Rudchenko Sergei, Scanlan Matthew, Kalantarov Gavreel, Yavelsky Victoria, Levy Chen, Estabrook Alison, Old Lloyd, Chan Gerald L, Lobel Leslie, Trakht Ilya
College of Physicians and Surgeons, Columbia University, 630 W, 168 St,, New York, NY 10032, USA.
BMC Cancer. 2008 Aug 24;8:248. doi: 10.1186/1471-2407-8-248.
We have been studying the native autoimmune response to cancer through the isolation of human monoclonal antibodies that are cancer specific from cancer patients. To facilitate this work we previously developed a fusion partner cell line for human lymphocytes, MFP-2, that fuses efficiently with both human lymph node lymphocytes and peripheral blood lymphocytes. Using this unique trioma fusion partner cell line we isolated a panel of autologous human monoclonal antibodies, from both peripheral blood and lymph node lymphocytes, which are representative of the native repertoire of anti-cancer specific antibodies from breast cancer patients.
The current study employs immunocytochemistry, immunohistochemistry, Western blot analysis as well as Northern blots, Scatchard binding studies and finally SEREX analysis for target antigen identification.
By application of an expression cloning technique known as SEREX, we determined that the target antigen for two monoclonal antibodies, 27.B1 and 27.F7, derived from lymph node B-cells of a breast cancer patient, is the PDZ domain-containing protein known as GIPC1. This protein is highly expressed not only in cultured human breast cancer cells, but also in primary and metastatic tumor tissues and its overexpression appears to be cancer cell specific. Confocal microscopy revealed cell membrane and cytoplasmic localization of the target protein, which is consistent with previous studies of this protein.
We have determined that GIPC1 is a novel breast cancer-associated immunogenic antigen that is overexpressed in breast cancer. Its role, however, in the initiation and/or progression of breast cancer remains unclear and needs further clarification.
我们一直在通过从癌症患者中分离出癌症特异性的人单克隆抗体来研究对癌症的天然自身免疫反应。为了便于开展这项工作,我们之前为人淋巴细胞开发了一种融合伙伴细胞系MFP - 2,它能与人类淋巴结淋巴细胞和外周血淋巴细胞高效融合。利用这种独特的三瘤融合伙伴细胞系,我们从外周血和淋巴结淋巴细胞中分离出了一组自体人单克隆抗体,这些抗体代表了乳腺癌患者抗癌特异性抗体的天然库。
当前研究采用免疫细胞化学、免疫组织化学、蛋白质印迹分析以及Northern印迹、Scatchard结合研究,最后通过SEREX分析来鉴定靶抗原。
通过应用一种名为SEREX的表达克隆技术,我们确定了来自一名乳腺癌患者淋巴结B细胞的两种单克隆抗体27.B1和27.F7的靶抗原是一种名为GIPC1的含PDZ结构域的蛋白质。这种蛋白质不仅在培养的人乳腺癌细胞中高度表达,而且在原发性和转移性肿瘤组织中也高度表达,其过表达似乎具有癌细胞特异性。共聚焦显微镜显示靶蛋白定位于细胞膜和细胞质,这与之前对该蛋白的研究一致。
我们已经确定GIPC1是一种在乳腺癌中过表达的新型乳腺癌相关免疫原性抗原。然而,其在乳腺癌发生和/或发展中的作用仍不清楚,需要进一步阐明。