Morra Francesco, Merolla Francesco, Zito Marino Federica, Catalano Rosaria, Franco Renato, Chieffi Paolo, Celetti Angela
Institute for the Experimental Endocrinology and Oncology, Research National Council, CNR, Naples, Italy.
Department of Medicine and Health Sciences "V. Tiberio", University of Molise, Campobasso, Italy.
Heliyon. 2021 Nov 15;7(11):e08399. doi: 10.1016/j.heliyon.2021.e08399. eCollection 2021 Nov.
Coiled-coil domain containing 6 (CCDC6) is a tumour suppressor gene involved in apoptosis and DNA damage response. CCDC6 is known to be functionally impaired upon gene fusions, somatic mutations, and altered protein turnover in several tumours. Testicular germ cell tumours are among the most common malignancies in young males. Despite the high cure rate, achieved through chemotherapy and/or surgery, drug resistance can still occur. In a human cellular model of testis Embryonal Carcinoma, the deficiency of CCDC6 was associated with defects in DNA repair via homologous recombination and sensitivity to PARP1/2 inhibitors. Same data were obtained in a panel of murine testicular cell lines, including Sertoli, Spermatogonia and Spermatocytes. In these cells, upon oxidative damage exposure, the absence of CCDC6 conferred tolerance to reactive oxygen species affecting regulated cell death pathways by apoptosis and ferroptosis. At molecular level, the loss of CCDC6 was associated with an enhancement of the xCT/SLC7A11 cystine antiporter expression which, by promoting the accumulation of ROS, interfered with the activation of ferroptosis pathway. In conclusion, our data suggest that the CCDC6 downregulation could aid the testis germ cells to be part of a pro-survival pathway that helps to evade the toxic effects of endogenous oxidants contributing to testicular neoplastic growth. Novel therapeutic options will be discussed.
卷曲螺旋结构域包含蛋白6(CCDC6)是一种参与细胞凋亡和DNA损伤反应的肿瘤抑制基因。已知CCDC6在多种肿瘤中因基因融合、体细胞突变和蛋白质周转改变而功能受损。睾丸生殖细胞肿瘤是年轻男性中最常见的恶性肿瘤之一。尽管通过化疗和/或手术治愈率很高,但仍可能出现耐药性。在睾丸胚胎癌的人类细胞模型中,CCDC6的缺乏与同源重组DNA修复缺陷以及对PARP1/2抑制剂的敏感性有关。在一组小鼠睾丸细胞系中也获得了相同的数据,包括支持细胞、精原细胞和精母细胞。在这些细胞中,暴露于氧化损伤后,CCDC6的缺失赋予了对活性氧的耐受性,活性氧通过凋亡和铁死亡影响受调控的细胞死亡途径。在分子水平上,CCDC6的缺失与xCT/SLC7A11胱氨酸反向转运体表达的增强有关,该转运体通过促进活性氧的积累干扰铁死亡途径的激活。总之,我们的数据表明,CCDC6的下调可能有助于睾丸生殖细胞成为促生存途径的一部分,该途径有助于逃避内源性氧化剂对睾丸肿瘤生长的毒性作用。将讨论新的治疗选择。