科學(xué)研究:
研究方向:
主要從事表觀遺傳學(xué)調(diào)控基因表達(dá),腫瘤分子生物學(xué)(主要為p53方向)以及細(xì)胞自噬的研究。
承擔(dān)科研項(xiàng)目情況:
科技部973項(xiàng)目子課題“上皮間質(zhì)轉(zhuǎn)換的機(jī)理及腫瘤侵襲轉(zhuǎn)移的細(xì)胞重編程機(jī)制 ”。 科技部973項(xiàng)目子課題“DNA甲基化異常與腫瘤發(fā)生發(fā)展”。科技部973項(xiàng)目子課題“p53功能與修飾的研究”。國(guó)家自然科學(xué)基金委“國(guó)家杰出青年基金”項(xiàng)目:“組蛋白重塑誘導(dǎo)核苷衍生物導(dǎo)致的細(xì)胞凋亡的研究” 。國(guó)家自然科學(xué)基金委重點(diǎn)項(xiàng)目;“NuRD復(fù)合物協(xié)同作用PRC2復(fù)合物調(diào)控腫瘤發(fā)生的研究” 。
1、國(guó)家自然科學(xué)基金重大項(xiàng)目(2021-2025),DNA復(fù)制相關(guān)DNA代謝調(diào)控基因組穩(wěn)態(tài)的機(jī)制研究(32090030)。
2、國(guó)家自然科學(xué)基金重大項(xiàng)目課題(2021-2025),DNA同源重組及DNA雙鏈斷裂修復(fù)的分子機(jī)制研究(32090033) 。
3、深圳市科技計(jì)劃基礎(chǔ)研究重點(diǎn)項(xiàng)目(2020-2023),靶向NAD+合成通路調(diào)控 DNA損傷修復(fù)的抗腫瘤機(jī)制研究(JCYJ20200109114214463)。
4、深圳灣實(shí)驗(yàn)室開(kāi)放基金項(xiàng)目(2019-2022),細(xì)胞脅迫應(yīng)激與機(jī)體穩(wěn)態(tài)及疾。⊿ZBL2019062801011)。
5、國(guó)家重點(diǎn)研發(fā)計(jì)劃:“蛋白質(zhì)機(jī)器與生命過(guò)程調(diào)控”重點(diǎn)專(zhuān)項(xiàng)首席科學(xué)家,2017.07-2022.06。
6、國(guó)家重點(diǎn)研發(fā)計(jì)劃項(xiàng)目:參與DNA損傷應(yīng)答的新型蛋白質(zhì)機(jī)器維持基因組穩(wěn)定性的機(jī)制研究,項(xiàng)目編號(hào):2017YFA0503900,2017-2022。
7、國(guó)際(地區(qū))合作與交流項(xiàng)目:組蛋白去乙;窼irtuin與p53相互調(diào)控的分子網(wǎng)絡(luò)及機(jī)制研究,項(xiàng)目編號(hào):81720108027,2018.01-2021.12。
8、 基礎(chǔ)學(xué)科布局項(xiàng)目:基20170306 放療耐受性腫瘤的再致敏研究。
9、廣東省科技廳重點(diǎn)實(shí)驗(yàn)室:廣東省基因組穩(wěn)定性與疾病防治重點(diǎn)實(shí)驗(yàn)室。
10、國(guó)家基金委重點(diǎn)項(xiàng)目:組蛋白甲基轉(zhuǎn)移酶G9a參與腫瘤細(xì)胞脂代謝的機(jī)制研究 (No:81530074) ,負(fù)責(zé)人,2016-2-2020。
11、國(guó)家基金委創(chuàng)新團(tuán)隊(duì):蛋白質(zhì)翻譯后修飾與腫瘤發(fā)生發(fā)展及轉(zhuǎn)移的分子機(jī)制研究 (No:81321003),負(fù)責(zé)人,2014-2019。
12、國(guó)家基金委重大計(jì)劃重點(diǎn)項(xiàng)目:組蛋白去乙;窼IRT6招募NuRD復(fù)合物參與DNA損傷應(yīng)激的分子機(jī)制研究(No:91319302),負(fù)責(zé)人,2014-2016。
13、國(guó)家基金委重大計(jì)劃重點(diǎn)項(xiàng)目:pRB介導(dǎo)NuRD 復(fù)合物與H3K4去甲基化相互作用的機(jī)制研究 (No: 90919030),負(fù)責(zé)人,2009-2012。
14、國(guó)家“973”計(jì)劃研究項(xiàng)目子課題:DNA 甲基化變化在惡性腫瘤發(fā)生發(fā)展及侵襲轉(zhuǎn)移中的作用,負(fù)責(zé)人,2005-2010。
15、國(guó)家“973”計(jì)劃研究項(xiàng)目子課題:DNA甲基化異常與腫瘤發(fā)生發(fā)展。
16、國(guó)家“973”計(jì)劃研究項(xiàng)目子課題:蛋白質(zhì)生成、折疊、組裝和降解的規(guī)律及其質(zhì)量控制。
17、國(guó)家“863”計(jì)劃研究項(xiàng)目:(B類(lèi)):腫瘤特異標(biāo)志物Pirh2磷酸化的鑒定及靶蛋白的設(shè)計(jì)與應(yīng)用,863計(jì)劃首席,2006。
18、國(guó)家自然基金委“杰出青年基金”腫瘤治療學(xué)基礎(chǔ) (No:30425017),2004。
19、國(guó)家杰出青年基金:染色質(zhì)重塑干擾核苷衍生物誘導(dǎo)的DNA損傷修復(fù)的機(jī)制研究,2004年。
主要學(xué)術(shù)成就:
