Nogueira Jeronimo A, Ono-Nita Suzane K, Nita Marcelo E, de Souza Marcelo M T, do Carmo Eliane P, Mello Evandro S, Scapulatempo Cristovan, Paranaguá-Vezozzo Denise C, Carrilho Flair J, Alves Venancio A F
Department of Gastroenterology, University of São Paulo School of Medicine, São Paulo, SP, Brazil.
BMC Cancer. 2009 Jun 26;9:204. doi: 10.1186/1471-2407-9-204.
Ser-249 TP53 mutation (249(Ser)) is a molecular evidence for aflatoxin-related carcinogenesis in Hepatocellular Carcinoma (HCC) and it is frequent in some African and Asian regions, but it is unusual in Western countries. HBV has been claimed to add a synergic effect on genesis of this particular mutation with aflatoxin. The aim of this study was to investigate the frequency of 249(Ser) mutation in HCC from patients in Brazil.
We studied 74 HCC formalin fixed paraffin blocks samples of patients whom underwent surgical resection in Brazil. 249(Ser) mutation was analyzed by RFLP and DNA sequencing. HBV DNA presence was determined by Real-Time PCR.
249(Ser) mutation was found in 21/74 (28%) samples while HBV DNA was detected in 13/74 (16%). 249Ser mutation was detected in 21/74 samples by RFLP assay, of which 14 were confirmed by 249(Ser) mutant-specific PCR, and 12 by nucleic acid sequencing. All HCC cases with p53-249ser mutation displayed also wild-type p53 sequences. Poorly differentiated HCC was more likely to have 249(Ser) mutation (OR = 2.415, 95% CI = 1.001 - 5.824, p = 0.05). The mean size of 249(Ser) HCC tumor was 9.4 cm versus 5.5 cm on wild type HCC (p = 0.012). HBV DNA detection was not related to 249(Ser) mutation.
Our results indicate that 249(Ser) mutation is a HCC important factor of carcinogenesis in Brazil and it is associated to large and poorly differentiated tumors.
249位丝氨酸(Ser-249)TP53突变是肝细胞癌(HCC)中黄曲霉毒素相关致癌作用的分子证据,在一些非洲和亚洲地区较为常见,但在西方国家并不常见。乙肝病毒(HBV)被认为会与黄曲霉毒素协同作用,促使这一特定突变的发生。本研究旨在调查巴西患者肝癌中249(Ser)突变的频率。
我们研究了74例在巴西接受手术切除的肝癌患者的福尔马林固定石蜡包埋组织样本。通过限制性片段长度多态性分析(RFLP)和DNA测序分析249(Ser)突变。采用实时聚合酶链反应(Real-Time PCR)检测HBV DNA的存在情况。
在21/74(28%)的样本中发现了249(Ser)突变,而在13/74(16%)的样本中检测到了HBV DNA。通过RFLP分析在21/74样本中检测到249Ser突变,其中14例经249(Ser)突变特异性PCR证实,12例经核酸测序证实。所有p53-249ser突变的肝癌病例也显示有野生型p53序列。低分化肝癌更易发生249(Ser)突变(比值比=2.415,95%置信区间=1.001 - 5.824,p = 0.05)。249(Ser)突变的肝癌肿瘤平均大小为9.4厘米,而野生型肝癌为5.5厘米(p = 0.012)。HBV DNA检测与249(Ser)突变无关。
我们的结果表明,249(Ser)突变是巴西肝癌发生的一个重要致癌因素,并且与肿瘤体积大及低分化有关。