Oncogenesis of Sarcomas, INSERM UMR1037 - Team 19, Cancer Research Center of Toulouse, France.
Institut Claudius Régaud, IUCT-Oncopole, Toulouse, France.
Cancer Res. 2020 Dec 1;80(23):5282-5290. doi: 10.1158/0008-5472.CAN-20-0512. Epub 2020 Oct 6.
The Complexity Index in Sarcomas (CINSARC) signature is a transcriptomic marker that identifies high-risk soft-tissue sarcomas and is associated with high metastatic potential. During the last decade, CINSARC has been successfully developed and validated and is currently being assessed in two prospective phase III clinical trials for stratification of therapy. Although the link between CINSARC expression and tumor aggressiveness is well established, questions remain about how CINSARC genes are regulated. In this study, we leveraged a The Cancer Genome Atlas multiomics study on sarcomas with complex genetics to appraise the association between CINSARC profile, genomic features, and two potential regulation mechanisms, DNA methylation and miRNA expression. CINSARC expression was associated with an increase of ploidy, intratumor heterogeneity, copy-number alteration, altered expression of 37 miRNAs, and a decrease of DNA methylation. These genetic changes are not independent, but rather act together to promote or repress CINSARC expression. These findings depict new insights into CINSARC regulation. SIGNIFICANCE: These findings demonstrate that CINSARC is associated with a variety of genomic aberrations that contribute to higher risk for metastasis and may serve as a prognostic factor in sarcomas and beyond.
肉瘤复杂性指数(CINSARC)特征是一种转录组标志物,可识别高危软组织肉瘤,并与高转移潜能相关。在过去十年中,CINSARC 已成功开发和验证,并正在两项前瞻性 III 期临床试验中评估其在治疗分层中的应用。尽管 CINSARC 表达与肿瘤侵袭性之间的联系已得到充分证实,但关于 CINSARC 基因如何调控的问题仍存在疑问。在这项研究中,我们利用癌症基因组图谱(TCGA)中具有复杂遗传学的肉瘤多组学研究,评估 CINSARC 特征与基因组特征以及两种潜在调控机制(DNA 甲基化和 miRNA 表达)之间的关联。CINSARC 的表达与倍性增加、肿瘤内异质性、拷贝数改变、37 个 miRNA 表达改变以及 DNA 甲基化减少相关。这些遗传变化不是独立的,而是共同作用,促进或抑制 CINSARC 的表达。这些发现为 CINSARC 的调控提供了新的见解。意义:这些发现表明,CINSARC 与多种导致转移风险增加的基因组异常相关,可能作为肉瘤及其他疾病的预后因素。