Tsujimoto H, Yura Y, Yoshioka Y, Kusaka J, Yoshida H, Sato M
Second Department of Oral and Maxillofacial Surgery, Tokushima University School of Dentistry, Japan.
J Oral Pathol Med. 1999 Jan;28(1):30-6. doi: 10.1111/j.1600-0714.1999.tb01991.x.
This study investigated whether epidermal growth factor (EGF) administration was capable of modifying salivary gland carcinogenesis. Two groups of mice were given 1 mg of 9,10-dimethyl-1,2-benzanthracene (DMBA) into the left submandibular gland, and then Group 1 mice received 2 microg of EGF and Group 2 mice received vehicle subcutaneously for 8 weeks. Mice in two other groups, 3 and 4, received either EGF or vehicle alone. Twelve weeks after the start of the experiment, the incidences of submandibular gland carcinomas in Groups 1 and 2 were 39% and 58%, respectively, although this difference was not statistically significant. Duct- and cyst-like structures and carcinomas in the left submandibular glands were weakly stained by anti-EGF receptor (EGFR) antibody. Immunoblot and reverse transcriptase polymerase chain reaction (RT-PCR) analyses revealed the expression of EGFR in the submandibular glands and carcinomas. However, EGFR was undetectable in YT cells that were derived from a submandibular gland undifferentiated carcinoma of a Group 2 mouse. These findings indicate that EGF does not promote tumor induction in mouse salivary gland carcinogenesis. This may be ascribed in part to the low expression level of EGFR in tumor cells.
本研究调查了给予表皮生长因子(EGF)是否能够改变唾液腺癌的发生。两组小鼠的左下颌下腺被注射1毫克的9,10 - 二甲基 - 1,2 - 苯并蒽(DMBA),然后第1组小鼠皮下注射2微克EGF,第2组小鼠皮下注射赋形剂,持续8周。另外两组,即第3组和第4组,分别单独接受EGF或赋形剂。实验开始12周后,第1组和第2组下颌下腺癌的发生率分别为39%和58%,尽管这一差异无统计学意义。左下颌下腺中的导管样和囊肿样结构以及癌组织被抗表皮生长因子受体(EGFR)抗体弱阳性染色。免疫印迹和逆转录聚合酶链反应(RT-PCR)分析显示EGFR在下颌下腺和癌组织中表达。然而,在源自第2组小鼠下颌下腺未分化癌的YT细胞中未检测到EGFR。这些发现表明,EGF在小鼠唾液腺癌发生过程中不促进肿瘤诱导。这可能部分归因于肿瘤细胞中EGFR的低表达水平。