camptothecin has been researched along with homocamptothecin in 53 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (7.55) | 18.2507 |
2000's | 26 (49.06) | 29.6817 |
2010's | 20 (37.74) | 24.3611 |
2020's | 3 (5.66) | 2.80 |
Authors | Studies |
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Bigg, DC; Camara, J; Demarquay, D; Harnett, J; Kasprzyk, PG; Lavergne, O; Lesueur-Ginot, L; Pla Rodas, F; Pommier, J; Pons, D; Prévost, G; Rolland, A; Schiano-Liberatore, AM; Ulibarri, G | 1 |
Bailly, C; Baroggi, N; Bigg, DC; Camara, J; Cazaux, JB; Coulomb, H; Demarquay, D; Huchet, M; Lanco, C; Lavergne, O; Le Breton, C; Manginot, E; Muller, N; Rolland, A | 1 |
Battistuzzi, G; Beretta, GL; Cabri, W; De Cesare, M; Giannini, G; Marastoni, E; Marzi, M; Pisano, C; Vesci, L; Zunino, F | 1 |
Huang, Q; Lu, W; Wang, L | 1 |
Bailly, C; Bigg, DC; Camara, J; Dassonneville, L; Demarquay, D; Kasprzyk, PG; Kiss, R; Lavergne, O; Lesueur-Ginot, L | 1 |
Agrawal, S; Chen, J; Chen, L; Le, LP; Oliver, P; Wang, H; Zeng, X; Zhang, R; Zhou, W | 1 |
Bailly, C; Bigg, DC; Coulomb, H; Dassonneville, L; Demarquay, D; Huchet, M; Lansiaux, A; Lavergne, O | 1 |
Bigg, DC; Bronckart, Y; Chaboteaux, C; da Costa, PM; Decaestecker, C; Gordover, L; Harper, L; Kiss, R; Lavergne, O; Lesueur-Ginot, L; Malonne, H; Philippart, P | 1 |
Pommier, Y; Takebayashi, Y; Urasaki, Y | 1 |
Bigg, DC; Demarquay, D; Kasprzyk, PG; Lavergne, O | 1 |
Bigg, DC; Chauvier, D; Chourpa, I; Manfait, M | 1 |
Bailly, C; Baldeyrou, B; Bigg, DC; Coulomb, H; Demarquay, D; Huchet, M; Laine, W; Lanco, C; Lavergne, O | 1 |
Wen, Z; Xiong, X; Zhu, Z | 1 |
Chauvier, D; Manfait, M; Morjani, H | 2 |
Li, P; Luo, L; Luo, Y; Peng, H; Tang, W | 1 |
Chen, HZ; Chen, Y; Ding, XQ; Kong, QY; Wang, AX | 1 |
Bailly, C | 1 |
Antony, S; Bates, SE; Kohlhagen, G; Medina-Pérez, WY; Nadjem, T; Pommier, Y; Robey, RW | 1 |
Yang, S; Zhang, WN | 1 |
Burke, TG; Curran, DP; Du, W; Jerina, DM; Kohlhagen, G; Laco, GS; Pommier, Y; Sayer, JM | 1 |
Chen, YT; Hong, GB; Jiang, RJ; Luo, JH; Xu, LF; Xu, LY; Zhou, JX | 1 |
Driver, RW; Yang, LX | 1 |
Chen, D; Chen, Y; Ding, XQ; Li, S; Wang, AX | 1 |
Agama, K; Anderson, BD; Antony, S; Bevins, R; Curran, DP; Pommier, Y; Tangirala, RS | 1 |
Althaus, M; Diolez, C; Manginot, E; Peters, R; Rolland, A; Veyrat, M | 1 |
Bailly, C; Bonte, JP; Dias, N; Foulon, C; Goossens, JF; Lansiaux, A; Mahieu, C; Principe, P; Vaccher, C | 1 |
Bates, SE; Guirouilh-Barbat, J; Liao, Z; Polgar, O; Pommier, Y; Robey, RW; To, KK | 1 |
Teicher, BA | 1 |
Che, X; Ji, H; Miao, Z; Shao, L; Sheng, C; Yao, J; You, L; Zhang, J; Zhang, M; Zhang, W | 1 |
Devaraj, S; Vadwai, V | 1 |
