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Microtubule stabilizing agents: Their molecular signaling consequences and the potential for enhancement by drug combination
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Accumulation of cyclin B1, activation of cyclin B1-dependent kinase and induction of programmed cell death in human epidermoid carcinoma KB cells treated with taxol
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19991008)83:2<151::aid-ijc1>3.0.co;2-5openalex-snapshot
Molecular effects of paclitaxel: Myths and reality (a critical review)
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Interleukin-8 serum level shift in patients with ovarian carcinoma undergoing paclitaxel-containing chemotherapy
inferredcites →https://doi.org/10.1002/1521-1878(200009)22:9<818::aid-bies7>3.0.co;2-6openalex-snapshot
Integrating the MAP kinase signal into the G1 phase cell cycle machinery
inferredcites →https://doi.org/10.1002/chin.199751201openalex-snapshot
ChemInform Abstract: Eleutherobin, a New Cytotoxin that Mimics Paclitaxel (Taxol) by Stabilizing Microtubules.
inferredcites →https://doi.org/10.1002/ijc.20878openalex-snapshot
Cyclooxygenase‐2 inhibitor celecoxib augments chemotherapeutic drug‐induced apoptosis by enhancing activation of caspase‐3 and ‐9 in prostate cancer cells
inferredcites →https://doi.org/10.1002/ijc.21325openalex-snapshot
Enhancement of antitumor activity of docetaxel by celecoxib in lung tumors
inferredcites →https://doi.org/10.1002/jcb.10699openalex-snapshot
Cell cycle checkpoints and their impact on anticancer therapeutic strategies
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Many actions of cyclooxygenase‐2 in cellular dynamics and in cancer
inferredcites →https://doi.org/10.1002/med.10038openalex-snapshot
Platinum‐based anticancer agents: Innovative design strategies and biological perspectives
inferredcites →https://doi.org/10.1006/excr.2001.5262openalex-snapshot
The Role of ERK 1/2 and p38 MAP-Kinase Pathways in Taxol-Induced Apoptosis in Human Ovarian Carcinoma Cells
inferredcites →https://doi.org/10.1006/excr.2001.5349openalex-snapshot
A Multistep Model for Paclitaxel-Induced Apoptosis in Human Breast Cancer Cell Lines
inferredcites →https://doi.org/10.1007/978-1-4615-1809-9_11openalex-snapshot
p27KIP1, an inhibitor of cyclin-dependent kinases
inferredcites →https://doi.org/10.1007/bf03401588openalex-snapshot
Taxol-Induced Mitotic Block Triggers Rapid Onset of a p53-Independent Apoptotic Pathway
inferredcites →https://doi.org/10.1007/s00018-002-8518-3openalex-snapshot
Expression of the anti-apoptotic gene survivin correlates with taxol resistance in human ovarian cancer
inferredcites →https://doi.org/10.1007/s000180050369openalex-snapshot
The stress-activated protein kinase pathways
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The immunological effects of taxanes
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Effects of paclitaxel on cytokine synthesis by unprimed human monocytes, T lymphocytes, and breast cancer cells
inferredcites →https://doi.org/10.1007/s002620050605openalex-snapshot
Paclitaxel up-regulates interleukin-8 synthesis in human lung carcinoma through an NF-κB- and AP-1-dependent mechanism
inferredcites →https://doi.org/10.1007/s00280-005-1009-0openalex-snapshot
Paclitaxel and gemcitabine combination in a biweekly schedule in patients with advanced non small-cell lung cancer: a phase i study
inferredcites →https://doi.org/10.1016/0024-3205(95)02233-3openalex-snapshot
Mechanism of action of the immunosuppressant rapamycin
inferredcites →https://doi.org/10.1016/0092-8674(94)90133-3openalex-snapshot
Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells
inferredcites →https://doi.org/10.1016/0092-8674(94)90256-9openalex-snapshot
A MAP kinase-dependent spindle assembly checkpoint in Xenopus egg extracts
inferredcites →https://doi.org/10.1016/j.canlet.2004.09.045openalex-snapshot
Paclitaxel/Taxol® sensitivity in human renal cell carcinoma is not determined by the p53 status
