Choy Edwin, MacConaill Laura E, Cote Gregory M, Le Long P, Shen Jacson K, Nielsen Gunnlaugur P, Iafrate Anthony J, Garraway Levi A, Hornicek Francis J, Duan Zhenfeng
Division of Hematology Oncology, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Sarcoma Biology Laboratory, Center for Sarcoma and Connective Tissue Oncology, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Center for Cancer Genome Discovery and Department of Medical Oncology, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS One. 2014 Jul 1;9(7):e101283. doi: 10.1371/journal.pone.0101283. eCollection 2014.
The molecular mechanisms underlying chordoma pathogenesis are unknown. We therefore sought to identify novel mutations to better understand chordoma biology and to potentially identify therapeutic targets. Given the relatively high costs of whole genome sequencing, we performed a focused genetic analysis using matrix-assisted laser desorption/ionization-time of flight mass spectrometer (Sequenom iPLEX genotyping). We tested 865 hotspot mutations in 111 oncogenes and selected tumor suppressor genes (OncoMap v. 3.0) of 45 human chordoma tumor samples. Of the analyzed samples, seven were identified with at least one mutation. Six of these were from fresh frozen samples, and one was from a paraffin embedded sample. These observations were validated using an independent platform using homogeneous mass extend MALDI-TOF (Sequenom hME Genotyping). These genetic alterations include: ALK (A877S), CTNNB1 (T41A), NRAS (Q61R), PIK3CA (E545K), PTEN (R130), CDKN2A (R58*), and SMARCB1 (R40*). This study reports on the largest comprehensive mutational analysis of chordomas performed to date. To focus on mutations that have the greatest chance of clinical relevance, we tested only oncogenes and tumor suppressor genes that have been previously implicated in the tumorigenesis of more common malignancies. We identified rare genetic changes that may have functional significance to the underlying biology and potential therapeutics for chordomas. Mutations in CDKN2A and PTEN occurred in areas of chromosomal copy loss. When this data is paired with the studies showing 18 of 21 chordoma samples displaying copy loss at the locus for CDKN2A, 17 of 21 chordoma samples displaying copy loss at PTEN, and 3 of 4 chordoma samples displaying deletion at the SMARCB1 locus, we can infer that a loss of heterozygosity at these three loci may play a significant role in chordoma pathogenesis.
脊索瘤发病机制的分子机制尚不清楚。因此,我们试图鉴定新的突变,以更好地理解脊索瘤生物学,并有可能确定治疗靶点。鉴于全基因组测序成本相对较高,我们使用基质辅助激光解吸/电离飞行时间质谱仪(Sequenom iPLEX基因分型)进行了重点基因分析。我们检测了45例人类脊索瘤肿瘤样本中111个癌基因和选定的肿瘤抑制基因(OncoMap v. 3.0)中的865个热点突变。在分析的样本中,有7个样本被鉴定出至少有一个突变。其中6个来自新鲜冷冻样本,1个来自石蜡包埋样本。这些观察结果通过使用均质质量延伸基质辅助激光解吸电离飞行时间质谱(Sequenom hME基因分型)的独立平台进行了验证。这些基因改变包括:ALK(A877S)、CTNNB1(T41A)、NRAS(Q61R)、PIK3CA(E545K)、PTEN(R130)、CDKN2A(R58*)和SMARCB1(R40*)。本研究报告了迄今为止对脊索瘤进行的最大规模的综合突变分析。为了关注具有最大临床相关性的突变,我们仅检测了先前与更常见恶性肿瘤的肿瘤发生有关的癌基因和肿瘤抑制基因。我们鉴定出了可能对脊索瘤潜在生物学和潜在治疗具有功能意义的罕见基因变化。CDKN2A和PTEN的突变发生在染色体拷贝缺失区域。当这些数据与显示21个脊索瘤样本中有18个在CDKN2A基因座显示拷贝缺失、21个脊索瘤样本中有17个在PTEN基因座显示拷贝缺失以及4个脊索瘤样本中有3个在SMARCB1基因座显示缺失的研究相结合时,我们可以推断这三个基因座的杂合性缺失可能在脊索瘤发病机制中起重要作用。