Cigrang Max, Obid Julian, Nogaret Maguelone, Seno Léane, Ye Tao, Davidson Guillaume, Catez Philippe, Berico Pietro, Capelli Clara, Marechal Clara, Zachayus Amélie, Elly Clémence, Guillen Navarro Marie Jose, Martinez Diez Marta, Santamaria Nunez Gema, Li Tsai-Kun, Compe Emmanuel, Avilés Pablo, Davidson Irwin, Egly Jean-Marc, Cuevas Carmen, Coin Frédéric
IGBMC, Institut de Génétique et de Biologie Moléculaire et Cellulaire Illkirch Cedex, C.U. Equipe Labélisée Ligue contre le Cancer, Strasbourg, France.
UMR7104, Illkirch, France.
Nat Commun. 2025 Jan 8;16(1):512. doi: 10.1038/s41467-024-55667-z.
The plasticity of cancer cells facilitates their ability to adopt heterogeneous differentiation states, posing a significant challenge to therapeutic interventions. Specific gene expression programs, driven in part by super-enhancers (SEs), underlie cancer cell states. Here we successfully inhibit SE-driven transcription in phenotypically distinct metastatic melanoma cells using next-generation synthetic ecteinascidins. Through functional genomic methodologies, we demonstrate that these compounds inhibit the expression of genes encoding lineage-specific or ubiquitous transcription factors/coactivators by selectively targeting the CpG-rich sequences within their promoters and/or enhancers. This prevents the formation of transcription factor/coactivator condensates necessary for SE-dependent gene expression. Consequently, these compounds exhibit cytotoxic activity across distinct subpopulations of metastatic melanoma cells and inhibit tumor proliferation, including those resistant to current therapies. These findings extend to other cancers, like small cell lung cancer, recently approved for ecteinascidin-based treatment. Overall, our study provides preclinical proof that pan-inhibition of SE-dependent genes with synthetic ecteinascidins is a promising therapeutic approach for tumors with heterogeneous transcriptional landscapes.
癌细胞的可塑性促进了它们采用异质分化状态的能力,这给治疗干预带来了重大挑战。部分由超级增强子(SEs)驱动的特定基因表达程序是癌细胞状态的基础。在这里,我们使用新一代合成海鞘素成功抑制了表型不同的转移性黑色素瘤细胞中SE驱动的转录。通过功能基因组学方法,我们证明这些化合物通过选择性靶向启动子和/或增强子内富含CpG的序列来抑制编码谱系特异性或普遍存在的转录因子/共激活因子的基因表达。这阻止了SE依赖性基因表达所需的转录因子/共激活因子凝聚物的形成。因此,这些化合物在转移性黑色素瘤细胞的不同亚群中表现出细胞毒性活性,并抑制肿瘤增殖,包括那些对当前疗法耐药的细胞。这些发现扩展到了其他癌症,如最近被批准基于海鞘素进行治疗的小细胞肺癌。总体而言,我们的研究提供了临床前证据,表明用合成海鞘素全面抑制SE依赖性基因是一种针对具有异质转录格局的肿瘤的有前景的治疗方法。