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癌症驱动基因异柠檬酸脱氢酶1/2(IDH1/2)、含Jumonji结构域的赖氨酸去甲基化酶1C/赖氨酸特异性去甲基化酶5C(JARID1C/KDM5C)以及含泛素羧基末端水解酶结构域的赖氨酸去甲基化酶6A/赖氨酸特异性去甲基化酶6A(UTX/KDM6A):癌症代谢中组蛋白去甲基化与缺氧重编程之间的相互作用

The cancer driver genes IDH1/2, JARID1C/ KDM5C, and UTX/ KDM6A: crosstalk between histone demethylation and hypoxic reprogramming in cancer metabolism.

作者信息

Chang Soojeong, Yim Sujin, Park Hyunsung

机构信息

Department of Life Science, University of Seoul, Seoul, 02504, Korea.

出版信息

Exp Mol Med. 2019 Jun 20;51(6):1-17. doi: 10.1038/s12276-019-0230-6.

DOI:10.1038/s12276-019-0230-6
PMID:31221981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6586683/
Abstract

Recent studies on mutations in cancer genomes have distinguished driver mutations from passenger mutations, which occur as byproducts of cancer development. The cancer genome atlas (TCGA) project identified 299 genes and 24 pathways/biological processes that drive tumor progression (Cell 173: 371-385 e318, 2018). Of the 299 driver genes, 12 genes are involved in histones, histone methylation, and demethylation (Table 1). Among these 12 genes, those encoding the histone demethylases JARID1C/KDM5C and UTX/KDM6A were identified as cancer driver genes. Furthermore, gain-of-function mutations in genes encoding metabolic enzymes, such as isocitrate dehydrogenases (IDH)1/2, drive tumor progression by producing an oncometabolite, D-2-hydroxyglutarate (D-2HG), which is a competitive inhibitor of α-ketoglutarate, O-dependent dioxygenases such as Jumonji domain-containing histone demethylases, and DNA demethylases. Studies on oncometabolites suggest that histone demethylases mediate metabolic changes in chromatin structure. We have reviewed the most recent findings regarding cancer-specific metabolic reprogramming and the tumor-suppressive roles of JARID1C/KDM5C and UTX/KDM6A. We have also discussed mutations in other isoforms such as the JARID1A, 1B, 1D of KDM5 subfamilies and the JMJD3/KDM6B of KDM6 subfamilies, which play opposing roles in tumor progression as oncogenes or tumor suppressors depending on the cancer cell type. Table 1 Cancer driver genes involved in epigenetics Pathways involved in epigenetics Driver genes Tumor suppressor/oncogene prediction (by 20/20+) Approved name Activity Cancer type Other driver genes in this pathways Histone modification KDM6A tsg Lysine demethylase 6A, UTX H3K27me2/3 demethylase BLCA, HNSC, KIRP, LUSC, PAAD, PANCAN, PRAD PPP6C SETD2 tsg SET domain-containing 2 H3K36 methyl transferase KIRC, KIRP, LGG, LUAD, MESO, PANCAN Chromatin histone modifiers KDM5C tsg Lysine demethylase 5C, JARID1C H3K4me2/3 demethylase KIRC, PANCAN ARID5B, CREBBP, EP300, KANSL1, MEN1, NCOR1, NSD1, SIN3A, WHSC1, ZMYM3 KMT2A tsg Lysine methyltransferase 2A H3K4 methyl transferase PANCAN KMT2B tsg Lysine methyltransferase 2B H3K4 methyl transferase PANCAN, UCEC KMT2C tsg Lysine methyltransferase 2C H3K4 methyl transferase BLCA, BRCA, CESC, PANCAN, UCEC KMT2D tsg Lysine methyltransferase 2D H3K4 methyl transferase BLCA, CESC, DLBC, ESCA, HNSC, LUSC, PANCAN, PRAD Chromatin (other) H3F3A Possible oncogene H3 histone family member 3A, H3.3A PANCAN AJUBA, ASXL1, ASXL2, ATF7IP, BCOR, CHD3, CHD4, CHD8, CTCF, NIPBL, NPM1 H3F3C - H3 histone family member 3C, H3.5 PANCAN HIST1H1E Possible oncogene HIST1H1E, H1.4 DLBC Possible tsg HIST1H1E, H1.4 LIHC Metabolism IDH1 Oncogene Isocitrate dehydrogenase (NADP(+)) 1 NADP-dependent IDH, Cytosolic CHOL, GBM, LAML, LGG, LIHC, PANCAN, PRAD, SKCM - IDH2 Oncogene Isocitrate dehydrogenase (NADP(+)) 2 NADP-dependent IDH, Mitochondrial LAML, LGG, PANCAN Among the 299 driver genes mentioned by Bailey et al., only the epigenetics-related pathways have been sorted out 20/20+: Classifies genes as an oncogene, tumor suppressor gene, or as a nondriver gene using Random Forests, http://2020plus.readthedocs.org BLCA (bladder urothelial carcinoma), BRCA (breast invasive carcinoma), CESC (cervical squamous cell carcinoma and endocervical adenocarcinoma), CHOL (cholangiocarcinoma), DLBC (lymphoid neoplasm diffuse large B-cell lymphoma), ESCA (esophageal carcinoma), GBM (glioblastoma multiforme), HNSC (head and neck squamous cell carcinoma), KIRC (kidney renal clear cell carcinoma), KIRP (kidney renal papillary cell carcinoma), LAML (acute myeloid leukemia), LGG (brain lower grade glioma), LIHC (liver hepatocellular carcinoma), LUAD (lung adenocarcinoma), LUSC (lung squamous cell carcinoma), MESO (mesothelioma), PAAD (pancreatic adenocarcinoma), PANCAN (Pan-cancer), PRAD (prostate adenocarcinoma), SKCM (skin cutaneous melanoma), THCA (thyroid carcinoma), UCEC (uterine corpus endometrial carcinoma).