Che, X; Cheng, P; Feng, H; Guo, W; Liu, W; Luo, C; Miao, Z; Sheng, C; Wang, W; Xu, Y; Yao, J; Zhang, J; Zhang, W; Zhu, L | 1 |
Che, X; Cheng, P; Guo, W; Liu, W; Miao, Z; Sheng, C; Wang, W; Yao, J; Zhang, W; Zhu, L | 1 |
Che, X; Cheng, P; Dong, G; Feng, H; Guo, W; Liu, W; Luo, C; Miao, Z; Sheng, C; Wang, J; Wang, W; Xu, Y; Yao, J; You, L; Zhang, J; Zhang, W; Zhou, L; Zhu, L | 1 |
Deng, Q; Hu, GX; Huang, YQ; Yuan, F; Yuan, K; Zhang, Y | 1 |
Cheng, P; Dong, G; Guo, W; Liu, W; Miao, Z; Sheng, C; Wang, S; Wang, W; Yao, J; Zhang, W; Zhang, Y; Zhu, L; Zhuang, C | 1 |
Cheng, P; Dong, G; Guo, W; Liu, W; Miao, Z; Sheng, C; Yao, J; Zhang, W; Zhang, Y; Zhu, L; Zhuang, C | 1 |
Cheng, P; Dong, G; Guo, W; Lei, N; Liu, W; Miao, Z; Sheng, C; Wang, S; Yao, J; Zhang, W; Zhang, Y; Zhu, L; Zhuang, C | 1 |
He, ZG; Pu, XH; Qin, YM; Sun, J; Zhang, P; Zhang, X | 1 |
Nie, F; Ran, ZH; Tong, JL; Xiao, SD; Xu, XT; Zhang, CP; Zhu, MM | 1 |
Chen, Y; Huang, Q; Lu, W; Luo, Y; Tong, L; Yu, S | 1 |
Cheng, P; Dong, G; Guo, W; Lei, N; Liu, W; Miao, Z; Sheng, C; Yao, J; Zhang, W; Zhang, X; Zhu, L; Zhuang, C | 1 |
Deng, LH; Tang, CY; Tu, LX; Wu, CB; Xu, YH | 1 |
Dong, G; Guo, W; Guo, Z; Liu, W; Miao, Z; Sheng, C; Yao, J; Zhang, H; Zhang, W; Zhu, L; Zhuang, C | 1 |
Ji, TF; Li, DZ; Li, YR; Liu, RH; Pan, XD; Wang, CY; Wang, YM | 1 |
Cao, R; Chen, X; Geng, M; Li, P; Wang, L | 1 |
Duan, Y; Gong, T; Liu, P; Sun, X; Wang, Q; Zhang, Z | 1 |
Chen, Y; Lu, W; Ma, L; Wang, L; Xie, S | 1 |
Fan, R; Guo, X; Li, D; Li, Z; Liu, Y; Song, C; Tang, X; Xu, H; Zhang, Y; Zhang, Z | 1 |
Gao, S; Li, L; Liu, T; Ma, Q; Miller-Kleinhenz, J; Qin, Z; Tian, R; Wang, G; Zhang, F; Zhu, L | 1 |
Chen, Q; Hu, J; Liu, J; Luo, X; Meng, Z; Ni, Z; Sun, Y; Tang, L; Wang, X; Xiang, F; Zhang, M; Zhang, Z; Zhu, L | 1 |
He, H; Li, X; Liu, D; Liu, J; Ma, Z; Tang, X; Wang, Y; Xu, Y | 1 |
Cao, P; Cheng, Y; Cui, J; Fan, S; Li, Y; Shang, Y; Yin, X; Zhang, H | 1 |
6 review(s) available for camptothecin and homocamptothecin
Article | Year |
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Evolution in medicinal chemistry of E-ring-modified Camptothecin analogs as anticancer agents.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Cell Survival; Chemistry, Pharmaceutical; Drug Screening Assays, Antitumor; Humans; Molecular Structure; Structure-Activity Relationship; Topoisomerase I Inhibitors | 2013 |
Homocamptothecins: E-ring modified CPT analogues.
Topics: Animals; Antineoplastic Agents; Camptothecin; Enzyme Inhibitors; Humans; Xenograft Model Antitumor Assays | 2000 |
Homocamptothecins: potent topoisomerase I inhibitors and promising anticancer drugs.
