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肿瘤抑制因子CCDC6通过逃避铁死亡参与活性氧耐受和肿瘤转化。

The tumour suppressor CCDC6 is involved in ROS tolerance and neoplastic transformation by evading ferroptosis.

作者信息

Morra Francesco, Merolla Francesco, Zito Marino Federica, Catalano Rosaria, Franco Renato, Chieffi Paolo, Celetti Angela

机构信息

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.

出版信息

Heliyon. 2021 Nov 15;7(11):e08399. doi: 10.1016/j.heliyon.2021.e08399. eCollection 2021 Nov.

DOI:10.1016/j.heliyon.2021.e08399
PMID:34841108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8605351/
Abstract

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.

摘要

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。

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本文引用的文献

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Coiled-Coil Domain-Containing (CCDC) Proteins: Functional Roles in General and Male Reproductive Physiology.卷曲螺旋结构域蛋白(CCDC):在一般和男性生殖生理学中的功能作用。
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Ferroptosis: molecular mechanisms and health implications.铁死亡:分子机制与健康关联。
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Testicular cancer: Determinants of cisplatin sensitivity and novel therapeutic opportunities.
MMP9 drives ferroptosis by regulating GPX4 and iron signaling.
基质金属蛋白酶9通过调节谷胱甘肽过氧化物酶4和铁信号传导来驱动铁死亡。
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A xCT role in tumour-associated ferroptosis shed light on novel therapeutic options.XCT在肿瘤相关铁死亡中的作用为新的治疗选择提供了线索。
Explor Target Antitumor Ther. 2022;3(5):570-581. doi: 10.37349/etat.2022.00101. Epub 2022 Oct 25.
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The disruption of the CCDC6 - PP4 axis induces a BRCAness like phenotype and sensitivity to PARP inhibitors in high-grade serous ovarian carcinoma.CCDC6-PP4 轴的破坏导致高级别浆液性卵巢癌中出现类似 BRCA 缺陷的表型和对 PARP 抑制剂的敏感性。
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NSCLC Mutated Isoforms of CCDC6 Affect the Intracellular Distribution of the Wild Type Protein Promoting Cisplatinum Resistance and PARP Inhibitors Sensitivity in Lung Cancer Cells.CCDC6的非小细胞肺癌突变异构体影响野生型蛋白的细胞内分布,促进肺癌细胞的顺铂耐药性和PARP抑制剂敏感性。
Cancers (Basel). 2019 Dec 21;12(1):44. doi: 10.3390/cancers12010044.
6
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Int J Mol Sci. 2019 Jun 25;20(12):3100. doi: 10.3390/ijms20123100.
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Cystine/glutamate antiporter xCT (SLC7A11) facilitates oncogenic RAS transformation by preserving intracellular redox balance.胱氨酸/谷氨酸反向转运蛋白 xCT(SLC7A11)通过维持细胞内氧化还原平衡促进致癌 RAS 转化。
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The molecular machinery of regulated cell death.调控细胞死亡的分子机制。
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