susceptibility.

作者信息

Cheng Sihang, Liu Jiaming, Zhang Yonggang, Lin Yifei, Liu Qinyu, Li Hong, Huang Jin, Zhang Peng

机构信息

Department of Urology, West China Hospital, Sichuan University Guoxuexiang 37, Chengdu 610041, Sichuan, China.

The Periodical Press of West China Hospital, Sichuan University Guoxuexiang 37, Chengdu 610041, Sichuan, China.

出版信息

Int J Clin Exp Pathol. 2014 Oct 15;7(11):8118-26. eCollection 2014.

PMID:25550860
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4270586/
Abstract

Bladder cancer (BCa) is the second most common urological malignancy, and the incidence of BCa has dramatically increased recently. Various toll-like receptors (TLRs) signaling pathway proteins were proven to be associated with BCa susceptibility. However, the effect of genetic variants in TLRs signaling pathway genes on risk of BCa has not been elucidated clearly. Previous studies mainly focused on the coding region of target genes, while in this study, polymorphisms in the non-coding region, microRNA (miRNA) binding sites were investigated as potential targets. We used bioinformatics approach to screen 100 BCa related TLRs signaling pathway genes. Candidate polymorphisms were select in this region and 8 polymorphisms were confirmed. Rs72552316, located at the 3'UTR of the TLR7 gene, exhibited significant association with risk of BCa, indicating a strong relationship with decreased risk of BCa (P ≤ 0.0001). Furthermore, no association was detected between all the polymorphisms and recurrence-free survival time of overall study population or non-muscle invasive BCa subgroups. In conclusion, rs72552316 in the miRNA binding sites of TLR7 might contribute to BCa susceptibility, and this finding provided new targets for high BCa risk population screening.

摘要

膀胱癌(BCa)是第二常见的泌尿系统恶性肿瘤,且其发病率近来急剧上升。各种Toll样受体(TLR)信号通路蛋白已被证明与BCa易感性相关。然而,TLR信号通路基因中的遗传变异对BCa风险的影响尚未得到明确阐明。以往的研究主要集中在靶基因的编码区,而在本研究中,非编码区、微小RNA(miRNA)结合位点的多态性被作为潜在靶点进行研究。我们采用生物信息学方法筛选了100个与BCa相关的TLR信号通路基因。在该区域选择了候选多态性位点,并确认了8个多态性位点。位于TLR7基因3'UTR的Rs72552316与BCa风险显著相关,表明其与BCa风险降低存在密切关系(P≤0.0001)。此外,在所有多态性位点与总体研究人群或非肌层浸润性BCa亚组的无复发生存时间之间未检测到关联。总之,TLR7的miRNA结合位点中的rs72552316可能与BCa易感性有关,这一发现为BCa高危人群筛查提供了新的靶点。