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首页> 外文期刊>Virchows Archiv >Expression of MAGE-C1/CT7 and selected cancer/testis antigens in ovarian borderline tumours and primary and recurrent ovarian carcinomas
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Expression of MAGE-C1/CT7 and selected cancer/testis antigens in ovarian borderline tumours and primary and recurrent ovarian carcinomas

机译:MAGE-C1 / CT7和某些癌/睾丸抗原在卵巢交界性肿瘤以及原发性和复发性卵巢癌中的表达

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MAGE-C1/CT7, NY-ESO-1, GAGE and MAGE-A4 are members of the cancer/testis (CT) antigen family, which have been proposed as potential targets for cancer immunotherapy. To determine the prevalence and biologic relevance of the novel CT antigen MAGE-C1/CT7 and other antigens, 36 ovarian borderline tumours (BTs), 230 primary ovarian carcinomas (OCs) and 80 recurrent OCs were immunohistochemically analysed using the monoclonal antibodies CT7-33 (MAGE-C1/CT7), E978 (NY-ESO-1), clone 26 (GAGE) and 57B (MAGE-A4). Positivity of at least one CT antigen was present in 39.5 % (81/205) of primary OC and in 50 % (26/52) of all recurrences. Expression of the novel CT antigen MAGE-C1/CT7 was most commonly seen with positivity in 24.5 % of primary and 35.1 % of recurrent OC. MAGE-A4, GAGE and NY-ESO-1 expressions were seen in 22.7, 13.9 and 7.1 % of primary and 22.6, 17.5 and 8.9 % of recurrent OC, respectively. Analysis of histological subtypes (serous, endometrioid, clear cell, mucinous and transitional) exhibited variable expression with negativity in all mucinous OC. High-grade serous OC revealed CT antigen expression in 5.6 to 28 % with MAGE-C1/CT7 being the most frequent, but without correlation with stage or overall survival. MAGE-C1/CT7 expression and coexpression of CT antigens were significantly correlated with grade of endometrioid OC. None of the BT showed CT antigen expression. No significant correlation was seen with stage, overall survival or response to chemotherapy. In summary, CT antigens are expressed in a certain subset of OC with no expression in BT or OC of mucinous histology. These findings may have implications for the design of polyvalent vaccination strategies for ovarian carcinomas.
机译:MAGE-C1 / CT7,NY-ESO-1,GAGE和MAGE-A4是癌症/睾丸(CT)抗原家族的成员,已被提议作为癌症免疫疗法的潜在靶标。为了确定新型CT抗原MAGE-C1 / CT7和其他抗原的患病率和生物学相关性,使用单克隆抗体CT7-33对36例卵巢交界性肿瘤(BTs),230例原发性卵巢癌(OCs)和80例复发性OCs进行了免疫组织化学分析。 (MAGE-C1 / CT7),E978(NY-ESO-1),克隆26(GAGE)和57B(MAGE-A4)。在原发性OC的39.5%(81/205)和所有复发的50%(26/52)中存在至少一种CT抗原阳性。最常见的是新型CT抗原MAGE-C1 / CT7的表达阳性,原发性OC的24.5%和复发性OC的35.1%。 MAGE-A4,GAGE和NY-ESO-1的表达分别占原发性OC的22.7%,13.9%和7.1%,复发性OC的22.6%,17.5%和8.9%。组织学亚型(浆液性,子宫内膜样,透明细胞,粘液性和过渡性)的分析显示,在所有粘液性OC中表达呈阴性。高级别浆液性OC显示CT抗原表达在5.6%至28%之间,其中MAGE-C1 / CT7是最常见的,但与阶段或总体生存率无关。 MAGE-C1 / CT7表达和CT抗原的共表达与子宫内膜样OC的等级显着相关。 BT均未显示CT抗原表达。与阶段,总体生存或对化疗的反应无明显相关性。总之,CT抗原在OC的某个子集中表达,而在粘液组织学的BT或OC中不表达。这些发现可能对卵巢癌多价疫苗接种策略的设计有影响。

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