Topics: Animals; Antineoplastic Agents; Camptothecin; DNA Topoisomerases, Type I; Drug Design; Drug Resistance, Neoplasm; Enzyme Inhibitors; Humans; Leukemia; Topoisomerase I Inhibitors | 2003 |
[Homocamptothecins--novel promising anticancer drugs as inhibitors of topoisomerase I].
Topics: Animals; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Camptothecin; DNA Damage; Humans; Irinotecan; Topoisomerase I Inhibitors; Topotecan; Tumor Cells, Cultured | 2004 |
Synthesis and pharmacology of new camptothecin drugs.
Topics: Animals; Antineoplastic Agents, Phytogenic; Camptothecin; Humans; Organosilicon Compounds | 2005 |
Next generation topoisomerase I inhibitors: Rationale and biomarker strategies.
Topics: Animals; Antineoplastic Agents; Biomarkers; Camptothecin; Carbazoles; Humans; Indenes; Indoles; Isoquinolines; Naphthyridines; Topoisomerase I Inhibitors | 2008 |
1 trial(s) available for camptothecin and homocamptothecin
Article | Year |
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[Preliminary clinical comparison of HLF and ELF regimen in the treatment of advanced gastric carcinoma in middle-aged and elderly patients].
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Camptothecin; Etoposide; Female; Fluorouracil; Humans; Leucovorin; Male; Middle Aged; Neoplasm Staging; Stomach Neoplasms | 2000 |
46 other study(ies) available for camptothecin and homocamptothecin
Article | Year |
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Homocamptothecins: synthesis and antitumor activity of novel E-ring-modified camptothecin analogues.
Topics: Animals; Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily B, Member 1; Benzoxepins; Camptothecin; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Female; Humans; Inhibitory Concentration 50; Male; Mice; Mice, Nude; Neoplasm Transplantation; Stereoisomerism; Structure-Activity Relationship; Topoisomerase I Inhibitors; Transplantation, Heterologous; Tumor Cells, Cultured | 1998 |
Topoisomerase I-mediated antiproliferative activity of enantiomerically pure fluorinated homocamptothecins.
Topics: Antineoplastic Agents; Camptothecin; DNA Topoisomerases, Type I; Dose-Response Relationship, Drug; HT29 Cells; Humans; Inhibitory Concentration 50; Stereoisomerism; Tumor Cells, Cultured | 2000 |
E-ring-modified 7-oxyiminomethyl camptothecins: Synthesis and preliminary in vitro and in vivo biological evaluation.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Cell Proliferation; DNA Topoisomerases, Type I; Enzyme Inhibitors; Humans; Inhibitory Concentration 50; Stereoisomerism; Structure-Activity Relationship; Xenograft Model Antitumor Assays | 2008 |
Homocamptothecin, an E-ring modified camptothecin with enhanced lactone stability, retains topoisomerase I-targeted activity and antitumor properties.
Topics: Animals; Antineoplastic Agents; Camptothecin; Cell Division; Disease Models, Animal; DNA; Drug Screening Assays, Antitumor; Drug Stability; Enzyme Inhibitors; HT29 Cells; Humans; K562 Cells; Lactones; Leukemia L1210; Leukemia, Experimental; Neoplasm Transplantation; Topoisomerase I Inhibitors; Transplantation, Heterologous; Tumor Cells, Cultured | 1999 |
MDM2 oncogene as a target for cancer therapy: An antisense approach.
Topics: Animals; Antineoplastic Agents; Camptothecin; Cell Division; Choriocarcinoma; Dose-Response Relationship, Drug; Doxorubicin; Drug Synergism; Female; Humans; Mice; Mice, Nude; Neoplasm Transplantation; Nuclear Proteins; Oligonucleotides, Antisense; Osteosarcoma; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-mdm2; Survival Rate; Tumor Cells, Cultured | 1999 |
Homocamptothecin, an E-ring-modified camptothecin analogue, generates new topoisomerase I-mediated DNA breaks.
Topics: Animals; Antineoplastic Agents; Camptothecin; Cell Survival; DNA Topoisomerases, Type I; DNA, Superhelical; Drug Resistance, Neoplasm; Enzyme Inhibitors; Leukemia P388; Mice; Structure-Activity Relationship; Topoisomerase I Inhibitors; Tumor Cells, Cultured | 1999 |
Homocamptothecin, an E-ring-modified camptothecin, exerts more potent antiproliferative activity than other topoisomerase I inhibitors in human colon cancers obtained from surgery and maintained in vitro under histotypical culture conditions.
