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通过二维(交叉)免疫电泳鉴定宫颈癌中的肿瘤相关抗原。

Identification of a tumor-associated antigen in cervical carcinoma by two dimensional (crossed) immunoelectrophoresis.

作者信息

Chiang W T, Alexander E R, Kenny G E

出版信息

J Natl Cancer Inst. 1977 Jan;58(1):43-8. doi: 10.1093/jnci/58.1.43.

DOI:10.1093/jnci/58.1.43
PMID:833863
Abstract

Two-dimensional immunoelectrophoresis was used to evaluate 8 cervical cancer speciments, 11 other gynecologic tumors, and 5 specimens of normal cervix. Antigens were water-soluble tissue extracts and antisera prepared in rabbits. When tested against antisera to cervical cancer, cancer antigens showed 14-17 precipitin lines whereas normal cervix showed 10-16. A single heavy heterogeneous precipitin line with an electrophoretic mobility of 0.58 relative to bovine albumin was observed in all cervical cancer specimens but not in normal cervical or other tumor specimens. Further evidence for the uniqueness of this antigen was sought by enhancement (addition of another antigen to the first phase of electrophoresis which increased the size of common peaks) and suppression (addition of another antiserum to the second phase, whereby the peak size of components to which both sera have antibody was decreased). The specific precipitin line was neither suppressed by the addition of antisera to normal tissue nor enhanced when normal tissue antigen was added to the tumor antigen preparation. More conclusively, adsorption of the tumor antiserum with normal tissue had no effect on the unique tumor-associated precipitin line, whereas all other precipitin lines were removed. This antigen was common to other cervical tumors because enhancement was demonstrated with three other cervical tumor specimens. The identification of a distinct and separate antigen associated with cervical carcinoma will permit further characterization and possible development of immunodiagnostic methods.

摘要

采用二维免疫电泳法对8份宫颈癌标本、11份其他妇科肿瘤标本及5份正常宫颈标本进行评估。抗原为水溶性组织提取物,抗血清由兔制备。用抗宫颈癌抗血清检测时,癌抗原显示14 - 17条沉淀线,而正常宫颈显示10 - 16条。在所有宫颈癌标本中均观察到一条单一的重异质沉淀线,相对于牛血清白蛋白,其电泳迁移率为0.58,而在正常宫颈或其他肿瘤标本中未观察到。通过增强(在电泳第一阶段添加另一种抗原,增加共同峰的大小)和抑制(在第二阶段添加另一种抗血清,从而降低两种血清均有抗体的成分的峰大小)来寻找该抗原独特性的进一步证据。添加正常组织抗血清时,特异性沉淀线未被抑制,向肿瘤抗原制剂中添加正常组织抗原时,特异性沉淀线也未增强。更具决定性的是,用正常组织吸附肿瘤抗血清对独特的肿瘤相关沉淀线没有影响,而所有其他沉淀线均被去除。该抗原在其他宫颈肿瘤中也存在,因为用另外三份宫颈肿瘤标本证实了增强现象。鉴定出与宫颈癌相关的独特且独立的抗原将有助于进一步表征并可能开发免疫诊断方法。

相似文献

1
Identification of a tumor-associated antigen in cervical carcinoma by two dimensional (crossed) immunoelectrophoresis.通过二维(交叉)免疫电泳鉴定宫颈癌中的肿瘤相关抗原。
J Natl Cancer Inst. 1977 Jan;58(1):43-8. doi: 10.1093/jnci/58.1.43.
2
Identification of beta-oncofetal antigen in cervical squamous cancer and its demonstration in neoplastic and normal tissues.宫颈鳞状癌中β-癌胚抗原的鉴定及其在肿瘤组织和正常组织中的显示
Cancer Res. 1978 May;38(5):1246-9.
3
Demonstration of tumor-associated antigens in human gynecologic malignancies.人类妇科恶性肿瘤中肿瘤相关抗原的显示
Am J Obstet Gynecol. 1973 Feb 1;115(3):387-93. doi: 10.1016/0002-9378(73)90595-4.
4
[A tumor-associated antigen of cervical cancer].[一种宫颈癌相关肿瘤抗原]
Eksp Onkol. 1986;8(2):48-51.
5
[Immunomorphological identification of an antigen associated with squamous cell carcinoma of the cervix uteri].[子宫颈鳞状细胞癌相关抗原的免疫形态学鉴定]
Eksp Onkol. 1988;10(5):33-5.
6
Immunohistochemical demonstration of tumor antigen TA-4 in gynecologic tumors.
Int J Gynecol Pathol. 1984;3(3):291-8. doi: 10.1097/00004347-198403000-00005.
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Radioimmunoassay for tumor antigen of human cervical squamous cell carcinoma.
Cancer. 1977 Oct;40(4):1621-8. doi: 10.1002/1097-0142(197710)40:4<1621::aid-cncr2820400435>3.0.co;2-i.
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Extraction and preliminary characterization of a human bronchogenic carcinoma antigen.一种人支气管源性癌抗原的提取及初步鉴定
Br J Cancer. 1975 Apr;31(4):379-86. doi: 10.1038/bjc.1975.77.
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Cervical carcinoma antigens in the diagnosis of human squamous cell carcinoma of the cervix.宫颈癌抗原在人宫颈鳞状细胞癌诊断中的应用
J Natl Cancer Inst. 1981 Mar;66(3):465-74.
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Tumor-associated antigens in gynecologic cancer.
Clin Obstet Gynecol. 1975 Dec;18(4):87-108. doi: 10.1097/00003081-197512000-00008.

引用本文的文献

1
Products of gynaecological neoplasms: clinical and pathological applications.妇科肿瘤产物:临床及病理应用
Arch Gynecol. 1980;229(4):311-23. doi: 10.1007/BF02108582.