Department of Clinical and Biological Sciences, University of Turin, Turin, Italy.
Cancer Prev Res (Phila). 2011 Jul;4(7):994-1001. doi: 10.1158/1940-6207.CAPR-10-0301.
Vaccines against oncoantigens halt early neoplastic lesions in several cancer-prone, genetically engineered mouse models, whereas their ability to prevent chemical carcinogenesis has not been explored. This is a significant issue, as exposure to chemical mutagens is responsible for a substantial percentage of cancers worldwide. Here, we show that the archetypal oncoantigen ERBB2 is transiently overexpressed in Syrian hamsters during the early stages of 7,12-dimethylbenz[α]anthracene (DMBA)-induced oral carcinogenesis. Repeated DNA vaccinations against ERBB2 significantly reduce the number, size, and severity of oral lesions in a manner directly proportional to the anti-ERBB2 antibody response. These results support the prospects of vaccines as a fresh strategy in the management of individuals at risk for exposure to defined carcinogenic agents.
针对癌抗原的疫苗可阻止几种易患癌症的基因工程小鼠模型中的早期肿瘤病变,而其预防化学致癌的能力尚未得到探索。这是一个重要的问题,因为接触化学诱变剂是全世界癌症的主要原因之一。在这里,我们发现 ERBB2 这一典型的癌抗原在叙利亚仓鼠接受 7,12-二甲基苯并[a]蒽(DMBA)诱导的口腔致癌作用的早期阶段会短暂过表达。针对 ERBB2 的重复 DNA 疫苗接种以与抗 ERBB2 抗体反应成正比的方式,显著减少了口腔病变的数量、大小和严重程度。这些结果支持将疫苗作为一种新策略用于管理接触特定致癌剂的高危人群。