• 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

MIR155HG 变异与汉族人群结直肠癌易感性分析。

Analysis of MIR155HG variants and colorectal cancer susceptibility in Han Chinese population.

机构信息

Surgical Oncology, The Second Affiliated Hospital of Hainan Medical College, Haikou, Hainan Province, China.

出版信息

Mol Genet Genomic Med. 2019 Aug;7(8):e778. doi: 10.1002/mgg3.778. Epub 2019 Jun 22.

DOI:10.1002/mgg3.778
PMID:31228357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6687631/
Abstract

BACKGROUND

MIR155HG plays an important role in malignant tumors, but it is rarely reported in the occurrence and development of colorectal cancer (CRC). This study investigated the effects of MIR155HG polymorphisms on CRC susceptibility from the perspective of molecular genetics.

METHODS

Eight SNPs in MIR155HG were selected and genotyped among 514 CRC cases and 510 healthy controls using the Agena MassARRAY platform. The associations between these SNPs and the CRC risk were evaluated under genetic models using conditional logistic regression analysis. The HaploReg v4.1 database was used for SNPs functional prediction.

RESULTS

The allele "C" of rs12482371 (p = 0.047), allele "C" of rs1893650 (p = 0.025), and the allele "A" of rs928883 (p = 0.037) in MIR155HG were significantly associated with CRC risk. Genetic model analysis revealed that rs12482371 and rs1893650 increased CRC risk; whereas rs928883 was associated with reduced CRC risk. Stratification analysis showed that rs9383938 was a protective factor in CRC patients under 60 years old. Rs12482371 and rs1893650 were associated with the CRC risk in females. Rs11911469 and rs34904192 may affect the clinical stage and lymph node metastasis. Moreover, the haplotypes CTT and GTC of LD block rs4143370|rs77218221|rs12482371, and the haplotypes CATGA and CACGG of LD block rs77699734|rs11911469|rs1893650|rs34904192|rs928883 were significantly associated with CRC risk.

CONCLUSION

This study revealed that MIR155HG SNPs were associated with CRC susceptibility and could be predictive biomarkers for CRC risk.

摘要

背景

MIR155HG 在恶性肿瘤中发挥着重要作用,但在结直肠癌(CRC)的发生和发展中却鲜有报道。本研究从分子遗传学角度探讨了 MIR155HG 多态性对 CRC 易感性的影响。

方法

在 514 例 CRC 病例和 510 例健康对照中,使用 Agena MassARRAY 平台选择 MIR155HG 中的 8 个 SNP 进行基因分型。采用条件逻辑回归分析,在遗传模型下评估这些 SNP 与 CRC 风险的相关性。使用 HaploReg v4.1 数据库对 SNP 功能进行预测。

结果

MIR155HG 中的 rs12482371 (p=0.047)、rs1893650 (p=0.025)和 rs928883 (p=0.037)的等位基因“C”与 CRC 风险显著相关。遗传模型分析显示,rs12482371 和 rs1893650 增加了 CRC 风险;而 rs928883 与降低 CRC 风险相关。分层分析显示,rs9383938 是 60 岁以下 CRC 患者的保护因素。rs12482371 和 rs1893650 与女性 CRC 风险相关。rs11911469 和 rs34904192 可能影响临床分期和淋巴结转移。此外,LD 块 rs4143370|rs77218221|rs12482371 的 CTT 和 GTC 单体型以及 LD 块 rs77699734|rs11911469|rs1893650|rs34904192|rs928883 的 CATGA 和 CACGG 单体型与 CRC 风险显著相关。

结论

本研究表明 MIR155HG SNP 与 CRC 易感性相关,可能是 CRC 风险的预测生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8408/6687631/daa3e4190fd6/MGG3-7-e778-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8408/6687631/daa3e4190fd6/MGG3-7-e778-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8408/6687631/daa3e4190fd6/MGG3-7-e778-g001.jpg

