Pandith Arshad A, Khan Nighat P, Rashid Nargis, Azad Niyaz, Zaroo Inam, Hafiz Adil, Siddiqi Mushtaq A
Department of Immunology and Molecular Medicine, Sher-I-Kashmir Institute of Medical Sciences, Soura, Srinagar, Kashmir, India 190011.
Tumour Biol. 2012 Aug;33(4):927-33. doi: 10.1007/s13277-012-0318-2. Epub 2012 Jan 17.
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.
康日癌仅在克什米尔地区(印度北部)被发现,是一种独特的热诱导皮肤鳞状细胞癌,它是由于克什米尔人在冬季使用康日(一种火盆)来抵御寒冷而导致的慢性持续性刺激所引发的。由于该癌症在这一地区具有独特性,其侵袭性康日癌的分子病因尚未完全明确。TP53基因的72位密码子多态性(Arg72Pro)已被发现与癌症易感性相关,但尚未在康日癌风险方面进行研究。本研究开展了一项病例对照研究,以确定TP53 Arg72Pro单核苷酸多态性的基因型分布,并阐明该单核苷酸多态性作为康日癌发生风险因素的可能作用。我们采用聚合酶链反应-限制性片段长度多态性方法,检测了106例康日癌患者的基因型分布,并与来自同一地理区域的200名无癌对照者进行比较。在对照组和康日癌患者之间观察到显著差异,优势比 = 2.02,95%置信区间 = 1.2 - 3.3(p = 0.01)。有趣的是,在高级别肿瘤中大量观察到脯氨酸形式(p < 0.05)。我们还发现变异等位基因(GC + CC)与男性受试者以及年龄大于45岁的患者存在显著关联(p < 0.05)。因此,从我们的研究中可以明显看出,Arg72Pro单核苷酸多态性与康日癌有关,并且罕见的、与脯氨酸相关的等位基因与康日癌的易感性较高有关。