inferredcites →https://doi.org/10.1016/j.ccr.2005.06.003openalex-snapshot
Induction of apoptosis by an inhibitor of the mitotic kinesin KSP requires both activation of the spindle assembly checkpoint and mitotic slippage
inferredcites →https://doi.org/10.1016/j.cub.2004.08.056openalex-snapshot
Mos Mediates the Mitotic Activation of p42 MAPK in Xenopus Egg Extracts
inferredcites →https://doi.org/10.1016/j.cyto.2003.10.004openalex-snapshot
Changes in plasma levels of inflammatory cytokines in response to paclitaxel chemotherapy
inferredcites →https://doi.org/10.1016/j.intimp.2003.08.007openalex-snapshot
The immunopharmacology of paclitaxel (Taxol®), docetaxel (Taxotere®), and related agents
inferredcites →https://doi.org/10.1016/j.lungcan.2004.11.004openalex-snapshot
Docetaxel and cyclooxygenase-2 inhibition with celecoxib for advanced non-small cell lung cancer progressing after platinum-based chemotherapy: a multicenter phase II trial
inferredcites →https://doi.org/10.1016/j.phrs.2004.03.007openalex-snapshot
mTOR: a protein kinase switching between life and death
inferredcites →https://doi.org/10.1016/s0006-2952(03)00255-7openalex-snapshot
The JNK, ERK and p53 pathways play distinct roles in apoptosis mediated by the antitumor agents vinblastine, doxorubicin, and etoposide
inferredcites →https://doi.org/10.1016/s0006-2952(98)00307-4openalex-snapshot
A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin
inferredcites →https://doi.org/10.1016/s0021-9258(18)35648-5openalex-snapshot
Human T-cell mitogen-activated protein kinase kinases are related to yeast signal transduction kinases.
inferredcites →https://doi.org/10.1016/s0026-895x(24)23058-3openalex-snapshot
Sequence-Dependent Potentiation of Paclitaxel-Mediated Apoptosis in Human Leukemia Cells by Inhibitors of the Mitogen-Activated Protein Kinase Kinase/Mitogen-Activated Protein Kinase Pathway
inferredcites →https://doi.org/10.1016/s0026-895x(24)23132-1openalex-snapshot
Selective Potentiation of Paclitaxel (Taxol)-Induced Cell Death by Mitogen-Activated Protein Kinase Kinase Inhibition in Human Cancer Cell Lines
inferredcites →https://doi.org/10.1016/s0026-895x(24)23261-2openalex-snapshot
Overexpression of p21waf1 Decreases G2-M Arrest and Apoptosis Induced by Paclitaxel in Human Sarcoma Cells Lacking Both p53 and Functional Rb Protein
inferredcites →https://doi.org/10.1016/s0092-8674(00)80255-xopenalex-snapshot
Kinetochore Localization of Murine Bub1 Is Required for Normal Mitotic Timing and Checkpoint Response to Spindle Damage
inferredcites →https://doi.org/10.1016/s0303-7207(01)00695-5openalex-snapshot
The mechanism of CSF arrest in vertebrate oocytes
inferredcites →https://doi.org/10.1016/s0304-3835(02)00722-xopenalex-snapshot
Down-regulation of Raf-1 kinase is associated with paclitaxel resistance in human breast cancer MCF-7/Adr cells
inferredcites →https://doi.org/10.1016/s0955-0674(97)80081-6openalex-snapshot
Coupling cell division and cell death to microtubule dynamics
inferredcites →https://doi.org/10.1016/s0955-0674(99)80036-2openalex-snapshot
Regulating the onset of mitosis
inferredcites →https://doi.org/10.1016/s0959-8049(00)00183-0openalex-snapshot
Sensitivity to paclitaxel is not related to p53-dependent apoptosis in ovarian cancer cells
inferredcites →https://doi.org/10.1016/s0960-9822(01)00045-8openalex-snapshot
Bub1 is activated by the protein kinase p90 Rsk during Xenopus oocyte maturation
inferredcites →https://doi.org/10.1016/s0960-9822(02)00894-1openalex-snapshot
The Spindle Checkpoint Kinase Bub1 and Cyclin E/Cdk2 Both Contribute to the Establishment of Meiotic Metaphase Arrest by Cytostatic Factor
inferredcites →https://doi.org/10.1016/s0962-8924(00)01880-8openalex-snapshot
Chromosomal passengers and the (aurora) ABCs of mitosis
inferredcites →https://doi.org/10.1016/s1074-5521(01)00055-2openalex-snapshot
The relationship between Taxol and (+)-discodermolide: synthetic analogs and modeling studies
inferredcites →https://doi.org/10.1016/s1074-7613(00)80428-8openalex-snapshot
ICE Family Proteases: Mediators of All Apoptotic Cell Death?