相似文献

1
Analysis of MIR155HG variants and colorectal cancer susceptibility in Han Chinese population.MIR155HG 变异与汉族人群结直肠癌易感性分析。
Mol Genet Genomic Med. 2019 Aug;7(8):e778. doi: 10.1002/mgg3.778. Epub 2019 Jun 22.
2
MiRNA155HG polymorphisms influenced the risk of liver cancer among the Han Chinese population.miRNA155HG 多态性影响汉族人群肝癌的发病风险。
BMC Med Genet. 2020 Jun 19;21(1):134. doi: 10.1186/s12881-020-01064-4.
3
The Single Nucleotide Polymorphisms rs4143370 and rs34904192 in MIR155HG Were Associated with Esophageal Cancer Risk in the Chinese Han Population.单核苷酸多态性 rs4143370 和 rs34904192 位于 MIR155HG 与中国汉族人群的食管癌风险相关。
Digestion. 2023;104(3):222-232. doi: 10.1159/000527751. Epub 2023 Jan 16.
4
Analysis of the relationship between MIR155HG variants and gastric Cancer susceptibility.MIR155HG 变异与胃癌易感性的关系分析。
BMC Gastroenterol. 2020 Jan 20;20(1):17. doi: 10.1186/s12876-020-1169-8.
5
Association of MIR17HG and MIR155HG gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China.中国北方人群中 MIR17HG 和 MIR155HG 基因变异与激素性股骨头坏死的关联。
J Orthop Surg Res. 2021 Nov 15;16(1):673. doi: 10.1186/s13018-021-02669-y.
6
IL1A polymorphisms is a risk factor for colorectal cancer in Chinese Han population: a case control study.白细胞介素 1A 多态性是中国汉族人群结直肠癌的危险因素:一项病例对照研究。
BMC Cancer. 2019 Feb 28;19(1):181. doi: 10.1186/s12885-019-5395-9.
7
C5orf66 rs4976270/rs639933 Are Associated with Colorectal Cancer Risk in Southern Chinese Han Population: A Case-Control Study.C5orf66 rs4976270/rs639933 与华南汉族人群结直肠癌风险相关:一项病例对照研究。
Digestion. 2022;103(2):103-115. doi: 10.1159/000518519. Epub 2021 Oct 12.
8
Association of miR-155 and MIR155HG polymorphisms with cancer risk: A meta-analysis.miR-155 和 MIR155HG 多态性与癌症风险的关联:荟萃分析。
J Cancer Res Ther. 2021 Nov;17(5):1209-1218. doi: 10.4103/jcrt.jcrt_913_21.
9
Genetic polymorphisms in the telomere length-related gene ACYP2 are associated with the risk of colorectal cancer in a Chinese Han population.端粒长度相关基因ACYP2的基因多态性与中国汉族人群患结直肠癌的风险相关。
Oncotarget. 2017 Feb 7;8(6):9849-9857. doi: 10.18632/oncotarget.14219.
10
Association between polymorphisms of MIR17HG and risk of colorectal cancer in the Chinese Han population.MIR17HG 多态性与中国汉族人群结直肠癌风险的关联。
Mol Genet Genomic Med. 2019 Jun;7(6):e667. doi: 10.1002/mgg3.667. Epub 2019 Apr 3.

引用本文的文献

1
Clinical significance of long non-coding RNA MIR155HG genetic variants and susceptibility to oral cancer.长链非编码RNA MIR155HG基因变异与口腔癌易感性的临床意义
Sci Rep. 2025 Mar 22;15(1):9956. doi: 10.1038/s41598-025-94661-3.
2
The relationship of miR-155 host gene polymorphism in the susceptibility of cancer: a systematic review and meta-analysis.miR-155宿主基因多态性与癌症易感性的关系:一项系统评价和荟萃分析。
Front Genet. 2025 Mar 6;16:1517513. doi: 10.3389/fgene.2025.1517513. eCollection 2025.
3
Association of HOTAIR, MIR155HG, TERC, miR-155, -196a2, and -146a Genes Polymorphisms with Papillary Thyroid Cancer Susceptibility and Prognosis.