Topics: Antineoplastic Agents; Biopsy; Camptothecin; Cell Division; Colon; Colonic Neoplasms; Culture Techniques; DNA Topoisomerases, Type I; Dose-Response Relationship, Drug; Doxorubicin; Enzyme Inhibitors; Etoposide; Humans; Irinotecan; Thymidine; Topoisomerase I Inhibitors; Topotecan; Tritium; Tumor Cells, Cultured | 2000 |
Activity of a novel camptothecin analogue, homocamptothecin, in camptothecin-resistant cell lines with topoisomerase I alterations.
Topics: Animals; Antineoplastic Agents; Camptothecin; Cricetinae; DNA Topoisomerases, Type I; DNA, Neoplasm; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Enzyme Stability; Humans; Inhibitory Concentration 50; Leukemia P388; Male; Mice; Point Mutation; Prostatic Neoplasms; Topoisomerase I Inhibitors; Tumor Cells, Cultured | 2000 |
Kinetics of in vitro hydrolysis of homocamptothecins as measured by fluorescence.
Topics: Antineoplastic Agents; Camptothecin; DNA; Hydrogen-Ion Concentration; Hydrolysis; Kinetics; Lactones; Spectrometry, Fluorescence | 2000 |
A novel B-ring modified homocamptothecin, 12-Cl-hCPT, showing antiproliferative and topoisomerase I inhibitory activities superior to SN-38.
Topics: Antibiotics, Antineoplastic; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Camptothecin; Cell Division; Cell Survival; DNA, Neoplasm; DNA, Superhelical; Doxorubicin; Enzyme Inhibitors; HT29 Cells; Humans; Irinotecan; Plasmids; Topoisomerase I Inhibitors | 2001 |
Ceramide involvement in homocamptothecin- and camptothecin-induced cytotoxicity and apoptosis in colon HT29 cells.
Topics: Antineoplastic Agents, Phytogenic; Apoptosis; Camptothecin; Caspases; Cell Survival; Ceramides; Colonic Neoplasms; Enzyme Inhibitors; Genes, p53; HT29 Cells; Humans; Lipids; Mutation; Sphingomyelin Phosphodiesterase; Sphingomyelins; trans-Golgi Network | 2002 |
[Cell cycle block and apoptosis in rabbit lens epithelial cells induced by hydroxycamptothecine].
Topics: Animals; Apoptosis; Camptothecin; Cell Cycle; Dose-Response Relationship, Drug; Enzyme Inhibitors; Epithelial Cells; Fas Ligand Protein; fas Receptor; Female; Lens, Crystalline; Male; Membrane Glycoproteins; Rabbits; S Phase | 2002 |
Homocamptothecin-daunorubicin association overcomes multidrug-resistance in breast cancer MCF7 cells.
Topics: Adenocarcinoma; Antibiotics, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Breast Neoplasms; Camptothecin; Carcinoma; Colonic Neoplasms; Daunorubicin; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Drug Synergism; Female; Flow Cytometry; Gene Expression Regulation, Neoplastic; Humans; In Vitro Techniques; Leukemia, Myeloid; Microbial Sensitivity Tests; Multidrug Resistance-Associated Proteins; Polymerase Chain Reaction; RNA, Neoplasm; Treatment Outcome; Tumor Cells, Cultured | 2002 |
[Anticancer effect of hydroxycampothecin on oral squamous carcinoma cell line].
Topics: Animals; Antineoplastic Agents; Apoptosis; Camptothecin; Carcinoma, Squamous Cell; Cell Cycle; Disease Models, Animal; Female; Humans; Male; Mice; Mice, Inbred BALB C; Mouth Neoplasms; Neoplasm Transplantation; Neoplasms, Experimental; Tumor Cells, Cultured; Xenograft Model Antitumor Assays | 2002 |
ABCG2 mediates differential resistance to SN-38 (7-ethyl-10-hydroxycamptothecin) and homocamptothecins.
Topics: ATP Binding Cassette Transporter, Subfamily G, Member 2; ATP-Binding Cassette Transporters; Camptothecin; Cell Line; Cell Line, Tumor; Cell Survival; Dose-Response Relationship, Drug; Drug Resistance, Neoplasm; Humans; Irinotecan; Neoplasm Proteins; Topoisomerase I Inhibitors | 2004 |
Analysis of human topoisomerase I inhibition and interaction with the cleavage site +1 deoxyguanosine, via in vitro experiments and molecular modeling studies.
