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端粒长度和 TERT 功能多态性与头颈部鳞状细胞癌的风险无关。

Telomere length and TERT functional polymorphisms are not associated with risk of squamous cell carcinoma of the head and neck.

机构信息

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2011 Dec;20(12):2642-5. doi: 10.1158/1055-9965.EPI-11-0890. Epub 2011 Oct 12.

DOI:10.1158/1055-9965.EPI-11-0890
PMID:21994403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3237736/
Abstract

BACKGROUND

Recent studies reported associations of the relative telomere length (RTL) and TERT variants with risk of several cancers, which have not been comprehensively investigated in squamous cell carcinoma of the head and neck (SCCHN).

METHODS

We detected RTL in peripheral blood lymphocytes and genotyped six selected functional single-nucleotide polymorphisms (SNP) of the TERT gene in 888 SCCHN cases and 885 cancer-free controls of non-Hispanic whites.

RESULTS

Overall, we did not observe significant associations between RTL and SCCHN risk (adjusted OR = 0.97; 95% CI = 0.80-1.17 for below versus above the median; P(trend) = 0.618) nor between the six TERT SNPs and SCCHN risk. We also found no associations between RTL and TERT SNPs.

CONCLUSIONS

Our results suggest that RTL and TERT functional polymorphisms may not play a major role in the etiology of SCCHN. Large prospective studies are needed to validate our findings.

IMPACT

Although our results suggest no association among RTL, TERT functional polymorphisms, and SCCHN risk, this study may contribute to future meta-analysis.

摘要

背景

最近的研究报告称,相对端粒长度(RTL)和 TERT 变体与多种癌症的风险相关,但这些关联在头颈部鳞状细胞癌(SCCHN)中尚未得到全面研究。

方法

我们检测了 888 例 SCCHN 病例和 885 例非西班牙裔白人无癌对照者外周血淋巴细胞中的 RTL,并对 TERT 基因的 6 个选定功能单核苷酸多态性(SNP)进行了基因分型。

结果

总体而言,我们未观察到 RTL 与 SCCHN 风险之间存在显著关联(校正后的 OR = 0.97;中位数以下与中位数以上相比;P(趋势)= 0.618),也未观察到 6 个 TERT SNP 与 SCCHN 风险之间存在关联。我们还未发现 RTL 与 TERT SNP 之间存在关联。

结论

我们的结果表明,RTL 和 TERT 功能多态性可能在 SCCHN 的发病机制中不起主要作用。需要进行大型前瞻性研究来验证我们的发现。

影响

尽管我们的结果表明 RTL、TERT 功能多态性与 SCCHN 风险之间没有关联,但这项研究可能有助于未来的荟萃分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd56/3237736/3046301f5bff/nihms331262f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd56/3237736/3046301f5bff/nihms331262f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd56/3237736/3046301f5bff/nihms331262f1.jpg

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PLoS One. 2011;6(6):e20466. doi: 10.1371/journal.pone.0020466. Epub 2011 Jun 10.
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Effects of MDM2 promoter polymorphisms and p53 codon 72 polymorphism on risk and age at onset of squamous cell carcinoma of the head and neck.MDM2 启动子多态性和 p53 密码子 72 多态性对头颈部鳞状细胞癌发病风险和发病年龄的影响。
Mol Carcinog. 2011 Sep;50(9):697-706. doi: 10.1002/mc.20806. Epub 2011 Jun 7.
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No association between TERT-CLPTM1L single nucleotide polymorphism rs401681 and mean telomere length or cancer risk.TERT-CLPTM1L 单核苷酸多态性 rs401681 与端粒平均长度或癌症风险之间没有关联。
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Telomere length in prospective and retrospective cancer case-control studies.前瞻性和回顾性癌症病例对照研究中的端粒长度。
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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.端粒酶逆转录酶(TERT)-跨膜蛋白1样蛋白(CLPTM1L)基因座处的序列变异与多种癌症类型相关。
Nat Genet. 2009 Feb;41(2):221-7. doi: 10.1038/ng.296. Epub 2009 Jan 18.
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