Turhal Nazim Serdar, Savaş Berna, Çoşkun Öznur, Baş Emine, Karabulut Bülent, Nart Deniz, Korkmaz Taner, Yavuzer Dilek, Demir Gökhan, Doğusoy Gülen, Artaç Mehmet
Department of Medical Oncology, Marmara University, Faculty of Medicine, 34722 Istanbul, Turkey.
Department of Pathology, Ankara University, Faculty of Medicine, 06100 Ankara, Turkey.
Mol Clin Oncol. 2015 Nov;3(6):1275-1279. doi: 10.3892/mco.2015.633. Epub 2015 Aug 31.
Hepatocellular carcinoma (HCC) is the fifth most common male-predominant type of cancer worldwide. There is no effective treatment regimen available for advanced-stage disease and chemotherapy is generally ineffective in these patients. The number of studies on the prevalence of K-Ras mutations in HCC patients is currently limited. A total of 58 patients from 6 comprehensive cancer centers in 4 metropolitan cities of Turkey were enrolled in this study. Each center committed to enroll approximately 10 random patients whose formalin-fixed paraffin-embedded tumor tissues were available for K-Ras, exon 2 genotyping. Two methods were applied based on the availability of adequate amounts of tumor DNA. In the first method, the samples were processed using TheraScreen. The genomic DNA was further used to detect the 7 most frequent somatic mutations (35G>A; 35G>C; 35G>T; 34G>A; 34G>C; 34G>T and 38G>A) in codons 12 and 13 in exon 2 of the K-Ras oncogene by quantitative polymerase chain reaction (PCR). In the second method, the genomic DNA was amplified by PCR using primers specific for K-Ras exon 2 with the GML SeqFinder Sequencing System's KRAS kit. The identified DNA sequence alterations were confirmed by sequencing both DNA strands in two independent experiments with forward and reverse primers. A total of 40 samples had adequate tumor tissue for the mutation analysis. A total of 33 (82.5%) of the investigated samples harbored no mutations in exon 2. All the mutations were identified via a direct sequencing technique, whereas none were identified by TheraScreen. In conclusion, in our patients, HCC exhibited a remarkably low (<20%) K-Ras mutation rate. Patients harboring K-Ras wild-type tumors may be good candidates for treatment with epidermal growth factor inhibitors, such as cetuximab.
肝细胞癌(HCC)是全球第五大最常见的以男性为主的癌症类型。对于晚期疾病,目前尚无有效的治疗方案,化疗对这些患者通常无效。目前关于HCC患者中K-Ras突变发生率的研究数量有限。本研究纳入了来自土耳其4个大城市6家综合癌症中心的58例患者。每个中心承诺纳入约10例随机患者,其福尔马林固定石蜡包埋的肿瘤组织可用于K-Ras第2外显子基因分型。根据肿瘤DNA的充足程度应用了两种方法。第一种方法是使用TheraScreen对样本进行处理。基因组DNA进一步用于通过定量聚合酶链反应(PCR)检测K-Ras癌基因第2外显子密码子12和13中的7种最常见的体细胞突变(35G>A;35G>C;35G>T;34G>A;34G>C;34G>T和38G>A)。第二种方法是使用GML SeqFinder测序系统的KRAS试剂盒,通过PCR使用针对K-Ras第2外显子的特异性引物扩增基因组DNA。通过在两个独立实验中使用正向和反向引物对两条DNA链进行测序,确认所鉴定的DNA序列改变。共有40个样本有足够的肿瘤组织用于突变分析。在被调查的样本中,共有33个(82.5%)在第2外显子中未发现突变。所有突变均通过直接测序技术鉴定,而TheraScreen未鉴定出任何突变。总之,在我们的患者中,HCC的K-Ras突变率极低(<20%)。携带K-Ras野生型肿瘤的患者可能是西妥昔单抗等表皮生长因子抑制剂治疗的良好候选者。