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胰腺癌中 E-选择素 S128R 基因多态性分析。

Analysis of E-Selectin S128R gene polymorphism in pancreatic cancer.

机构信息

First Propaedeutic Surgical Department, Hippocration University Hospital, University of Athens, Athens, Greece.

出版信息

J Surg Oncol. 2010 Nov 1;102(6):604-7. doi: 10.1002/jso.21648.

DOI:10.1002/jso.21648
PMID:20607758
Abstract

BACKGROUND

E-selectin, an intercellular adhesion molecule that plays important roles in metastasis of tumor cells, has a polymorphism in exon 4 that results in the substitution of a serine by an arginine within the extracellular domain of the receptor, which increases its affinity for ligands. No evidence exist on the role of E-selectin polymorphism in pancreatic cancer.

METHODS

Eighty pancreatic cancer patients and 160 cases of normal healthy control subjects were investigated for genotype and allelic frequencies of S128R polymorphism of E-selectin gene by PCR-RFLPs.

RESULTS

The frequencies for "AA," "CA," and "CC" genotypes were 46.25%, 50%, and 3.75% in patients, and 63.75%, 26.9%, and 9.4% in healthy subjects, respectively. The "C" carriers group of patients ("CA + CC" genotype) and the "C" allele were over-represented among the pancreatic cancer cases (P = 0.012 and 0.096, respectively). Advanced T stage, the presence of lymph node and other adverse pathologic characteristics were not significantly correlated with either the "CA + CC" genotype group of patients or the presence of "C" allele.

CONCLUSIONS

E-selectin S128R "C" allele may confer an increased susceptibility to pancreatic cancer development, while its carriage status does not appear to be related to the aggressive features of this malignancy.

摘要

背景

E-选择素是一种细胞间黏附分子,在肿瘤细胞转移中发挥重要作用,其外显子 4 中的一个多态性导致受体细胞外结构域中丝氨酸被精氨酸取代,从而增加了其与配体的亲和力。目前尚无关于 E-选择素多态性在胰腺癌中作用的证据。

方法

通过 PCR-RFLPs 方法,对 80 例胰腺癌患者和 160 例正常健康对照者的 E-选择素基因 S128R 多态性的基因型和等位基因频率进行了研究。

结果

患者中“AA”、“CA”和“CC”基因型的频率分别为 46.25%、50%和 3.75%,健康对照组分别为 63.75%、26.9%和 9.4%。患者中“C”携带者组(“CA+CC”基因型)和“C”等位基因的频率均高于胰腺癌病例(P=0.012 和 0.096)。晚期 T 分期、淋巴结转移和其他不良病理特征与患者的“CA+CC”基因型组或“C”等位基因均无显著相关性。

结论

E-选择素 S128R“C”等位基因可能增加了胰腺癌发生的易感性,但其携带状态似乎与这种恶性肿瘤的侵袭性特征无关。

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