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在乳腺癌患者血清中,抗体W1检测到的一种高分子量抗原水平升高。

Elevated levels of a high molecular weight antigen detected by antibody W1 in sera from breast cancer patients.

作者信息

Linsley P S, Ochs V, Laska S, Horn D, Ring D B, Frankel A E, Brown J P

出版信息

Cancer Res. 1986 Oct;46(10):5444-50.

PMID:2428478
Abstract

A novel screening assay was used to test 13 previously described antibreast cancer antibodies for those which recognize antigens elevated in serum of breast cancer patients. Binding of three of these antibodies to breast or lung carcinoma cells was inhibited to a significantly greater extent by tumor patient serum than by normal serum, suggesting that the antigens might be useful serum markers. Two of these antibodies, W1 and W9, were shown to recognize nonoverlapping epitopes on a high molecular weight molecule(s) purified from serum from breast cancer patients. A sensitive double determinant immunoassay was developed to measure W1 antigen levels in sera from a total of 389 cancer patients and controls. Forty seven % (37 of 79) of individuals having breast cancer showed elevated serum levels of the W1 antigen, whereas only 4% (1 of 25) of normal controls and 2% (1 of 47) of patients hospitalized for nonmalignant disorders showed elevated levels. These differences were statistically significant (P less than 0.001). The percentage of breast cancer patients showing elevated serum levels was greater for individuals with metastatic disease. Statistically significant numbers of lung, ovarian, and prostate, but not colon, cancer patients also had elevated serum levels of the W1 antigen. These data suggest that measurement of the W1 antigen in serum might provide clinically useful information on the course of metastatic breast and other cancers.

摘要

一种新型筛选试验被用于检测13种先前描述的抗乳腺癌抗体,以寻找那些能识别乳腺癌患者血清中升高抗原的抗体。与正常血清相比,肿瘤患者血清对其中三种抗体与乳腺癌或肺癌细胞结合的抑制作用显著更强,这表明这些抗原可能是有用的血清标志物。其中两种抗体W1和W9被证明可识别从乳腺癌患者血清中纯化出的高分子量分子上不重叠的表位。开发了一种灵敏的双决定簇免疫测定法来检测总共389名癌症患者和对照血清中的W1抗原水平。47%(79例中的37例)乳腺癌患者血清中W1抗原水平升高,而正常对照中只有4%(25例中的1例),因非恶性疾病住院的患者中只有2%(47例中的1例)出现升高水平。这些差异具有统计学意义(P小于0.001)。有转移疾病的乳腺癌患者血清水平升高的比例更高。在肺癌、卵巢癌和前列腺癌患者中,血清W1抗原水平升高的人数具有统计学意义,但结肠癌患者中没有。这些数据表明,检测血清中的W1抗原可能为转移性乳腺癌和其他癌症的病程提供临床上有用的信息。

相似文献

1
Elevated levels of a high molecular weight antigen detected by antibody W1 in sera from breast cancer patients.在乳腺癌患者血清中,抗体W1检测到的一种高分子量抗原水平升高。
Cancer Res. 1986 Oct;46(10):5444-50.
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Detection of antigens recognized by a novel monoclonal antibody in tissue and serum from patients with breast cancer.在乳腺癌患者的组织和血清中检测一种新型单克隆抗体识别的抗原。
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Demonstration of elevated anti-Lewis antibodies in sera of cancer patients using a carcinoembryonic antigen-polyethylene glycol immunoassay.使用癌胚抗原-聚乙二醇免疫测定法证明癌症患者血清中抗Lewis抗体升高。
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Heritable variation in expression of multiple tumor associated epitopes on a high molecular weight mucin-like antigen.一种高分子量粘蛋白样抗原上多种肿瘤相关表位表达的可遗传变异。
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引用本文的文献

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Hum Reprod. 2006 Nov;21(11):2783-93. doi: 10.1093/humrep/del164. Epub 2006 Sep 22.
2
Antigen forks: bispecific reagents that inhibit cell growth by binding selected pairs of tumor antigens.抗原叉:通过结合选定的肿瘤抗原对来抑制细胞生长的双特异性试剂。
Cancer Immunol Immunother. 1994 Jul;39(1):41-8. doi: 10.1007/BF01517179.
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Epitope expression on the breast epithelial mucin.
Breast Cancer Res Treat. 1992;24(2):103-13. doi: 10.1007/BF01961243.
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Analysis of a heterogeneous group of human breast carcinoma associated glycoproteins bearing the Tn determinant.对一组携带Tn决定簇的人乳腺癌相关糖蛋白的异质性分析。
Breast Cancer Res Treat. 1994;32(2):139-52. doi: 10.1007/BF00665765.
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Purification and biochemical characterisation of a novel breast carcinoma associated mucin-like glycoprotein defined by antibody 3E1.2.由抗体3E1.2鉴定的一种新型乳腺癌相关粘蛋白样糖蛋白的纯化及生化特性分析
Br J Cancer. 1989 Apr;59(4):544-53. doi: 10.1038/bjc.1989.111.
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Diagnostic ability of different human milk fat globule antigens in breast cancer.
Breast Cancer Res Treat. 1990 May;15(3):161-74. doi: 10.1007/BF01806353.
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Purification and characterisation of a breast-cancer-associated glycoprotein not expressed in normal breast and identified by monoclonal antibody 83D4.一种与乳腺癌相关的糖蛋白的纯化与特性分析,该糖蛋白在正常乳腺中不表达且由单克隆抗体83D4鉴定。
Br J Cancer. 1991 Mar;63(3):390-8. doi: 10.1038/bjc.1991.91.