Graduate Institute of Biomedical Sciences, Chang Gung University, Tao-Yuan, Taiwan.
Genes Chromosomes Cancer. 2011 May;50(5):358-69. doi: 10.1002/gcc.20861. Epub 2011 Feb 22.
Oral squamous cell carcinoma (OSCC) has the highest rate of increase among male cancers in Taiwan. An understanding of the molecular pathogenesis of this disease as well as the development of prognostic markers for the clinical management of this disease is very important. Thus, a systematic loss of heterozygosity (LOH) analysis was performed to define minimally deleted regions (MDRs) in 63 male OSCCs using 400 polymorphic microsatellite markers. For increasing reliability, genomic DNA was extracted from >90% tumor cells that had been purified by LCM, and only when a microsatellite marker provided LOH information in >30% of the OSCCs was there considered to be successful allelotyping. A correlation of the various MDRs with clinicopathological parameters and prognosis was carried out. In total, 32 MDRs were identified and ten were noted as novel. In addition, six MDRs were found to be associated with cigarette smoking. Among these markers, a loss of MDR c7r2 (7q32.2-q35) was significantly associated with poor disease-free survival (DFS) and ten MDRs were associated with allelic imbalance (AI) in tumors. Among the latter, a loss of MDR c14r1 (14q24.2-q32.12) and c11r1 (11q13.4-q25) had a synergistic effect on poor DFS and were able to reduce further the DFS rate in patients with MDR c7r2 loss. Taken together, the results generated in this study provide new insights that help with exploring the molecular mechanisms associated with OSCC tumorigenesis and cigarette smoking. They also should aid the development of potential prognostic markers for the clinical management of OSCC.
口腔鳞状细胞癌 (OSCC) 在台湾男性癌症中发病率增长最快。了解这种疾病的分子发病机制以及为这种疾病的临床管理开发预后标志物非常重要。因此,使用 400 个多态微卫星标记物对 63 例男性 OSCC 进行了系统的杂合性丢失 (LOH) 分析,以定义最小缺失区域 (MDR)。为了提高可靠性,从通过 LCM 纯化的 >90%肿瘤细胞中提取基因组 DNA,并且只有当微卫星标记物在 >30%的 OSCC 中提供 LOH 信息时,才认为是成功的等位基因分型。对各种 MDR 与临床病理参数和预后的相关性进行了研究。总共鉴定出 32 个 MDR,其中 10 个是新的。此外,还发现 6 个 MDR 与吸烟有关。在这些标记物中,MDR c7r2 (7q32.2-q35) 的丢失与无病生存期 (DFS) 差显著相关,10 个 MDR 与肿瘤中的等位基因失衡 (AI) 相关。在后者中,MDR c14r1 (14q24.2-q32.12) 和 c11r1 (11q13.4-q25) 的丢失与较差的 DFS 具有协同作用,并且能够进一步降低 MDR c7r2 丢失患者的 DFS 率。总之,本研究的结果提供了新的见解,有助于探索与 OSCC 肿瘤发生和吸烟相关的分子机制。它们还应该有助于开发用于 OSCC 临床管理的潜在预后标志物。