Photo of Aaron Goldman,  PhD

Aaron Goldman, PhD

Brigham And Women's Hospital

Brigham And Women's Hospital
Phone: (520) 975-4804


agoldman@bwh.harvard.edu

Aaron Goldman, PhD

Brigham And Women's Hospital

EDUCATIONAL TITLES

  • Instructor, Medicine, Harvard Medical School
  • Instructor in Medicine, Medicine, Brigham And Women's Hospital
  • Associate Bioengineer, Engineering in Medicine, Brigham And Women's Hospital

DF/HCC PROGRAM AFFILIATION

Research Abstract

I have been in the field of medical pharmacology, translational medicine and oncology research for almost 20 years. Our overarching goal is to elucidate why and how therapy resistance develops so we can easily target and overcome these mechanisms using engineering principles. To do this, we interrogate the entire biological ecosystem using novel in-vitro, in-vivo and ex-vivo models that bring together stromal, immune and neoplastic or diseased cells.

A primary philosophy of our group is that interdisciplinary science and collaboration will drive innovation and cures for disease including cancer. To practice this philosophy, we bring together biologists, clinicians, physicists, chemical engineers and mathematicians to provide a complete picture of drug resistance. Using these diverse set of skills, our team was the first to identify the dynamic role that clonal cooperation contributes to therapy resistance under drug pressure in heterogeneous cancers. We were also the first to describe how non-cancer stem cells contribute to a new model of drug-induced resistance.

A second major component of our research philosophy is to engineer therapeutic solutions. Our team has a long history of deploying nanoscale technology to develop new drugs that exploit pharmacokinetic deficiencies of new or clinical small molecules and can deliver combinations of drugs to difficult-to-access tissues and cells. These discoveries and innovations have resulted in more than 10 patents and patent applications that have been or are being licensed into industry. Translating therapeutic solutions to the clinic is a major driver of our group motivation.

Our group is also heavily invested in our next generation of scientists, and we put a keen focus on nurturing an environment in which students can thrive. Although we are a small group, our team is ambitious, eager to learn, and constantly seeking to build our knowledge and be successful scientists!

Publications from Harvard Catalyst Profiles

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  • Mirzaei S, Gholami MH, Hashemi F, Zabolian A, Farahani MV, Hushmandi K, Zarrabi A, Goldman A, Ashrafizadeh M, Orive G. Advances in understanding the role of P-gp in doxorubicin resistance: Molecular pathways, therapeutic strategies, and prospects. Drug Discov Today 2021. PubMed
  • Saha T, Mondal J, Khiste S, Lusic H, Hu ZW, Jayabalan R, Hodgetts KJ, Jang H, Sengupta S, Eunice Lee S, Park Y, Lee LP, Goldman A. Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer. Nanophotonics 2021; 10:3063-3073. PubMed
  • Przedborski M, Smalley M, Thiyagarajan S, Goldman A, Kohandel M. Systems biology informed neural networks (SBINN) predict response and novel combinations for PD-1 checkpoint blockade. Commun Biol 2021; 4:877. PubMed
  • Craig M, Jenner AL, Namgung B, Lee LP, Goldman A. Engineering in Medicine To Address the Challenge of Cancer Drug Resistance: From Micro- and Nanotechnologies to Computational and Mathematical Modeling. Chem. Rev. 2020. PubMed
  • Smalley M, Przedborski M, Thiyagarajan S, Pellowe M, Verma A, Brijwani N, Datta D, Jain M, Shanthappa BU, Kapoor V, Gopinath KS, Doval DC, Sabitha KS, Taroncher-Oldenburg G, Majumder B, Majumder P, Kohandel M, Goldman A. Integrating Systems Biology and an Ex Vivo Human Tumor Model Elucidates PD-1 Blockade Response Dynamics. iScience 2020; 23:101229. PubMed
  • Smalley M, Natarajan SK, Mondal J, Best D, Goldman D, Shanthappa B, Pellowe M, Dash C, Saha T, Khiste S, Ramadurai N, Eton EO, Smalley JL, Brown A, Thayakumar A, Rahman M, Arai K, Kohandel M, Sengupta S, Goldman A. Nanoengineered Disruption of Heat Shock Protein 90 Targets Drug-Induced Resistance and Relieves Natural Killer Cell Suppression in Breast Cancer. Cancer Res 2020; 80:5355-5366. PubMed
  • Craig M, Kaveh K, Woosley A, Brown AS, Goldman D, Eton E, Mehta RM, Dhawan A, Arai K, Rahman MM, Chen S, Nowak MA, Goldman A. Cooperative adaptation to therapy (CAT) confers resistance in heterogeneous non-small cell lung cancer. PLoS Comput. Biol. 2019; 15:e1007278. PubMed
  • Kumar N, Prasad P, Jash E, Jayasundar S, Singh I, Alam N, Murmu N, Somashekhar SP, Goldman A, Sehrawat S. cAMP regulated EPAC1 supports microvascular density, angiogenic and metastatic properties in a model of triple negative breast cancer. Carcinogenesis 2018; 39:1245-1253. PubMed
  • Goldman A, Majumder B, Dhawan A, Ravi S, Goldman D, Kohandel M, Majumder PK, Sengupta S. Temporally sequenced anticancer drugs overcome adaptive resistance by targeting a vulnerable chemotherapy-induced phenotypic transition. Nat Commun 2015; 6:6139. PubMed