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Interfering with S100B-effector protein interactions for cancer therapy

期刊

DRUG DISCOVERY TODAY
卷 25, 期 9, 页码 1754-1761

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ELSEVIER SCI LTD
DOI: 10.1016/j.drudis.2020.07.010

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资金

  1. Hong Kong Baptist University [FRG2/17-18/003]
  2. Health and Medical Research Fund [HMRF/14150561]
  3. National Natural Science Foundation of China (China) [21775131]
  4. Hong Kong Baptist University Century Club Sponsorship Scheme 2019
  5. Interdisciplinary Research Matching Scheme [RC-IRMS/16-17/03]
  6. Interdisciplinary Research Clusters Matching Scheme [RC-IRCs/17-18/03]
  7. SKLEBA [SKLP_1920_P02]
  8. HKBU Strategic Development Fund [SKLP_1920_P02]
  9. Science and Technology Development Fund, Macau SAR [0072/2018/A2]
  10. University of Macau [MYRG2018-00187-ICMS, MYRG-201900002-ICMS]
  11. [C5026-16G]

向作者/读者索取更多资源

S100 calcium-binding protein B (S100B) is overexpressed in various malignant tumors, where it regulates cancer cell proliferation and metabolism by physical interactions with other molecules. Interfering with S100B-effector protein interactions is a potential strategy to treat malignant tumors. Although some S100B inhibitors have been discovered by virtual screening (VS), most target the S100B-p53 interaction. Hence, there is scope for the discovery of other S100B-effector protein interaction modulators for malignant tumors. In this review, we provide an overview of S100B-effector protein interaction inhibitor discovery using VS and discuss promising S100B-effector protein interaction targets that permit in silico analysis for drug discovery.

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