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谷胱甘肽S-转移酶胎盘型在人胃癌中的癌胚表达。

Oncofetal expression of glutathione S-transferase placental form in human stomach carcinomas.

作者信息

Tsutsumi M, Sugisaki T, Makino T, Miyagi N, Nakatani K, Shiratori T, Takahashi S, Konishi Y

出版信息

Jpn J Cancer Res. 1987 Jul;78(7):631-3.

PMID:3114191
Abstract

The content of glutathione S-transferase placental form (GST-pi) was immunohistochemically analyzed in 100 cases of human stomach carcinoma of various histological types and compared with the content in the stomach mucosa of the human fetus, infant and adult. High levels of GST-pi content were demonstrated in all stomach carcinomas except for signet ring cell carcinomas. High levels were also present in surface mucous cells and glandular cells of the stomach from a fetus aged 18 weeks, whereas only the parietal cells of fundic glands in the adult stomach showed slight staining for GST-pi. These results indicate that the phenotypic expression of GST-pi in human stomach carcinoma is oncofetal in character.

摘要

采用免疫组织化学方法分析了100例不同组织学类型的人胃癌中谷胱甘肽S-转移酶胎盘型(GST-pi)的含量,并与人类胎儿、婴儿及成人胃黏膜中的含量进行比较。除印戒细胞癌外,所有胃癌中均显示出高水平的GST-pi含量。18周龄胎儿胃的表面黏液细胞和腺细胞中也存在高水平的GST-pi,而成年胃中仅胃底腺的壁细胞显示出轻微的GST-pi染色。这些结果表明,GST-pi在人胃癌中的表型表达具有肿瘤胎儿性特征。

相似文献

1
Oncofetal expression of glutathione S-transferase placental form in human stomach carcinomas.谷胱甘肽S-转移酶胎盘型在人胃癌中的癌胚表达。
Jpn J Cancer Res. 1987 Jul;78(7):631-3.
2
Human placental form of glutathione S-transferase (GST-pi) as a new immunohistochemical marker for human colonic carcinoma.人胎盘型谷胱甘肽S-转移酶(GST-pi)作为人结肠癌的一种新的免疫组织化学标志物。
Jpn J Cancer Res. 1986 Mar;77(3):226-9.
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Immunohistochemical determination of glutathione S-transferases in gastric carcinomas and in adjacent normal gastric epithelium.
Anticancer Res. 1996 Mar-Apr;16(2):565-71.
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Elevation of the placental glutathione S-transferase form (GST-pi) in tumor tissues and the levels in sera of patients with cancer.肿瘤组织中胎盘型谷胱甘肽S-转移酶(GST-pi)的升高及癌症患者血清中的水平。
Cancer Res. 1989 Sep 15;49(18):5225-9.
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Immunohistochemical detection of the placental form of glutathione S-transferase in dysplastic and neoplastic human uterine cervix lesions.
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[Expression of pi glutathione S-transferase in intestinal metaplasia and its relationship with Helicobacter pylori infection].[π谷胱甘肽S转移酶在肠化生中的表达及其与幽门螺杆菌感染的关系]
Zhonghua Yi Xue Za Zhi. 2002 Aug 10;82(15):1033-6.
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[Expression and significance of MRP, GST-pi, Topo IIalpha, and LRP in gastric carcinoma].[多药耐药相关蛋白、谷胱甘肽S转移酶π、拓扑异构酶Ⅱα及肺耐药蛋白在胃癌中的表达及意义]
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[Value of immunohistochemical investigation of anti-GST-pi antibody in the early diagnosis of gastric carcinoma and precancerous lesion].[抗谷胱甘肽 S-转移酶π抗体免疫组化检测在胃癌及癌前病变早期诊断中的价值]
Zhonghua Zhong Liu Za Zhi. 1989 Mar;11(2):114-6.
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Glutathione S-transferase-pi in malignant tissues and plasma of human colorectal and gastric cancers.人结直肠癌和胃癌恶性组织及血浆中的谷胱甘肽S-转移酶π
J Cancer Res Clin Oncol. 2002 Feb;128(2):91-5. doi: 10.1007/s00432-001-0300-7. Epub 2001 Dec 13.
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Silencing and CpG island methylation of GSTP1 is rare in ordinary gastric carcinomas but common in Epstein-Barr virus-associated gastric carcinomas.谷胱甘肽S-转移酶P1(GSTP1)的沉默和CpG岛甲基化在普通胃癌中少见,但在爱泼斯坦-巴尔病毒相关胃癌中常见。
Anticancer Res. 2005 Nov-Dec;25(6B):4013-9.

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Discovery of tumor markers for gastric cancer by proteomics.蛋白质组学发现胃癌的肿瘤标志物。
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2
Immunohistochemical localization of glutathione S-transferase-pi in human colorectal polyps.谷胱甘肽S-转移酶π在人结肠息肉中的免疫组织化学定位
World J Gastroenterol. 2008 Jul 14;14(26):4179-84. doi: 10.3748/wjg.14.4179.
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Overexpression of glutathione S-transferase pi messenger RNA and its relationship to gene amplification in head and neck squamous cell carcinoma.
谷胱甘肽S-转移酶π信使核糖核酸在头颈部鳞状细胞癌中的过表达及其与基因扩增的关系。
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Glutathione-related enzymes, glutathione and multidrug resistance.谷胱甘肽相关酶、谷胱甘肽与多药耐药性
Cytotechnology. 1993;12(1-3):155-70. doi: 10.1007/BF00744663.
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The expression of placental-type glutathione S-transferase (GST-pi) in human cutaneous squamous cell carcinoma and normal human skin.
Virchows Arch. 1995;425(6):589-92. doi: 10.1007/BF00199348.
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Glutathione S-transferases and hepatocarcinogenesis.谷胱甘肽S-转移酶与肝癌发生
Jpn J Cancer Res. 1988 May;79(5):556-72. doi: 10.1111/j.1349-7006.1988.tb00022.x.