Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
In vitro anti-cancer activity and structure-activity relationships of natural products isolated from fruits of Panax ginseng.
|
Cancer Chemother Pharmacol
|
2006
|
2.33
|
2
|
MDM2 is a negative regulator of p21WAF1/CIP1, independent of p53.
|
J Biol Chem
|
2004
|
1.93
|
3
|
Antisense therapy targeting MDM2 oncogene in prostate cancer: Effects on proliferation, apoptosis, multiple gene expression, and chemotherapy.
|
Proc Natl Acad Sci U S A
|
2003
|
1.87
|
4
|
MDM2 and human malignancies: expression, clinical pathology, prognostic markers, and implications for chemotherapy.
|
Curr Cancer Drug Targets
|
2005
|
1.83
|
5
|
Wnt/beta-catenin signaling pathway as a novel cancer drug target.
|
Curr Cancer Drug Targets
|
2004
|
1.72
|
6
|
Proteasome activator PA28 gamma regulates p53 by enhancing its MDM2-mediated degradation.
|
EMBO J
|
2008
|
1.65
|
7
|
Curcumin, a dietary component, has anticancer, chemosensitization, and radiosensitization effects by down-regulating the MDM2 oncogene through the PI3K/mTOR/ETS2 pathway.
|
Cancer Res
|
2007
|
1.60
|
8
|
The MDM2-p53 pathway revisited.
|
J Biomed Res
|
2013
|
1.52
|
9
|
Stabilization of E2F1 protein by MDM2 through the E2F1 ubiquitination pathway.
|
Oncogene
|
2005
|
1.51
|
10
|
Experimental therapy of hepatoma with artemisinin and its derivatives: in vitro and in vivo activity, chemosensitization, and mechanisms of action.
|
Clin Cancer Res
|
2008
|
1.47
|
11
|
Antisense, RNAi, and gene silencing strategies for therapy: mission possible or impossible?
|
Drug Discov Today
|
2008
|
1.37
|
12
|
Ginsenosides as Anticancer Agents: In vitro and in vivo Activities, Structure-Activity Relationships, and Molecular Mechanisms of Action.
|
Front Pharmacol
|
2012
|
1.35
|
13
|
RYBP stabilizes p53 by modulating MDM2.
|
EMBO Rep
|
2008
|
1.33
|
14
|
Dihydroartemisinin induces apoptosis and sensitizes human ovarian cancer cells to carboplatin therapy.
|
J Cell Mol Med
|
2008
|
1.32
|
15
|
Experimental therapy of prostate cancer with novel natural product anti-cancer ginsenosides.
|
Prostate
|
2008
|
1.31
|
16
|
p53-independent activities of MDM2 and their relevance to cancer therapy.
|
Curr Cancer Drug Targets
|
2005
|
1.30
|
17
|
Genistein, a dietary isoflavone, down-regulates the MDM2 oncogene at both transcriptional and posttranslational levels.
|
Cancer Res
|
2005
|
1.30
|
18
|
Pretreatment with dexamethasone increases antitumor activity of carboplatin and gemcitabine in mice bearing human cancer xenografts: in vivo activity, pharmacokinetics, and clinical implications for cancer chemotherapy.
|
Clin Cancer Res
|
2004
|
1.25
|
19
|
Experimental therapy of human prostate cancer by inhibiting MDM2 expression with novel mixed-backbone antisense oligonucleotides: in vitro and in vivo activities and mechanisms.
|
Prostate
|
2003
|
1.22
|
20
|
Preclinical characterization of AEG35156/GEM 640, a second-generation antisense oligonucleotide targeting X-linked inhibitor of apoptosis.
|
Clin Cancer Res
|
2006
|
1.22
|
21
|
MSP-RON signalling in cancer: pathogenesis and therapeutic potential.
|
Nat Rev Cancer
|
2013
|
1.17
|
22
|
In vitro and in vivo anticancer activity of novel synthetic makaluvamine analogues.
