SIPA1基因多态性与埃及女性乳腺癌风险:一项初步研究

A. Mackawy, O. Megahed
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The present study relied on the hypothesis that Sipa1 gene may be contributed to the risk of breast cancer occurrence and aggressiveness as well.Objective: We aimed to examine the association of SIPA1 single nucleotide polymorphisms (SNPs) and human breast cancer incidence and prognosis in Egyptian female patients.Patient and Methods: Two common SNPs (rs3741378 C>T and rs746429 A>G) were genotyped in 80 Egyptian females; 50 patients with breast cancer and 30 breast carcinoma free females.Results: The rs3741378 TT genotype enhanced the incidence of breast carcinoma in comparison with the genotypes rs3741378 CC and TC (X2=7.08, P=0.029), Sipa 1 rs3741378 T allele had a high frequency in BC cases compared to controls (OR (95%)=2.593 (1.339-5.02), P=0.04). Sipa 1 rs3741378 TT genotype also displayed significant association with clinical stages, grades and lymph node metastasis (X2=12.73, P=0.013), (X2=10.88, P=0.028), (X2=6.534, P=0.010; OR (95%)=0.324 [0.134-0.781]), respectively. 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摘要

背景:已知多种基因影响肿瘤转移,但种系遗传多态性对肿瘤易感性和转移的影响尚不清楚。信号诱导增殖相关基因1 (SIPA1)被认为是乳腺癌(BC)转移过程中的一个修饰因子。Sipa - 1基因的分子研究表明其在细胞粘附调节和转移调节中具有重要作用。目前的研究基于Sipa1基因可能与乳腺癌发生和侵袭性风险有关的假设。目的:探讨SIPA1单核苷酸多态性(snp)与埃及女性乳腺癌发病率和预后的关系。患者和方法:对80名埃及女性的两个常见snp (rs3741378 C>T和rs746429 A>G)进行基因分型;50例乳腺癌患者和30例无乳腺癌女性。结果:与rs3741378 CC和TC基因型相比,rs3741378 TT基因型增加了乳腺癌的发病率(X2=7.08, P=0.029), sipa1 rs3741378 T等位基因在BC病例中出现的频率高于对照组(OR (95%)=2.593 (1.339 ~ 5.02), P=0.04)。Sipa 1 rs3741378 TT基因型与临床分期、分级、淋巴结转移也有显著相关性(X2=12.73, P=0.013)、(X2=10.88, P=0.028)、(X2=6.534, P=0.010;OR(95%)=0.324[0.134-0.781])。指出携带rs3741378 TT基因型的患者具有更高的肿瘤进展率和晚期肿瘤分级。相反,在rs746429 A>G中没有检测到这些关联。结论:我们的研究结果表明Sipa1启动子rs3741378 C>T SNP与BC风险和进展有关,可能被认为是BC风险和进展的预测性生物标志物。
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SIPA1 Gene Polymorphisms And The Risk Of Breast Carcinoma Among The Egyptian Females: A Pilot Study
Background: Multiple genes are known to influence the cancer metastasis but the effect of the germline heritable genetic polymorphisms on the predisposition and metastasis is not yet well known. Signal-induced proliferation associated gene1 (SIPA1) was considered as a modifying factor in the breast carcinoma (BC) metastasis process. Molecular studies on Sipa 1 gene suggested its essential role as cell adhesion regulator and metastasis modulator. The present study relied on the hypothesis that Sipa1 gene may be contributed to the risk of breast cancer occurrence and aggressiveness as well.Objective: We aimed to examine the association of SIPA1 single nucleotide polymorphisms (SNPs) and human breast cancer incidence and prognosis in Egyptian female patients.Patient and Methods: Two common SNPs (rs3741378 C>T and rs746429 A>G) were genotyped in 80 Egyptian females; 50 patients with breast cancer and 30 breast carcinoma free females.Results: The rs3741378 TT genotype enhanced the incidence of breast carcinoma in comparison with the genotypes rs3741378 CC and TC (X2=7.08, P=0.029), Sipa 1 rs3741378 T allele had a high frequency in BC cases compared to controls (OR (95%)=2.593 (1.339-5.02), P=0.04). Sipa 1 rs3741378 TT genotype also displayed significant association with clinical stages, grades and lymph node metastasis (X2=12.73, P=0.013), (X2=10.88, P=0.028), (X2=6.534, P=0.010; OR (95%)=0.324 [0.134-0.781]), respectively. Pointing to those patients carrying the rs3741378 TT genotype had a higher tumor progression rate with advanced tumor grades. Oppositely, these associations could not be detected for rs746429 A>G.Conclusion: Our results suggest that the Sipa1 promoter rs3741378 C>T SNP was contributed to BC risk and progression, which may be considered as a foretelling biomarker of BC risk and progression.
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