Wei Li, PhD

Professor of Dermatology

Director, MSS Graduate Program

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Overview

Dr. Li research focuses on the following topics: 1) Identification of the “driver genes” for wound healing, 2) Identification of tumor-secreted molecules as drug targets for TNBCs (triple negative breast cancers). 3) Signal transduction to understand the cell motility signaling, which initiates at the cell surface, propagates via cytosolic signaling networks and executes by newly expressed and secreted gene products.

His experimental model systems are less manipulated primary human skin cells, whose migration is essential for both physiological processes, such as skin wound healing, and pathological occurrence, such as skin cancer, PDX models for TNBCs and pig models for wound healing.

Awards

  • USC Stevens Center for Innovation: Technology Commercialization Award, 2017
     – 2017
  • USC Stevens Center for Innovation: Technology Commercialization Award, 2018
     – 2018
  • USA: Elected Member, National Academy of Inventors, 2017
     – pre.

Education and Training

  • Xinjiang University, Urumqi, China — B.S. — 1982 — General Biology
  • CUSBEA, Guangzhou, China — English Certificate — 1984 — English
  • Albert Einstein College of Medicine, New York City, NY — Ph.D. — 1991 — Biochemistry and Molecular Biology
  • New York University Medical Center, New York City, NY — Postdoctoral Research — 1993 — Signal Transduction

Research Funding

  • Development of Extracellular Heat Shock Protein-90 as a Novel Topical Wound Healing
    NIH · R01AR059853 · Jul 1, 2011 – Apr 30, 2018 · Role: Principal Investigator
  • Mechanisms of Human Dermal Fibroblast Migration
    NIH · R01GM067100 · Jan 1, 2003 – Apr 30, 2021 · Role: Principal Investigator
  • Signal Transduction of Human Keratinocyte Migration
    NIH · R01GM066193 · Jul 1, 2002 – May 31, 2013 · Role: Principal Investigator
  • STUDIES OF A NOVEL SH2/SH3-CONTAINING CELLULAR ONCOGENE
    NIH · R01CA065567 · Aug 15, 1995 – Apr 30, 2001 · Role: Principal Investigator

Research Keywords

  • big molecule drug development, wound healing, breast cancer

Publications

  • Extracellular Heat Shock Protein-90 (eHsp90): Everything You Need to Know. Biomolecules. 2022 06 29; 12(7).. View in PubMed
  • Extracellular Hsp90α, which participates in vascular inflammation, is a novel serum predictor of atherosclerosis in type 2 diabetes. BMJ Open Diabetes Res Care. 2022 01; 10(1).. View in PubMed
  • Heterogeneous Responses and Isoform Compensation the Dim Therapeutic Window of Hsp90 ATP-Binding Inhibitors in Cancer. Mol Cell Biol. 2022 02 17; 42(2):e0045921.. View in PubMed
  • Correction to: Heat shock protein-90alpha (Hsp90α) stabilizes hypoxia-inducible factor-1α (HIF-1α) in support of spermatogenesis and tumorigenesis. Cancer Gene Ther. 2021 Sep; 28(9):1071-1072.. View in PubMed
  • Publisher Correction: Heat shock protein-90alpha (Hsp90α) stabilizes hypoxia-inducible factor-1α (HIF-1α) in support of spermatogenesis and tumorigenesis. Cancer Gene Ther. 2021 Sep; 28(9):1073.. View in PubMed
  • Heat shock protein-90alpha (Hsp90α) stabilizes hypoxia-inducible factor-1α (HIF-1α) in support of spermatogenesis and tumorigenesis. Cancer Gene Ther. 2021 09; 28(9):1058-1070.. View in PubMed
  • Wound Healing Driver Gene and Therapeutic Development: Political and Scientific Hurdles. Adv Wound Care (New Rochelle). 2021 08; 10(8):415-435.. View in PubMed
  • Tumour-Secreted Hsp90α on External Surface of Exosomes Mediates Tumour – Stromal Cell Communication via Autocrine and Paracrine Mechanisms. Sci Rep. 2019 10 22; 9(1):15108.. View in PubMed
  • Extracellular and Non-Chaperone Function of Heat Shock Protein-90α Is Required for Skin Wound Healing. J Invest Dermatol. 2018 02; 138(2):423-433.. View in PubMed
  • PRAS40 Connects Microenvironmental Stress Signaling to Exosome-Mediated Secretion. Mol Cell Biol. 2017 Oct 01; 37(19).. View in PubMed