Ewha Research Center for Systems Biology, Seoul, Korea.
Genes Chromosomes Cancer. 2012 Jun;51(6):590-7. doi: 10.1002/gcc.21945. Epub 2012 Feb 15.
An increasing number of chromosomal aberrations is being identified in solid tumors providing novel biomarkers for various types of cancer and new insights into the mechanisms of carcinogenesis. We applied next generation sequencing technique to analyze the transcriptome of the non-small cell lung carcinoma (NSCLC) cell line H2228 and discovered a fusion transcript composed of multiple exons of ALK (anaplastic lymphoma receptor tyrosine kinase) and PTPN3 (protein tyrosine phosphatase, nonreceptor Type 3). Detailed analysis of the genomic structure revealed that a portion of genomic region encompassing Exons 10 and 11 of ALK has been translocated into the intronic region between Exons 2 and 3 of PTPN3. The key net result appears to be the null mutation of one allele of PTPN3, a gene with tumor suppressor activity. Consistently, ectopic expression of PTPN3 in NSCLC cell lines led to inhibition of colony formation. Our study confirms the utility of next generation sequencing as a tool for the discovery of somatic mutations and has led to the identification of a novel mutation in NSCLC that may be of diagnostic, prognostic, and therapeutic importance.
越来越多的染色体异常正在实体瘤中被发现,为各种类型的癌症提供了新的生物标志物,并为癌症发生的机制提供了新的见解。我们应用下一代测序技术分析了非小细胞肺癌(NSCLC)细胞系 H2228 的转录组,发现了一个由 ALK(间变性淋巴瘤受体酪氨酸激酶)和 PTPN3(蛋白酪氨酸磷酸酶,非受体型 3)多个外显子组成的融合转录本。对基因组结构的详细分析表明,ALK 的外显子 10 和 11 的一部分基因组区域已易位到 PTPN3 的内含子 2 和 3 之间。关键的净结果似乎是 PTPN3 的一个等位基因的无效突变,PTPN3 是一种具有肿瘤抑制活性的基因。一致地,在 NSCLC 细胞系中外源表达 PTPN3 导致集落形成的抑制。我们的研究证实了下一代测序作为发现体细胞突变的工具的实用性,并导致鉴定出 NSCLC 中的一种新突变,该突变可能具有诊断、预后和治疗意义。