Kaur Sukhwinder, Momi Navneet, Chakraborty Subhankar, Wagner David G, Horn Adam J, Lele Subodh M, Theodorescu Dan, Batra Surinder K
Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
PLoS One. 2014 Mar 26;9(3):e92742. doi: 10.1371/journal.pone.0092742. eCollection 2014.
Radical changes in both expression and glycosylation pattern of transmembrane mucins have been observed in various malignancies. We and others have shown that MUC1 and MUC4, two transmembrane mucins, play a sentinel role in cell signaling events that drive several epithelial malignancies. In the present study, we investigated the expression profile of MUC1 and MUC4 in the non-neoplastic bladder urothelium, in various malignant neoplasms of bladder and in bladder carcinoma cell lines.
Immunohistochemistry was performed on tissue sections from the urinary bladder biopsies, resection samples and tissue microarrays (TMAs) with monoclonal antibodies specific for MUC1 and MUC4. We also investigated their expression in bladder carcinoma cell lines by RT-PCR and immunoblotting.
MUC1 is expressed on the apical surface or in umbrella cells of the normal non-neoplastic bladder urothelium. Strong expression of MUC1 was also observed in urothelial carcinoma (UC). MUC1 staining increased from normal urothelium (n = 27, 0.35±0.12) to urothelial carcinoma (UC, n = 323, H-score, 2.4±0.22, p≤0.0001). In contrast to MUC1, MUC4 was expressed in all the layers of non-neoplastic bladder urothelium (n = 14, 2.5±0.28), both in the cell membrane and cytoplasm. In comparison to non-neoplastic urothelium, the loss of MUC4 expression was observed during urothelial carcinoma (n = 211, 0.56±0.06). However, re-expression of MUC4 was observed in a subset of metastatic cases of urothelial carcinoma (mean H-score 0.734±0.9).
The expression of MUC1 is increased while that of MUC4 decreased in UC compared to the normal non-neoplastic urothelium. Expression of both MUC1 and MUC4, however, are significantly higher in urothelial carcinoma metastatic cases compared to localized UC. These results suggest differential expression of MUC1 and MUC4 during development and progression of bladder carcinoma.
在多种恶性肿瘤中均观察到跨膜黏蛋白的表达和糖基化模式发生了根本性变化。我们和其他研究人员已表明,两种跨膜黏蛋白MUC1和MUC4在驱动多种上皮性恶性肿瘤的细胞信号传导事件中发挥着哨兵作用。在本研究中,我们调查了MUC1和MUC4在非肿瘤性膀胱尿路上皮、膀胱各种恶性肿瘤以及膀胱癌细胞系中的表达谱。
使用针对MUC1和MUC4的单克隆抗体对膀胱活检组织切片、切除样本和组织微阵列(TMA)进行免疫组织化学检测。我们还通过逆转录聚合酶链反应(RT-PCR)和免疫印迹法研究了它们在膀胱癌细胞系中的表达。
MUC1在正常非肿瘤性膀胱尿路上皮的顶端表面或伞细胞中表达。在尿路上皮癌(UC)中也观察到MUC1的强表达。MUC1染色从正常尿路上皮(n = 27,0.35±0.12)增加到尿路上皮癌(UC,n = 323,H评分,2.4±0.22,p≤0.0001)。与MUC1相反,MUC4在非肿瘤性膀胱尿路上皮的所有层(n = 14,2.5±0.28)中均有表达,在细胞膜和细胞质中均有表达。与非肿瘤性尿路上皮相比,在尿路上皮癌期间观察到MUC4表达缺失(n = 211,0.56±0.06)。然而,在一部分尿路上皮癌转移病例中观察到MUC4重新表达(平均H评分0.734±0.9)。
与正常非肿瘤性尿路上皮相比,UC中MUC1的表达增加而MUC4的表达降低。然而,与局限性UC相比,MUC1和MUC4在尿路上皮癌转移病例中的表达均显著更高。这些结果表明MUC1和MUC4在膀胱癌发生和发展过程中存在差异表达。