主要從事腫瘤學(xué),生化與分子生物學(xué)的基礎(chǔ)研究。在腫瘤發(fā)生的機(jī)制研究和腫瘤的分子治療領(lǐng)域作出了較為突出的貢獻(xiàn)。在DNA甲基化導(dǎo)致腫瘤發(fā)生的基礎(chǔ)研究中,提出了“臨近位點(diǎn)阻礙說(shuō)”對(duì)表觀遺傳導(dǎo)致基因失活的機(jī)理研究提出了新的理論,并發(fā)表在國(guó)際著名生物學(xué)雜志Mol Cell Biol上。在腫瘤的分子治療的機(jī)制研究中,建立了“核苷衍生物并用組蛋白乙;T導(dǎo)腫瘤細(xì)胞凋亡”的模型,受到國(guó)際該領(lǐng)域的重視和好評(píng),并大量被引用。作者以該模型為研究中心, 相繼以第一作者或通訊作者身份發(fā)表了多篇高質(zhì)量的科學(xué)論文,分別發(fā)表在Cancer Research, Journal of Biological Chemistry, Oncogene, Human Molecular Genetics上。并且發(fā)現(xiàn)BMP3B基因?yàn)榉伟┘?xì)胞中與甲基化相關(guān)聯(lián)的新的抑癌基因,并發(fā)表在Neoplasia 和 Oncogene等雜志上。在國(guó)際主流學(xué)術(shù)刊物如Nature, Nature Cell Biology, PNAS等發(fā)表了多篇論文,在腫瘤與生物醫(yī)學(xué)主要學(xué)術(shù)期刊上發(fā)表了70多篇SCI論文。2010年在Nature Cell Biology上首次論證了轉(zhuǎn)錄因子FOXO1在細(xì)胞漿內(nèi)的特異功能:誘導(dǎo)細(xì)胞自噬發(fā)生。2006,2008,2010年及2011年在Molecular &Cellular Biology, Journal of Biological Chemistry,Nature 和PNAS上闡述了腫瘤抑制因子p53的乙酰化修飾與其功能的關(guān)系;2008年在Molecular &Cellular Biology上論證了組蛋白修飾可能參與指導(dǎo)DNA甲基化及基因表達(dá)的過(guò)程。
1. 發(fā)現(xiàn)在氧化應(yīng)激或饑餓時(shí),轉(zhuǎn)錄因子FoxO1啟動(dòng)腫瘤細(xì)胞自噬過(guò)程
該過(guò)程與III類(lèi)組蛋白去乙酰化酶SIRT2密切相關(guān)。腫瘤細(xì)胞在未處理的情況下,SIRT2與FoxO1相互作用使得FoxO1保持在去乙;癄顟B(tài)。但在各種應(yīng)激情況下,SIRT2與FoxO1脫開(kāi),使得FoxO1乙酰化,并結(jié)合到自噬的重要蛋白Atg7,從而啟動(dòng)細(xì)胞自噬。該項(xiàng)研究將參與表觀遺傳的重要修飾酶的功能在應(yīng)激情況下與腫瘤細(xì)胞自噬有機(jī)的聯(lián)系起來(lái),于2010年發(fā)表在《Nat Cell Biol》上。
2. 代謝相關(guān)的p53功能方面的研究
發(fā)現(xiàn)p53能夠下調(diào)在糖異生過(guò)程中兩種重要限速酶:磷酸烯醇型丙酮酸羧激酶(PCK1)和葡萄糖6-磷酸酶(G6PC) 的表達(dá)。細(xì)胞水平我們證實(shí)了p53能夠引起叉頭框轉(zhuǎn)錄因子(FOXO1)的核輸出,而FOXO1正是PCK1和G6PC的轉(zhuǎn)錄激活因子。因而p53能夠抑制FOXO1依賴(lài)性的糖異生。進(jìn)一步的研究表明, p53可以直接激活NAD(+)依賴(lài)的組蛋白去乙酰化酶Sirtuin 6(SIRT6)的表達(dá)。SIRT6與FoxO1的相互作用會(huì)引起FoxO1的去乙酰進(jìn)而引起FOXO1轉(zhuǎn)位到胞漿。C57Bl/J6小鼠以及肝臟條件性敲除SIRT6的小鼠也證實(shí)了p53介導(dǎo)的FOXO1出核,下調(diào)PCK1和G6PC進(jìn)而調(diào)節(jié)血糖的實(shí)驗(yàn)結(jié)果。該工作2014年發(fā)表在《PNAS》上。
3. DNA損傷應(yīng)答的研究
腫瘤細(xì)胞在化療藥物阿霉素處理后,組蛋白甲基化酶SET7/9與另一個(gè)組蛋白甲基化酶SUV39H1相互作用, 并導(dǎo)致SUV39H1甲基化。甲基化的SUV39H1活性明顯下降,從而使異染色質(zhì)結(jié)構(gòu)變得松散,DNA易于碎裂。該項(xiàng)研究成果部分解釋了抗癌化療的機(jī)制并有機(jī)地與表觀遺傳的分子機(jī)制有效聯(lián)系起來(lái)。該工作2013年發(fā)表在《PNAS》上。
4. 發(fā)現(xiàn)SET7/9調(diào)節(jié)組蛋白去乙酰化酶SIRT1對(duì)p53乙;,影響p53功能
DNA損傷后,SET7/9和SIRT1相互作用顯著增強(qiáng),SET7/9對(duì)p53進(jìn)行甲基化修飾同時(shí)抑制了SIRT1對(duì)p53的作用,提高了p53乙;健ET7/9不僅可以直接對(duì)p53進(jìn)行甲基化修飾,還作為一個(gè)關(guān)鍵調(diào)節(jié)分子,通過(guò)調(diào)節(jié)SIRT1-p53相互作用,從而間接調(diào)節(jié)p53功能。該工作2011年發(fā)表在《PNAS》上。
科研成果:
1. 組蛋白去乙;敢种苿┮种颇[瘤細(xì)胞增殖的機(jī)制研究 朱衛(wèi)國(guó); 趙穎; 王海英; 楊洋; 于宇; 廖文娟; 馮京南; 王麗娜 【科技成果】北京大學(xué)基礎(chǔ)醫(yī)學(xué)院 2009-06-01
2. 組蛋白去乙;傅淖饔脵C(jī)制 朱衛(wèi)國(guó) 第五屆“藥明康德生命化學(xué)研究獎(jiǎng)”。
發(fā)明專(zhuān)利:
[1]程永現(xiàn), 朱衛(wèi)國(guó), 晏永明, 康天舒, 谷金科, 陸小鵬. 一種小分子化合物及其制備方法與應(yīng)用[P]. 廣東省: CN117623929A, 2024-03-01.
