Torabi Keyvan, Miró Rosa, Fernández-Jiménez Nora, Quintanilla Isabel, Ramos Laia, Prat Esther, del Rey Javier, Pujol Núria, Killian J Keith, Meltzer Paul S, Fernández Pedro Luis, Ried Thomas, Lozano Juan José, Camps Jordi, Ponsa Immaculada
Unitat de Biologia Cellular i Genètica Mèdica, Departament de Biologia Cellular, Fisiologia i Immunologia, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Catalonia 08193, Spain.
Unitat de Biologia Cellular i Genètica Mèdica, Departament de Biologia Cellular, Fisiologia i Immunologia, Facultat de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Catalonia 08193, Spain, Institut de Biotecnologia i Biomedicina, Universitat Autònoma de Barcelona, Bellaterra, Catalonia 08193, Spain.
Carcinogenesis. 2015 Oct;36(10):1103-10. doi: 10.1093/carcin/bgv115. Epub 2015 Aug 4.
Colorectal cancer (CRC) is characterized by specific patterns of copy number alterations (CNAs), which helped with the identification of driver oncogenes and tumor suppressor genes (TSGs). More recently, the usage of single nucleotide polymorphism arrays provided information of copy number neutral loss of heterozygosity, thus suggesting the occurrence of somatic uniparental disomy (UPD) and uniparental polysomy (UPP) events. The aim of this study is to establish an integrative profiling of recurrent UPDs/UPPs and CNAs in sporadic CRC. Our results indicate that regions showing high frequencies of UPD/UPP mostly coincide with regions typically involved in genomic losses. Among them, chromosome arms 3p, 5q, 9q, 10q, 14q, 17p, 17q, 20p, 21q and 22q preferentially showed UPDs/UPPs over genomic losses suggesting that tumor cells must maintain the disomic state of certain genes to favor cellular fitness. A meta-analysis using over 300 samples from The Cancer Genome Atlas confirmed our findings. Several regions affected by recurrent UPDs/UPPs contain well-known TSGs, as well as novel candidates such as ARID1A, DLC1, TCF7L2 and DMBT1. In addition, VCAN, FLT4, SFRP1 and GAS7 were also frequently involved in regions of UPD/UPP and displayed high levels of methylation. Finally, sequencing and fluorescence in situ hybridization analysis of the gene APC underlined that a somatic UPD event might represent the second hit to achieve biallelic inactivation of this TSG in colorectal tumors. In summary, our data define a profile of somatic UPDs/UPPs in sporadic CRC and highlights the importance of these events as a mechanism to achieve the inactivation of TSGs.
结直肠癌(CRC)具有特定的拷贝数改变(CNA)模式,这有助于识别驱动癌基因和肿瘤抑制基因(TSG)。最近,单核苷酸多态性阵列的应用提供了拷贝数中性杂合性缺失的信息,从而提示了体细胞单亲二体(UPD)和单亲多体(UPP)事件的发生。本研究的目的是建立散发性CRC中复发性UPD/UPP和CNA的综合图谱。我们的结果表明,显示高频率UPD/UPP的区域大多与通常涉及基因组缺失的区域重合。其中,染色体臂3p、5q、9q、10q、14q、17p、17q、20p、21q和22q优先显示UPD/UPP而非基因组缺失,这表明肿瘤细胞必须维持某些基因的二体状态以利于细胞适应性。使用来自癌症基因组图谱的300多个样本进行的荟萃分析证实了我们的发现。几个受复发性UPD/UPP影响的区域包含知名的TSG,以及ARID1A、DLC1、TCF7L2和DMBT1等新的候选基因。此外,VCAN、FLT4、SFRP1和GAS7也经常参与UPD/UPP区域并显示出高水平的甲基化。最后,对基因APC的测序和荧光原位杂交分析强调,体细胞UPD事件可能代表在结直肠癌肿瘤中实现该TSG双等位基因失活的第二次打击。总之,我们的数据定义了散发性CRC中体细胞UPD/UPP的图谱,并突出了这些事件作为实现TSG失活机制的重要性。