Kellermann Michele G, Sobral Lays M, da Silva Sabrina Daniela, Zecchin Karina G, Graner Edgard, Lopes Marcio A, Kowalski Luis Paulo, Coletta Ricardo D
Department of Oral Diagnosis, School of Dentistry, State University of Campinas, Piracicaba, São Paulo, Brazil.
Oral Oncol. 2008 May;44(5):509-17. doi: 10.1016/j.oraloncology.2007.07.001. Epub 2007 Sep 7.
Several lines of evidence demonstrated that the stroma surrounding the tumors plays an important role in the growth and progression of several neoplasms, including oral squamous cell carcinomas (OSCC). We evaluated the presence of myofibroblasts in OSCC and determined whether their presence is associated with clinicopathological features of the tumors. We also investigated the mutual paracrine effects of tumor cells and myofibroblasts on fibroblast-myofibroblast transdifferentiation and tumor cell proliferation. Immunohistochemical analysis showed the approximately 60% of the OSCCs contained myofibroblasts in the stroma of the tumor. Abundant presence of myofibroblasts significantly correlated with N stage, disease stage, regional recurrence, and proliferative potential of the tumor cells. Using OSCC cell lines and primary oral normal fibroblasts (ONF), we demonstrated that tumor cells induced transdifferentiation of ONFs to myofibroblasts via secretion of transforming growth factor-beta 1 (TGF-beta 1). In turn, myofibroblasts secreted factors that stimulated OSCC cell proliferation, as revealed by measuring BrdU incorporation and Ki67 expression. The results of the study suggest that during tumor invasion OSCC-derived TGF-beta 1 promote fibroblast-myofibroblast transdifferentiation, and that tumor cellular proliferation can be induced by factors released from myofibroblasts, which may favor tumor growth.
多项证据表明,肿瘤周围的基质在包括口腔鳞状细胞癌(OSCC)在内的多种肿瘤的生长和进展中起着重要作用。我们评估了OSCC中肌成纤维细胞的存在情况,并确定它们的存在是否与肿瘤的临床病理特征相关。我们还研究了肿瘤细胞与肌成纤维细胞对成纤维细胞-肌成纤维细胞转分化和肿瘤细胞增殖的相互旁分泌作用。免疫组织化学分析显示,约60%的OSCC肿瘤基质中含有肌成纤维细胞。肌成纤维细胞的大量存在与N分期、疾病分期、区域复发以及肿瘤细胞的增殖潜能显著相关。利用OSCC细胞系和原代口腔正常成纤维细胞(ONF),我们证明肿瘤细胞通过分泌转化生长因子-β1(TGF-β1)诱导ONF转分化为肌成纤维细胞。反过来,肌成纤维细胞分泌的因子可刺激OSCC细胞增殖,这通过测量BrdU掺入和Ki67表达得以揭示。研究结果表明,在肿瘤侵袭过程中,OSCC来源的TGF-β1促进成纤维细胞-肌成纤维细胞转分化,并且肌成纤维细胞释放的因子可诱导肿瘤细胞增殖,这可能有利于肿瘤生长。