David E. Cobrinik, MD, PhD

Professor of Research Ophthalmology and Cancer Biology

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Overview

Our research seeks to improve understanding of retinal development and its relationship to retinal diseases. This goal stems from my long interest in a childhood retinal tumor called retinoblastoma, a cancer that develops in response to inactivation of the RB1 tumor suppressor gene and loss of functional pRB protein. One of our goals is to understand why cells of the retina but not other tissues routinely form cancers in response to pRB loss, and to use this knowledge to develop more effective therapies for retinoblastoma and other RB1-mutant cancers. We recently found that retinoblastomas arise from cone photoreceptor precursors, and that cone precursor-specific proliferation-related signaling pathways collaborate with pRB loss to enable tumorigenesis. This finding suggests that cone precursors signaling pathways can be targeted to suppress retinoblastoma development. Current studies aim to 1) define developmental signaling pathways that sensitize retinal cells to Rb loss, 2) define the step-by-step events through which Rb loss converts normal retinal cells to malignant retinoblastomas, and 3) target novel vulnerabilities in the pRB-deficient cone precursor circuitry.

With our colleagues at the CHLA Vision Center we also model retinal development and diseases using human pluripotent stem cells. We can produce normal-appearing developing retinas in vitro, opening the door to previously unimagined vision research opportunities. Current efforts aim to define similarities and differences between human retina produced in vitro and in vivo, and to thereby improve the verisimilitude of the in vitro retinal development model.

Awards

  • International Society for Genetic Eye Diseases and Retinoblastoma: The Ellsworth Lecture, 2023
  • James S. McDonnell Foundation: James S. McDonnell Scholar, 1996
     – 1999
  • Susan G. Komen Breast Cancer Foundation: Susan G. Komen Foundation Postdoctoral Fellow, 1992
     – 1995
  • American Cancer Society: ACS Postdoctoral Fellow, 1989
     – 1992
  • American Cancer Society: Joseph S. Silber Pre-doctoral Fellow, 1983
  • Amherst College: Oscar E. Schotté Award for Biological Research, 1982

Education and Training

  • Amherst College, Amherst, MA — BA — 05/1982 — Biology
  • Case Western Reserve University, Cleveland, OH — MD, PhD — 05/1989 — Biochemistry, Medicine
  • Whitehead Institute, Cambridge, MA — Postdoctoral — 1995 — Cancer Biology

Publications

  • Expression of HER2 in the eye and the potential for on-target side effects with antibody-drug conjugates. Sci Rep. 2026 May 07; 16(1).. View in PubMed
  • Trio exome sequencing of an optic nerve hypoplasia cohort reveals evidence for polygenic architecture. Ophthalmic Genet. 2025 12; 46(6):581-593.. View in PubMed
  • Identification and characterization of early human photoreceptor states and cell-state-specific retinoblastoma-related features. Elife. 2025 Aug 06; 13.. View in PubMed
  • Chevreul: an R bioconductor package for exploratory analysis of full-length single cell sequencing. GigaByte. 2025; 2025:gigabyte158.. View in PubMed
  • Chevreul: An R Bioconductor Package for Exploratory Analysis of Full-Length Single Cell Sequencing. bioRxiv. 2025 Jun 01.. View in PubMed
  • Identification and characterization of early human photoreceptor states and cell-state-specific retinoblastoma-related features. bioRxiv. 2025 Apr 24.. View in PubMed
  • Phenotypic Biomarkers of Aqueous Extracellular Vesicles from Retinoblastoma Eyes. Int J Mol Sci. 2024 Oct 30; 25(21).. View in PubMed
  • Retinoblastoma Origins and Destinations. N Engl J Med. 2024 04 18; 390(15):1408-1419.. View in PubMed
  • Aberrant gene expression yet undiminished retinal ganglion cell genesis in iPSC-derived models of optic nerve hypoplasia. Ophthalmic Genet. 2024 02; 45(1):1-15.. View in PubMed
  • Episodic live imaging of cone photoreceptor maturation in GNAT2-EGFP retinal organoids. Dis Model Mech. 2023 11 01; 16(11).. View in PubMed