课题组简介
1、景永奎教授课题组:
本课题组主要研究方向为抗肿瘤新药物作用靶点的确认、癌细胞分化诱导剂和凋亡促进剂的寻找及其机制研究。建立了以肿瘤特异性分子靶标研究新型抗癌药物的技术平台,从事抗肿瘤活性指导下天然活性化合物的提取分离、结构修饰。在新抗肿瘤活性化合物的发现以及联合用药法案的建立方面取得了突出的成绩,发现了多个药物候选活性化合物。在《Blood》、《Leukemia》、《Clinical Cancer Research》、《Cancer Research》等学术刊物上发表学术论文130余篇,被他引4000多次。申请发明专利24项,取得国际专利4件,中国专利16件。主持10项美国NIH和癌症研究基金会支持项目。先后两次获得国家自然科学基金海外青年学者合作研究基金资助,参与6项重大新药创制科技重大专项课题、6项国家自然科学基金等国家级项目的研究工作。
2、主持或参加科研项目(课题)及人才计划项目情况:
1. 重大新药创制”科技重大专项,2017ZX09101002-007,抗多药耐肿瘤新青蒿素衍生物DHX-11的临床前研究,2017/03-2020/12,参与。
2. 国家自然科学基金面上项目,31570350,藤黄属植物中作用于PI3K/Akt/mTOR通路的抗前列腺癌活性成分及作用机制研究,2016/01-2019/12,参与。
3. Samuel Waxman Cancer Research foundation资助项目,Development of α, β-unsaturated carbonyl compounds as novel anti-leukemia agents,2019/07-2019/06,主持。
4. 重大新药创制”科技重大专项,2012ZX09103-101-023,抗多药耐药肿瘤新药DHX-11的研究与开发,2012/01-2015/12,参与。
5. 国家自然科学基金,81072533,JZY03及其类似物的抗癌作用机理和构效关系研究,2011/01-2013/12,参与。
6. 国家自然科学基金项目海外及港澳学者合作研究基金项目,81028015,c-FLIP作为取代环戊酮类抗肿瘤活性化合物的分子靶标的研究,2011/01-2012/12,主持。
7. 国家科技部国际科技合作项目,2009DFA31200,基于特异性分子靶标的抗肿瘤药物筛选平台的建立与新型抗肿瘤药物的开发,2009/01-2011/12,主持。
8. 重大新药创制”科技重大专项“十一五”课题,2009ZX09103-080,新型抗肿瘤活性化合物PTZ-09的研究与开发,2009/01-2011/03,参与。
3、代表性论文:
(1) Rui Wang, Ying Li, Ping Gong, Janice Gabrilove, Samuel Waxman and Yongkui Jing. Arsenic Trioxide and Sorafenib Induce Synthetic Lethality of FLT3-ITD Acute Myeloid Leukemia Cells. Mol Cancer Ther. 2018 Sep; 17(9):1871-1880
(2) Ping Gong(#), Kun Li, Ying Li(#), Dan Liu, Linxiang,Zhao, Yongkui,Jing(#), HDAC and Ku70 axis-an effective target for apoptosis induction by a new 2-cyano-3-oxo-1,9-dien glycyrrhetinic acid analogue. Cell Death and Disease, (2018)9:623
(3) Rui Wang(#) ; Lijuan Xia; Janice Gabrilove; Samuel Waxman;Yongkui Jing(*), Sorafenib inhibition of Mcl-1 accelerates ATRA induced apoptosis in differentiationresponsive AML cells Clinical Cancer Research 2016.3.1 22(5): 1211~1221
(4) Guyue Liu(#); Rui Wang; Yuetong Wang; Pengzhan Li; Guisen Zhao; Linxiang,Zhao; Yongkui Jing(*), Ethacrynic acid oxadiazole analogs induce apoptosis in malignant hematologic cells through downregulation of Mcl-1 and c-FLIP, which was attenuated by GSTP1-1,Molecular Cancer Therapeutics,2013.9 12(9):1837~1847
(5) Rui Wang(#) ; Lijuan Xia; Janice Gabrilove; Samuel Waxman;Yongkui Jing(*), Downregulation of Mcl-1 through GSK-3β activation contributes to arsenic trioxide-induced apoptosis in acute myeloid leukemia cells, Leukemia 2013.2,27(2)
(6) Rui Wang(#); Changda Liu; Lijuan Xia; Guisen Zhao; Janice Gabrilove;Samuel Waxman; Yongkui Jing(*), Ethacrynic acid and a derivative enhance apoptosis in arsenic trioxide-treated myeloid leukemia and lymphoma cells: the role of glutathione S-transferase P1-1, Clinical Cancer Research, 2012.12.15,18(24): 6690~6701
(7) Yang X, Liu G, Li H, Zhang Y, Song D, Li C, Wang R, Liu B, Liang W, Jing YK, Zhao G. Novel oxadiazole analogues derived from ethacrynic acid: design, synthesis, and structure-activity relationships in inhibiting the activity of glutathione S-transferase P1-1 and cancer cell proliferation. J Med Chem. 2010, 53:1015-22
(8) Min Lu(#); Lijuan Xia; Huiming Hua; Yongkui Jing(*), Acetyl-keto-beta-boswellic acid induces apoptosis through a death receptor 5-mediated pathway in prostate cancer cells, Cancer Research, 2008.2.15, 68(4): 1180~1186
