Identification of Autoantibodies for α and γ-Enolase in Serum from a Patient with Melanoma.

Japanese clinical medicine Pub Date : 2011-07-17 Print Date: 2011-01-01 DOI:10.4137/JCM.S6256
Yui Hiura, Toyofumi Nakanishi, Miki Tanioka, Takayuki Takubo, Shinichi Moriwaki
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引用次数: 3

Abstract

Melanoma is one of lethal malignant skin tumors and the sole effective cure for the disease can be achieved by surgical resection of primary tumor and early diagnosis for melanoma is crucial for patients' prognosis. Detection of novel tumor-related antibodies would aid in the diagnosis of early-stage cancer, in the detection of recurrence and in the development of a more effective immunotherapy. In the middle of the exploration of a candidate of biomarker for melanoma by proteomics-base technique, we encountered the coexistence of autoantibodies for α-enolase and γ-enolase in serum derived from a patient with melanoma, who had received the repeated treatments with alkylating agents and interferon β. Although melanoma is known to be a highly antigenic tumor, it is still unclear why these autoantibodies appeared. To evaluate the usefulness in detecting the circulating α-enolase or γ-enolase autoantibodies in serum from melanoma patients for biomarkers for tumor progression, more studies are needed.

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黑色素瘤患者血清α和γ烯醇化酶自身抗体的鉴定。
黑色素瘤是致死性皮肤恶性肿瘤之一,手术切除原发肿瘤是唯一有效的治疗方法,早期诊断对患者预后至关重要。检测新的肿瘤相关抗体将有助于早期癌症的诊断,检测复发和开发更有效的免疫疗法。在利用蛋白质组学技术探索黑色素瘤候选生物标志物的过程中,我们在一名黑色素瘤患者的血清中发现α-烯醇化酶和γ-烯醇化酶的自身抗体共存,该患者接受了烷基化剂和干扰素β的反复治疗。虽然已知黑色素瘤是一种高度抗原的肿瘤,但目前尚不清楚为什么会出现这些自身抗体。为了评估检测黑色素瘤患者血清中循环α-烯醇化酶或γ-烯醇化酶自身抗体作为肿瘤进展生物标志物的有效性,还需要进行更多的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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