Matta Ajay, Bahadur Sudhir, Duggal Ritu, Gupta Siddhartha D, Ralhan Ranju
Department of Biochemistry, All India Institute of Medical Sciences, Ansari Nagar, New Delhi -110029, India.
BMC Cancer. 2007 Sep 2;7:169. doi: 10.1186/1471-2407-7-169.
The functional and clinical significance of 14-3-3 proteins in human cancers remain largely undetermined. Earlier, we have reported differential expression of 14-3-3zeta mRNA in oral squamous cell carcinoma (OSCC) by differential display.
The clinical relevance of 14-3-3zeta protein in oral tumorigenesis was determined by immunohistochemistry in paraffin embedded sections of oral pre-malignant lesions (OPLs), OSCCs and histologically normal oral tissues and corroborated by Western Blotting. Co-immunoprecipitation assays were carried out to determine its association with NFkappaB, beta-catenin and Bcl-2.
Intense immunostaining of 14-3-3zeta protein was observed in 61/89 (69%) OPLs and 95/120 (79%) OSCCs. Immunohistochemistry showed significant increase in expression of 14-3-3zeta protein from normal mucosa to OPLs to OSCCs (ptrend < 0.001). Significant increase in expression of 14-3-3zeta protein was observed as early as in hyperplasia (p = 0.009), with further elevation in moderate and severe dysplasia, that was sustained in OSCCs. These findings were validated by Western blotting. Using Co-immunoprecipitation, we demonstrated that 14-3-3zeta protein binds to NFkappaB, beta-catenin and Bcl-2, suggesting its involvement in cellular signaling, leading to proliferation of oral cancer cells.
Our findings suggest that over-expression of 14-3-3zeta is an early event in oral tumorigenesis and may have an important role in its development and progression. Thus, 14-3-3zeta may serve as an important molecular target for designing novel therapy for oral cancer.
14-3-3蛋白在人类癌症中的功能和临床意义在很大程度上仍未明确。此前,我们通过差异显示技术报道了口腔鳞状细胞癌(OSCC)中14-3-3ζ mRNA的差异表达。
通过免疫组织化学法检测石蜡包埋的口腔癌前病变(OPL)、OSCC和组织学正常的口腔组织切片中14-3-3ζ蛋白在口腔肿瘤发生中的临床相关性,并通过蛋白质印迹法进行确证。进行免疫共沉淀试验以确定其与核因子κB(NFκB)、β-连环蛋白和Bcl-2的关联。
在61/89(69%)的OPL和95/120(79%)的OSCC中观察到14-3-3ζ蛋白的强烈免疫染色。免疫组织化学显示从正常黏膜到OPL再到OSCC,14-3-3ζ蛋白的表达显著增加(趋势p<0.001)。早在增生阶段就观察到14-3-3ζ蛋白表达显著增加(p = 0.009),在中度和重度发育异常中进一步升高,并在OSCC中持续存在。这些发现通过蛋白质印迹法得到验证。通过免疫共沉淀,我们证明14-3-3ζ蛋白与NFκB、β-连环蛋白和Bcl-2结合,表明其参与细胞信号传导,导致口腔癌细胞增殖。
我们的研究结果表明,14-3-3ζ的过表达是口腔肿瘤发生的早期事件,可能在其发展和进展中起重要作用。因此,14-3-3ζ可能作为设计口腔癌新疗法的重要分子靶点。