inferredcites →https://doi.org/10.1016/s1097-2765(00)80157-4openalex-snapshot
Overexpression of ErbB2 Blocks Taxol-Induced Apoptosis by Upregulation of p21Cip1, which Inhibits p34Cdc2 Kinase
inferredcites →https://doi.org/10.1016/s1535-6108(02)00084-3openalex-snapshot
A p34cdc2 survival checkpoint in cancer
inferredcites →https://doi.org/10.1016/s1535-6108(02)00235-0openalex-snapshot
AURORA-A amplification overrides the mitotic spindle assembly checkpoint, inducing resistance to Taxol
inferredcites →https://doi.org/10.1021/bi9515127openalex-snapshot
Discodermolide, A Cytotoxic Marine Agent That Stabilizes Microtubules More Potently Than Taxol,
inferredcites →https://doi.org/10.1021/ja00738a045openalex-snapshot
Plant antitumor agents. VI. Isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia
inferredcites →https://doi.org/10.1021/ja9717828openalex-snapshot
Eleutherobin, a New Cytotoxin that Mimics Paclitaxel (Taxol) by Stabilizing Microtubules
inferredcites →https://doi.org/10.1021/np020219mopenalex-snapshot
Five New Discodermolide Analogues from the Marine SpongeDiscodermiaSpecies
inferredcites →https://doi.org/10.1023/a:1006327729228openalex-snapshot
Gemcitabine in Non-Small Cell Lung Cancer (NSCLC)
inferredcites →https://doi.org/10.1023/a:1009652412399openalex-snapshot
Activation of MAD 2 checkprotein and persistence of cyclin B1/CDC 2 activity associate with paclitaxel-induced apoptosis in human nasopharyngeal carcinoma cells
inferredcites →https://doi.org/10.1023/a:1024369220605openalex-snapshot
Docetaxel–Anthracycline Combinations in Metastatic Breast Cancer
inferredcites →https://doi.org/10.1038/10533openalex-snapshot
Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo
inferredcites →https://doi.org/10.1038/25141openalex-snapshot
Control of apoptosis and mitotic spindle checkpoint by survivin
inferredcites →https://doi.org/10.1038/277665a0openalex-snapshot
Promotion of microtubule assembly in vitro by taxol
inferredcites →https://doi.org/10.1038/35085604openalex-snapshot
A MAP kinase-dependent actin checkpoint ensures proper spindle orientation in fission yeast
inferredcites →https://doi.org/10.1038/ncb1022openalex-snapshot
Phosphorylation of Cdc20 is required for its inhibition by the spindle checkpoint
inferredcites →https://doi.org/10.1038/nm0897-917openalex-snapshot
A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma
inferredcites →https://doi.org/10.1038/nrc1503openalex-snapshot
Targeting the mitogen-activated protein kinase cascade to treat cancer
inferredcites →https://doi.org/10.1038/nrc1714openalex-snapshot
On the road to cancer: aneuploidy and the mitotic checkpoint
inferredcites →https://doi.org/10.1038/nrd1279openalex-snapshot
The IKK NF-κB system: a treasure trove for drug development
inferredcites →https://doi.org/10.1038/nrm830openalex-snapshot
IAP proteins: blocking the road to death's door
inferredcites →https://doi.org/10.1038/sj.bjc.6600788openalex-snapshot
Reversal of Taxol resistance in hepatoma by cyclosporin A: involvement of the PI-3 kinase-AKT 1 pathway
inferredcites →https://doi.org/10.1038/sj.cgt.7700096openalex-snapshot
Alteration of drug chemosensitivity caused by the adenovirus-mediated transfer of the wild-type p53 gene in human lung cancer cells
inferredcites →https://doi.org/10.1038/sj.leu.2401449openalex-snapshot
Mitogen-activated protein kinase pathway is dispensable for microtubule-active drug-induced Raf-1/Bcl-2 phosphorylation and apoptosis in leukemia cells
inferredcites →https://doi.org/10.1038/sj.onc.1201469openalex-snapshot
