Per3 VNTR基因型可以预测土耳其人群膀胱癌患者的总生存率

Z. Yeğin, F. Ozen, İ. Yıldırım, Yasin Altinisik, A. Yıldırım
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引用次数: 0

摘要

昼夜节律基因已被证明通过协调各种细胞过程在肿瘤的发生和进展中发挥重要作用。尽管在表达水平和遗传变异分析上的昼夜节律紊乱与许多癌症类型的风险增加有关,但尚未研究PER3 VNTR在膀胱肿瘤发生中的潜在作用。在这项研究中,我们旨在评估PER3 VNTR在膀胱癌形成易感性方面的作用。我们的第二个目标是揭示膀胱癌队列中PER3基因型与临床病理相关性之间的可能关联,从而评估膀胱癌预后的结果。在这项病例对照研究中,招募了116名患者和120名健康对照者。采用标准盐析法从外周血中分离DNA,用PCR技术检测PER3 VNTR变异(ins/del多态性),区分5重复等位基因(401 bp)和4重复等位基因(347 bp)。虽然本探索性分析没有提供PER3 VNTR在膀胱癌发病中的作用的证据,但它使我们能够对膀胱癌患者的预后进行风险评估。PER3 4/4基因型患者组(进展和膀胱切除术阳性)和PER3 4/5基因型患者组(复发、进展和膀胱切除术阳性)患者的生存时间缩短。本研究的结果强烈建议在不同人群和种族的更大样本中进行调查和验证,以推广潜在的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PER3 VNTR GENOTYPES MAY PREDICT OVERALL SURVIVAL IN BLADDER CANCER PATIENTS IN THE TURKISH POPULATION
Circadian genes were proven to play significant roles in tumor development and progression via coordinating various cellular processes. Though circadian rhythm disturbances both on the level of expression and genetic variant analysis have been associated with increased risk for many cancer types, none has investigated the potential effect of PER3 VNTR in bladder tumorigenesis yet. In this study, we aimed to assess PER3 VNTR’s effect in terms of creating susceptibility to bladder carcinoma formation. Our second target was to enlighten the possible associations between PER3 genotypes and clinicopathological correlations in bladder carcinoma cohort and thus evaluate outcomes in bladder carcinoma prognosis. In this case-control study, 116 patients and 120 healthy controls were recruited. DNA was isolated from peripheral blood using the standard salting-out procedure and PER3 VNTR variants (ins/del polymorphism) were determined with PCR technique to distinguish the 5-repeats allele (401 bp) from the 4-repeats allele (347 bp). Though this exploratory analysis did not provide evidence supporting the role of PER3 VNTR in the onset of bladder carcinoma, it enabled us to make a risk assessment for the prognosis of bladder carcinoma patients. The survival times of patients decreased in the patient group (progression and cystectomy positive) for PER3 4/4 genotype and (recurrence, progression and cystectomy positive) for PER3 4/5 genotype. Results presented in this study are highly recommended to be investigated and validated in larger samples in different populations and ethnicities to generalize potential clinical utility.
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