[2]朱衛(wèi)國(guó), 程永現(xiàn), 康天舒, 晏永明, 陸小鵬, 黃金波. 一種小分子化合物YZL-51N在制備SIRT7選擇性抑制劑中的應(yīng)用[P]. 廣東省: CN117357507A, 2024-01-09.
[3]朱衛(wèi)國(guó). 一種高通量大規(guī)模篩選組蛋白修飾結(jié)合蛋白質(zhì)的方法[P]. 廣東省: CN113588856B, 2023-07-21.
[4]康天舒, 朱衛(wèi)國(guó), 賀靜. 一種檢測(cè)SIRT7酶活性的熒光多肽底物[P]. 廣東省: CN113880922B, 2023-06-13.
[5]朱衛(wèi)國(guó), 黃金波, 張俊, 許文超. 組蛋白去乙;8選擇性降解劑、制備方法及其在抗腫瘤活性中的應(yīng)用[P]. 廣東省: CN114409638B, 2023-02-14.
[6]文赫, 朱衛(wèi)國(guó), 劉向宇. 一種評(píng)價(jià)組蛋白賴(lài)氨酸去甲基轉(zhuǎn)移酶活性的方法[P]. 廣東省: CN109825551B, 2022-08-02.
[7]文赫, 朱衛(wèi)國(guó), 李曉帆, 田媛, 王慧. 基于核磁共振氫譜的LSD1的活性檢測(cè)方法及其應(yīng)用[P]. 廣東省: CN112098448B, 2022-05-20.
[8]朱衛(wèi)國(guó), 黃金波, 張俊, 許文超. 組蛋白去乙;8選擇性降解劑、制備方法及其在抗腫瘤活性中的應(yīng)用[P]. 廣東省: CN114409638A, 2022-04-29.
[9]文赫, 朱衛(wèi)國(guó), 舒明慧, 陳嘉儀, 李曉帆. 基于一維HNCO核磁共振光譜檢測(cè)SIRTs去乙酰化酶活性的方法及應(yīng)用[P]. 廣東省: CN114414608A, 2022-04-29.
[10]朱衛(wèi)國(guó), 黃金波, 吳丹丹, 白曉康. 一種3-多氟烷基化取代咪唑[1,2-a]并吡啶的簡(jiǎn)易合成方法[P]. 廣東省: CN112851670B, 2022-01-04.
[11]康天舒, 朱衛(wèi)國(guó), 賀靜. 一種檢測(cè)SIRT7酶活性的熒光多肽底物[P]. 廣東省: CN113880922A, 2022-01-04.
[12]朱衛(wèi)國(guó). 一種高通量大規(guī)模篩選組蛋白修飾結(jié)合蛋白質(zhì)的方法[P]. 廣東省: CN113588856A, 2021-11-02.
[13]朱衛(wèi)國(guó), 黃金波, 吳丹丹, 白曉康. 一種3-多氟烷基化取代咪唑[1,2-a]并吡啶的簡(jiǎn)易合成方法[P]. 廣東省: CN112851670A, 2021-05-28.
[14]文赫, 朱衛(wèi)國(guó), 李曉帆, 田媛, 王慧. 基于核磁共振氫譜的LSD1的活性檢測(cè)方法及其應(yīng)用[P]. 廣東省: CN112098448A, 2020-12-18.
[16]文赫, 朱衛(wèi)國(guó), 劉向宇. 一種評(píng)價(jià)組蛋白賴(lài)氨酸去甲基轉(zhuǎn)移酶活性的方法[P]. 廣東省: CN109825551A, 2019-05-31.
論文專(zhuān)著:
在國(guó)內(nèi)外重要雜志上發(fā)表50余篇文章。
出版專(zhuān)著:
1. DNA REPLICATION- Damage and Replication stress responses. 沈萍 王海英 朱衛(wèi)國(guó)
2.論著名稱(chēng):“分子細(xì)胞生物學(xué)”第3版,第二章“表觀遺傳調(diào)控部分”,朱衛(wèi)國(guó)、文赫、朱騫,高等教育出版社,2019年8月。
3. 論著名稱(chēng):“承續(xù)的魅力:令人著迷的表觀遺傳學(xué)”第1版,第一章“組蛋白修飾”部分,朱衛(wèi)國(guó)、文赫、朱騫,科學(xué)出版社,2018年11月。
發(fā)表英文論文: 帶*號(hào)的為責(zé)任作者
1. Zhu Q, Yang Q, Lu X, Wang H, Tong L, Li Z, Liu G, Bao Y, Xu X, Gu L, Yuan J, Zhu WG*. SETD2-mediated H3K14 trimethylation promotes ATR activation and stalled replication fork restart in response to DNA replication stress. Proc Natl Acad Sci USA. 2021, 118(23):e2011278118. doi: 10.1073/pnas.2011278118.
2. Hou T, Cao Z, Zhang J, Tang M, Tian Y, Li Y, Lu X, Chen Y, Wang H, Wei FZ, Wang L, Yang Y, Zhao Y, Wang Z, Wang H, Zhu WG*. SIRT6 coordinates with CHD4 to promote chromatin relaxation and DNA repair.Nucleic Acids Res. 2020, 48(6):2982-3000.
