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MAGE - A3的核过表达水平预示着前列腺癌患者的预后不良。

Nuclear overexpression levels of MAGE-A3 predict poor prognosis in patients with prostate cancer.

作者信息

Khalvandi Azadeh, Abolhasani Maryam, Madjd Zahra, Shekarabi Mehdi, Kourosh-Arami Masoumeh, Mohsenzadegan Monireh

机构信息

Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Hasheminejad Kidney Center, Iran University of Medical Sciences, Tehran, Iran.

出版信息

APMIS. 2021 Jun;129(6):291-303. doi: 10.1111/apm.13132. Epub 2021 Apr 13.

Abstract

Melanoma antigen gene A3 (MAGE-A3) is one of the most immunogenic cancer testis antigens and is common in various types of cancers. In this study, for the first time, we performed immunohistochemical analysis to evaluate the expression of MAGE-A3 in 153 prostate tissue samples including prostate cancer (PCa), benign prostatic hyperplasia (BPH), and high-grade prostatic intraepithelial neoplasia (HPIN). Increased both nuclear and cytoplasmic expression of MAGE-A3 was significantly found in PCa tissues compared with both HPIN and BPH tissues (nuclear expression at p = 0.011, and cytoplasmic expression at p = 0.034; for both comparisons p < 0.0001, respectively). A significant correlation was observed between higher nuclear and cytoplasmic expressions of MAGE-A3 with Gleason score (p < 0.0001 and 0.006, respectively). Increased expression of MAGE-A3 was associated with shorter biochemical recurrence-free survival (BCR-FS) and disease-free survival (DFS) of patients (p = 0.042 and = 0.0001, respectively). In multivariate analysis, nuclear expression of MAGE-A3 and Gleason score (≤7 vs >7) was independent predictors of the DFS (both; p = 0.019). Nuclear expression of MAGE-A3 was also significantly related to BCR-FS (p = 0.015). MAGE-A3 can be considered as a predictor for poor prognosis and an option for vaccine immunotherapy in patients with PCa.

摘要

黑色素瘤抗原基因A3(MAGE-A3)是免疫原性最强的癌睾丸抗原之一,在多种癌症中普遍存在。在本研究中,我们首次进行免疫组织化学分析,以评估MAGE-A3在153例前列腺组织样本中的表达,这些样本包括前列腺癌(PCa)、良性前列腺增生(BPH)和高级别前列腺上皮内瘤变(HPIN)。与HPIN和BPH组织相比,在PCa组织中显著发现MAGE-A3的核表达和细胞质表达均增加(核表达p = 0.011,细胞质表达p = 0.034;两种比较的p值均分别<0.0001)。观察到MAGE-A3较高的核表达和细胞质表达与Gleason评分之间存在显著相关性(分别为p < 0.0001和0.006)。MAGE-A3表达增加与患者较短的无生化复发生存期(BCR-FS)和无病生存期(DFS)相关(分别为p = 0.042和= 0.0001)。在多变量分析中,MAGE-A3的核表达和Gleason评分(≤7 vs >7)是DFS的独立预测因子(两者;p = 0.019)。MAGE-A3的核表达也与BCR-FS显著相关(p = 0.015)。MAGE-A3可被视为PCa患者预后不良的预测指标和疫苗免疫治疗的选择。

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