Topics: Binding Sites; Camptothecin; Deoxyguanosine; DNA; DNA Topoisomerases, Type I; Humans; Hydrophobic and Hydrophilic Interactions; Ligands; Models, Molecular; Nucleic Acid Conformation; Protein Binding; Static Electricity; Thermodynamics; Topoisomerase I Inhibitors | 2004 |
[Efficacy of selective continuous transarterial infusion chemotherapy on advanced pancreatic cancer].
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Camptothecin; Carboplatin; Deoxycytidine; Doxorubicin; Female; Fluorouracil; Gemcitabine; Humans; Infusion Pumps, Implantable; Infusions, Intra-Arterial; Leucovorin; Liver Neoplasms; Lymphatic Metastasis; Male; Middle Aged; Neoplasm Staging; Pancreatic Neoplasms; Remission Induction; Survival Rate | 2004 |
[Antitumor effects of ring-closed and ring-opened hydroxycamptothecin on oral squamous carcinoma cell line Tca8113].
Topics: Animals; Antineoplastic Agents, Phytogenic; Apoptosis; Camptothecin; Carcinoma, Squamous Cell; Cell Cycle; Cell Line, Tumor; Humans; Lactones; Mice; Mice, Inbred BALB C; Mice, Nude; Mouth Neoplasms; Neoplasm Transplantation | 2005 |
Synthesis and biological assays of E-ring analogs of camptothecin and homocamptothecin.
Topics: Antineoplastic Agents; Biological Assay; Camptothecin; Cell Line, Tumor; Cell Proliferation; DNA; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Humans; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Structure; Structure-Activity Relationship; Topoisomerase Inhibitors | 2006 |
Practical formal total syntheses of the homocamptothecin derivative and anticancer agent diflomotecan via asymmetric acetate aldol additions to pyridine ketone substrates.
Topics: Aldehydes; Antineoplastic Agents; Camptothecin; Heterocyclic Compounds, 4 or More Rings; Ketones; Pyridines | 2006 |
Chiral capillary electrophoretic determination of the enantiomeric purity of homocamptothecin derivatives, promising antitumor topoisomerase I inhibitors, using highly sulfated CDs and fluorescence detection.
Topics: Antineoplastic Agents; beta-Cyclodextrins; Buffers; Camptothecin; Electrophoresis, Capillary; Enzyme Inhibitors; Spectrometry, Fluorescence; Spectrophotometry, Ultraviolet; Stereoisomerism; Sulfates; Temperature; Topoisomerase I Inhibitors | 2006 |
Reduced expression of DNA topoisomerase I in SF295 human glioblastoma cells selected for resistance to homocamptothecin and diflomotecan.
Topics: Camptothecin; Cell Line, Tumor; DNA Topoisomerases, Type I; Down-Regulation; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Gene Expression Regulation, Enzymologic; Glioblastoma; Humans; Topoisomerase I Inhibitors | 2008 |
New homocamptothecins: synthesis, antitumor activity, and molecular modeling.
Topics: Antineoplastic Agents; Binding Sites; Camptothecin; Cell Line, Tumor; Cell Survival; DNA Topoisomerases, Type I; Humans; Imaging, Three-Dimensional; Imines; Methylation; Models, Molecular; Molecular Structure; Protein Binding; Pyridines; Quantitative Structure-Activity Relationship; Solubility; Water | 2008 |
Insilico analysis of homocamptothecin (hCPT) analogues for anti-tumour activity.
Topics: Antineoplastic Agents; Camptothecin; Molecular Structure; Monte Carlo Method | 2009 |
Synthesis and evaluation of 9-benzylideneamino derivatives of homocamptothecin as potent inhibitors of DNA topoisomerase I.
Topics: Antineoplastic Agents; Benzylidene Compounds; Camptothecin; Cell Line, Tumor; DNA; DNA Topoisomerases, Type I; Enzyme Inhibitors; Humans; Inhibitory Concentration 50; Structure-Activity Relationship; Topoisomerase I Inhibitors | 2010 |
Trifluoromethyl-promoted homocamptothecins: synthesis and biological activity.