3. Tang M, Li Z, Zhang C, Lu X, Tu B, Cao Z, Li Y, Chen Y, JInag L, Wang H, Wang L, Wang J, Liu B, Xu X, Wang H, Zhu WG*. SIRT7-mediated ATM deacetylation is essential for its deactivation and DNA damage repair. Science Advances., 2019, 5: eaav 1118.
4. Li Z, Li Y, Tang M, Peng B, Lu X, Yang Q, Zhu Q, Hou T, Li M, Liu C, Wang L, Xu X, Zhao Y, Wang H, Yang Y, Zhu WG*. Destabilization of linker histone H1.2 is essential for ATM activation and DNA damage repair.Cell Res. 2018, 28(7):756-770.
5.Yang Q, Zhu Q, Lu X, Du Y, Cao L, Shen C, Hou T, Li M, Li Z, Liu C, Wu D, Xu X, Wang L, Wang H, Zhao Y, Yang Y, Zhu WG*. (2017) G9a coordinates with the RPA complex to promote DNA damage repair and cell survival. Proc Natl Acad Sci USA. 2017,114(30):E6054-E6063.
6. Cao LL, Wei F, Du Y, Song B, Wang D, Shen C, Lu X, Cao Z, Yang Q, Gao Y, Wang L, Zhao Y, Wang H, Yang Y, Zhu WG* (2016). ATM-mediated KDM2A phosphorylation is required for the DNA damage repair. Oncogene 35(3): 402.
7. Wang Y, Zhang N, Zhang L, Li R, Fu W, Ma K, Li X, Wang L, Wang J, Zhang H, Gu W, Zhu WG*, Zhao Y*. Autophagy Regulates Chromatin Ubiquitination in DNA Damage Response through Elimination of SQSTM1/p62. Mol Cell. 2016, 63(1):34-48.
8. Wei FZ, Cao Z, Wang X, Wang H, Cai MY, Li T, Hattori N, Wang D, Du Y, Song B, Cao LL, Shen C, Wang L, Wang H, Yang Y, Xie D, Wang F, Ushijima T, Zhao Y*, Zhu WG*. Epigenetic regulation of autophagy by the methyltransferase EZH2 through an MTOR-dependent pathway. Autophagy. 2015 Nov;11(12):2309-22. doi: 10.1080/15548627.2015.1117734.
9. Cao LL, Wei F, Du Y, Song B, Wang D, Shen C, Lu X, Cao Z, Yang Q, Gao Y, Wang L, Zhao Y, Wang H, Yang Y, Zhu WG*. ATM-mediated KDM2A phosphorylation is requiredfor the DNA damage repair. Oncogene. 2015 Mar 30. doi: 10.1038/onc.2015.81. [Epubahead of print]
10.Wu D, Liu J, Wu B, Tu B, Zhu WG, Luo J. The Batten disease gene CLN3 confers resistance to endoplasmic reticulum stress induced by tunicamycin. Biochemical and Biophysical Research Communications [Internet]. 2014;(1):115-120.
11. Wang Y, Qiu B, Liu J, Zhu WG, Zhu S. Cocaine- and amphetamine-regulated transcript facilitates the neurite outgrowth in cortical neurons after oxygen and glucose deprivation through PTN-dependent pathway. Neuroscience. 2014 Sep 26;277:103-10.
12. Yi J, Huang X, Yang Y, Zhu WG, Gu W, Luo J. Regulation of histone acetyltransferase TIP60 function by histone deacetylase 3.J Biol Chem. 2014 Oct 9. pii: jbc.M114.575266.
13. Li T, Song B, Wu Z, Lu M, Zhu WG*. Systematic identification of Class I HDAC substrates. Brief Bioinform. 2014 Nov;15(6):963-972.
14.Yao Y, Yang Y, Zhu WG*.Sirtuins: Nodes connecting aging, metabolism and tumorigenesis. Current Pharmaceutical Design. 2014,20(11):1614-1624.
15.Li Z, Zhu WG*. Targeting histone deacetylases for cancer therapy: From molecular mechanisms to clinical implications. International Journal of Biological Sciences. 2014;(7):757-770.
16.Zhang P, Tu B, Wang H, Cao Z, Tang M, Zhang C, Gu B, Li Z, Wang L, Yang Y, Zhao Y, Wang H, Luo J, Deng CX, Gao B, Roeder RG, Zhu WG*. Tumor suppressor p53 cooperates with SIRT6 to regulate gluconeogenesis by promoting FoxO1 nuclear exclusion. Proceedings of the National Academy of Sciences of the United States of America [Internet]. 2014;111(29):10684-10689.
17.Li L, Zhang Z-G, Lei H, Wang C, Wu L-P, Wang J-Y, Fu F-Y, Zhu W-G, Wu L-L. Angiotensin II Reduces Cardiac AdipoR1 Expression through AT1 Receptor/ROS/ERK1/2/c-Myc Pathway. PLoS ONE [Internet]. 2013;(1).
18.Zhao Y*, Li X, Ma K, Yang J, Zhou J, Fu W, Wei F, Wang L, Zhu WG*. The axis of MAPK1/3-XBP1u-FOXO1 controls autophagic dynamics in cancer cells. Autophagy [Internet]. 2013;(5):794-796.
19.Wang D, Zhou J, Liu X, Lu D, Shen C, Du Y, Wei FZ, Song B, Lu X, Yu Y, Wang L, Zhao Y, Wang H, Yang Y, Akiyama Y, Zhang H, Zhu WG*. Methylation of SUV39H1 by SET7/9 results in heterochromatin relaxation and genome instability. Proceedings of the National Academy of Sciences of the United States of America [Internet]. 2013;(14):5516-5521.