|
Clin Cancer Res
|
2009
|
1.13
|
23
|
Differential effects of ginsenosides on NO and TNF-alpha production by LPS-activated N9 microglia.
|
Int Immunopharmacol
|
2006
|
1.13
|
24
|
Natural product ginsenoside 25-OCH3-PPD inhibits breast cancer growth and metastasis through down-regulating MDM2.
|
PLoS One
|
2012
|
1.09
|
25
|
Novel ginsenosides 25-OH-PPD and 25-OCH3-PPD as experimental therapy for pancreatic cancer: anticancer activity and mechanisms of action.
|
Cancer Lett
|
2009
|
1.07
|
26
|
Chemotherapy and chemosensitization of non-small cell lung cancer with a novel immunomodulatory oligonucleotide targeting Toll-like receptor 9.
|
Mol Cancer Ther
|
2006
|
1.05
|
27
|
Anti-lung cancer effects of novel ginsenoside 25-OCH(3)-PPD.
|
Lung Cancer
|
2009
|
1.00
|
28
|
Knockdown of ribosomal protein S7 causes developmental abnormalities via p53 dependent and independent pathways in zebrafish.
|
Int J Biochem Cell Biol
|
2011
|
1.00
|
29
|
Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications.
|
Med Res Rev
|
2014
|
0.98
|
30
|
Anti-Inflammatory Agents for Cancer Therapy.
|
Mol Cell Pharmacol
|
2009
|
0.98
|
31
|
Divergent synthetic nucleotide motif recognition pattern: design and development of potent immunomodulatory oligodeoxyribonucleotide agents with distinct cytokine induction profiles.
|
Nucleic Acids Res
|
2003
|
0.98
|
32
|
Arylsulfonamide KCN1 inhibits in vivo glioma growth and interferes with HIF signaling by disrupting HIF-1α interaction with cofactors p300/CBP.
|
Clin Cancer Res
|
2012
|
0.97
|
33
|
Experimental therapy of ovarian cancer with synthetic makaluvamine analog: in vitro and in vivo anticancer activity and molecular mechanisms of action.
|
PLoS One
|
2011
|
0.96
|
34
|
miRNAs in cancer prevention and treatment and as molecular targets for natural product anticancer agents.
|
Curr Cancer Drug Targets
|
2013
|
0.96
|
35
|
A novel synthetic iminoquinone, BA-TPQ, as an anti-breast cancer agent: in vitro and in vivo activity and mechanisms of action.
|
Breast Cancer Res Treat
|
2009
|
0.95
|
36
|
Sustained expression of the RON receptor tyrosine kinase by pancreatic cancer stem cells as a potential targeting moiety for antibody-directed chemotherapeutics.
|
Mol Pharm
|
2011
|
0.94
|
37
|
Radiosensitization by antisense anti-MDM2 mixed-backbone oligonucleotide in in vitro and in vivo human cancer models.
|
Clin Cancer Res
|
2004
|
0.94
|
38
|
Recent advances in validating MDM2 as a cancer target.
|
Anticancer Agents Med Chem
|
2009
|
0.94
|
39
|
FBA-TPQ, a novel marine-derived compound as experimental therapy for prostate cancer.
|
Invest New Drugs
|
2009
|
0.93
|
40
|
Synthesis and in vitro anti-lung cancer activity of novel 1, 3, 4, 8-tetrahydropyrrolo [4, 3, 2-de]quinolin-8(1H)-one alkaloid analogs.
|
Med Chem
|
2009
|
0.93
|
41
|
Dexamethasone as a chemoprotectant in cancer chemotherapy: hematoprotective effects and altered pharmacokinetics and tissue distribution of carboplatin and gemcitabine.
|
Cancer Chemother Pharmacol
|
2004
|
0.93
|
42
|
Small-molecule inhibitor BMS-777607 induces breast cancer cell polyploidy with increased resistance to cytotoxic chemotherapy agents.
