Designed BH3 Peptides with High Affinity and Specificity for Targeting Mcl-1 in Cells-Reference-Cited by-同舟云学术

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Designed BH3 Peptides with High Affinity and Specificity for Targeting Mcl-1 in Cells

Published:2014-07-23 Issue:9 Volume:9 Page:1962-1968
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Foight Glenna Wink¹,Ryan Jeremy A.²,Gullá Stefano V.¹,Letai Anthony²³,Keating Amy E.¹

Affiliation:

1. Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States

2. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02215, United States

3. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States

Funder

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Molecular Medicine,General Medicine,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cb500340w

Reference36 articles.

1. The landscape of somatic copy-number alteration across human cancers

2. Sensitivity to antitubulin chemotherapeutics is regulated by MCL1 and FBW7

3. Inducing apoptosis and enhancing chemosensitivity to Gemcitabine via RNA interference targeting Mcl-1 gene in pancreatic carcinoma cell

4. Distinct BH3 domains either sensitize or activate mitochondrial apoptosis, serving as prototype cancer therapeutics

5. Substantial Susceptibility of Chronic Lymphocytic Leukemia to BCL2 Inhibition: Results of a Phase I Study of Navitoclax in Patients With Relapsed or Refractory Disease

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