High-throughput dynamic BH3 profiling may quickly and accurately predict effective therapies in solid tumors

Author:

Bhola Patrick D.12ORCID,Ahmed Eman1,Guerriero Jennifer L.1ORCID,Sicinska Ewa1,Su Emily1ORCID,Lavrova Elizaveta1,Ni Jing1,Chipashvili Otari1ORCID,Hagan Timothy1ORCID,Pioso Marissa S.1,McQueeney Kelley1,Ng Kimmie1,Aguirre Andrew J.13,Cleary James M.1,Cocozziello David3ORCID,Sotayo Alaba1ORCID,Ryan Jeremy1ORCID,Zhao Jean J.134,Letai Anthony123ORCID

Affiliation:

1. Dana-Farber Cancer Institute, Boston, MA 02215, USA.

2. Laboratory of Systems Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

3. Broad Institute, Cambridge, MA 02115, USA.

4. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02215, USA.

Abstract

Effective treatments might be identified by rapidly profiling drug sensitivities in patient biopsies from solid tumors.

Funder

National Institutes of Health

U.S. Department of Defense

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

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