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

  • Cell-Free DNA Tumor Fraction in the Aqueous Humor Is Associated With Therapeutic Response in Retinoblastoma Patients. Transl Vis Sci Technol. 2020 09; 9(10):30.. View in PubMed
  • Simultaneous identification of clinically relevant RB1 mutations and copy number alterations in aqueous humor of retinoblastoma eyes. Ophthalmic Genet. 2020 12; 41(6):526-532.. View in PubMed
  • Variability in retinoblastoma genome stability is driven by age and not heritability. Genes Chromosomes Cancer. 2020 10; 59(10):584-590.. View in PubMed
  • Chromosome 6p Amplification in Aqueous Humor Cell-Free DNA Is a Prognostic Biomarker for Retinoblastoma Ocular Survival. Mol Cancer Res. 2020 08; 18(8):1166-1175.. View in PubMed
  • Corrigendum to “Conservative management of retinoblastoma: Challenging orthodoxy without compromising the state of metastatic grace. “Alive, with good vision and no comorbidity”” [Prog. Retina Eye Res. 73 (2019) 100764]. Prog Retin Eye Res. 2020 Apr 08; 100857.. View in PubMed
  • Improved third-generation lentiviral packaging with pLKO.1C vectors. Biotechniques. 2020 06; 68(6):349-352.. View in PubMed
  • Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods. Mitochondrion. 2020 03; 51:97-103.. View in PubMed
  • Conservative management of retinoblastoma: Challenging orthodoxy without compromising the state of metastatic grace. “Alive, with good vision and no comorbidity”. Prog Retin Eye Res. 2019 11; 73:100764.. View in PubMed
  • A novel thyroid hormone receptor isoform, TRβ2-46, promotes SKP2 expression and retinoblastoma cell proliferation. J Biol Chem. 2019 02 22; 294(8):2961-2969.. View in PubMed
  • Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors. Proc Natl Acad Sci U S A. 2018 10 02; 115(40):E9391-E9400.. View in PubMed