NSUN2酰化通过增强gclc依赖性谷胱甘肽合成驱动癌细胞对铁凋亡的抵抗。

IF 10.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kaifeng Niu , Zixiang Chen , Mengge Li , Guannan Ma , Yuchun Deng , Ji Zhang , Di Wei , Jiaqi Wang , Yongliang Zhao
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引用次数: 0

摘要

乳酸介导的靶蛋白乳酸化是一种具有深远生物学功能的新型翻译后修饰。RNA 5-甲基胞嘧啶(m5C)修饰具有动态和可逆性,表明其甲基转移酶NSUN2的活性受到积极调节。然而,NSUN2的活性是如何响应肿瘤微环境中的酸性条件,进而调控癌细胞存活的,目前尚不清楚。在这里,我们证明NSUN2的活性通过乳酸介导的赖氨酸508的乳酸化而增强,然后以谷氨酸-半胱氨酸连接酶催化亚基(GCLC) mRNA为靶点,促进GCLC m5C的形成和mRNA的稳定。激活的GCLC在胃癌细胞中诱导更高水平的细胞内GSH,并伴有脂质过氧化降低和对多柔比星(Dox)诱导铁死亡的抗性表型。具体来说,当NSUN2 K508R或GCLC C-A突变体(5个胞嘧啶位点)被引入癌细胞时,NSUN2乳酸化-GCLC- gsh通路的作用几乎消失。我们进一步确定催化亚基N-α-乙酰转移酶10 (NAA10)是NSUN2的乳酸转移酶,乳酸处理大大增强了它们的关联和随后的NSUN2活化。综上所述,我们的研究结果令人信服地阐明了NAA10-NSUN2-GCLC的信号轴在酸性条件下能有效拮抗铁凋亡,因此,靶向NSUN2的乳酸化可能是改善癌症患者预后的有效策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

NSUN2 lactylation drives cancer cell resistance to ferroptosis through enhancing GCLC-dependent glutathione synthesis

NSUN2 lactylation drives cancer cell resistance to ferroptosis through enhancing GCLC-dependent glutathione synthesis
Lactate-mediated lactylation on target proteins is recently identified as the novel posttranslational modification with profound biological functions. RNA 5-methylcytosine (m5C) modification possesses dynamic and reversible nature, suggesting that activity of its methyltransferase NSUN2 is actively regulated. However, how NSUN2 activity is response to acidic condition in tumor microenvironment and then regulates cancer cell survival remain to be clarified. Here, we demonstrate that NSUN2 activity is enhanced by lactate-mediated lactylation at lysine 508, which then targets glutamate-cysteine ligase catalytic subunit (GCLC) mRNA to facilitates GCLC m5C formation and mRNA stabilization. The activated GCLC induces higher level of intracellular GSH accompanied by decreased lipid peroxidation and resistant phenotype to ferroptosis induction by doxorubicin (Dox) in gastric cancer cells. Specifically, the effect of NSUN2 lactylation-GCLC-GSH pathway is nearly lost when NSUN2 K508R or GCLC C-A mutant (five cytosine sites) was introduced into the cancer cells. We further identify the catalytic subunit N-α-acetyltransferase 10 (NAA10) as the lactytransferase of NSUN2, and lactate treatment substantially enhances their association and consequent NSUN2 activation. Taken together, our findings convincingly elucidate the signaling axis of NAA10-NSUN2-GCLC that potently antagonizes the ferroptosis under acidic condition, and therefore, targeting NSUN2 lactylation might be an effective strategy in improving the prognosis of cancer patients.
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来源期刊
Redox Biology
Redox Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
19.90
自引率
3.50%
发文量
318
审稿时长
25 days
期刊介绍: Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease. Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.
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