Novel Functions of Lysine Demethylases as Mitochondrial Gatekeepers

Ling-Yu Wang, Hung‐Jung Wang, Chiu‐Lien Hung, Wen-Ching Wang, D. Ann, H. Kung
{"title":"Novel Functions of Lysine Demethylases as Mitochondrial Gatekeepers","authors":"Ling-Yu Wang, Hung‐Jung Wang, Chiu‐Lien Hung, Wen-Ching Wang, D. Ann, H. Kung","doi":"10.18143/JWMS_V2I2_1974","DOIUrl":null,"url":null,"abstract":"There is considerable evidence that KDMs, lysine demethylases, are oncogenic drivers for cancers. We have focused on KDM4A (Wang et al., Cell Reports, 2016) and KDM8 (Wang et al., PNAS, 2014) in prostate carcinogenesis. Both KDM4A and KDM8 are overexpressed in prostate cancers and their overexpressions confer castration-resistance as well as therapy-resistance. KDM4A demethylates H3K9me3 and H3K36me2/3, whereas KDM8 demethylates H3K36me2 (Hsia et al., PNAS, 2010). They both are coactivators of AR and when overexpressed, activate androgen response genes. Here, we report that they have additional novel functions as the gate keepers of mitochondria. Pyruvate flow into mitochondria is important for TCA cycle and oxidative phosphorylation, which is regulated by two key kinases PKM2 (pyruvate kinase M2) and PDKs (pyruvate dehydrogenase kinases). Cytosolic PKM2, the predominant form in tumor cells, is responsible for the synthesis of pyruvate, the level of which dictates the flow to mitochondria or to lactate. PDK1 to 4 negatively regulate the conversion of pyruvate to acetyl-coA by phosphorylating pyruvate dehydrogenase. We have shown that KDM8 associates with PKM2 and effectively translocates PKM2 into the nucleus, where KDM8/PKM2 serve as coactivator of HIF-1a. The consequence of this translocation is the decrease of cytosolic PKM2 activity and the increase of the expression of glycolytic enzymes, resulting in the limited pyruvate flow into mitochondria. At the same time, it favors the anabolic pathways and the biosynthesis of macromolecules, required for metabolic adaptation of tumor cells. KDM4, as we reported recently, serves as an E2F1 coactivator enhances the expression of PDK1 and PDK3, which also limits the flow of pyruvate to acetyl-coA and oxidative phosphorylation. Thus, both KDM8 and KDM4A work in concert to deflect pyruvate from mitochondria in favor of tumor metabolism. The detailed mechanisms and their implications in cancer therapies will be discussed.","PeriodicalId":266249,"journal":{"name":"Journal of World Mitochondria Society","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of World Mitochondria Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18143/JWMS_V2I2_1974","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

There is considerable evidence that KDMs, lysine demethylases, are oncogenic drivers for cancers. We have focused on KDM4A (Wang et al., Cell Reports, 2016) and KDM8 (Wang et al., PNAS, 2014) in prostate carcinogenesis. Both KDM4A and KDM8 are overexpressed in prostate cancers and their overexpressions confer castration-resistance as well as therapy-resistance. KDM4A demethylates H3K9me3 and H3K36me2/3, whereas KDM8 demethylates H3K36me2 (Hsia et al., PNAS, 2010). They both are coactivators of AR and when overexpressed, activate androgen response genes. Here, we report that they have additional novel functions as the gate keepers of mitochondria. Pyruvate flow into mitochondria is important for TCA cycle and oxidative phosphorylation, which is regulated by two key kinases PKM2 (pyruvate kinase M2) and PDKs (pyruvate dehydrogenase kinases). Cytosolic PKM2, the predominant form in tumor cells, is responsible for the synthesis of pyruvate, the level of which dictates the flow to mitochondria or to lactate. PDK1 to 4 negatively regulate the conversion of pyruvate to acetyl-coA by phosphorylating pyruvate dehydrogenase. We have shown that KDM8 associates with PKM2 and effectively translocates PKM2 into the nucleus, where KDM8/PKM2 serve as coactivator of HIF-1a. The consequence of this translocation is the decrease of cytosolic PKM2 activity and the increase of the expression of glycolytic enzymes, resulting in the limited pyruvate flow into mitochondria. At the same time, it favors the anabolic pathways and the biosynthesis of macromolecules, required for metabolic adaptation of tumor cells. KDM4, as we reported recently, serves as an E2F1 coactivator enhances the expression of PDK1 and PDK3, which also limits the flow of pyruvate to acetyl-coA and oxidative phosphorylation. Thus, both KDM8 and KDM4A work in concert to deflect pyruvate from mitochondria in favor of tumor metabolism. The detailed mechanisms and their implications in cancer therapies will be discussed.
赖氨酸去甲基酶作为线粒体看门人的新功能
有相当多的证据表明赖氨酸去甲基化酶是癌症的致癌驱动因素。我们重点研究了KDM4A (Wang et al., Cell Reports, 2016)和KDM8 (Wang et al., PNAS, 2014)在前列腺癌发生中的作用。KDM4A和KDM8在前列腺癌中都过表达,它们的过表达导致去势抵抗和治疗抵抗。KDM4A使H3K9me3和H3K36me2/3去甲基化,而KDM8使H3K36me2去甲基化(Hsia等,PNAS, 2010)。它们都是AR的共激活因子,当过表达时,激活雄激素反应基因。在这里,我们报道了它们作为线粒体的看门人具有额外的新功能。丙酮酸进入线粒体对于TCA循环和氧化磷酸化是重要的,这是由两个关键激酶PKM2(丙酮酸激酶M2)和PDKs(丙酮酸脱氢酶激酶)调节的。胞质PKM2是肿瘤细胞中的主要形式,负责丙酮酸的合成,其水平决定了流向线粒体或乳酸的流动。PDK1至4通过磷酸化丙酮酸脱氢酶负向调节丙酮酸转化为乙酰辅酶a。我们已经证明KDM8与PKM2结合并有效地将PKM2转运到细胞核中,在细胞核中KDM8/PKM2作为HIF-1a的共激活因子。这种易位的结果是胞质内PKM2活性的降低和糖酵解酶表达的增加,导致丙酮酸流入线粒体的受限。同时,它有利于肿瘤细胞代谢适应所需的合成代谢途径和大分子的生物合成。正如我们最近报道的那样,KDM4作为E2F1共激活因子增强PDK1和PDK3的表达,这也限制了丙酮酸向乙酰辅酶a的流动和氧化磷酸化。因此,KDM8和KDM4A协同作用,使丙酮酸从线粒体中转移,有利于肿瘤代谢。详细的机制及其在癌症治疗中的意义将被讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信