Involvement of p21 in mitotic exit after paclitaxel treatment in MCF-7 breast adenocarcinoma cell line
inferredcites →https://doi.org/10.1038/sj.onc.1202569openalex-snapshot
The inhibitors of apoptosis (IAPs) and their emerging role in cancer
inferredcites →https://doi.org/10.1038/sj.onc.1203768openalex-snapshot
Paclitaxel sensitivity of breast cancer cells with constitutively active NF-κB is enhanced by IκBα super-repressor and parthenolide
inferredcites →https://doi.org/10.1038/sj.onc.1204083openalex-snapshot
Development of anticancer drugs targeting the MAP kinase pathway
inferredcites →https://doi.org/10.1038/sj.onc.1204487openalex-snapshot
Low concentrations of paclitaxel induce cell type-dependent p53, p21 and G1/G2 arrest instead of mitotic arrest: molecular determinants of paclitaxel-induced cytotoxicity
inferredcites →https://doi.org/10.1038/sj.onc.1204751openalex-snapshot
Damaged microtubules can inactivate BCL-2 by means of the mTOR kinase
inferredcites →https://doi.org/10.1038/sj.onc.1205848openalex-snapshot
The function of multiple IκB : NF-κB complexes in the resistance of cancer cells to Taxol-induced apoptosis
inferredcites →https://doi.org/10.1038/sj.onc.1206175openalex-snapshot
Paclitaxel induces inactivation of p70 S6 kinase and phosphorylation of Thr421 and Ser424 via multiple signaling pathways in mitosis
inferredcites →https://doi.org/10.1038/sj.onc.1206954openalex-snapshot
Small-molecule cyclin-dependent kinase modulators
inferredcites →https://doi.org/10.1038/sj.onc.1207188openalex-snapshot
The MAP kinase pathway is required for entry into mitosis and cell survival
inferredcites →https://doi.org/10.1038/sj.onc.1207374openalex-snapshot
The spindle checkpoint, aneuploidy, and cancer
inferredcites →https://doi.org/10.1038/sj.onc.1209088openalex-snapshot
The Akt/PKB pathway: molecular target for cancer drug discovery
inferredcites →https://doi.org/10.1038/sj.onc.1209097openalex-snapshot
Akt-dependent transformation: there is more to growth than just surviving
inferredcites →https://doi.org/10.1042/bj20041415openalex-snapshot
Essential tension and constructive destruction: the spindle checkpoint and its regulatory links with mitotic exit
inferredcites →https://doi.org/10.1046/j.1525-1438.2000.00003.xopenalex-snapshot
Cytokines IL-1beta, IL-2, IL-6, IL-8, MCP-1, GM-CSF and TNFalpha in patients with epithelial ovarian cancer and their relationship to treatment with paclitaxel
inferredcites →https://doi.org/10.1053/j.seminoncol.2003.08.012openalex-snapshot
CI-1040 (PD184352), a targeted signal transduction inhibitor of MEK (MAPKK)
inferredcites →https://doi.org/10.1073/pnas.132275599openalex-snapshot
Enhanced microtubule-dependent trafficking and p53 nuclear accumulation by suppression of microtubule dynamics
inferredcites →https://doi.org/10.1073/pnas.240390697openalex-snapshot
Regulation of apoptosis at cell division by p34 cdc2 phosphorylation of survivin
inferredcites →https://doi.org/10.1073/pnas.77.3.1561openalex-snapshot
Taxol stabilizes microtubules in mouse fibroblast cells.
inferredcites →https://doi.org/10.1073/pnas.90.18.8319openalex-snapshot
Mitogen-activated protein kinases p42mapk and p44mapk are required for fibroblast proliferation.
inferredcites →https://doi.org/10.1073/pnas.91.18.8329openalex-snapshot
Mos oncogene product associates with kinetochores in mammalian somatic cells and disrupts mitotic progression.
inferredcites →https://doi.org/10.1073/pnas.92.19.8881openalex-snapshot
Association of mitogen-activated protein kinase with the microtubule cytoskeleton.
