Ansamycin antibiotics inhibit Akt activation and cyclin D expression in breast cancer cells that overexpress HER2
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Summary
In murine xenograft models, non-toxic doses of 17-AAG markedly reduced the expression of HER2 and phosphorylation of Akt and inhibited tumor growth and may be useful for the treatment of Her2 driven tumors.
- Type
- article
- Published
- 2002-02-14
- Cited by
- 279
- References
- 33
- Access
- Open access
- OpenAlex
- https://openalex.org/W2001215449
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:943513
Keywords
Protein kinase B, Biology, PI3K/AKT/mTOR pathway, Cancer research, Cyclin D
References
- Heregulin‐dependent regulation of HER2/neu oncogenic signaling by heterodimerization with HER3.
- Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN.
- Pharmacologic shifting of a balance between protein refolding and degradation mediated by Hsp90.
- Polyubiquitination and Proteasomal Degradation of the p185c-erbB-2 Receptor Protein-tyrosine Kinase Induced by Geldanamycin*
- The protein kinase encoded by the Akt proto-oncogene is a target of the PDGF-activated phosphatidylinositol 3-kinase.
- Cyclin D Expression Is Controlled Post-transcriptionally via a Phosphatidylinositol 3-Kinase/Akt-dependent Pathway*
- Geldanamycin, a heat shock protein 90-binding benzoquinone ansamycin, inhibits steroid-dependent translocation of the glucocorticoid receptor from the cytoplasm to the nucleus.
- The PI3K-PDK1 connection: more than just a road to PKB.
- The hsp90-based Chaperone System: Involvement in Signal Transduction from a Variety of Hormone and Growth Factor Receptors
- Sensitivity of Mature ErbB2 to Geldanamycin Is Conferred by Its Kinase Domain and Is Mediated by the Chaperone Protein Hsp90*
- An immunotherapeutic approach to treatment of breast cancer: focus on trastuzumab plus paclitaxel
- Stable and specific binding of heat shock protein 90 by geldanamycin disrupts glucocorticoid receptor function in intact cells.
- Phosphorylation of Ser-241 is essential for the activity of 3-phosphoinositide-dependent protein kinase-1: identification of five sites of phosphorylation in vivo.
- Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin
- Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
- Modulation of Akt kinase activity by binding to Hsp90.
- The hsp90-binding Antibiotic Geldanamycin Decreases Raf Levels and Epidermal Growth Factor Signaling without Disrupting Formation of Signaling Complexes or Reducing the Specific Enzymatic Activity of Raf Kinase*
- Mammalian p50Cdc37 is a protein kinase-targeting subunit of Hsp90 that binds and stabilizes Cdk4.
- PKB/Akt: connecting phosphoinositide 3-kinase to cell survival and beyond.
- Inhibitory effects of combinations of HER-2/neu antibody and chemotherapeutic agents used for treatment of human breast cancers
Cited by
- Heat shock protein 90 as a molecular target for cancer therapeutics.
- Survival-signaling pathway as a promising target for cancer chemotherapy
- The mechanisms and managements of hormone-therapy resistance in breast and prostate cancers.
- Targeting hypoxia and angiogenesis through HIF-1alpha inhibition
- A Multi-Pronged Modulation of Signaling Pathways in Targeting Breast Cancer Stem Cells.
- INTEGRATION OF HSP90 INHIBITION IN COMBINATIONAL IMMUNOTHERAPIES TARGETING RECEPTOR TYROSINE KINASE EPHA2
- Novel Agents for the Prevention of Breast Cancer: Targeting Transcription Factors and Signal Transduction Pathways
- From the bench to the bed side: PI3K pathway inhibitors in clinical development.
- HSP90 inhibitors for cancer therapy and overcoming drug resistance.
- Signal transduction mediated by cyclin D1: from mitogens to cell proliferation: a molecular target with therapeutic potential.
- Régulation de l’activité transcriptionnelle des récepteurs des estrogènes (ER) par le récepteur à chimiokine CXCR4 et les récepteurs à activité tyrosine kinase ErbB2 et ErbB3
- Geldanamycin treatment reduces neovascularization in a mouse model of retinopathy of prematurity
- Black tea polyphenols induce human leukemic cell cycle arrest by inhibiting Akt signaling
- Estudio del valor patogénico de la expresión y ruta de señalización de KIT e IGF1R en Sarcoma de Ewing: ¿nuevas posibles dianas terapeúticas?
- The ErbB2 receptor and breast carcinoma cell migration : memo is a novel mediator of cell motility
- Heat Shock Protein 90 Is Critical for Regulation of Phenotype and Functional Activity of Human T Lymphocytes and NK Cells
- Inhibition of heat shock protein 90 function down-regulates Akt kinase and sensitizes tumors to Taxol.
- Heat shock protein 90 inhibition by 17-allylamino-17- demethoxygeldanamycin: a novel therapeutic approach for treating hormone-refractory prostate cancer.
- ErbBs inhibition by lapatinib blocks tumor growth in an orthotopic model of human testicular germ cell tumor
- Functional Interactions Between Par-1b Protein Kinase and RNF41 E3 Ubiquitin Ligase
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