...
首页> 外文期刊>Indian Journal of Pathology and Microbiology >Molecular mechanisms of tobacco induced oral and oropharyngeal cancer: Results of a tissue microarray and immunohistochemistry-based study from a tertiary cancer center in India
【24h】

Molecular mechanisms of tobacco induced oral and oropharyngeal cancer: Results of a tissue microarray and immunohistochemistry-based study from a tertiary cancer center in India

机译:烟草诱发口腔和口咽癌症的分子机制:组织微阵列和印度高等教育中心的免疫组织化学研究结果

获取原文

摘要

Background: It is well established that chronic exposure to tobacco induces head and neck cancers but the exact etiopathogenesis is not known. Though studies have shown expression of TIMP1, EPS8 and AXL in cancers, their role in tobacco-induced cancers is not known. We aimed this study to evaluate the role of these molecules in oral and oropharyngeal squamous cell cancers (SCC). Materials and Methods: In this single institutional study, 31 patients of oral and oropharyngeal SCC with history of chewing tobacco were included. Smokers were excluded from the study. After informed consent biopsies were taken from affected and contralateral normal mucosa. Paraffin blocks were made and tissue microarray (TMA) were constructed using these blocks. Immunohistochemistry (IHC) for TIMP1, EPS8, AXL kinase was carried out on these tissue microarrays. The intensity of staining was scored from 0 to 3+, related to expression of each of the three molecules. Results: The expression of TIMP1, EPS8 and AXL kinase was significantly more in the cancerous mucosa versus non-cancerous mucosa (P = 0.000 in all three) in oral and oropharyngeal SCC exposed to chewing tobacco. Conclusion: Immunohistochemical expression of these molecular markers in oral and oropharyngeal SCC correlated with their molecular based studies. Significant IHC expression of TIMP1, EPS8 and AXL establishes their role in the pathogenesis of oral and oropharyngeal squamous cell carcinomas. Novel targeted therapies may be researched that can detect and target these molecules at an earlier stage of pathogenesis of these tumors.
机译:背景:很好地确立了慢性暴露于烟草诱导头部和颈部癌症,但确切的病因发生器未知。虽然研究表明癌症中TIMP1,EPS8和AXL的表达,但它们在烟草诱导的癌症中的作用是未知的。我们旨在评估这些分子在口腔和口咽鳞状细胞癌症(SCC)中的作用。材料和方法:在这项单一制度研究中,包括31例口腔和口咽患者,患有咀嚼烟草的历史。吸烟者被排除在研究之外。经过知情的同意活检,受影响和对侧正常粘膜。制备石蜡块,使用这些嵌段构建组织微阵列(TMA)。在这些组织微阵列上进行IMP1,EPS8,AXL激酶的免疫组织化学(IHC)。染色的强度从0到3 +评分,与三种分子中的每一个的表达有关。结果:在口服和口咽SCC暴露于咀嚼烟草的口腔和口咽SCC中,TiMP1,EPS8和AXL激酶的表达在癌症粘膜上具有显着更多的癌粘膜(P = 0.00)。结论:口服和口咽SCC中这些分子标记的免疫组织化学表达与其分子基研究相关。 TIMP1,EPS8和AXL的重要IHC表达在口腔和口咽鳞状细胞癌的发病机制中建立了它们的作用。可以研究新的靶向疗法,其可以在这些肿瘤的发病机制的早期阶段检测和靶向这些分子。

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