Mullard Mathilde, Cadé Marie, Morice Sarah, Dupuy Maryne, Danieau Geoffroy, Amiaud Jérome, Renault Sarah, Lézot Frédéric, Brion Régis, Thepault Rose Anne, Ory Benjamin, Lamoureux François, Corre Isabelle, Brounais-LeRoyer Bénédicte, Rédini Françoise, Verrecchia Franck
INSERM, UMR1238 "Bone Sarcomas and Remodeling of Calcified Tissues", Nantes University, F44035 Nantes, France.
Centre de Recherche en Cancérologie et Immunologie Nantes Angers, INSERM UMR1232, Nantes University, F44035 Nantes, France.
Cancers (Basel). 2020 Nov 19;12(11):3438. doi: 10.3390/cancers12113438.
Osteosarcoma (OS) and Ewing's sarcoma (ES) are the most common malignant bone tumors in children and adolescents. In many cases, the prognosis remains very poor. The Sonic hedgehog (SHH) signaling pathway, strongly involved in the development of many cancers, regulate transcription via the transcriptional factors Gli1-3. In this context, RNAseq analysis of OS and ES cell lines reveals an increase of some major compounds of the SHH signaling cascade in ES cells, such as the transcriptional factor Gli1. This increase leads to an augmentation of the transcriptional response of Gli1 in ES cell lines, demonstrating a dysregulation of Gli1 signaling in ES cells and thus the rationale for targeting Gli1 in ES. The use of a preclinical model of ES demonstrates that GANT61, an inhibitor of the transcriptional factor Gli1, reduces ES primary tumor growth. In vitro experiments show that GANT61 decreases the viability of ES cell, mainly through its ability to induce caspase-3/7-dependent cell apoptosis. Taken together, these results demonstrates that GANT61 may be a promising therapeutic strategy for inhibiting the progression of primary ES tumors.
骨肉瘤(OS)和尤因肉瘤(ES)是儿童和青少年中最常见的恶性骨肿瘤。在许多情况下,预后仍然很差。 Sonic hedgehog(SHH)信号通路在许多癌症的发生发展中起着重要作用,它通过转录因子Gli1-3调节转录。在这种情况下,对OS和ES细胞系的RNAseq分析显示,ES细胞中SHH信号级联的一些主要成分增加,例如转录因子Gli1。这种增加导致ES细胞系中Gli1的转录反应增强,表明ES细胞中Gli1信号失调,因此有理由在ES中靶向Gli1。使用ES的临床前模型表明,转录因子Gli1的抑制剂GANT61可减少ES原发性肿瘤的生长。体外实验表明,GANT61主要通过诱导caspase-3/7依赖性细胞凋亡来降低ES细胞的活力。综上所述,这些结果表明GANT61可能是抑制原发性ES肿瘤进展的一种有前景的治疗策略。