本文引用的文献

1
lncRNAs in Non-Malignant Tissue Have Prognostic Value in Colorectal Cancer.非恶性组织中的 lncRNAs 在结直肠癌中具有预后价值。
Int J Mol Sci. 2018 Sep 8;19(9):2672. doi: 10.3390/ijms19092672.
2
MicroRNA-155 acts as a tumor suppressor in colorectal cancer by targeting CTHRC1 .微小RNA-155通过靶向CTHRC1在结直肠癌中发挥肿瘤抑制作用。
Oncol Lett. 2018 Apr;15(4):5561-5568. doi: 10.3892/ol.2018.8069. Epub 2018 Feb 16.
3
Deep intronic mutations and human disease.内含子深处的突变与人类疾病。
HOTAIR、MIR155HG、TERC、miR-155、-196a2和-146a基因多态性与甲状腺乳头状癌易感性及预后的相关性
Cancers (Basel). 2024 Jan 23;16(3):485. doi: 10.3390/cancers16030485.
4
Regulatory Roles of Noncoding RNAs in the Progression of Gastrointestinal Cancers and Health Disparities.非编码 RNA 在胃肠道癌进展和健康差异中的调控作用。
Cells. 2022 Aug 7;11(15):2448. doi: 10.3390/cells11152448.
5
Association of MIR17HG and MIR155HG gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China.中国北方人群中 MIR17HG 和 MIR155HG 基因变异与激素性股骨头坏死的关联。
J Orthop Surg Res. 2021 Nov 15;16(1):673. doi: 10.1186/s13018-021-02669-y.
6
LncRNA MIR155HG induces M2 macrophage polarization and drug resistance of colorectal cancer cells by regulating ANXA2.长链非编码 RNA MIR155HG 通过调节 ANXA2 诱导结直肠癌细胞 M2 巨噬细胞极化和耐药性。
Cancer Immunol Immunother. 2022 May;71(5):1075-1091. doi: 10.1007/s00262-021-03055-7. Epub 2021 Sep 25.
7
MiRNA155HG polymorphisms influenced the risk of liver cancer among the Han Chinese population.miRNA155HG 多态性影响汉族人群肝癌的发病风险。
BMC Med Genet. 2020 Jun 19;21(1):134. doi: 10.1186/s12881-020-01064-4.
Hum Genet. 2017 Sep;136(9):1093-1111. doi: 10.1007/s00439-017-1809-4. Epub 2017 May 12.
4
Blocking MIR155HG/miR-155 axis inhibits mesenchymal transition in glioma.阻断 MIR155HG/miR-155 轴抑制胶质瘤中的间充质转化。
Neuro Oncol. 2017 Sep 1;19(9):1195-1205. doi: 10.1093/neuonc/nox017.
5
Loss of oncogenic miR-155 in tumor cells promotes tumor growth by enhancing C/EBP-β-mediated MDSC infiltration.肿瘤细胞中致癌性miR-155的缺失通过增强C/EBP-β介导的髓源性抑制细胞浸润来促进肿瘤生长。
Oncotarget. 2016 Mar 8;7(10):11094-112. doi: 10.18632/oncotarget.7150.
6
Association of Tag SNPs and Rare CNVs of the MIR155HG/miR-155 Gene with Epilepsy in the Chinese Han Population.中国汉族人群中MIR155HG/miR - 155基因的标签单核苷酸多态性和罕见拷贝数变异与癫痫的关联
Biomed Res Int. 2015;2015:837213. doi: 10.1155/2015/837213. Epub 2015 Sep 6.
7
The updated incidences and mortalities of major cancers in China, 2011.2011年中国主要癌症的最新发病率和死亡率。
Chin J Cancer. 2015 Sep 14;34(11):502-7. doi: 10.1186/s40880-015-0042-6.
8
Association of colorectal cancer susceptibility variants with esophageal cancer in a Chinese population.中国人群中结直肠癌易感性变异与食管癌的关联
World J Gastroenterol. 2015 Jun 14;21(22):6898-904. doi: 10.3748/wjg.v21.i22.6898.
9
LncRNAs: New Players in Apoptosis Control.长链非编码RNA:细胞凋亡调控中的新角色
Int J Cell Biol. 2014;2014:473857. doi: 10.1155/2014/473857. Epub 2014 Jan 30.
10
Genetic association of PLCE1, C11orf92-C11orf93, and NOC3L with colorectal cancer risk in the Han population.PLCE1、C11orf92 - C11orf93和NOC3L与汉族人群结直肠癌风险的遗传关联。
Tumour Biol. 2014 Mar;35(3):1813-7. doi: 10.1007/s13277-013-1242-9. Epub 2013 Oct 22.