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/1eb58d81f8dc/12276_2019_230_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/fc3f50c9ceb6/12276_2019_230_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/00934764f386/12276_2019_230_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/1eb58d81f8dc/12276_2019_230_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/fc3f50c9ceb6/12276_2019_230_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/00934764f386/12276_2019_230_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cb/6586683/1eb58d81f8dc/12276_2019_230_Fig3_HTML.jpg
摘要

近期对癌症基因组突变的研究已将驱动突变与乘客突变区分开来,乘客突变是癌症发展的副产物。癌症基因组图谱(TCGA)项目鉴定出了299个驱动肿瘤进展的基因以及24条通路/生物过程(《细胞》173: 371 - 385 e318, 2018)。在这299个驱动基因中,有12个基因参与组蛋白、组蛋白甲基化和去甲基化过程(表1)。在这12个基因中,编码组蛋白去甲基酶JARID1C/KDM5C和UTX/KDM6A的基因被鉴定为癌症驱动基因。此外,编码代谢酶的基因,如异柠檬酸脱氢酶(IDH)1/2的功能获得性突变,通过产生一种致癌代谢物D - 2 - 羟基戊二酸(D - 2HG)来驱动肿瘤进展,D - 2 - 羟基戊二酸是α - 酮戊二酸的竞争性抑制剂,可抑制诸如含Jumonji结构域的组蛋白去甲基酶和DNA去甲基酶等α - 酮戊二酸依赖性双加氧酶。对致癌代谢物的研究表明,组蛋白去甲基酶介导染色质结构的代谢变化。我们回顾了关于癌症特异性代谢重编程以及JARID1C/KDM5C和UTX/KDM6A的肿瘤抑制作用的最新研究结果。我们还讨论了其他亚型的突变,如KDM5亚家族的JARID1A、1B、1D以及KDM6亚家族的JMJD3/KDM6B,它们在肿瘤进展中根据癌细胞类型作为癌基因或肿瘤抑制基因发挥相反作用。表1 参与表观遗传学的癌症驱动基因 参与表观遗传学的通路 驱动基因 肿瘤抑制基因/癌基因预测(通过20/20 +) 批准名称 活性 癌症类型 该通路中的其他驱动基因 组蛋白修饰 KDM6A 肿瘤抑制基因 赖氨酸去甲基酶6A,UTX H3K27me2/3去甲基酶 膀胱癌、头颈部鳞状细胞癌、肾乳头状细胞癌、肺鳞状细胞癌、胰腺癌、泛癌、前列腺癌 PPP6C SETD2 肿瘤抑制基因 SET结构域包含蛋白2 H3K36甲基转移酶 肾透明细胞癌、肾乳头状细胞癌、脑低级别胶质瘤、肺腺癌、间皮瘤、泛癌 染色质组蛋白修饰剂 KDM5C 肿瘤抑制基因 赖氨酸去甲基酶5C,JARID1C H3K4me2/3去甲基酶 肾透明细胞癌、泛癌 ARID5B、CREBBP、EP300、KANSL1、MEN1(多发性内分泌肿瘤1型)、NCOR1(核受体辅阻遏蛋白1)、NSD1(核受体结合SET结构域蛋白1)、SIN3A、WHSC1(Wolf - Hirschhorn综合征候选基因1)、ZMYM3 KMT2A 肿瘤抑制基因 赖氨酸甲基转移酶2A H3K4甲基转移酶 泛癌 KMT2B 肿瘤抑制基因 赖氨酸甲基转移酶2B H3K4甲基转移酶 泛癌、子宫内膜癌 KMT2C 肿瘤抑制基因 赖氨酸甲基转移酶2C H3K4甲基转移酶 膀胱癌、乳腺癌、子宫颈癌、泛癌、子宫内膜癌 KMT2D 肿瘤抑制基因 赖氨酸甲基转移酶2D H3K4甲基转移酶 膀胱癌、子宫颈癌、弥漫性大B细胞淋巴瘤、食管癌、头颈部鳞状细胞癌、肺鳞状细胞癌、泛癌、前列腺癌 染色质(其他) H3F3A 可能的癌基因 H3组蛋白家族成员3A,H3.3A 泛癌 AJUBA、ASXL1、ASXL2、ATF7IP、BCOR、CHD3、CHD4、CHD8、CTCF、NIPBL、NPM1 H3F3C - H3组蛋白家族成员3C,H3.5 泛癌 HIST1H1E 可能的癌基因 HIST1H1E,H1.4 弥漫性大B细胞淋巴瘤 可能的肿瘤抑制基因 HIST1H1E,H1.4 肝细胞癌 代谢 IDH1 癌基因 异柠檬酸脱氢酶(NADP(+))1 NADP依赖性异柠檬酸脱氢酶,胞质 胆管癌(肝内胆管癌)、多形性胶质母细胞瘤、急性髓系白血病、脑低级别胶质瘤、肝细胞癌、泛癌、前列腺癌、皮肤黑色素瘤 - IDH2 癌基因 异柠檬酸脱氢酶(NADP(+))2 NADP依赖性异柠檬酸脱氢酶,线粒体 急性髓系白血病、脑低级别胶质瘤、泛癌 在贝利等人提到的299个驱动基因中,只有与表观遗传学相关的通路已通过20/20 +进行分类:使用随机森林将基因分类为癌基因、肿瘤抑制基因或非驱动基因,http://2020plus.readthedocs.org 膀胱癌(膀胱尿路上皮癌)、乳腺癌(乳腺浸润性癌)、子宫颈癌(宫颈鳞状细胞癌和宫颈内膜腺癌)、胆管癌(肝内胆管癌)、弥漫性大B细胞淋巴瘤、食管癌、多形性胶质母细胞瘤、头颈部鳞状细胞癌、肾透明细胞癌、肾乳头状细胞癌、急性髓系白血病、脑低级别胶质瘤、肝细胞癌、肺腺癌、肺鳞状细胞癌、间皮瘤、胰腺癌、泛癌、前列腺癌、皮肤黑色素瘤、甲状腺癌、子宫内膜癌

