Department of Ocular Pathology, Dr. R. P. Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.
Department of Biochemistry, AIIMS, New Delhi, India.
Clin Transl Oncol. 2018 Dec;20(12):1592-1603. doi: 10.1007/s12094-018-1895-3. Epub 2018 May 23.
Uveal melanoma, although a rare form of cancer, is the most common primary malignancy of the eye in adults. Nuclear factor-κB (NF-κB) is a transcription factor that transactivates genes involved in the regulation of cell growth, apoptosis, angiogenesis, and metastasis, but the molecular mechanisms that negatively regulate NF-κB activation are not fully understood. NF-κB can also be activated by DNA damage pathway through NEMO protein. Therefore, the objective of this study is to elucidate the role of NEMO/IKKγ protein in uveal melanoma patients.
Seventy-five formalin-fixed paraffin-embedded prospective tissues of uveal melanoma were included in the present study. These cases were reviewed and investigated for the expression of NEMO/IKKγ protein by immunohistochemistry and validated by western blotting along with the qRT-PCR for mRNA expression. Expression levels were correlated with the clinicopathological parameters and patients' outcome.
Immunohistochemistry showed cytoplasmic expression of NEMO/IKKγ expression in only 22 out of 75 (29.33%) cases. This result was confirmed by western blotting, and correlated well with the immunohistochemical expression of NEMO/IKKγ protein (48 kDa). In addition, downregulation of this gene was found in 87.93% of the cases when compared with the normal tissues. On statistical analysis, loss of NEMO/IKKγ protein was correlated with neovascularization, high mitotic count, and presence of vascular loop (p < 0.05). There was less overall survival rate with low expression of NEMO/IKKγ protein in patients with uveal melanoma.
This was the first study suggesting the relevant role of NEMO/IKKγ protein, and highlights the prognostic significance with outcome in uveal melanoma patients. This protein might be used as a screening biomarker in these patients after large-scale validation and translational studies.
葡萄膜黑色素瘤虽然是一种罕见的癌症,但却是成年人眼部最常见的原发性恶性肿瘤。核因子-κB(NF-κB)是一种转录因子,可激活参与细胞生长、凋亡、血管生成和转移调节的基因,但负调节 NF-κB 激活的分子机制尚未完全阐明。NF-κB 也可以通过 NEMO 蛋白被 DNA 损伤途径激活。因此,本研究的目的是阐明 NEMO/IKKγ 蛋白在葡萄膜黑色素瘤患者中的作用。
本研究纳入了 75 例福尔马林固定石蜡包埋的葡萄膜黑色素瘤前瞻性组织。通过免疫组织化学法检测 NEMO/IKKγ 蛋白的表达,并通过 Western 印迹和 qRT-PCR 验证 mRNA 表达,对这些病例进行了回顾性分析。同时,还对表达水平与临床病理参数和患者预后的关系进行了研究。
免疫组织化学显示,75 例病例中仅有 22 例(29.33%)出现细胞质 NEMO/IKKγ 表达。Western 印迹证实了这一结果,并与 NEMO/IKKγ 蛋白的免疫组织化学表达(48 kDa)很好地相关。此外,与正常组织相比,87.93%的病例发现该基因下调。统计学分析显示,NEMO/IKKγ 蛋白缺失与新生血管形成、高有丝分裂计数和血管环存在相关(p < 0.05)。葡萄膜黑色素瘤患者中 NEMO/IKKγ 蛋白低表达与总生存率降低相关。
这是首次研究表明 NEMO/IKKγ 蛋白具有相关性,并强调了其在葡萄膜黑色素瘤患者预后中的意义。该蛋白可能在大规模验证和转化研究后,作为这些患者的筛查生物标志物。