inferredcites →https://doi.org/10.1073/pnas.95.7.3896openalex-snapshot
Taxane-mediated gene induction is independent of microtubule stabilization: Induction of transcription regulators and enzymes that modulate inflammation and apoptosis
inferredcites →https://doi.org/10.1073/pnas.96.15.8493openalex-snapshot
Retention of the Bub3 checkpoint protein on lagging chromosomes
inferredcites →https://doi.org/10.1073/pnas.96.7.3775openalex-snapshot
Deletion of the loop region of Bcl-2 completely blocks paclitaxel-induced apoptosis
inferredcites →https://doi.org/10.1073/pnas.96.8.4256openalex-snapshot
A common pharmacophore for cytotoxic natural products that stabilize microtubules
inferredcites →https://doi.org/10.1074/jbc.270.35.20235openalex-snapshot
Characterization of the Taxol Binding Site on the Microtubule
inferredcites →https://doi.org/10.1074/jbc.273.21.13280openalex-snapshot
An Analysis of Mek1 Signaling in Cell Proliferation and Transformation
inferredcites →https://doi.org/10.1074/jbc.273.43.28253openalex-snapshot
Paclitaxel (Taxol)-induced Gene Expression and Cell Death Are Both Mediated by the Activation of c-Jun NH2-terminal Kinase (JNK/SAPK)
inferredcites →https://doi.org/10.1074/jbc.274.53.37990openalex-snapshot
Characterization of the Taxol Binding Site on the Microtubule
inferredcites →https://doi.org/10.1074/jbc.275.20.14838openalex-snapshot
Microtubule-interfering Agents Stimulate the Transcription of Cyclooxygenase-2
inferredcites →https://doi.org/10.1074/jbc.c000684200openalex-snapshot
MEK Inhibition Enhances Paclitaxel-induced Tumor Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m301481200openalex-snapshot
Regulation of Cyclooxgenase-2 mRNA Stability by Taxanes
inferredcites →https://doi.org/10.1074/jbc.m313709200openalex-snapshot
Inhibition of NFκB Increases the Efficacy of Cisplatin in in Vitro and in Vivo Ovarian Cancer Models
inferredcites →https://doi.org/10.1080/07853890310017053openalex-snapshot
Non steroidal anti‐inflammatory drugs and COX‐2 inhibitors as anti‐cancer therapeutics: hypes, hopes and reality
inferredcites →https://doi.org/10.1083/jcb.136.5.1091openalex-snapshot
MAP Kinase Is Required for the Spindle Assembly Checkpoint but Is Dispensable for the Normal M Phase Entry and Exit in Xenopus Egg Cell Cycle Extracts
inferredcites →https://doi.org/10.1083/jcb.137.2.433openalex-snapshot
A Role for Mitogen-activated Protein Kinase in the Spindle Assembly Checkpoint in XTC Cells
inferredcites →https://doi.org/10.1083/jcb.141.5.1181openalex-snapshot
Localization of Mad2 to Kinetochores Depends on Microtubule Attachment, Not Tension
inferredcites →https://doi.org/10.1083/jcb.142.6.1533openalex-snapshot
Activation of the MKK/ERK Pathway during Somatic Cell Mitosis: Direct Interactions of Active ERK with Kinetochores and Regulation of the Mitotic 3F3/2 Phosphoantigen
inferredcites →https://doi.org/10.1083/jcb.151.7.1575openalex-snapshot
Human Survivin Is a Kinetochore-Associated Passenger Protein
inferredcites →https://doi.org/10.1083/jcb.200208091openalex-snapshot
Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores
inferredcites →https://doi.org/10.1083/jcb.200208092openalex-snapshot
The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore–microtubule attachment and in maintaining the spindle assembly checkpoint
inferredcites →https://doi.org/10.1091/mbc.10.4.947openalex-snapshot
Taxol Suppresses Dynamics of Individual Microtubules in Living Human Tumor Cells
inferredcites →https://doi.org/10.1093/carcin/bgh087openalex-snapshot
Id-1-induced Raf/MEK pathway activation is essential for its protective role against taxol-induced apoptosis in nasopharyngeal carcinoma cells
inferredcites →https://doi.org/10.1093/emboj/cdg307openalex-snapshot
Survivin is required for a sustained spindle checkpoint arrest in response to lack of tension
inferredcites →https://doi.org/10.1093/jjco/hyi130openalex-snapshot
Oxaliplatin, a Potent Inhibitor of Survivin, Enhances Paclitaxel-induced Apoptosis and Mitotic Catastrophe in Colon Cancer Cells
inferredcites →https://doi.org/10.1093/jnci/djg058openalex-snapshot
Enhancing Radiotherapy With Cyclooxygenase-2 Enzyme Inhibitors: A Rational Advance?
