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Bcl-2 编码区单核苷酸多态性与结直肠癌发生及预后的关系:一项病例对照研究。

Association of single nucleotide polymorphisms in the coding region of Bcl-2 with the occurrence and prognosis of colorectal cancer: A case-control study.

机构信息

Department of Laboratory, Yantai Yuhuangding Hospital, Yantai 264000, Shandong, China.

Department of Pediatrics, Yantai Yuhuangding Hospital, Yantai 264000, Shandong, China.

出版信息

Cancer Biomark. 2017;18(4):433-439. doi: 10.3233/CBM-160378.

DOI:10.3233/CBM-160378
PMID:28106544
Abstract

OBJECTIVE

To investigate the relationship of single nucleotide polymorphisms in the coding region of Bcl-2 with the occurrence and prognosis of colorectal cancer (CRC).

METHODS

Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay was used detect Bcl-2 gene polymorphisms (rs1800477A/G and rs1801018A/G) in 185 patients with CRC (case group) and 177 healthy subjects (control group). The relationships of Bcl-2 gene polymorphisms with clinicopathological features and prognosis of CRC patients were analyzed.

RESULTS

The frequency of GG genotype and G allele of rs1800477A/G in the case group were significantly higher than those in the control group (both P < 0.05). The GG genotype of rs1800477A/G was associated with lymph node metastasis and Dukes' staging of CRC (both P < 0.05). Haplotype analysis demonstrated that the case group had decreased frequency of GA haplotype, but increased frequency of GG haplotype in comparisons to the control group (GA: P = 0.014; GG: P = 0.003). Kaplan-Meier survival analysis showed that the risk of death (within 5 years) in patients carrying GG genotype (rs1800477A/G) was 2.159 as much as that in patients carrying AA + GA genotype. Multivariate analyses showed that Dukes' staging and GG genotype of rs1800477A/G are risk factors for poor prognosis in CRC (Dukes' staging: P = 0.001; GG genotype: P = 0.034).

CONCLUSION

Bcl-2 rs1800477A/G polymorphism may be related to the occurrence of CRC, and GG genotype could be a risk factor of poor prognosis in CRC.

摘要

目的

探讨 Bcl-2 编码区单核苷酸多态性与结直肠癌(CRC)发生发展及预后的关系。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测 185 例 CRC 患者(病例组)和 177 例健康对照者(对照组)的 Bcl-2 基因多态性(rs1800477A/G 和 rs1801018A/G),分析 Bcl-2 基因多态性与 CRC 患者临床病理特征及预后的关系。

结果

病例组 rs1800477A/G 中 GG 基因型和 G 等位基因频率显著高于对照组(均 P<0.05)。rs1800477A/G 的 GG 基因型与 CRC 的淋巴结转移和 Dukes 分期有关(均 P<0.05)。单体型分析显示,与对照组相比,病例组 GA 单体型频率降低,而 GG 单体型频率增加(GA:P=0.014;GG:P=0.003)。Kaplan-Meier 生存分析显示,携带 GG 基因型(rs1800477A/G)的患者死亡风险(5 年内)是携带 AA+GA 基因型患者的 2.159 倍。多因素分析显示,Dukes 分期和 rs1800477A/G 的 GG 基因型是 CRC 预后不良的危险因素(Dukes 分期:P=0.001;GG 基因型:P=0.034)。

结论

Bcl-2 rs1800477A/G 多态性可能与 CRC 的发生有关,GG 基因型可能是 CRC 预后不良的危险因素。

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