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Expression of Cyclooxygenase-2 in Human Transitional Cell Carcinoma of the Urinary Bladder

机译:环氧合酶-2在膀胱膀胱移行细胞癌中的表达

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摘要

Recent studies suggest that expression of cyclooxygenase-2 (Cox-2) is elevated in transitional cell carcinoma (TCC) of the urinary bladder and that inhibition of Cox-2 activity suppresses bladder cancer in experimental animal models. We have investigated the expression of Cox-2 protein in human TCCs (n = 85), in in situ carcinomas (Tis) of the urinary bladder (n = 17), and in nonneoplastic urinary bladder samples (n = 16) using immunohistochemistry. Cox-2 immunoreactivity was detected in 66% (67 of 102) of the carcinomas, whereas only 25% (4 of 16) of the nonneoplastic samples were positive (P 90% of the tumor cells positive) than the invasive carcinomas (10%) (P < 0.05). However, several invasive TCCs exhibited the strongest intensity of Cox-2 staining in the invading cells, whereas other parts of the tumor were virtually negative. Finally, strong Cox-2 positivity was also found in nonneoplastic ulcerations (2 of 2) and in inflammatory pseudotumors (2 of 2), in which the immunoreactivity localized to the nonepithelial cells. Taken together, our data suggest that Cox-2 is highly expressed in noninvasive bladder carcinomas, whereas the highest expression of invasive tumors associated with the invading cells, and that Cox-2 may also have a pathophysiological role in nonneoplastic conditions of the urinary bladder, such as ulcerations and inflammatory pseudotumors.
机译:最近的研究表明,在膀胱移行细胞癌(TCC)中,环氧合酶2(Cox-2)的表达升高,而抑制Cox-2活性可以抑制实验动物模型中的膀胱 癌症。我们已经研究了膀胱原位癌(n = 17)在人TCC(n = 85)中Cox-2蛋白的表达(n = 85),以及使用免疫组织化学方法在非肿瘤性 膀胱样本中(n = 16)。在 癌,而非肿瘤性 样本中只有25%(16个中的4个)呈阳性(P 90%的肿瘤细胞呈阳性),而浸润性癌(10%)为阳性(P <0.05)。但是,一些 侵袭性TCC在侵袭的细胞中显示出最强的Cox-2染色强度,而肿瘤的其他部分实际上是阴性的。最后,在非肿瘤性溃疡(2个中的2个)和炎性 假性肿瘤(2个中的2个)中也发现了强Cox-2阳性,其中免疫反应性局限在 到非上皮细胞。两者合计,我们的数据表明 Cox-2在非侵袭性膀胱癌中高表达, 与与侵袭相关的侵袭性肿瘤的表达最高。细胞,并且Cox-2在膀胱非肿瘤状态下也可能具有病理生理作用,例如溃疡和炎性假瘤。

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  • 来源
    《American Journal of Pathology》 |2001年第3期|849-853|共5页
  • 作者单位

    From the Departments of Pathology,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland|Obstetrics and Gynecology,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland;

    Surgery,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland;

    Obstetrics and Gynecology,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland;

    and Clinical Chemistry,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland;

    From the Departments of Pathology,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland;

    Surgery,Helsinki University Central Hospital and the Haartman Institute, University of Helsinki, Helsinki, Finland;

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