Topics: Animals; Antineoplastic Agents; Camptothecin; Cell Line, Tumor; DNA; DNA Topoisomerases, Type I; Halogenation; Humans; Male; Mice; Topoisomerase I Inhibitors | 2010 |
Phosphate ester derivatives of homocamptothecin: synthesis, solution stabilities and antitumor activities.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Cell Proliferation; Drug Design; Drug Screening Assays, Antitumor; Drug Stability; Esters; Humans; Hydrogen-Ion Concentration; Inhibitory Concentration 50; Molecular Structure; Pharmaceutical Solutions; Phosphates; Structure-Activity Relationship | 2010 |
[Effect of hydroxycamptothecin (HCPT) on proliferation and apoptosis of rat hepatic stellate cells].
Topics: Animals; Apoptosis; Camptothecin; Cell Line; Cell Proliferation; Hepatic Stellate Cells; Rats | 2010 |
Synthesis and biological evaluation of novel 7-acyl homocamptothecins as Topoisomerase I inhibitors.
Topics: Antineoplastic Agents; Camptothecin; Cell Proliferation; Crystallography, X-Ray; DNA Topoisomerases, Type I; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; Humans; Models, Molecular; Molecular Structure; Stereoisomerism; Structure-Activity Relationship; Topoisomerase I Inhibitors; Tumor Cells, Cultured | 2011 |
Synthesis of 9-(heteroarylmethylidene)amino derivatives of homocamptothecin with biological activities.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Cell Proliferation; DNA Topoisomerases, Type I; Drug Screening Assays, Antitumor; Humans; Neoplasms; Topoisomerase I Inhibitors | 2011 |
Synthesis and biological evaluation of novel homocamptothecins conjugating with dihydropyrimidine derivatives as potent topoisomerase I inhibitors.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Cell Proliferation; DNA Topoisomerases, Type I; HCT116 Cells; Humans; Neoplasms; Pyrimidines; Topoisomerase I Inhibitors | 2011 |
[Pharmaceutical evaluation of hydroxycamptothecin nanosuspensions with the action of inhibiting P-gp].
Topics: Antineoplastic Agents, Phytogenic; ATP Binding Cassette Transporter, Subfamily B, Member 1; Biological Availability; Calorimetry, Differential Scanning; Camptothecin; Cyclosporine; Drug Carriers; Drug Compounding; Microscopy, Electron, Transmission; Nanoparticles; Particle Size; Solubility; Suspensions; X-Ray Diffraction | 2011 |
MicroRNA 506 regulates expression of PPAR alpha in hydroxycamptothecin-resistant human colon cancer cells.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Colonic Neoplasms; Drug Resistance, Neoplasm; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Humans; MicroRNAs; PPAR alpha; Reverse Transcriptase Polymerase Chain Reaction | 2011 |
Synthesis and biological evaluation of new homocamptothecin analogs.
Topics: Antineoplastic Agents; Camptothecin; Cell Line, Tumor; Cell Proliferation; Chemistry Techniques, Synthetic; DNA Topoisomerases, Type I; Drug Stability; Humans; Structure-Activity Relationship; Topoisomerase I Inhibitors | 2012 |
Synthesis and biological evaluation of 7-alkenyl homocamptothecins as potent topoisomerase I inhibitors.
Topics: Antineoplastic Agents; Apoptosis; Camptothecin; Cell Line, Tumor; DNA; DNA Cleavage; DNA Topoisomerases, Type I; Humans; Topoisomerase I Inhibitors; Topotecan | 2012 |
[In vivo imaging in tumor-bearing animals and pharmacokinetics of PEGylated liposomes modified with RGD cyclopeptide].
Topics: Animals; Area Under Curve; Camptothecin; Diagnostic Imaging; Drug Delivery Systems; Female; Fluorescent Dyes; Hep G2 Cells; Humans; Liposomes; Liver Neoplasms; Male; Mice; Mice, Inbred BALB C; Mice, Nude; Neoplasm Transplantation; Oligopeptides; Polyethylene Glycols; Random Allocation; Rats; Rats, Sprague-Dawley; Spectroscopy, Near-Infrared; Tissue Distribution | 2012 |
Synthesis and biological assays of 9-(acylamino) homocamptothecins as DNA topoisomerase I inhibitors.
Topics: Animals; Apoptosis; Binding Sites; Camptothecin; Catalytic Domain; Cell Line, Tumor; DNA Cleavage; DNA Topoisomerases, Type I; Enzyme Activation; HCT116 Cells; Humans; Lung Neoplasms; Mice; Mice, Nude; Molecular Docking Simulation; Structure-Activity Relationship; Topoisomerase I Inhibitors; Transplantation, Heterologous | 2013 |
Synthesis and cytotoxicity of novel 20-O-linked homocamptothecin ester derivatives as potent topoisomerase I inhibitors.