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Front Mol Neurosci. 2018 Apr 4;11:104. doi: 10.3389/fnmol.2018.00104. eCollection 2018.
6
In vivo CRISPR screening unveils histone demethylase UTX as an important epigenetic regulator in lung tumorigenesis.体内 CRISPR 筛选揭示组蛋白去甲基酶 UTX 是肺癌发生中的一个重要表观遗传调控因子。
Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):E3978-E3986. doi: 10.1073/pnas.1716589115. Epub 2018 Apr 9.
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Comprehensive Characterization of Cancer Driver Genes and Mutations.全面描绘癌症驱动基因和突变。
Cell. 2018 Apr 5;173(2):371-385.e18. doi: 10.1016/j.cell.2018.02.060.
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Loss of KDM6A Activates Super-Enhancers to Induce Gender-Specific Squamous-like Pancreatic Cancer and Confers Sensitivity to BET Inhibitors.KDM6A 缺失激活超级增强子诱导性别特异性胰腺鳞癌,并赋予 BET 抑制剂敏感性。
Cancer Cell. 2018 Mar 12;33(3):512-526.e8. doi: 10.1016/j.ccell.2018.02.003.
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Utx loss causes myeloid transformation.Utx 缺失导致髓系转化。
Leukemia. 2018 Jun;32(6):1458-1465. doi: 10.1038/s41375-018-0011-6. Epub 2018 Feb 2.
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Transcription factor-dependent 'anti-repressive' mammalian enhancers exclude H3K27me3 from extended genomic domains.转录因子依赖性的“抗抑制”哺乳动物增强子可将H3K27me3排除在扩展的基因组区域之外。
Genes Dev. 2017 Dec 1;31(23-24):2391-2404. doi: 10.1101/gad.308536.117. Epub 2018 Jan 10.