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| Authors | Naoise C Synnott, Matthias R Bauer, Stephen F. Madden, Alyson M. Murray, Rut Klinger, Norma O'Donovan, Darran O'Connor, William M. Gallagher, John Crown, Alan R Fersht, Michael J. Duffy | ||||||||||||
| Title | Targeting mutant p53 with PK11007: A new approach for the treatment of patients with triple-negative breast cancer? | ||||||||||||
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| URL | http://abstracts.asco.org/199/AbstView_199_189403.html | ||||||||||||
| Abstract Text | J Clin Oncol 35, 2017 (suppl; abstr e14099) | ||||||||||||
| Molecular Profile | Treatment Approach |
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| Gene Name | Source | Synonyms | Protein Domains | Gene Description | Gene Role |
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| Therapy Name | Drugs | Efficacy Evidence | Clinical Trials |
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| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
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| Gene | Variant | Impact | Protein Effect | Variant Description | Associated with drug Resistance |
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| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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| TP53 mutant | breast cancer | sensitive | PK11007 | Preclinical - Cell culture | Actionable | In a preclinical study, TP53-mutated breast cancer cell lines demonstrated increased sensitivity to PK11007 compared to TP53-wild type cells in culture, regardless of Esr1 and Erbb2 (Her2) status (J Clin Oncol 35, 2017 (suppl; abstr e14099)). | detail... |