Topics: Antineoplastic Agents; Camptothecin; Drug Screening Assays, Antitumor; Esters; Humans; Inhibitory Concentration 50; KB Cells; Molecular Structure; Structure-Activity Relationship; Topoisomerase I Inhibitors | 2013 |
The association between chemosensitivity and Pgp, GST-π and Topo II expression in gastric cancer.
Topics: Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily B, Member 1; Camptothecin; Cells, Cultured; Cisplatin; DNA Topoisomerases, Type II; Doxorubicin; Drug Resistance, Neoplasm; Fluorouracil; Gastric Mucosa; Glutathione S-Transferase pi; Humans; In Vitro Techniques; Mitomycin; Stomach; Stomach Neoplasms | 2013 |
Uptake mechanism and endosomal fate of drug-phospholipid lipid nanoparticles in subcutaneous and in situ hepatoma.
Topics: Animals; Camptothecin; Carcinoma, Hepatocellular; Cell Line, Tumor; Diffusion; Endosomes; Liposomes; Male; Mice; Mice, Inbred C57BL; Nanocapsules; Organ Specificity; Phospholipids; Tissue Distribution | 2014 |
Design, synthesis and biological evaluation of novel homocamptothecin analogues as potent antitumor agents.
Topics: Animals; Antineoplastic Agents; Camptothecin; Cell Proliferation; Dose-Response Relationship, Drug; Drug Design; HT29 Cells; Humans; Mice; Molecular Structure; Neoplasms, Experimental; Structure-Activity Relationship; Xenograft Model Antitumor Assays | 2015 |
A pH-responsive prodrug delivery system of 10-HCPT for controlled release and tumor targeting.
Topics: Animals; Antineoplastic Agents, Phytogenic; Camptothecin; Carbon-13 Magnetic Resonance Spectroscopy; Cell Line, Tumor; Delayed-Action Preparations; Drug Carriers; Drug Delivery Systems; Drug Liberation; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Endocytosis; Humans; Hydrogen-Ion Concentration; Mice, Inbred BALB C; Micelles; Neoplasms; Prodrugs; Proton Magnetic Resonance Spectroscopy; Rats; Solubility; Spectrometry, Fluorescence; Tissue Distribution | 2017 |
Theranostic Hyaluronic Acid-Iron Micellar Nanoparticles for Magnetic-Field-Enhanced in vivo Cancer Chemotherapy.
Topics: Administration, Intravenous; Animals; Apoptosis; Camptothecin; Cell Line, Tumor; Drug Carriers; Female; Ferric Compounds; Humans; Hyaluronan Receptors; Hyaluronic Acid; Magnetic Fields; Magnetic Resonance Imaging; Mice; Mice, Nude; Micelles; Nanoparticles; Neoplasms; Positron-Emission Tomography; Theranostic Nanomedicine | 2018 |
Decreasing Arl4c expression by inhibition of AKT signal in human lung adenocarcinoma cells.
Topics: A549 Cells; Adenocarcinoma; Adenocarcinoma of Lung; ADP-Ribosylation Factors; Blotting, Western; Camptothecin; Cell Line, Tumor; Chromones; Gene Expression Regulation, Neoplastic; Gene Knockdown Techniques; Humans; Leupeptins; Lung Neoplasms; Morpholines; Proto-Oncogene Proteins c-akt; Signal Transduction; Smoking | 2020 |
Hydroxycamptothecin (HCPT)-loaded PEGlated lipid-polymer hybrid nanoparticles for effective delivery of HCPT: QbD-based development and evaluation.
Topics: Animals; Camptothecin; Cell Line, Tumor; Drug Carriers; Mice; Nanoparticles; Particle Size; Polymers; Rats; Rats, Sprague-Dawley | 2022 |
Fluorescent Imaging-Guided Chemo- and Photodynamic Therapy of Hepatocellular Carcinoma with HCPT@NMOFs-RGD Nanocomposites.
Topics: Animals; Camptothecin; Carcinoma, Hepatocellular; Humans; Liver Neoplasms; Mice; Nanocomposites; Oligopeptides; Photochemotherapy; Zebrafish | 2022 |