Rad18 在维持胶质母细胞瘤增殖方面的非催化功能

Nour El-Houda Benbahouche, Chames Kermi, Aurore Siegfried, Lenka Sefancikova, Jean-Marc Pascussi, Julie Pannequin, Jerome Moreaux, Jean-Philippe Hugnot, Marie-Bernadette Delisle, Elizabeth Moyal, Emmanuelle Uro-Coste, Domenico Maiorano
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摘要

Rad18 E3 泛素连接酶是 DNA 损伤耐受性的一个关键调节因子,它还具有修复 DNA 双股断裂的功能。Rad18 在侵袭性脑癌胶质母细胞瘤中过度表达,其下调会使胶质母细胞瘤细胞对 DNA 损伤剂敏感。我们在这里发现,在没有外部损伤的情况下,Rad18 对胶质母细胞瘤细胞的增殖起着至关重要的作用,这与它的催化活性无关。在没有明显 DNA 损伤的情况下,Rad18 的下调会导致细胞周期停滞在细胞周期的 G1 阶段。我们还发现,Rad18 对胶质母细胞瘤干细胞的自我更新和存活以及肿瘤在小鼠体内的正交异种移植的生长至关重要。我们还发现,Rad18 表达的增加会促进转化细胞的生长,并诱导致癌转化的特征。总之,这些数据表明 Rad18 这一非基本基因是胶质母细胞瘤增殖所必需的基因,也是使胶质母细胞瘤对治疗敏感的关键靶点。
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A non-catalytic function for Rad18 in sustaining glioblastoma proliferation
The Rad18 E3 ubiquitin ligase is a key regulator of DNA damage tolerance that also functions in repair of DNA double strand breaks. Rad18 is overexpressed in the aggressive brain cancer glioblastoma and its downregulation sensitizes glioblastoma cells to DNA damaging agents. Here we show that Rad18 has an essential role in glioblastoma cells proliferation in the absence of external damage, which is independent of its catalytic activity. Rad18 downregulation leads to cell cycle arrest in the G1 phase of the cell cycle in the absence of apparent DNA damage. We also show that Rad18 is essential for glioblastoma stem cells self-renewal and survival, and the growth of tumor orthotropic xenografts in mice. We also show that increased Rad18 expression enhances the growth of transformed cells and induces features of oncogenic transformation. Altogether, these data propose Rad18, a non-essential gene, as a gene essential for GBM proliferation and a key target to sensitize glioblastoma to therapy.
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