|
Mol Cancer Ther
|
2013
|
0.91
|
43
|
Immunomodulatory oligonucleotides as novel therapy for breast cancer: pharmacokinetics, in vitro and in vivo anticancer activity, and potentiation of antibody therapy.
|
Mol Cancer Ther
|
2006
|
0.91
|
44
|
Preclinical evaluation of anticancer efficacy and pharmacological properties of FBA-TPQ, a novel synthetic makaluvamine analog.
|
Mar Drugs
|
2012
|
0.91
|
45
|
MDM2 promotes proteasomal degradation of p21Waf1 via a conformation change.
|
J Biol Chem
|
2010
|
0.90
|
46
|
Synthetic oligodeoxynucleotides containing deoxycytidyl-deoxyguanosine dinucleotides (CpG ODNs) and modified analogs as novel anticancer therapeutics.
|
Curr Pharm Des
|
2005
|
0.90
|
47
|
Potent CpG oligonucleotides containing phosphodiester linkages: in vitro and in vivo immunostimulatory properties.
|
Biochem Biophys Res Commun
|
2002
|
0.90
|
48
|
Anti-tumor efficacy of a novel antisense anti-MDM2 mixed-backbone oligonucleotide in human colon cancer models: p53-dependent and p53-independent mechanisms.
|
Mol Med
|
2002
|
0.90
|
49
|
Dexamethasone as a chemosensitizer for breast cancer chemotherapy: potentiation of the antitumor activity of adriamycin, modulation of cytokine expression, and pharmacokinetics.
|
Int J Oncol
|
2007
|
0.90
|
50
|
Structure-activity relationship and substrate-dependent phenomena in effects of ginsenosides on activities of drug-metabolizing P450 enzymes.
|
PLoS One
|
2008
|
0.90
|
51
|
Transcription factor NFAT1 activates the mdm2 oncogene independent of p53.
|
J Biol Chem
|
2012
|
0.88
|
52
|
Intensive anti-inflammatory therapy with dexamethasone in patients with non-small cell lung cancer: effect on chemotherapy toxicity and efficacy.
|
Cancer Chemother Pharmacol
|
2008
|
0.87
|
53
|
A downstream kinase of the mammalian target of rapamycin, p70S6K1, regulates human double minute 2 protein phosphorylation and stability.
|
J Cell Physiol
|
2006
|
0.87
|
54
|
KCN1, a novel synthetic sulfonamide anticancer agent: in vitro and in vivo anti-pancreatic cancer activities and preclinical pharmacology.
|
PLoS One
|
2012
|
0.86
|
55
|
Extracellular activity of cyclic AMP-dependent protein kinase as a biomarker for human cancer detection: distribution characteristics in a normal population and cancer patients.
|
Cancer Epidemiol Biomarkers Prev
|
2007
|
0.86
|
56
|
Mode conversion based on forward stimulated Brillouin scattering in a hybrid phononic-photonic waveguide.
|
Opt Express
|
2014
|
0.85
|
57
|
JKA97, a novel benzylidene analog of harmine, exerts anti-cancer effects by inducing G1 arrest, apoptosis, and p53-independent up-regulation of p21.
|
PLoS One
|
2012
|
0.85
|
58
|
Experimental therapy for lung cancer: umbilical cord-derived mesenchymal stem cell-mediated interleukin-24 delivery.
|
Curr Cancer Drug Targets
|
2013
|
0.85
|
59
|
Antisense oligonucleotide targeted to RIalpha subunit of cAMP-dependent protein kinase (GEM231) enhances therapeutic effectiveness of cancer chemotherapeutic agent irinotecan in nude mice bearing human cancer xenografts: in vivo synergistic activity, pharmacokinetics and host toxicity.
