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Impact of codon 72 Arg > Pro single nucleotide polymorphism in TP53 gene in the risk of kangri cancer: a case control study in Kashmir.

机译:TP53基因密码子72 Arg> Pro单核苷酸多态性对患kangri癌症的影响:克什米尔的病例对照研究。

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摘要

Kangri cancer found only in Kashmir (north India) is a unique thermally induced squamous cell carcinoma of the skin that develops because of chronic and persistent irritation due to the use of a kangri (a brazier) by the Kashmiri people to combat the chilling cold temperature during winter. Being unique to this region, the molecular etiology of the invasive kangri cancer is not known fully. The TP53 gene, codon 72 polymorphism (Arg72Pro), has been found to be associated with cancer susceptibility but has not been investigated in kangri cancer risk. A case control study was conducted to find the genotype distribution of TP53 Arg72Pro SNP and to elucidate the possible role of this SNP as risk factor in kangri cancer development. Using the polymerase chain reaction-restriction fragment length polymorphism approach, we tested the genotype distribution of 106 kangri cancer patients in comparison with 200 cancer-free controls from the same geographical region. A significant difference was observed between the control and kangri cancer patients with odds ratio = 2.02 and 95% confidence interval = 1.2-3.3 (p = 0.01). Interestingly, the proline form was abundantly observed in advanced-grade tumors (p < 0.05). We also found a significant association of the variant allele (GC?+?CC) with male subjects and patients >45 years of age (p < 0.05). Thus, it is evident from our study that Arg72Pro SNP is implicated in kangri cancer and that the rare, proline-related allele is connected with higher susceptibility to kangri cancer.
机译:仅在克什米尔(印度北部)发现的Kangri癌是一种独特的热诱导皮肤鳞状细胞癌,由于克什米尔人使用kangri(火盆)来对抗寒冷的低温而引起的长期持续刺激而发展在冬天。对于该区域而言,浸润性kangri癌的分子病因学尚不完全清楚。 TP53基因,密码子72多态性(Arg72Pro),已被发现与癌症的易感性有关,但尚未在坎格里患癌症的风险中进行过研究。进行了一项病例对照研究,以发现TP53 Arg72Pro SNP的基因型分布,并阐明该SNP作为坎格瑞癌症发展中的危险因素的可能作用。使用聚合酶链反应-限制性片段长度多态性方法,我们测试了106名坎格瑞癌症患者的基因型分布,并比较了来自同一地理区域的200名无癌对照。在对照组和袋鼠癌患者之间观察到显着差异,优势比= 2.02,95%置信区间= 1.2-3.3(p = 0.01)。有趣的是,脯氨酸形式在晚期肿瘤中被大量观察到(p <0.05)。我们还发现,变异等位基因(GC?+?CC)与男性受试者和年龄> 45岁的患者之间存在显着相关性(p <0.05)。因此,从我们的研究中可以明显看出,Arg72Pro SNP与坎格里氏癌有关,而稀有的脯氨酸相关等位基因与坎格里氏癌的易感性有关。

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