20.Dai X-Y, Zhao M-M, Cai Y, Guan Q-C, Zhao Y, Guan Y, Kong W, Zhu W-G, Xu M-J, Wang X. Phosphate-induced autophagy counteracts vascular calcification by reducing matrix vesicle release. Kidney International [Internet]. 2013;(6):1042-1051.
21.Yang J, Carra S, Zhu W-G, Kampinga HH. The regulation of the autophagic network and its implications for human disease. International Journal of Biological Sciences [Internet]. 2013;(10):1121-1133.
22.Zhao Y, Li X, Cai MY, Ma K, Yang J, Zhou J, Fu W, Wei FZ, Wang L, Xie D, Zhu WG*. . XBP-1u suppresses autophagy by promoting the degradation of FoxO1 in cancer cells. Cell Res. 2013, 23(4): 491-507.
23.Li T, Du Y, Wang L, Huang L, Li W, Lu M, Zhang X, Zhu W-G. Characterization and prediction of lysine (K)-acetyl-transferase specific acetylation sites. Molecular and Cellular Proteomics. 2012;(1).
24.Klionsky DJ, Abdalla FC, Abeliovich H, Abraham RT, Acevedo-Arozena A, Adeli K, Agholme L, Agnello M, Agostinis P, Aguirre-Ghiso JA, Zhu W-G,et al. Guidelines for the use and interpretation of assays for monitoring autophagy. Autophagy. 2012;8(4):445-544.
25.Zhou J, Liao W, Yang J, Ma K, Li X, Wang Y, Wang D, Wang L, Zhang Y, Yin Y, Zhao Y, Zhu WG*. FOXO3 induces FOXO1-dependent autophagy by activating the AKT1 signaling pathway. Autophagy [Internet]. 2012;(12):1712-1723.
26.Yu Y, Wu J, Wang Y, Zhao T, Ma B, Liu Y, Fang W, Zhu W-G, Zhang H. Kindlin 2 forms a transcriptional complex with β-catenin and TCF4 to enhance Wnt signalling. EMBO Reports [Internet]. 2012;(8):750-758.
27.Zhu WG*. Methylation of FoxO3 regulates neuronal cell death. Acta Pharmacologica Sinica [Internet]. 2012;33(5):577-.
28.Gu B, Zhu WG*.Surf the Post-translational Modification Network of p53 Regulation. International Journal of Biological Sciences [Internet]. 2012;(5):672-684.
29.Zheng Z, Li L, Liu X, Wang D, Tu B, Wang L, Wang H, Zhu W-G*. 5-Aza-2′-deoxycytidine reactivates gene expression via degradation of pRb pocket proteins. FASEB Journal [Internet]. 2012;26(1):449-459.
30.Tingting Li, Yipeng Du, Likun Wang, Lei Huang, Wenlin Li, Ming Lu, Xuegong Zhang, Wei-Guo Zhu*. Characterization and prediction of lysine (K)-acetyl-transferase specific acetylation sites. Mol Cell Proteomics. 11(1):M111.011080.
31.Tong Z-T, Cai M-Y, Wang X-G, Kong L-L, Mai S-J, Liu Y-H, Zhang H-B, Liao Y-J, Zheng F, Zhu W, et al. EZH2 supports nasopharyngeal carcinoma cell aggressiveness by forming a co-repressor complex with HDAC1/HDAC2 and Snail to inhibit E-cadherin. Oncogene [Internet]. 2012;(5):583-594.
32.Haiying Wang, Wen Zhou, Zhixing Zheng, Ping Zhang, Bo Tu, Qihua He and Wei-Guo Zhu*. The HDAC inhibitor depsipeptide transactivates the p53/p21 pathway by inducing DNA damage. DNA Repair [Internet]. 2012;11(2):146-156.
33.Song B-Y, Zhu W-G. [Advances in effector protein of histone methylation]. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji [Internet]. 2011;(4):285-292.
34.Zhao Y, Wang Y, Zhu W-G*. Applications of post-translational modifications of FoxO family proteins in biological functions. Journal of Molecular Cell Biology [Internet]. 2011;(5):276-282.
35.Wang C, Wang Y, McNutt MA, Zhu W-G. Autophagy process is associated with anti-neoplastic function. Acta Biochimica et Biophysica Sinica [Internet]. 2011;(6):425-432.
36.Yang J, Zhao Y, Ma K, Jiang FJ, Liao W, Zhang P, Zhou J, Tu B, Wang L, Kampinga HH, Xie Z, Zhu WG*. Deficiency of hepatocystin induces autophagy through an mTOR-dependent pathway. Autophagy [Internet]. 2011;(7):748-759.
37.Liu X, Wang D, Zhao Y, Tu B, Zheng Z, Wang L, Wang H, Gu W, Roeder RG, Zhu W-G*. Methyltransferase Set7/9 regulates p53 activity by interacting with Sirtuin 1 (SIRT1). Proceedings of the National Academy of Sciences of the United States of America [Internet]. . 2011, 108(5):1925-1930.
38.Yang W-J, Wang D-L, Zhu W-G. [Mechanism of regulating deacetylase SIRT1 expression and activity.]. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji [Internet]. 2010;(10):1003-1008.
39.Zhao Y, Wang L, Yang J, Zhang P, Ma K, Zhou J, Liao W, Zhu W-G. Anti-neoplastic activity of the cytosolic FoxO1 results from autophagic cell death. Autophagy [Internet]. 2010;(7):988-990.
40.Zhao Y, Yang J, Liao W, Liu X, Zhang H, Wang S, Wang D, Feng J, Yu L, Zhu W-G. Cytosolic FoxO1 is essential for the induction of autophagy and tumour suppressor activity. Nature Cell Biology [Internet]. 2010;(7):665-675.
