首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Polymorphisms of transforming growth factor beta 1 (RS#1800468 and RS#1800471) and esophageal squamous cell carcinoma among Zhuangese population, China.
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Polymorphisms of transforming growth factor beta 1 (RS#1800468 and RS#1800471) and esophageal squamous cell carcinoma among Zhuangese population, China.

机译:中国壮族人群转化生长因子β1(RS#1800468和RS#1800471)与食管鳞状细胞癌的多态性。

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Epidemiological evidence has shown two polymorphisms (namely RS#1800468G>A and RS#1800471G>C) of transforming growth factor-beta 1 (TGF-β1) gene may be involved in the cancer development. However, their role in the carcinogenic process of esophageal squamous cell carcinoma (ESCC) has been less well elaborated. We conducted a hospital-based case-control study including 391 ESCC cases and 508 controls without any evidence of tumors to evaluate the association between these two polymorphisms and ESCC risk and prognosis for Zhuangese population by means of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and amplification refractory mutation system (ARMS)-PCR techniques. We found that individuals with the genotypes with RS#1800471 C allele (namely RS#1800471-GC or -CC) had an increased risk of ESCC than those without above genotypes (namely RS#1800471-GG, adjusted odds ratio 3.26 and 5.65, respectively). Further stratification analysis showed that this polymorphism was correlated with tumor histological grades and TNM (tumor, node, and metastasis) stage, and modified the serum levels of TGF-β1. Additionally, RS#1800471 polymorphism affected ESCC prognosis (hazard ratio, 3.40), especially under high serum levels of TGF-β1 conditions. However, RS#1800468 polymorphism was not significantly related to ESCC risk. These findings indicated that TGF-β1 RS#1800471G>C polymorphism may be a genetic modifier for developing ESCC in Zhuangese population.
机译:流行病学证据表明,转化生长因子-β1(TGF-β1)基因的两个多态性(即RS#1800468G> A和RS#1800471G> C)可能参与了癌症的发展。但是,它们在食管鳞状细胞癌(ESCC)致癌过程中的作用尚未得到很好的阐述。我们进行了一项基于医院的病例对照研究,包括391例ESCC病例和508例无肿瘤证据的对照,以通过聚合酶链反应-限制性片段长度多态性评估这两个多态性与壮族人群ESCC风险和预后的关系( PCR-RFLP)和扩增难治性突变系统(ARMS)-PCR技术。我们发现具有RS#1800471 C等位基因基因型的个体(即RS#1800471-GC或-CC)比没有以上基因型个体的RSCC风险(即RS#1800471-GG,调整后的优势比为3.26和5.65,分别)。进一步的分层分析表明,该多态性与肿瘤的组织学分级和TNM(肿瘤,淋巴结转移)有关,并改变了血清TGF-β1的水平。此外,RS#1800471多态性影响ESCC的预后(危险比,3.40),尤其是在高血清TGF-β1条件下。但是,RS#1800468多态性与ESCC风险没有显着相关。这些发现表明,TGF-β1RS#1800471G> C多态性可能是在壮族人群中发展ESCC的遗传修饰子。

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