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欧洲人群胃癌中的雌激素和孕激素受体以及pS2和ERD5抗原

Estrogen and progesterone receptors and pS2 and ERD5 antigens in gastric carcinomas from the European population.

作者信息

Chaubert P, Bouzourene H, Saraga E

机构信息

Institut Universitaire de Pathologie, Lausanne, Switzerland.

出版信息

Mod Pathol. 1996 Mar;9(3):189-93.

PMID:8685212
Abstract

We examined immunohistochemically 50 gastric carcinomas from European patients for estrogen receptors, progesterone receptors, and hormone-receptor-related proteins pS2 and ERD5. Unlike gastric carcinomas from non-Europeans reported previously, the carcinomas of the present series were all negative for estrogen and progesterone receptors. One-half of them, however, expressed pS2, and three-fourths were positive for ERD5. pS2 expression was significantly more frequent in carcinomas of the diffuse type than in those of the intestinal type and in advanced carcinomas compared with early ones. Our results indicate that pS2 and ERD5 are estrogen independent in the stomach. The possibility that estrogen and progesterone receptor status could be different in gastric carcinomas from Occidental and non-Occidental patients is discussed.

摘要

我们采用免疫组织化学方法检测了50例欧洲患者的胃癌组织,以检测雌激素受体、孕激素受体以及与激素受体相关的蛋白pS2和ERD5。与先前报道的非欧洲人胃癌不同,本系列研究中的胃癌雌激素和孕激素受体均为阴性。然而,其中一半表达pS2,四分之三ERD5呈阳性。弥漫型胃癌中pS2表达明显高于肠型胃癌,进展期胃癌高于早期胃癌。我们的结果表明,胃中pS2和ERD5与雌激素无关。本文还讨论了西方和非西方患者胃癌中雌激素和孕激素受体状态可能存在差异的可能性。

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Mod Pathol. 1996 Mar;9(3):189-93.
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Turk Patoloji Derg. 2021;37(3):203-211. doi: 10.5146/tjpath.2021.01529.
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Expression profile and prognostic role of sex hormone receptors in gastric cancer.性激素受体在胃癌中的表达谱及预后作用。
BMC Cancer. 2012 Dec 2;12:566. doi: 10.1186/1471-2407-12-566.
3
Androgen receptor (AR) expression is an independent unfavorable prognostic factor in gastric cancer.雄激素受体(AR)表达是胃癌中一个独立的不良预后因素。
J Cancer Res Clin Oncol. 2004 May;130(5):253-8. doi: 10.1007/s00432-003-0531-x. Epub 2004 Feb 13.
4
Loss of pS2 protein expression is an early event of intestinal-type gastric cancer.pS2蛋白表达缺失是肠型胃癌的早期事件。
Jpn J Cancer Res. 1998 Mar;89(3):278-82. doi: 10.1111/j.1349-7006.1998.tb00559.x.