|
Int J Oncol
|
2002
|
0.85
|
60
|
Radiolabeled 2'-fluorodeoxyuracil-beta-D-arabinofuranoside (FAU) and 2'-fluoro-5-methyldeoxyuracil-beta -D-arabinofuranoside (FMAU) as tumor-imaging agents in mice.
|
Cancer Chemother Pharmacol
|
2002
|
0.85
|
61
|
CpG penta- and hexadeoxyribonucleotides as potent immunomodulatory agents.
|
Biochem Biophys Res Commun
|
2003
|
0.85
|
62
|
Japonicone A suppresses growth of Burkitt lymphoma cells through its effect on NF-κB.
|
Clin Cancer Res
|
2013
|
0.84
|
63
|
Pathogenesis of RON receptor tyrosine kinase in cancer cells: activation mechanism, functional crosstalk, and signaling addiction.
|
J Biomed Res
|
2013
|
0.84
|
64
|
Synergistic activities of MET/RON inhibitor BMS-777607 and mTOR inhibitor AZD8055 to polyploid cells derived from pancreatic cancer and cancer stem cells.
|
Mol Cancer Ther
|
2013
|
0.84
|
65
|
Antisense-based cancer therapeutics: are we there yet?
|
Expert Opin Emerg Drugs
|
2006
|
0.84
|
66
|
T40214/PEI complex: a potent therapeutics for prostate cancer that targets STAT3 signaling.
|
Prostate
|
2008
|
0.84
|
67
|
Pharmacokinetics and tissue distribution of 25-hydroxyprotopanaxadiol, an anti-cancer compound isolated from Panax ginseng, in athymic mice bearing xenografts of human pancreatic tumors.
|
Eur J Drug Metab Pharmacokinet
|
2010
|
0.83
|
68
|
Disulfiram is a direct and potent inhibitor of human O6-methylguanine-DNA methyltransferase (MGMT) in brain tumor cells and mouse brain and markedly increases the alkylating DNA damage.
|
Carcinogenesis
|
2013
|
0.83
|
69
|
Experimental therapy for colon cancer: anti-cancer effects of TLR9 agonism, combination with other therapeutic modalities, and dependence upon p53.
|
Int J Oncol
|
2007
|
0.83
|
70
|
Preclinical pharmacology of BA-TPQ, a novel synthetic iminoquinone anticancer agent.
|
Mar Drugs
|
2010
|
0.83
|
71
|
Chemosensitization and radiosensitization of human cancer by antisense anti-MDM2 oligonucleotides: in vitro and in vivo activities and mechanisms.
|
Ann N Y Acad Sci
|
2003
|
0.83
|
72
|
Experimental therapy of prostate cancer with an immunomodulatory oligonucleotide: effects on tumor growth, apoptosis, proliferation, and potentiation of chemotherapy.
|
Prostate
|
2006
|
0.82
|
73
|
Antisense anti-MDM2 oligonucleotides as a novel approach to the treatment of glioblastoma multiforme.
|
Anticancer Res
|
2002
|
0.81
|
74
|
Oncogenes as novel targets for cancer therapy (part III): transcription factors.
|
Am J Pharmacogenomics
|
2005
|
0.81
|
75
|
Concurrent chemoradiation therapy with cisplatin and paclitaxel for locally advanced non-small cell lung cancer: long-term follow-up of a phase I trial.
|
Lung Cancer
|
2002
|
0.81
|
76
|
Novel MDM2 p53-independent functions identified through RNA silencing technologies.
|
Ann N Y Acad Sci
|
2005
|
0.80
|
77
|
Oncogenes as novel targets for cancer therapy (part IV): regulators of the cell cycle and apoptosis.
|
Am J Pharmacogenomics
|
2005
|
0.80
|
78
|
Advances in translational pharmacological investigations in identifying and validating molecular targets of natural product anticancer agents.
|
Curr Cancer Drug Targets
|
2013
|
0.80
|
79
|
Identification of the ZAK-MKK4-JNK-TGFβ signaling pathway as a molecular target for novel synthetic iminoquinone anticancer compound BA-TPQ.