41.Dai D-P, Zhou X-Y, Xiao Y, Xu F, Sun F-C, Ji F-S, Zhang Z-X, Hu J-H, Guo J, Zheng J-D, Zhu W-G,et al. Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population. European Journal of Clinical Investigation [Internet]. 2010;(8):669-677.
42.Chen D, Shan J, Zhu W-G, Qin J, Gu W. Transcription-independent ARF regulation in oncogenic stress-mediated p53 responses. Nature [Internet]. 2010;(7288):624-627.
43.Yang Y, Zhao Y, Liao W, Yang J, Wu L, Zhung Z, Yu Y, Zhou W, Li L, Feng J, Zhu W,et al. Acetylation of Fox01 activates b i m expression to induce apoptosis in response to Histone deacetylase inhibitor depsipeptide treatment12 www.neoplasia.com. Neoplasia [Internet]. 2009;(4):313-324.
44.Zhou W, Zhu W-G. The changing face of HDAC inhibitor depsipeptide. Current Cancer Drug Targets [Internet]. 2009;(1):91-100.
45.Liao W, McNutt MA, Zhu W-G. The comet assay: A sensitive method for detecting DNA damage in individual cells. Methods [Internet]. 2009;(1):46-53.
46.SU Y, Wang X, Zhu W-G. DNA methyltransferases: the role in regulation of gene expression and biological processes. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji [Internet]. 2009;(11):1087-1093.
47.Yu Y, Cai J-P, Tu B, Wu L, Zhao Y, Liu X, Li L, McNutt MA, Feng J, He Q, Zhu W,et al. Proliferating cell nuclear antigen is protected from degradation by forming a complex with MutT homolog2. Journal of Biological Chemistry [Internet]. 2009;(29):19310-19320.
48.Wang X, Zhu W-G. Advances in histone methyltransferases and histone demethylases. Ai zheng = Aizheng = Chinese journal of cancer [Internet]. 2008;(10):1018-1025.
49.Wang H, Zhao Y, Li L, McNutt MA, Wu L, Lu S, Yu Y, Zhou W, Feng J, Chai G, Zhu W,et al. An ATM- and Rad3-related (ATR) signaling pathway and a phosphorylation- acetylation cascade are involved in activation of p53/p21Waf1/Cip1 in response to 5-Aza-2′-deoxycytidine treatment. Journal of Biological Chemistry [Internet]. 2008;(5):2564-2574.
50.Chai G, Li L, Zhou W, Wu L, Zhao Y, Wang D, Lu S, Yu Y, Wang H, McNutt MA, Zhu W ,et al. HDAC inhibitors act with 5-aza-2′-deoxycytidine to inhibit cell proliferation by suppressing removal of incorporated abases in lung cancer cells. PLoS ONE [Internet]. 2008, 3:e2445.
51.Wu L-P, Wang X, Li L, Zhao Y, Lu S, Yu Y, Zhou W, Liu X, Yang J, Zheng Z, et al. Histone deacetylase inhibitor depsipeptide activates silenced genes through decreasing both CpG and H3K9 methylation on the promoter. Molecular and Cellular Biology [Internet]. 2008;(10):3219-3235.
52.Duan S, Yao Z, Hou D, Wu Z, Zhu W-G, Wu M. Phosphorylation of Pirh2 by Calmodulin-dependent kinase II impairs its ability to ubiquitinate p53. EMBO Journal [Internet]. 2007;(13):3062-3074.
53.Yang Y, Ikezoe T, Zheng Z, Taguchi H, Koeffler PH, Zhu W-G. Saw Palmetto induces growth arrest and apoptosis of androgen-dependent prostate cancer LNCaP cells via inactivation of STAT 3 and androgen receptor signaling. International Journal of Oncology [Internet]. 2007;(3):593-600.
54.Zhao Y, Lu S, Wu L, Chai G, Wang H, Chen Y, Sun J, Yu Y, Zhou W, Zheng QH, et al. Acetylation of p53 at lysine 373/382 by the histone deacetylase inhibitor depsipeptide induces expression of p21Waf1/Cip1. Molecular and Cellular Biology [Internet]. 2006;(7):2782-2790.
55.Xie W, Jiang P, Miao L, Zhao Y, Zhimin Z, Qing L, Zhu W-G, Wu M. Novel link between E2F1 and Smac/DIABLO: Proapoptotic Smac/DIABLO is transcriptionally upregulated by E2F1. Nucleic Acids Research [Internet]. 2006;(7):2046-2055.
56.Zheng QH, Ma LW, Zhu WG, Zhang ZY, Tong T. p21Waf1/Cip1 plays a critical role in modulating senescence through changes of DNA methylation. Journal of Cellular Biochemistry [Internet]. 2006;(5):1230-1248.
57.Yang Y, Ikezoe T, Nishioka C, Taguchi T, Zhu W-G, Koeffler PH, Taguchi H. ZD6474 induces growth arrest and apoptosis of GIST-T1 cells, which is enhanced by concomitant use of sunitinib. Cancer Science [Internet]. 2006;(12):1404-1409.
58.Cai G-lin, Zhu W-guo. DNA damage and repair. Zhonghua zhong liu za zhi [Chinese journal of oncology]. [Internet]. 2005;(10):577-580.
59.Zhu W-G, Hileman T, Ke Y, Wang P, Lu S, Duan W, Dai Z, Tong T, Villalona-Calero MA, Plass C, et al. 5-Aza-2′-deoxycytidine Activates the p53/p21Waf1/Cip1 Pathway to Inhibit Cell Proliferation. Journal of Biological Chemistry [Internet]. 2004;(15):15161-15166.
60.Dai Z, Popkie AP, Zhu W-G, Timmers CD, Raval A, Tannehill-Gregg S, Morrison CD, Auer H, Kratzke RA, Niehans G, et al. Bone morphogenetic protein 3B silencing in non-small-cell lung cancer. Oncogene [Internet]. 2004;(20):3521-3529.
