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BH3-Mimetic Drugs: Blazing the Trail for New Cancer Medicines

期刊

CANCER CELL
卷 34, 期 6, 页码 879-891

出版社

CELL PRESS
DOI: 10.1016/j.ccell.2018.11.004

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资金

  1. National Health and Medical Research Council (NHMRC), Australia [NHMRC 1101378]
  2. NHMRC [1086291, 1116937, 1113133, 1143105, 1126843, 1117089]
  3. Cancer Council Victoria [1086157, 1147328, 1102104]
  4. Leukemia Foundation Australia
  5. VCA [MCRF 17028]
  6. Leukemia & Lymphoma Society Special Center of Research [7015-18]
  7. Medical Research Future Fund [1141460]
  8. VCA
  9. Australian Cancer Research Foundation
  10. National Health and Medical Research Council of Australia [1143105, 1126843, 1117089, 1116937, 1086291] Funding Source: NHMRC

向作者/读者索取更多资源

Defects in apoptotic cell death can promote cancer and impair responses of malignant cells to anti-cancer therapy. Pro-survival BCL-2 proteins prevent apoptosis by keeping the cell death effectors, BAX and BAK, in check. The BH3-only proteins initiate apoptosis by neutralizing the pro-survival BCL-2 proteins. Structural analysis and medicinal chemistry led to the development of small-molecule drugs that mimic the function of the BH3-only proteins to kill cancer cells. The BCL-2 inhibitor venetoclax has been approved for treatment of refractory chronic lymphocytic leukemia and this drug and inhibitors of pro-survival MCL-1 and BCL-XL are being tested in diverse malignancies.

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