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黑色素瘤相关抗原作为黑色素瘤的信使核糖核酸检测标志物

Melanoma-associated antigens as messenger RNA detection markers for melanoma.

作者信息

Sarantou T, Chi D D, Garrison D A, Conrad A J, Schmid P, Morton D L, Hoon D S

机构信息

John Wayne Cancer Institute at Saint John's Hospital and Health Center, Santa Monica, California 90404, USA.

出版信息

Cancer Res. 1997 Apr 1;57(7):1371-6.

PMID:9102226
Abstract

Melanoma is heterogeneous for its biological properties and melanoma-associated antigens (MAAs). This diversity is partially observed in the expression of the MAAs involved with the melanin synthesis pathway. We therefore developed a sensitive multimarker reverse transcription-PCR plus Southern blot assay using five MAAs as molecular markers to detect primary and metastatic melanoma cells. Melanoma cell lines, melanocytes (cultured), primary and metastatic malignant melanoma tissues, and blood from patients with American Joint Committee on Cancer stage I-IV melanoma were assessed for tyrosinase, tyrosinase-related proteins 1 and 2, Pmel 17, and MART-1/Melan-A. All of the MAA mRNA markers were expressed in 100% of melanoma cell lines and cultured melanocytes, 74% of primary and metastatic tumors (excluding tumor-draining lymph nodes), 43% of tumor-involved lymph nodes, and 43% of patients' bloods. Hypomelanotic melanoma tissues expressed a lower frequency of individual mRNA markers. Overall, at least one mRNA marker was expressed in more than 86% of specimens assayed. Normal tissue specimens from patients and blood from normal volunteer donors were negative for MAA mRNA expression. The multimarker MAA reverse transcription-PCR plus Southern blot analysis was more reliable and sensitive than a single-molecular marker assay for the detection of melanoma cells. This molecular assay can also provide information on MAA mRNA expression of metastatic melanoma cells that may assist in monitoring the therapeutic efficacy of active specific immunotherapy toward specific MAA-bearing melanomas.

摘要

黑色素瘤在生物学特性和黑色素瘤相关抗原(MAA)方面具有异质性。这种多样性部分体现在参与黑色素合成途径的MAA的表达上。因此,我们开发了一种灵敏的多标记逆转录PCR加Southern印迹分析方法,使用五种MAA作为分子标记来检测原发性和转移性黑色素瘤细胞。对黑色素瘤细胞系、(培养的)黑素细胞、原发性和转移性恶性黑色素瘤组织以及美国癌症联合委员会I-IV期黑色素瘤患者的血液进行酪氨酸酶、酪氨酸酶相关蛋白1和2、Pmel 17以及MART-1/黑色素A的评估。所有MAA mRNA标记在100%的黑色素瘤细胞系和培养的黑素细胞、74%的原发性和转移性肿瘤(不包括引流肿瘤的淋巴结)、43%的肿瘤累及淋巴结以及43%的患者血液中均有表达。色素减退性黑色素瘤组织中单个mRNA标记的表达频率较低。总体而言,在所检测的标本中,超过86%至少表达一种mRNA标记。患者的正常组织标本和正常志愿者捐赠者的血液中MAA mRNA表达呈阴性。多标记MAA逆转录PCR加Southern印迹分析在检测黑色素瘤细胞方面比单分子标记分析更可靠、更灵敏。这种分子检测还可以提供转移性黑色素瘤细胞MAA mRNA表达的信息,这可能有助于监测针对特定携带MAA的黑色素瘤的主动特异性免疫治疗的疗效。

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