61.Duan W, Gao L, Druhan LJ, Zhu W-G, Morrison C, Otterson GA, Villalona-Calero MA. Expression of Pirh2, a newly identified ubiquitin protein ligase, in lung cancer. Journal of the National Cancer Institute [Internet]. 2004;(22):1718-1721.
62.Dai Z, Zhu W-G, Morrison CD, Brena RM, Smiraglia DJ, Raval A, Wu Y-Z, Rush LJ, Ross P, Molina JR, et al. A comprehensive search for DNA amplification in lung cancer identifies inhibitors of apoptosis cIAP1 and cIAP2 as candidate oncogenes. Human Molecular Genetics [Internet]. 2003;(7):791-801.
63.Zhu W-G, Otterson GA. The interaction of histone deacetylase inhibitors and DNA methyltransferase inhibitors in the treatment of human cancer cells. Current Medicinal Chemistry - Anti-Cancer Agents [Internet]. 2003;(3):187-199.
64.Zhu W-G, Srinivasan K, Dai Z, Duan W, Druhan LJ, Ding H, Yee L, Villalona-Calero MA, Plass C, Otterson GA. Methylation of adjacent CpG sites affects Sp1/Sp3 binding and activity in the p21Cip1 promoter. Molecular and Cellular Biology [Internet]. 2003;(12):4056-4065.
65.Ding H, Duan W, Zhu W-G, Ju R, Srinivasan K, Otterson GA, Villalona-Calero MA. p21 response to DNA damage induced by genistein and etoposide in human lung cancer cells. Biochemical and Biophysical Research Communications [Internet]. 2003;(4):950-956.
66.Duan W, Ding H, Subler MA, Zhu W-G, Zhang H, Stoner GD, Windle JJ, Otterson GA, Villalona-Calero MA. Lung-specific expression of human mutant p53-273H is associated with a high frequency of lung adenocarcinoma in transgenic mice. Oncogene [Internet]. 2002;(51):7831-7838.
67.Duan W, Ding H, Zhu W-G, Srinivasan K, Otterson GA, Villalona-Calero MA. RT-PCR heteroduplex analysis permits differentiation of transgene and host gene expression in a transgenic animal model. BioTechniques [Internet]. 2002;(1):58-66.
68.Zhu W-G, Dai Z, Ding H, Srinivasan K, Hall J, Duan W, Villalona-Calero MA, Plass C, Otterson GA. Increased expression of unmethylated CDKN2D by 5-aza-2′-deoxycytidine in human lung cancer cells. Oncogene [Internet]. 2001;(53):7787-7796.
69.Zhu W-G, Lakshmanan RR, Beal MD, Otterson GA. DNA methyltransferase inhibition enhances apoptosis induced by histone deacetylase inhibitors. Cancer Research [Internet]. 2001;(4):1327-1333.
70.Dai Z, Lakshmanan RR, Zhu W-G, Smiraglia DJ, Rush LJ, Frühwald MC, Brena RM, Li B, Wright FA, Ross P, et al. Global methylation profiling of lung cancer identifies novel methylated genes. Neoplasia [Internet]. 2001;(4):314-323.
71.Zhu W-G, Seno JD, Beck BD, Dynlacht JR. Translocation of MRE11 from the nucleus to the cytoplasm as a mechanism of radiosensitization by heat. Radiation Research [Internet]. 2001;(1):95-102.
72.Zhu W-G, Roberts ZV, Dynlacht JR. Heat-induced modulation of lamin B content in two different cell lines. Journal of Cellular Biochemistry [Internet]. 1999;(4):620-628.
73.Dynlacht JR, Story MD, Zhu W-G, Danner J. Lamin B is a prompt heat shock protein. Journal of Cellular Physiology [Internet]. 1999;(1):28-34.
74.Chen WR, Zhu W-G, Dynlacht JR, Liu H, Nordquist RE. Long-term tumor resistance induced by laser photo-immunotherapy. International Journal of Cancer [Internet]. 1999;(5):808-812.
75.Zhu W-G, Antoku S, Sasaki H, Dynlacht JR. Post-irradiation exposure to HBSS enhances apoptosis in FM3A cells. Anticancer Research [Internet]. 1998;(6 A):4043-4049.
76.Sasaki H, Yatagai F, Kanai T, Furusawa Y, Hanaoka F, Zhu W-G, Mehnati P. Dependence of induction of interphase death of Chinese hamster ovary cells exposed to accelerated heavy ions on linear energy transfer. Radiation Research [Internet]. 1997;(5):449-454.
77.Zhu W-G, Aramaki R, Cai Y, Antoku S. Promotion of heat-induced apoptosis in FM3A cells by protease inhibitors. Biochemical and Biophysical Research Communications [Internet]. 1996;(3):924-931.
78.Zhu W-G, Antoku S, Kura S, Aramaki R, Nakamura K, Sasaki H. Enhancement of hyperthermic killing in L5178Y cells by protease inhibitors. Cancer Research [Internet]. 1995;(4):739-742.
