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Expression of MAGE-C1/CT7 and MAGE-C2/CT10 Predicts Lymph Node Metastasis in Melanoma Patients

机译:MAGE-C1 / CT7和MAGE-C2 / CT10的表达预测黑色素瘤患者的淋巴结转移

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摘要

MAGE-C1/CT7 and MAGE-C2/CT10 are members of the large MAGE family of cancer-testis (CT) antigens. CT antigens are promising targets for immunotherapy in cancer because their expression is restricted to cancer and germ line cells and a proportion of cancer patients presents with immune responses against CT antigens, which clearly demonstrates their immunogenicity. This study investigates the expression of MAGE-C1/CT7 and MAGE-C2/CT10 in primary and metastatic melanoma. Immunohistochemical staining of tissue microarrays that consisted of 59 primary malignant melanomas of the skin, 163 lymph node and distant melanoma metastases and 68 melanoma cell lines was performed. We found MAGE-C1/CT7 expression in 15 out of 50 (24%) primary melanomas and 15 out of 50 (24%) cell lines, whereas MAGE-C2/CT10 was detected in 17 out of 51 (33%) primary melanomas and 14 out of 68 (17%) cell lines. MAGE-C1/CT7 and MAGE-C2/CT10 were both detected in 40% of melanoma metastases. Patients with MAGE-C1/CT7 or MAGE-C2/CT10 positive primary melanoma had significantly more lymph node metastases (p = 0.005 and p<0.001, resp.). Prediction of lymph node metastasis by MAGE-C1/CT7 and MAGE-C2/CT10 was independent of tumor cell proliferation rate (Ki67 labeling index) in a multivariate analysis (p = 0.01). Our results suggest that the expression of MAGE-C1/CT7 and MAGE-C2/CT10 in primary melanoma is a potent predictor of sentinel lymph node metastasis.
机译:MAGE-C1 / CT7和MAGE-C2 / CT10是大型MAGE癌-睾丸(CT)抗原家族的成员。 CT抗原是癌症免疫疗法的有希望的靶标,因为它们的表达仅限于癌和种系细胞,并且一部分癌症患者表现出针对CT抗原的免疫反应,这清楚地证明了其免疫原性。本研究调查了MAGE-C1 / CT7和MAGE-C2 / CT10在原发性和转移性黑色素瘤中的表达。进行组织微阵列的免疫组织化学染色,该阵列由59例皮肤原发性恶性黑色素瘤,163个淋巴结和远处的黑色素瘤转移以及68个黑色素瘤细胞系组成。我们发现MAGE-C1 / CT7在50个(24%)原发性黑素瘤中有15个和50个(24%)的细胞系中有15个表达,而MAGE-C2 / CT10在51个(33%)的原发性黑素瘤中有17个被检测到68个细胞系中有14个(17%)。在40%的黑色素瘤转移中均检测到MAGE-C1 / CT7和MAGE-C2 / CT10。 MAGE-C1 / CT7或MAGE-C2 / CT10阳性的原发性黑色素瘤患者的淋巴结转移明显更多(p = 0.005,p <0.001)。在多变量分析中,MAGE-C1 / CT7和MAGE-C2 / CT10对淋巴结转移的预测与肿瘤细胞增殖率(Ki67标记指数)无关(p = 0.01)。我们的结果表明,原发性黑色素瘤中MAGE-C1 / CT7和MAGE-C2 / CT10的表达是前哨淋巴结转移的有效预测因子。

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