Search Results - "Hait, W N"
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1
Silencing of stathmin induces tumor-suppressor function in breast cancer cell lines harboring mutant p53
Published in Oncogene (15-02-2007)“…Cancers harboring dominant-negative p53 mutations are often aggressive and difficult to treat. Direct attempts to restore wild-type p53 function have produced…”
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2
Activity and regulation by growth factors of calmodulin-dependent protein kinase III (elongation factor 2-kinase) in human breast cancer
Published in British journal of cancer (01-01-1999)“…Calmodulin-dependent protein kinase III (CaM kinase III, elongation factor-2 kinase) is a unique member of the Ca2+/CaM-dependent protein kinase family…”
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3
The expression of drug resistance gene products during the progression of human prostate cancer
Published in Clinical cancer research (01-06-1998)“…Prostate cancer progresses from a localized disease to a widely disseminated malignancy. Each step along this progression pathway involves multiple genetic…”
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4
Activation of phospholipase C induces the expression of the multidrug resistance (MDR1) gene through the Raf-MAPK pathway
Published in Molecular pharmacology (01-10-2001)“…Resistance to multiple, unrelated cancer chemotherapeutic drugs can be mediated by P-glycoprotein, the MDR1 gene product. Numerous substances, including…”
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5
The role of MAP4 expression in the sensitivity to paclitaxel and resistance to vinca alkaloids in p53 mutant cells
Published in Oncogene (26-03-1998)“…Mutations in p53 change the sensitivity to cancer chemotherapeutic drugs. Whereas many drugs, including the vinca alkaloids, often become less effective when…”
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6
Phase I Clinical and Pharmacologic Study of 13-cis-Retinoic Acid, Interferon Alfa, and Paclitaxel in Patients With Prostate Cancer and Other Advanced Malignancies
Published in Journal of clinical oncology (01-07-1999)“…Recent studies demonstrate that retinoids decrease expression of the anti-apoptotic protein bcl-2, enhance the effect of chemotherapy, and act synergistically…”
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7
Structural features determining activity of phenothiazines and related drugs for inhibition of cell growth and reversal of multidrug resistance
Published in Molecular pharmacology (01-01-1989)“…Phenothiazines and structurally related compounds inhibit cellular proliferation and sensitize multidrug-resistant (MDR) cells to chemotherapeutic agents. To…”
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8
DNA damage increases sensitivity to Vinca alkaloids and decreases sensitivity to taxanes through p53-dependent repression of microtubule-associated protein 4
Published in Cancer research (Chicago, Ill.) (01-08-1999)“…Taxanes and Vinca alkaloids are among the most active classes of drugs in the treatment of cancer. Yet, fewer than 50% of previously untreated patients…”
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9
The Prognostic and Predictive Values of ECD-HER-2
Published in Clinical cancer research (01-09-2001)“…The search for a simple, sensitive test to reliably determine prognosis and predict response to therapy in patients with cancer is an important area of…”
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10
Calmodulin: a potential target for cancer chemotherapeutic agents
Published in Journal of clinical oncology (01-06-1986)“…Calmodulin is a ubiquitous, calcium-binding protein that is responsible for many of the intracellular actions of calcium. Recent evidence suggests that…”
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11
Effect of anti-calmodulin drugs on the growth and sensitivity of C6 rat glioma cells to bleomycin
Published in Anticancer research (01-09-1994)“…Antipsychotic drugs that bind to and inhibit the action of calmodulin also inhibit cellular proliferation. In addition these drugs are cytotoxic to most…”
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12
Biochemical correlates of the antitumor and antimitochondrial properties of gossypol enantiomers
Published in Molecular pharmacology (01-06-1990)“…Racemic gossypol has been shown to have antitumor properties that may be due to its ability to uncouple tumor mitochondria or to its inhibitory effects on a…”
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13
Cellular and biochemical characterization of thioxanthenes for reversal of multidrug resistance in human and murine cell lines
Published in Cancer research (Chicago, Ill.) (15-03-1990)“…We have previously shown that phenothiazines sensitize multidrug resistant (MDR) cells to chemotherapeutic drugs in a manner related to specific structural…”
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14
Disruption of the EF-2 kinase/Hsp90 protein complex : A possible mechanism to inhibit glioblastoma by geldanamycin
Published in Cancer research (Chicago, Ill.) (15-05-2001)“…Glioblastoma multiforme is the most treatment-resistant brain tumor. Elongation factor-2 (EF-2) kinase (calmodulin kinase III) is a unique protein kinase that…”
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15
Pharmacology of drugs that alter multidrug resistance in cancer
Published in Pharmacological reviews (01-09-1990)Get more information
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16
Clinical and Biologic Activity of an Estrogenic Herbal Combination (PC-SPES) in Prostate Cancer
Published in The New England journal of medicine (17-09-1998)“…Herbal therapies are unconventional treatments in wide use for many diseases. They are sold as nutritional supplements for numerous illnesses, including the…”
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17
Structure-activity relationships of phenothiazines and related drugs for inhibition of protein kinase C
Published in Molecular pharmacology (01-11-1991)“…Phenothiazines are known to inhibit the activity of protein kinase C. To identify structural features that determine inhibitory activity against the enzyme, we…”
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18
Modulation of resistance to alkylating agents in cancer cell by gossypol enantiomers
Published in Cancer letters (01-01-1991)“…Several cell lines resistant to alkylating agents possess increased activity of glutathione-S-transferase (GST) drug detoxifying enzymes. Inhibition of certain…”
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19
Sensitivity of K562 human chronic myelogenous leukemia blast cells transfected with a human multidrug resistance cDNA to cytotoxic drugs and differentiating agents
Published in The Journal of clinical investigation (01-05-1993)“…The blast crisis of chronic myelogenous leukemia (CML) is refractory to most forms of cancer chemotherapy, but may be amenable to drugs that differentiate…”
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20
Terfenadine (Seldane): a new drug for restoring sensitivity to multidrug resistant cancer cells
Published in Biochemical pharmacology (26-01-1993)“…In our efforts to identify clinically effective drugs for reversing multidrug resistance (MDR) mediated by P-glycoprotein, we tested terfenadine for anti-MDR…”
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