Smela M E, Currier S S, Bailey E A, Essigmann J M
Department of Chemistry and Division of Bioengineering and Environmental Health Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Carcinogenesis. 2001 Apr;22(4):535-45. doi: 10.1093/carcin/22.4.535.
Dietary exposure to aflatoxin B(1) (AFB(1)) is associated with an increased incidence of hepatocellular carcinoma (HCC), especially in populations in which exposure to hepatitis B virus (HBV) is a common occurrence. Most HCC samples from people living where HBV is prevalent have one striking mutational hotspot: a GC-->TA transversion at the third position of codon 249 of the p53 gene. In this review, the chemical reaction of an electrophilic derivative of aflatoxin with specific DNA sequences is examined, along with the types of mutations caused by AFB(1) and the sequence context dependence of those mutations. An attempt is made to assign the source of these mutations to specific chemical forms of AFB(1)-DNA damage. In addition, epidemiological and experimental data are examined regarding the synergistic effects of AFB(1) and HBV on HCC formation and the predominance of one hotspot GC-->TA transversion in the p53 gene of affected individuals.
膳食中黄曲霉毒素B1(AFB1)暴露与肝细胞癌(HCC)发病率增加有关,尤其是在乙型肝炎病毒(HBV)暴露常见的人群中。来自HBV流行地区人群的大多数HCC样本有一个显著的突变热点:p53基因密码子249第三位的GC→TA颠换。在本综述中,研究了黄曲霉毒素亲电衍生物与特定DNA序列的化学反应,以及AFB1引起的突变类型和这些突变的序列上下文依赖性。试图将这些突变的来源归因于AFB1-DNA损伤的特定化学形式。此外,还研究了关于AFB1和HBV对HCC形成的协同作用以及受影响个体p53基因中一个热点GC→TA颠换占优势的流行病学和实验数据。