發(fā)表中文期刊論文:
1 深圳大學(xué)醫(yī)學(xué)部專(zhuān)題簡(jiǎn)介 朱衛(wèi)國(guó) 中國(guó)科學(xué):生命科學(xué) 2018-01-20
2 精準(zhǔn)醫(yī)學(xué)的臨床部署:頂層架構(gòu)設(shè)計(jì)及關(guān)鍵信息技術(shù) 王宇;王心慰;劉爽;楊之輝;朱衛(wèi)國(guó);弓孟春 轉(zhuǎn)化醫(yī)學(xué)雜志 2017-12-18
3 甲基化和乙;揎椩谀[瘤發(fā)生發(fā)展中的作用 湯明; 李治明; 陸小鵬; 朱衛(wèi)國(guó) 生命科學(xué) 2017-11-08 06:51
4 Sirtuins家族蛋白參與DNA損傷修復(fù)的研究進(jìn)展 郭葦; 劉勤獻(xiàn); 湯明; 朱衛(wèi)國(guó); 王海英 中國(guó)科學(xué):生命科學(xué) 2017-06-20
5 細(xì)胞自噬通過(guò)清除SQSTM1/p62調(diào)控DNA損傷引起的染色質(zhì)泛素化 Yanan Wang;Nan Zhang;Luyao Zhang;Ran Li;Wan Fu;Ke Ma;Xue Li;Lina Wang;Jiadong Wang;Hongquan Zhang;Wei Gu;朱衛(wèi)國(guó);趙穎 科學(xué)新聞 2017-04-25
6 蛋白質(zhì)翻譯后修飾在蛋白質(zhì)-蛋白質(zhì)相互作用中的調(diào)控作用 侯天云; 陸小鵬; 朱衛(wèi)國(guó) 科學(xué)通報(bào) 2017-03-20
7 胚胎發(fā)育的精細(xì)表觀遺傳調(diào)控 朱衛(wèi)國(guó) 中國(guó)科學(xué):生命科學(xué) 2016-12-20
8 乙;揎棇(duì)p53功能調(diào)控的新機(jī)制 朱衛(wèi)國(guó) 中國(guó)科學(xué):生命科學(xué) 2016-12-20
9 Histone modifications and DNA damage responses 朱衛(wèi)國(guó) 中國(guó)生物化學(xué)與分子生物學(xué)會(huì)2016年全國(guó)學(xué)術(shù)會(huì)議論文集 2016-10-20 中國(guó)會(huì)議
10 β-catenin的翻譯后修飾及其作用 申長(zhǎng)春; 朱衛(wèi)國(guó) 中國(guó)科學(xué):生命科學(xué) 2015-11-20
11 含有多種酶活性的SIRT5蛋白在細(xì)胞代謝中的功能 楊鑫; 劉博雅; 朱衛(wèi)國(guó); 羅建沅 中國(guó)科學(xué):生命科學(xué) 2015-11-20
12 五彩繽紛的蛋白質(zhì)翻譯后修飾 朱衛(wèi)國(guó) 中國(guó)科學(xué):生命科學(xué) 2015-11-20
13 大漠回歸的靈魂書(shū)寫(xiě)——對(duì)話(huà)雪漠 朱衛(wèi)國(guó);雪漠;陳彥瑾;張曉琴;張凡;劉鎮(zhèn)偉 甘肅廣播電視大學(xué)學(xué)報(bào) 2015-02-15
14 “表觀遺傳學(xué)研究進(jìn)展專(zhuān)刊”編者寄語(yǔ) 朱衛(wèi)國(guó); 宋旭; 張根發(fā); 李紹武 遺傳 2014-03-15
15 組蛋白修飾與疾病 朱衛(wèi)國(guó) 中國(guó)生理學(xué)會(huì)腎臟生理專(zhuān)業(yè)委員會(huì)第二屆學(xué)術(shù)年會(huì)論文匯編 2013-05-23 中國(guó)會(huì)議
16 胞漿中Fox01引起細(xì)胞自噬進(jìn)而發(fā)揮抑制腫瘤的功能 趙穎;楊靜;廖文娟;劉向宇;張輝;王杉;王冬來(lái);馮京南;俞立;朱衛(wèi)國(guó) 中華醫(yī)學(xué)會(huì)腫瘤學(xué)分會(huì)第七屆全國(guó)中青年腫瘤學(xué)術(shù)會(huì)議——中華醫(yī)學(xué)會(huì)腫瘤學(xué)分會(huì)“中華腫瘤 明日之星”大型評(píng)選活動(dòng)暨中青年委員全國(guó)遴選論文匯編 2011-11-25 中國(guó)會(huì)議
17 細(xì)胞自噬與腫瘤發(fā)生的關(guān)系 王寵; 張萍; 朱衛(wèi)國(guó) 中國(guó)生物化學(xué)與分子生物學(xué)報(bào) 2010-11-20
18 組蛋白甲基化修飾效應(yīng)分子的研究進(jìn)展 宋博研; 朱衛(wèi)國(guó) 遺傳 2011-04-15
19 乙酰轉(zhuǎn)移酶Tip60在轉(zhuǎn)錄調(diào)控及DNA損傷應(yīng)答中作用的研究進(jìn)展 彭媛; 涂博; 朱衛(wèi)國(guó) 生理科學(xué)進(jìn)展 2011-02-25
20 DNA甲基轉(zhuǎn)移酶的表達(dá)調(diào)控及主要生物學(xué)功能 蘇玉; 王溪; 朱衛(wèi)國(guó) 遺傳 2009-11-15
21 去乙;窼IRT1的表達(dá)及活性調(diào)控機(jī)制 楊文嘉; 王冬來(lái); 朱衛(wèi)國(guó) 遺傳 2010-10-15
22 p53修飾及其相互作用的研究進(jìn)展 黃潔; 劉向宇; 朱衛(wèi)國(guó) 科學(xué)通報(bào) 2009-09-30
23 組蛋白甲基化酶及去甲基化酶的研究進(jìn)展 王溪; 朱衛(wèi)國(guó) 癌癥 2008-10-05
24 DNA的損傷與修復(fù) 柴國(guó)林; 朱衛(wèi)國(guó) 中華腫瘤雜志 2005-10-30
25 DNA甲基化的生物學(xué)應(yīng)用及檢測(cè)方法進(jìn)展 武立鵬; 朱衛(wèi)國(guó) 中華檢驗(yàn)醫(yī)學(xué)雜志 2004-07-30