(9) Rui Wang(#); Chunmin Li; Dandan Song; Guisen Zhao; Linxiang Zhao; Yongkui Jing(*), Ethacrynic Acid Butyl-Ester Induces Apoptosis in Leukemia Cells through a Hydrogen Peroxide–Mediated Pathway Independent of Glutathione S-Transferase P1-1 Inhibition, Cancer Research, 2007.8.15, 67(16): 7856~7864
(10) Chen D, Chan R, Waxman S, Jing YK. Buthionine sulfoximine enhancement of arsenic trioxide-induced apoptosis in leukemia and lymphoma cells is mediated via activation of JNK and upregulation of death receptors. Cancer Research, 2006 66:11416-23
(11) Lijuan Xia(#); Elisa Wurmbach; Samuel Waxman; Yongkui Jing(*), Upregulati on of Bfl-1/A1 in leukemia cells undergoing differentiation by all-trans retinoic acid treatment attenuates chemotherapeutic agent-induced apoptosis, Leukemia, 2006.3.30, 20(6): 1009~1016
(12) Jing YK, Hellinger N, Xia L, Monks A, Sausville EA, Zelent A, Waxman S. Benzodithiophenes induce differentiation and apoptosis in human leukemia cells. Cancer Research, 2005, 65:7847-55
(13) Lu M, Mira-y-Lopez R, Nakajo S, Nakaya K and Jing YK. Evidence for a linear gene regulatory network linking estrogen receptor a, retinoic acid receptor a, and cellular retinoic acid binding protein II expression in human breast cells. Oncogene, 2005, 24:4362-9
(14) Xia L, Chen D, Han R, Fang QC, Waxman S and Jing YK. Boswellic acid acetate induces apoptosis through caspase-mediated pathways in acute myeloid leukemia. Molecular Cancer Therapeutics, 2005, 4:381-388
(15) Lu M, Xia LJ, Luo D,Waxman S and Jing YK. Dual effects of glutathione-s-transferase p on As2O3 action in prostate cancer cells: enhancement of growth inhibition and inhibition of apoptosis. Oncogene. 2004, 23:3945-52
(16) Jing YK, Xia LJ, Lu M and Waxman S. The cleavage product ∆PML-RARa contributes to all-trans retinoic acid-mediated differentiation in acute promyelocytic leukemia cells. Oncogene 2003, 22:4083-91
(17) Yongkui Jing(#)(*) ; Lijuan Xia; Samuel Waxman, Targeted removal of PML-RARα protein is required prior to inhibition of histone deacetylase for overcoming all-trans retinoic acid differentiation resistance in acute promyelocytic leukemia, Blood, 2002.8.1, 100(3): 1008~1013
(18) Yongkui Jing(#)(*) ; Long Wang; Lijuan Xia; Guoqiang Chen; Zhu Chen;Wilson H. Miller; Samuel Waxman, Combined effect of all-trans retinoic acid and arsenic trioxide in acute promyelocytic leukemia cells in vitro and in vivo, Blood, 2001.1.1, 97(1): 264~269
(19) Jing YK, Dai J, Chalmers-Redman R.E, Tatton W.G., Waxman S. Arsenic trioxidase selectively induces acute promyelocytic leukemia cell apoptosis via a hydrogen peroxide-dependent pathway. Blood 1999, 94:2102-2111
(20) Jing YK, Waxman S and Mira-y-Lopez R. The cellular retinoic acid-binding protein II (CRABPII) is a positive regulator of retinoic acid signaling in breast cancer cells. Cancer Research. 1997, 57:1668-1672
4、实验室平台介绍:
本实验室注重研究抗肿瘤药物的前沿领域,有浓厚的学术追求氛围和严谨的科研创新态度,同时在学校多学科交叉、融合的研究平台上开拓多方向的科研探索思路。本实验室现有科研助理1人,博士后1人,在读硕、博士生共计18人,定期举行一些团体活动,重视和支持每一位同学的爱好和兴趣发展。学术上的互帮互助,生活上的团结友爱,造就了我们向心力强、团结一致的课题组。热忱期待每一位热爱科研的同学加入!
景永奎教授实验室电话:024-23986975
E-mail: jingyk@syphu.edu.cn
所招专业: 100706药理学(博士)、100706药理学(硕士)、105504药学(药理学方向)(硕士)
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