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The application and prospect of CDK4/6 inhibitors in malignant solid tumors
Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors, which block the transition from the G1 to S phase of the cell cycle by interfering with Rb phosphorylation and E2F release, have shown potent antitumor activity and manageable toxicity in HR+/HER2− breast cancer patients. Some clinical trials involvin...
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| Опубликовано в: : | J Hematol Oncol |
|---|---|
| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2020
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7195725/ https://ncbi.nlm.nih.gov/pubmed/32357912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13045-020-00880-8 |
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