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本文引用的文献

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Significant association of XPD codon 312 single nucleotide polymorphism with bladder cancer susceptibility in Taiwan.台湾地区XPD基因第312位密码子单核苷酸多态性与膀胱癌易感性的显著关联。
Anticancer Res. 2009 Oct;29(10):3903-7.
2
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Anticancer Res. 2009 Oct;29(10):3897-901.
3
Significant association of Ku80 single nucleotide polymorphisms with colorectal cancer susceptibility in Central Taiwan.台湾中部地区Ku80单核苷酸多态性与结直肠癌易感性的显著关联。
Anticancer Res. 2009 Jun;29(6):2239-42.
4
Significant association of Ku80 single nucleotide polymorphisms with bladder cancer susceptibility in Taiwan.
Anticancer Res. 2009 Apr;29(4):1275-9.
5
Association between DNA double strand break gene Ku80 polymorphisms and oral cancer susceptibility.Ku80 基因双链断裂点多态性与口腔癌易感性的关系。
Oral Oncol. 2009 Sep;45(9):789-93. doi: 10.1016/j.oraloncology.2008.12.002. Epub 2009 Feb 13.
6
Oral cancer and genetic polymorphism of DNA double strand break gene Ku70 in Taiwan.台湾口腔癌与 DNA 双链断裂基因 Ku70 遗传多态性。
Oral Oncol. 2008 Nov;44(11):1047-51. doi: 10.1016/j.oraloncology.2008.02.008. Epub 2008 May 19.
7
A novel single nucleotide polymorphism in XRCC4 gene is associated with oral cancer susceptibility in Taiwanese patients.XRCC4基因中的一种新型单核苷酸多态性与台湾患者的口腔癌易感性相关。
Oral Oncol. 2008 Sep;44(9):898-902. doi: 10.1016/j.oraloncology.2007.11.007. Epub 2008 Mar 4.
8
A novel single nucleotide polymorphism in XRCC4 gene is associated with gastric cancer susceptibility in Taiwan.XRCC4基因中的一种新型单核苷酸多态性与台湾地区的胃癌易感性相关。
Ann Surg Oncol. 2008 Feb;15(2):514-8. doi: 10.1245/s10434-007-9674-3. Epub 2007 Nov 7.
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A novel single nucleotide polymorphism in ERCC6 gene is associated with oral cancer susceptibility in Taiwanese patients.ERCC6基因中的一种新型单核苷酸多态性与台湾患者口腔癌易感性相关。
Oral Oncol. 2008 Jun;44(6):582-6. doi: 10.1016/j.oraloncology.2007.07.006. Epub 2007 Oct 22.
10
Genetic analysis of caveolin-1 and eNOS genes in colorectal cancer.结直肠癌中小窝蛋白-1和内皮型一氧化氮合酶基因的遗传分析。
Oncol Rep. 2006 Aug;16(2):353-9.

台湾腔蛋白-1 多态性与结直肠癌易感性的相关性研究。

Association of Caveolin-1 polymorphisms with colorectal cancer susceptibility in Taiwan.

机构信息

Mei-Due Yang, Chao-Hsiang Chang, Hwei-Chung Wang, Department of Surgery, China Medical University Hospital, 2 Yuh-Der Road, Taichung 404, Taiwan, China.

出版信息

World J Gastrointest Oncol. 2010 Aug 15;2(8):326-31. doi: 10.4251/wjgo.v2.i8.326.

DOI:10.4251/wjgo.v2.i8.326
PMID:21160894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2999679/
Abstract

AIM

To investigate the association of Caveolin-1 (Cav-1) polymorphisms with colorectal cancer (CRC) risk in a central Taiwanese population.

METHODS

Three hundred and sixty-two patients with colorectal cancer and the same number of recruited age- and gender-matched healthy controls were genotyped. And only those matches with all single nucleotide polymorphisms data (case/control = 362/362) were selected for final analyzing.

RESULTS

There were significant differences between CRC and control groups in the distributions of their genotypes (P = 1.6 × 10(-12) and 3.0 × 10(-4)) and allelic frequencies (P = 2.3 × 10(-13) and 4.0 × 10(-5)) in the Cav-1 G14713A (rs3807987) and T29107A (rs7804372) polymorphisms respectively. As for the haplotype analysis, those who had GG/AT or GG/AA at Cav-1 G14713A/T29107A showed a 0.68-fold (95% CI: 0.48-0.98) decreased risk of CRC compared to those with GG/TT, while those of any other combinations were of increased risk. There were joint effects of Cav-1 G14713A and T29107A genotype with smoking status on individual CRC susceptibility.

CONCLUSION

This is the first report providing evidence of Cav-1 being involved in CRC and it may be novel useful genomic markers for early detection of CRC.

摘要

目的

在台湾中部人群中研究窖蛋白-1(Cav-1)多态性与结直肠癌(CRC)风险的相关性。

方法

362 例结直肠癌患者和相同数量的年龄和性别匹配的健康对照者进行基因分型。只有那些具有所有单核苷酸多态性数据的匹配者(病例/对照=362/362)被选择进行最终分析。

结果

CRC 组和对照组在 Cav-1 G14713A(rs3807987)和 T29107A(rs7804372)多态性的基因型分布(P=1.6×10(-12)和 3.0×10(-4))和等位基因频率(P=2.3×10(-13)和 4.0×10(-5))方面存在显著差异。对于单倍型分析,Cav-1 G14713A/T29107A 处 GG/AT 或 GG/AA 的个体发生 CRC 的风险降低了 0.68 倍(95%CI:0.48-0.98),而任何其他组合的个体发生 CRC 的风险增加。Cav-1 G14713A 和 T29107A 基因型与吸烟状态对个体 CRC 易感性存在联合作用。

结论

这是首个报道窖蛋白-1 参与结直肠癌的研究,它可能是 CRC 早期检测的新的有用的基因组标记物。