Cancer Institute, University of Mississippi Medical Center, Jackson, MS, USA.
Sci Rep. 2013;3:2331. doi: 10.1038/srep02331.
Metastasis-associated protein 1 (MTA1), a negative epigenetic modifier, plays a critical role in prostate cancer (PCa) progression. We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archival PCa specimens from University of Mississippi Medical Center and University of Iowa. We found that nuclear MTA1 overexpression was positively correlated with the severity of disease progression reaching its highest levels in metastatic PCa. Nuclear MTA1 overexpression was significantly associated with Gleason > 7 tumors in African Americans but not in Caucasians. It was also a predictor of recurrent disease. We concluded that MTA1 nuclear overexpression may be a prognostic indicator and a future therapeutic target for aggressive PCa in African American men. Our findings may be useful for categorizing African American patients with a higher probability of recurrent disease and metastasis from those who are likely to remain metastasis-free.
转移相关蛋白 1(MTA1)是一种负性表观遗传修饰物,在前列腺癌(PCa)的进展中发挥关键作用。我们假设原发肿瘤组织中 MTA1 的过度表达可以预测 PCa 的侵袭性和转移。我们对密西西比大学医学中心和爱荷华大学的前列腺癌标本进行了 MTA1 的免疫组织化学染色。我们发现核 MTA1 的过度表达与疾病进展的严重程度呈正相关,在转移性 PCa 中达到最高水平。核 MTA1 的过度表达在非裔美国人中与 Gleason>7 肿瘤显著相关,但在白种人中则不然。它也是复发性疾病的预测因子。我们得出结论,核 MTA1 的过度表达可能是预测指标,也是治疗非裔美国男性侵袭性 PCa 的未来靶点。我们的发现可能有助于将更有可能发生疾病复发和转移的非裔美国患者与那些可能保持无转移的患者进行分类。