inferredcites →https://doi.org/10.1096/fasebj.9.9.7601337openalex-snapshot
The MAPK signaling cascade
inferredcites →https://doi.org/10.1097/00007890-199110000-00014openalex-snapshot
DISCODERMOLIDE—A NEW, MARINE-DERIVED IMMUNOSUPPRESSIVE COMPOUND
inferredcites →https://doi.org/10.1097/00007890-199110000-00015openalex-snapshot
DISCODERMOLIDE—A NEW, MARINE-DERIVED IMMUNOSUPPRESSIVE COMPOUND
inferredcites →https://doi.org/10.1097/00130404-200505000-00007openalex-snapshot
The Combination of the Selective Cyclooxygenase-2 Inhibitor Celecoxib with Weekly Paclitaxel Is a Safe and Active Second-Line Therapy for Non-Small Cell Lung Cancer
inferredcites →https://doi.org/10.1097/01.cad.0000131681.21637.b2openalex-snapshot
The clinical development of new mitotic inhibitors that stabilize the microtubule
inferredcites →https://doi.org/10.1101/gad.13.22.2905openalex-snapshot
Cellular survival: a play in three Akts
inferredcites →https://doi.org/10.1111/j.1582-4934.2005.tb00361.xopenalex-snapshot
Survivin as a target for new anticancer interventions
inferredcites →https://doi.org/10.1124/mol.52.4.613openalex-snapshot
The Microtubule-Stabilizing Agent Discodermolide Competitively Inhibits the Binding of Paclitaxel (Taxol) to Tubulin Polymers, Enhances Tubulin Nucleation Reactions More Potently than Paclitaxel, and Inhibits the Growth of Paclitaxel-Resistant Cells
inferredcites →https://doi.org/10.1124/mol.61.1.105openalex-snapshot
IκB Kinase Activation Is Involved in Regulation of Paclitaxel-Induced Apoptosis in Human Tumor Cell Lines
inferredcites →https://doi.org/10.1126/science.1411546openalex-snapshot
The Primary Structure of MEK, a Protein Kinase that Phosphorylates the ERK Gene Product
inferredcites →https://doi.org/10.1126/science.275.5298.343openalex-snapshot
An Information-Intensive Approach to the Molecular Pharmacology of Cancer
inferredcites →https://doi.org/10.1126/science.282.5392.1312openalex-snapshot
Requirement for MAPK Activation for Normal Mitotic Progression in Xenopus Egg Extracts
inferredcites →https://doi.org/10.1126/science.286.5445.1741openalex-snapshot
Phosphorylation and Regulation of Raf by Akt (Protein Kinase B)
inferredcites →https://doi.org/10.1126/science.8052857openalex-snapshot
Transformation of Mammalian Cells by Constitutively Active MAP Kinase Kinase
inferredcites →https://doi.org/10.1128/mcb.13.4.2546openalex-snapshot
Mos stimulates MAP kinase in Xenopus oocytes and activates a MAP kinase kinase in vitro.
