Chen Dan, Yang Kai, Zhang Guodong, Mei Jie, Xiang Li
Department of Oral and Maxillofacial Surgery, the First Affiliated Hospital, Chongqing Medical University, Chongqing 400016, P.R. China.
Oncol Lett. 2011 Mar;2(2):265-271. doi: 10.3892/ol.2010.228. Epub 2010 Dec 23.
7,12-Dimethylbenz(a)-anthracene (DMBA)-induced oral buccal mucosa squamous cell carcinoma in Syrian golden hamsters was used to establish precancerous lesions. Agilent rat whole-genome microarray and biological information analysis were used to screen for genes related to key diseases during the transformation of normal buccal mucosa to precancerous lesions in golden hamsters. DMBA acetone solution (0.5%) was used to establish a model of precancerous lesions in oral buccal mucosa in golden hamsters. The results showed that a total of 1331 genes were differentially expressed, including 1278 known, 53 unknown, 747 up-regulated and 584 down-regulated genes. Analysis revealed a total of 14 gene interaction pathways that significantly associated with the 1278 known differentially expressed genes (P<0.05). In conclusion, the occurrence of precancerous lesions in the oral buccal mucosa of golden hamsters was caused by a number of genetic changes that resulted in changes to their respective pathways. Key candidate genes for the formation of precancerous lesions in oral buccal mucosa included Cyp2b13, Orc1L, casp8, CCL5, CXCL12, CCL20, Serping1, P518/Qrfp, F5, TFPI, Vcam1, Fn1, Angpt2, Lcp2, Cxadr, Lyn, Hck, Btk, RGD1564385/fes, Vav1 and IL5ra.
采用7,12-二甲基苯并(a)蒽(DMBA)诱导叙利亚金黄地鼠口腔颊黏膜鳞状细胞癌以建立癌前病变模型。运用安捷伦大鼠全基因组微阵列及生物信息分析,筛选金黄地鼠正常颊黏膜向癌前病变转化过程中与关键疾病相关的基因。用0.5%的DMBA丙酮溶液建立金黄地鼠口腔颊黏膜癌前病变模型。结果显示,共有1331个基因差异表达,其中包括1278个已知基因、53个未知基因、747个上调基因和584个下调基因。分析发现共有14条基因相互作用通路与1278个已知差异表达基因显著相关(P<0.05)。综上所述,金黄地鼠口腔颊黏膜癌前病变的发生是由一些基因变化引起的,这些变化导致了各自通路的改变。口腔颊黏膜癌前病变形成的关键候选基因包括Cyp2b13、Orc1L、casp8、CCL5、CXCL12、CCL20、Serping1、P518/Qrfp、F5、TFPI、Vcam1、Fn1、Angpt2、Lcp2、Cxadr、Lyn、Hck、Btk、RGD1564385/fes、Vav1和IL5ra。