|
Curr Cancer Drug Targets
|
2013
|
0.79
|
80
|
Mesenchymal stem cells modified to express lentivirus TNF-α Tumstatin(45-132) inhibit the growth of prostate cancer.
|
J Cell Mol Med
|
2011
|
0.79
|
81
|
Recent advances in experimental molecular therapeutics for malignant gliomas.
|
Curr Med Chem Anticancer Agents
|
2004
|
0.79
|
82
|
Preclinical pharmacology of 2-methoxyantimycin A compounds as novel antitumor agents.
|
Cancer Chemother Pharmacol
|
2005
|
0.79
|
83
|
Overexpression of annexin a1 induced by terephthalic acid calculi in rat bladder cancer.
|
Proteomics
|
2007
|
0.78
|
84
|
Preclinical pharmacology of novel indolecarboxamide ML-970, an investigative anticancer agent.
|
Cancer Chemother Pharmacol
|
2012
|
0.78
|
85
|
Antisense anti-MDM2 mixed-backbone oligonucleotides enhance therapeutic efficacy of topoisomerase I inhibitor irinotecan in nude mice bearing human cancer xenografts: In vivo activity and mechanisms.
|
Int J Oncol
|
2002
|
0.78
|
86
|
Preclinical pharmacology of epothilone D, a novel tubulin-stabilizing antitumor agent.
|
Cancer Chemother Pharmacol
|
2005
|
0.77
|
87
|
Phase-I dose escalation and sequencing study of docetaxel and continuous infusion topotecan in patients with advanced malignancies.
|
Cancer Chemother Pharmacol
|
2005
|
0.77
|
88
|
Development and validation of a rapid HPLC method for quantitation of SP-141, a novel pyrido[b]indole anticancer agent, and an initial pharmacokinetic study in mice.
|
Biomed Chromatogr
|
2014
|
0.77
|
89
|
Oncogenes as novel targets for cancer therapy (part II): Intermediate signaling molecules.
|
Am J Pharmacogenomics
|
2005
|
0.77
|
90
|
A phase I study of bi-weekly administration of 24-h gemcitabine followed by 24-h irinotecan in patients with solid tumors.
|
Cancer Chemother Pharmacol
|
2007
|
0.76
|
91
|
Oncogenes as novel targets for cancer therapy (part I): growth factors and protein tyrosine kinases.
|
Am J Pharmacogenomics
|
2005
|
0.76
|
92
|
Preclinical pharmacology of the novel antitumor agent adaphostin, a tyrphostin analog that inhibits bcr/abl.
|
Cancer Chemother Pharmacol
|
2005
|
0.75
|
93
|
Antisense approaches in drug discovery and development.
|
Prog Drug Res
|
2005
|
0.75
|
94
|
Analysis of threshold current of uniaxially tensile stressed bulk Ge and Ge/SiGe quantum well lasers.
|
Opt Express
|
2017
|
0.75
|
95
|
Anti-cancer molecular targets of natural products.
|
Curr Cancer Drug Targets
|
2013
|
0.75
|
96
|
Human tumor xenografts in mouse as a model for evaluating therapeutic efficacy of monoclonal antibodies or antibody-drug conjugate targeting receptor tyrosine kinases.
|
Methods Mol Biol
|
2015
|
0.75
|
97
|
Design and analysis of a CMOS-compatible distributed Bragg reflector laser based on highly uniaxial tensile stressed germanium.
|
Opt Express
|
2017
|
0.75
|
98
|
Determination of desoxyepothilone B in nude mice plasma by liquid-liquid extraction and reversed-phase high-performance liquid chromatography.
|
J Pharm Biomed Anal
|
2006
|
0.75
|
99
|
Analysis of acousto-optic interaction based on forward stimulated Brillouin scattering in hybrid phononic-photonic waveguides.
|
Opt Express
|
2016
|
0.75
|