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Analysis of cyclooxygenase 2 (COX-2) expression during malignant melanoma progression.

机译:恶性黑色素瘤进展过程中环氧合酶2(COX-2)表达的分析。

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Cyclooxygenase 2 (COX-2) is an inducible enzyme involved in the production of prostaglandins and thromboxanes during inflammation. There are now several lines of evidence indicating that increased expression of COX-2 plays a functional role in the development and progression of malignant epithelial cancers. However, there is only limited data regarding the role of COX-2 in melanoma pathogenesis. In the present work, we retrospectively examined lesions through out the development of melanoma and metastatic disease (dysplastic nevi n = 10, melanoma in situ n = 4, stage II melanoma n = 10, stage III n = 4, stage IV n = 3, stage V n = 2, melanoma metastasis lymph nodes n = 13 metastasis to other sites n = 3). COX-2 was consistently observed in keratinocytes, dermal fibroblasts, and inflammatory cells in regions adjacent to benign evi and primary cutaneous melanomas. However, no COX-2 staining was detected in the nevi nor in the primary skin melanoma cells. In addition, COX-2 was undetected in all vertical and radial growth phase cases Interestingly, 13 out of 13 of the lymph node metastasis expressed extremely high levels of COX-2 in overlying epithelium and inflammatory cells, and COX-2 was strongly detected in the metastatic cancer cells per se. For additional information on the expression of COX-2 in malignant melanoma, we determined the expression of COX-2 protein in several different melanoma cell lines. We found that 3We found that 5 out of 7 of the melanoma cells over expressed COX-2 compared to normal melanocytes. Collectively, these data suggest that COX-2 may play a functional role in metastases of melanoma, and treatment with COX-2 inhibitors may be efficacious for malignant melanoma.
机译:环氧合酶2(COX-2)是一种可诱导的酶,参与炎症过程中前列腺素和血栓烷的产生。现在有几条证据表明,COX-2表达的增加在恶性上皮癌的发生和发展中起着功能性作用。但是,关于COX-2在黑色素瘤发病机理中的作用的数据很少。在本研究中,我们回顾性研究了黑色素瘤和转移性疾病发展的病变(增生性痣n = 10,原位黑色素瘤n = 4,II期黑色素瘤n = 10,III期n = 4,IV期n = 3 ,阶段V n = 2,黑色素瘤转移淋巴结n = 13转移至其他部位n = 3)。在与良性evi和原发性皮肤黑素瘤相邻的区域的角质形成细胞,真皮成纤维细胞和炎性细胞中始终观察到COX-2。但是,在痣和原发性皮肤黑素瘤细胞中均未检测到COX-2染色。此外,在所有垂直和径向生长期病例中均未检测到COX-2。有趣的是,在13个淋巴结转移中,有13个在上皮和炎性细胞中表达了极高水平的COX-2,而在淋巴结转移中,强烈检测到了COX-2。转移癌细胞本身。有关COX-2在恶性黑色素瘤中表达的更多信息,我们确定了COX-2蛋白在几种不同的黑色素瘤细胞系中的表达。我们发现3我们发现与正常黑色素细胞相比,7个黑色素瘤细胞中有5个过度表达了COX-2。总体而言,这些数据表明,COX-2可能在黑色素瘤转移中发挥功能性作用,并且用COX-2抑制剂治疗可能对恶性黑色素瘤有效。

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