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62例日本隐睾症患者中INSL3和LGR8/GREAT的突变及多态性分析

Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism.

作者信息

Yamazawa Kazuki, Wada Yuka, Sasagawa Isoji, Aoki Katsuya, Ueoka Katsuhiko, Ogata Tsutomu

机构信息

Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan.

出版信息

Horm Res. 2007;67(2):73-6. doi: 10.1159/000096089. Epub 2006 Oct 6.

Abstract

BACKGROUND/AIMS: Although insulin-like factor 3 (INSL3) and its receptor leucine-rich repeat-containing G protein-coupled receptor 8/G protein-coupled receptor affecting testis descent (LGR8/GREAT) are essential for the gubernacular development, mutations of INSL3 and LGR8/GREAT are infrequent in patients with cryptorchidism (CO), and there is no report documenting a positive association of CO with a polymorphism in INSL3 or LGR8/GREAT. Here, we further examined the relevance of INSL3 and LGR8/GREAT mutations and polymorphisms to the development of CO.

METHODS

Sixty-two Japanese CO patients and 60 fertile males were studied. INSL3 was analyzed by direct sequencing and restriction enzyme digestion, and LGR8/GREAT was examined by denaturing high-performance liquid chromatography followed by direct sequencing for exons with abnormal chromatogram patterns.

RESULTS

No definitive mutation was identified in both genes. Six polymorphisms were detected in INSL3 or LGR8/GREAT and Thr/Thr genotype of Ala60Thr polymorphism in INSL3 was strongly associated with CO (p=0.0024, odds ratio=5.3, 95% confidence interval=1.7-17).

CONCLUSION

The results, in conjunction with the previous data, suggest that mutations of INSL3 and LGR8/GREAT remain rare, and that the Thr/Thr genotype of Ala60Thr polymorphism in INSL3 may constitute a susceptibility factor for the development of CO.

摘要

背景/目的:尽管胰岛素样因子3(INSL3)及其受体富含亮氨酸重复序列的G蛋白偶联受体8/影响睾丸下降的G蛋白偶联受体(LGR8/GREAT)对睾丸引带发育至关重要,但隐睾症(CO)患者中INSL3和LGR8/GREAT的突变并不常见,且尚无报道记录CO与INSL3或LGR8/GREAT多态性之间存在正相关。在此,我们进一步研究了INSL3和LGR8/GREAT突变及多态性与CO发生发展的相关性。

方法

对62例日本CO患者和60例有生育能力的男性进行研究。通过直接测序和限制性酶切分析INSL3,通过变性高效液相色谱法检测LGR8/GREAT,然后对色谱图异常的外显子进行直接测序。

结果

在两个基因中均未鉴定出明确的突变。在INSL3或LGR8/GREAT中检测到6种多态性,INSL3中Ala60Thr多态性的Thr/Thr基因型与CO密切相关(p = 0.0024,优势比 = 5.3,95%置信区间 = 1.7 - 17)。

结论

这些结果与先前的数据表明,INSL3和LGR8/GREAT的突变仍然很少见,并且INSL3中Ala60Thr多态性的Thr/Thr基因型可能是CO发生发展的一个易感因素。

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