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血管内皮生长因子基因多态性与肾细胞癌风险:来自八项病例对照研究的证据。

Vascular endothelial growth factor gene polymorphisms and the risk of renal cell carcinoma: Evidence from eight case-control studies.

作者信息

Gong Mancheng, Dong Wenjing, Shi Zhirong, Qiu Shaopeng, Yuan Runqiang

机构信息

Department of Urology, Zhongshan Affiliated Hospital of Sun Yat-sen University, Zhongshan, Guangdong 528403, China.

Department of Oncology, Zhongshan Affiliated Hospital of Sun Yat-sen University, Zhongshan, Guangdong 528403, China.

出版信息

Oncotarget. 2017 Jan 31;8(5):8447-8458. doi: 10.18632/oncotarget.14263.

Abstract

BACKGROUND

Vascular endothelial growth factor (VEGF) protein plays important role in renal cell carcinoma (RCC) development and progression. VEGF gene polymorphisms can alter the protein concentrations and might be associated with renal cell carcinoma risk. However, the results of studies investigating the association between VEGF polymorphisms and renal cell carcinoma risk are inconsistent. Thus, a meta-analysis was performed.

METHODS

We selected eligible studies via electronic searches. Only high-quality studies were included based on specific inclusion criteria and the Newcastle-Ottawa Scale (NOS).

RESULTS

Eight studies primarily focusing on seven polymorphisms were included in our meta-analysis. Our results showed dramatically high risks for renal cell carcinoma were found regarding most genetic models and alleles of the +936C/T polymorphism (except CT vs. CC). In addition, significant increased renal cell carcinoma risks were found regarding all genetic models and alleles of the -2578C/A polymorphism. However, no significant associations were found between renal cell carcinoma risk and the +1612G/A, -460T/C, -634G/C, -405G/C or -1154G/A polymorphisms.

CONCLUSIONS

Our meta-analysis indicates that the +936C/T and -2578C/A polymorphisms of VEGF are associated with an increased risk for renal cell carcinoma. Additional rigorous analytical studies are needed to confirm our results.

摘要

背景

血管内皮生长因子(VEGF)蛋白在肾细胞癌(RCC)的发生和发展中起重要作用。VEGF基因多态性可改变蛋白浓度,并可能与肾细胞癌风险相关。然而,关于VEGF多态性与肾细胞癌风险之间关联的研究结果并不一致。因此,进行了一项荟萃分析。

方法

我们通过电子检索筛选符合条件的研究。仅纳入基于特定纳入标准和纽卡斯尔-渥太华量表(NOS)的高质量研究。

结果

我们的荟萃分析纳入了八项主要关注七种多态性的研究。我们的结果显示,对于大多数遗传模型以及+936C/T多态性的等位基因(CT与CC比较除外),肾细胞癌风险显著升高。此外,对于-2578C/A多态性的所有遗传模型和等位基因,肾细胞癌风险均显著增加。然而,未发现肾细胞癌风险与+1612G/A、-460T/C、-634G/C、-405G/C或-1154G/A多态性之间存在显著关联。

结论

我们的荟萃分析表明,VEGF的+936C/T和-2578C/A多态性与肾细胞癌风险增加相关。需要更多严格的分析研究来证实我们的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1691/5352413/4e4cd80da950/oncotarget-08-8447-g001.jpg

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