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辐射后肉瘤与散发性肉瘤的基因组和转录组比较。

Genomic and transcriptomic comparison of post-radiation versus sporadic sarcomas.

机构信息

Inserm U1218, Institut Bergonié, Bordeaux, France.

University of Bordeaux, F-33000, Bordeaux, France.

出版信息

Mod Pathol. 2019 Dec;32(12):1786-1794. doi: 10.1038/s41379-019-0300-2. Epub 2019 Jun 26.

Abstract

Post-radiation sarcomas are rare secondary cancers arising from radiation therapies. To date, few genetic specificities have been described for such malignancies and the oncogenesis of sarcomas with complex genetics (both sporadic and post-radiation) remains largely misunderstood. We performed genomic and transcriptomic analyses on 77 post-radiation sarcomas using DNA-array and RNA sequencing. Consequently, we were able to investigate changes in copy number variations, transcriptome profiling, fusion gene expression, and mutational landscapes. We compare these data to a reference cohort of 93 sporadic sarcomas. At genomic level, similar chromosomal complexity was observed both in post-radiation and sporadic sarcomas with complex genetics. We found more frequent CDKN2A and CDKN2B (coding for p14/p16 and p15 proteins, respectively; at 9p21.3) losses in post-radiation (71%) than in sporadic tumors (39%; P = 6.92e-3). Among all detected fusion genes and punctual variations, few specificities were observed between these groups and such alterations are not able to drive a strong and specific oncogenesis. Recurrent MYC amplifications (96%) and KDR variants (8%) were detected in post-radiation angiosarcomas, in agreement with the literature. Transcriptomic analysis of such angiosarcomas revealed two distinct groups harboring different genomic imbalances (in particular gains of 17q24.2-17qter) with different clinical courses according to patient's vital status. Differential gene expression analysis permitted to focus on the immune response as a potential actor to tumor aggressiveness. Histochemistry validated a lower inflammation and lower immune infiltrate at tumor periphery for highly aggressive angiosarcomas. Our results provide new genomic and transcriptomic information about post-radiation sarcomas. The techniques we used (RNA-seq and DNA-arrays) did not highlight major differences in sarcomas with complex genetics depending on the radiation context, revealing similar patterns of transcriptomic profiles and chromosomal copy number variations. Additional characterizations, particularly whole genome sequencing, could measure changes in DNA following radiation therapy in such malignancies and may precise their oncogenesis.

摘要

放射性肉瘤是一种罕见的继发癌症,由放射治疗引起。迄今为止,对于此类恶性肿瘤,很少有特定的遗传特征被描述,并且具有复杂遗传学(包括散发性和放射性后)的肉瘤的致癌机制在很大程度上仍未被理解。我们使用 DNA 芯片和 RNA 测序对 77 例放射性肉瘤进行了基因组和转录组分析。因此,我们能够研究拷贝数变异、转录组谱、融合基因表达和突变景观的变化。我们将这些数据与 93 例散发性肉瘤的参考队列进行了比较。在基因组水平上,我们观察到具有复杂遗传学的放射性后和散发性肉瘤具有相似的染色体复杂性。我们发现,与散发性肿瘤(39%;P=6.92e-3)相比,放射性肉瘤中更频繁地出现 CDKN2A 和 CDKN2B(分别编码 p14/p16 和 p15 蛋白;位于 9p21.3)缺失(71%)。在所有检测到的融合基因和点突变中,这两组之间观察到的特异性很少,并且这些改变不能驱动强烈和特异的致癌作用。在放射性血管肉瘤中检测到反复出现的 MYC 扩增(96%)和 KDR 变体(8%),与文献一致。对这些血管肉瘤的转录组分析揭示了两组具有不同基因组失衡(特别是 17q24.2-17qter 的增益)的不同亚组,根据患者的生存状态,具有不同的临床过程。差异基因表达分析使我们能够关注免疫反应作为肿瘤侵袭性的潜在因素。组织化学验证了高度侵袭性血管肉瘤的肿瘤外周区炎症和免疫浸润较低。我们的结果提供了有关放射性肉瘤的新的基因组和转录组信息。我们使用的技术(RNA-seq 和 DNA 芯片)没有突出显示具有复杂遗传学的肉瘤之间的主要差异,这取决于放射治疗的背景,揭示了相似的转录组谱和染色体拷贝数变异模式。其他特征,特别是全基因组测序,可以测量此类恶性肿瘤在放射治疗后 DNA 的变化,并可能精确其致癌机制。

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