(1) G9a stimulates CRC growth by inducing p53 Lys373 dimethylation-dependent activation of Plk1, Theranostics, 2018, 第 11 作者
(2) G9a regulates breast cancer growth by modulating iron homeostasis through the repression of ferroxidase hephaestin, Nat Commun, 2017, 第 11 作者
(3) Polymeric immunoglobulin receptor promotes tumor growth in hepatocellular carcinoma, Hepatology, 2017, 第 4 作者
(4) Evaluation of in vitro and in vivo activity of a multityrosine kinase inhibitor, AL3810, against human thyroid cancer, Acta Pharmacol Sin, 2017, 第 11 作者
(5) Down-regulation of G9a triggers DNA damage response and inhibits colorectal cancer cells proliferation, Oncotarget, 2015, 第 11 作者
(6) Design, synthesis and biological evaluation of novel homocamptothecin analogues as potent antitumor agents, Bioorg Med Chem., 2015, 第 11 作者
(7) G226, a new ETP derivative, triggers DNA damage, and apoptosis via ROS generation, Acta Pharmacol Sin, 2014, 第 11 作者
(8) G226, a novel epipolythiodioxopiperazine derivative, induces autophagy and caspase-dependent apoptosis in human breast cancer cells in vitro., Acta Pharmacol Sin, 2014, 第 11 作者
(9) Design, synthesis and biological evaluation of 4-demethyl-4-deoxypodophyllotoxin derivatives as novel tubulin and histone deacetylase dual inhibitors, RSC Advances, 2014, 第 11 作者
(10) Suzuki coupling based synthesis and in vitro cytotoxic evaluation of 7-heteroaryl-substituted camptothecin analogs, Bioorg Med Chem Lett, 2014, 第 11 作者
(11) JNK signaling maintains the mesenchymal properties of multi-drug resistant human epidermoid carcinoma KB cells through snail and twist1, BMC Cancer, 2013, 第 11 作者
(12) Oligomannurarate sulfate inhibits CXCL12/SDF-1-mediated proliferation and invasion of human tumor cells in vitro, Acta Pharmacol Sin, 2013, 第 11 作者
(13) The discovery and optimization of novel dual inhibitors of topoisomerase II and histone deacetylase, Bioorg Med Chem, 2013, 第 11 作者
(14) The discovery of colchicine-SAHA hybrids as a new class of antitumor agents, Bioorg Med Chem, 2013, 第 11 作者
(15) Synthesis and biological evaluation of new homocamptothecin analogues., Eur J Med Chem, 2012, 第 11 作者
(16) AL3810, a multi-tyrosine kinase inhibitor, exhibits potent anti-angiogenic and antitumor activity via targeting VEGFR, FGFR, PDGFR, J Cell Mol Med, 2012, 第 2 作者
(17) Combined Src and ER blockade impairs human breast cancer proliferation in vitro and in vivo., Breast Cancer Res Treat, 2011, 第 1 作者
(18) Reversal of multidrug resistance by reduction-sensitive linear cationic click polymer/iMDR1-pDNA complex nanoparticles., Biomaterials, 2011, 第 4 作者
(19) Design, synthesis and biological evaluation of substituted 11H-benzo[a]carbazole-5-carboxamides as novel antitumor agents, Eur J Med Chem, 2011, 第 4 作者
(20) Oligomannurarate sulfate, a novel antimitotic agent, exerts anti-cancer activity by binding to tubulin on novel site. , Cancer Biol Ther., 2010, 第 2 作者
(21) Increased accumulation of hypoxia-inducible factor-1α with reduced transcriptional activity mediates the antitumor effect of triptolide, Mol Cancer, 2010, 第 11 作者
(22) The characteristics and performance of a multifunctional nanoassembly system for the co-delivery of docetaxel and iSur-pDNA in a mouse hepatocellular carcinoma model., Biomaterials., 2010, 第 3 作者
(23) Oligomannurarate sulfate blocks tumor growth by inhibiting NF-kappaB activation., Acta Pharmacol Sin. , 2010, 第 2 作者
(24) Combined Src and aromatase inhibition impairs human breast cancer growth in vivo and bypass pathways are activated in AZD0530 resistant tumors., Clin Cancer Res, 2009, 第 1 作者
(25) Salvicine inactivates beta 1 integrin and inhibits adhesion of MDA-MB-435 cells to fibronectin via reactive oxygen species signaling., Mol Cancer Res, 2008, 第 2 作者
(26) SH-7, a new synthesized shikonin derivative, exerting its potent antitumor activities as a topoisomerase inhibitor, Inter J Cancer, 2006, 第 1 作者
(27) The p53 pathway is synergized by p38 MAPK signaling to mediate 11,11’-dideoxyverticillin-induced G2/M arrest, FEBS Lett, 2005, 第 1 作者
(28) Antiangiogenic activity of 11,11’-dideoxyverticillin, a natural product isolated from the fungus Shiraia bambusicola, Biochem Biophys Res Commun, 2005, 第 1 作者