...
首页> 外文期刊>Oral oncology >Mutual paracrine effects of oral squamous cell carcinoma cells and normal oral fibroblasts: induction of fibroblast to myofibroblast transdifferentiation and modulation of tumor cell proliferation.
【24h】

Mutual paracrine effects of oral squamous cell carcinoma cells and normal oral fibroblasts: induction of fibroblast to myofibroblast transdifferentiation and modulation of tumor cell proliferation.

机译:口腔鳞状细胞癌细胞与正常口腔成纤维细胞的旁分泌相互作用:诱导成纤维细胞向成肌纤维细胞转分化并调节肿瘤细胞的增殖。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

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.
机译:一些证据表明,肿瘤周围的基质在包括口腔鳞状细胞癌(OSCC)在内的几种肿瘤的生长和进展中起着重要作用。我们评估了成肌纤维细胞在OSCC中的存在,并确定它们的存在是否与肿瘤的临床病理特征有关。我们还调查了肿瘤细胞和成纤维细胞对成纤维细胞-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在肿瘤的基质中含有成肌纤维细胞。肌成纤维细胞的大量存在与肿瘤细胞的N期,疾病期,局部复发和增殖潜力显着相关。使用OSCC细胞系和原发性口腔正常成纤维细胞(ONF),我们证明了肿瘤细胞通过分泌转化生长因子-β1(TGF-β1)诱导了ONFs向肌纤维母细胞的转分化。反过来,如通过测量BrdU掺入和Ki67表达所揭示的,肌成纤维细胞分泌的因子刺激OSCC细胞增殖。研究结果表明,在肿瘤侵袭过程中,源自OSCC的TGF-β1促进了成纤维细胞-肌成纤维细胞的转分化,并且肿瘤细胞增殖可以由成肌纤维细胞释放的因子诱导,这可能有利于肿瘤的生长。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号