inferredcites →https://doi.org/10.1128/mcb.17.9.5097openalex-snapshot
Identification of Tumor-Specific Paclitaxel (Taxol)-Responsive Regulatory Elements in the Interleukin-8 Promoter
inferredcites →https://doi.org/10.1128/mcb.18.2.1055openalex-snapshot
Characterization of the p53-Dependent Postmitotic Checkpoint following Spindle Disruption
inferredcites →https://doi.org/10.1146/annurev.immunol.14.1.649openalex-snapshot
THE NF-κB AND IκB PROTEINS: New Discoveries and Insights
inferredcites →https://doi.org/10.1146/annurev.med.48.1.353openalex-snapshot
THE DEVELOPMENT AND CLINICAL UTILITY OF THE TAXANE CLASS OF ANTIMICROTUBULE CHEMOTHERAPY AGENTS
inferredcites →https://doi.org/10.1152/ajplung.00233.2002openalex-snapshot
Pathophysiological roles of interleukin-8/CXCL8 in pulmonary diseases
inferredcites →https://doi.org/10.1158/0008-5472.can-04-2538openalex-snapshot
Survivin Deregulation in β-Tubulin Mutant Ovarian Cancer Cells Underlies Their Compromised Mitotic Response to Taxol
inferredcites →https://doi.org/10.1158/0008-5472.can-04-4391openalex-snapshot
Enhancement of the Therapeutic Efficacy of Taxol by the Mitogen-Activated Protein Kinase Kinase Inhibitor CI-1040 in Nude Mice Bearing Human Heterotransplants
inferredcites →https://doi.org/10.1158/1078-0432.ccr-04-0958openalex-snapshot
Inhibition of Inhibitor of Nuclear Factor-κB Phosphorylation Increases the Efficacy of Paclitaxel in in Vitro and in Vivo Ovarian Cancer Models
inferredcites →https://doi.org/10.1158/1078-0432.ccr-040020openalex-snapshot
Preclinical and Clinical Development of the Cyclin-Dependent Kinase Inhibitor Flavopiridol
inferredcites →https://doi.org/10.1158/1078-0432.ccr-05-0108openalex-snapshot
Chemotherapy Induces the Expression of Cyclooxygenase-2 in Non–Small Cell Lung Cancer
inferredcites →https://doi.org/10.1158/1535-7163.1605.3.12openalex-snapshot
Akt up-regulation increases resistance to microtubule-directed chemotherapeutic agents through mammalian target of rapamycin
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Potentiation of paclitaxel-induced apoptosis by the novel cyclin-dependent kinase inhibitor NU6140: a possible role for survivin down-regulation
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A Comparison of Signaling Activities Induced by Taxol and Desoxyepothilone B
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Epothilones: Mechanism of Action and Biologic Activity
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A phase I pharmacokinetic (PK) trial of XAA296A (Discodermolide) administered every 3 wks to adult patients with advanced solid malignancies
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Survivin is required for stable checkpoint activation in taxol-treated HeLa cells
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Bub1 is required for kinetochore localization of BubR1, Cenp-E, Cenp-F and Mad2, and chromosome congression
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The interplay between cyclin-B–Cdc2 kinase (MPF) and MAP kinase during maturation of oocytes
inferredcites →https://doi.org/10.1242/jcs.115.3.575openalex-snapshot
Survivin exists in immunochemically distinct subcellular pools and is involved in spindle microtubule function
inferredcites →https://doi.org/10.1634/theoncologist.4-3-241openalex-snapshot
Gemcitabine: Single-Agent and Combination Therapy in Non-Small Cell Lung Cancer
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inferredcites →https://doi.org/10.2174/0929867053363180openalex-snapshot
NF-κB in Human Disease: Current Inhibitors and Prospects for De Novo Structure Based Design of Inhibitors
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Taxol and colchicine increase LPS-induced pro-IL-1 beta production, but do not increase IL-1 beta secretion. A role for microtubules in the regulation of IL-1 beta production.
inferredcites →https://doi.org/10.4049/jimmunol.164.5.2769openalex-snapshot
IL-8 Reduced Tumorigenicity of Human Ovarian Cancer In Vivo Due to Neutrophil Infiltration
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Sequence Dependent Exposure of Mammary Carcinoma Cells to Taxotere® and the MEK1/2 Inhibitor U0126 Causes Enhanced Cell Killing In Vitro
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The Microtubule Stabilizing Agent Discodermolide is a Potent Inducer of Accelerated Cell Senescence
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Epothilons A and B: Antifungal and Cytotoxic Compounds from Sorangium cellulosum (Myxobacteria). Production, Physico-chemical and Biological Properties.
What points at this work
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Cell Type Variation in Responses to Antimitotic Drugs that Target Microtubules and Kinesin-5
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P18/Stathmin1 is regulated by miR-31 in ovarian cancer in response to taxane
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Total Synthesis of Otteliones Possessing Powerful Tubulin Polymerization Inhibitory Activity
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Development of tumour therapies : from target validation of TTLL12 to tests of a small molecule XRP44X in pre-clinical models of cancer
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The diagnostic and therapeutic role of the stromal cell-derived factor (SDF)-1/CXCR4 axis in breast cancer metastasis
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