Faculty

John J. Bissler, MD

Clark D. West Endowed Chair of Nephrology
Associate Professor
Associate Program Director for Research and Academic Careers

Related Links
Cincinnati Children's: Director, Nephrology Fellowship Training Program
Cincinnati Children's: Associate Program Director of Research and Academic Careers
Cincinnati Children's Annual Report: Profile of Intelligent Hemofiltration System developed by Dr. Bissler
BTG News Release: Technology Developed at Cincinnati Children's to Significantly Benefit Adults and Children on Dialysis
University of Cincinnati: Member of the Interdisciplinary Graduate Program in Cell and Molecular Biology

Education and Training

  • BS, Kent State University
  • MD, Northeastern Ohio University
  • Pediatrics, Children's Hospital Medical Center, Akron
  • Pediatric Nephrology, Children's Hospital Medical Center, Cincinnati
  • William Cooper Procter Research Scholar, Cincinnati Children's Research Foundation, Cincinnati

Clinical Interests

Hemofiltration and autosomal dominant polycystic kidney disease

Research Interests

Dr. Bissler has two major research focuses. His basic science interests revolve around DNA biochemistry and the role of intrinsic DNA instability leading to disease. His work has identified several inherited diseases that have renal involvement that can be explained by alternative DNA structure mutagenesis. These structures include A-B helix transitions, cruciform extrusion and triplex DNA formation. His major focus is on DNA directed mutagenesis within the PKD1 gene. Mutations in this gene lead to autosomal dominant polycystic kidney disease.

Dr. Bissler's clinical research focus revolves around the computerization of hemodialysis and hemofiltration. Specifically, Drs. Bissler and Marios Polycarpou at the Department of Electrical and Computer Engineering, University of Cincinnati, are working with adaptive and intelligent control systems as applied to pediatric nephrology procedures. These control algorithms can both control and learn from experience smoothing procedures with easing of physician and nurse time demands.

Dr. Bissler attends the Tuberous Sclerosis Clinic in Cincinnati. This clinic has over 300 patients, making it one of the largest TS clinics in the world. Dr. Bissler cares for the renal component of this disease process. Furthermore, in conjunction with Dr. David Franz, Director of the Tuberous Sclerosis Clinic and Dr. Frank McCormack, Pulmonologist who specializes in the lymphangioleiomyomatosis, Dr. Bissler is conducting a clinical trial in hopes to discover a pharmacological treatment for the renal lesion of TS.

Dr. Bissler is also on the faculty of the Interdisciplinary Graduate Program in Cell and Molecular Biology at the University of Cincinnati.

Representative Recent Publications

Funding

    DNA Structure and Mutagenesis

  1. DNA Replication Fork: Pausing, Recombination and Disease
    Agency: NIH (R01 DK061458)
    PI: John J. Bissler, MD
    Dates/Effort: 5/1/03-4/30/08 (25%)
    Total Direct Costs: $1,025,002
    Goal: To investigate the contribution of alternative DNA secondary structures to replication fork arrest and induction of recombination. No overlap.

    Utility of Rapamycin for the Treatment of Renal Angiomyolipomas

  2. Utility of Rapamycin for the Treatment of Renal Angiomyolipomas
    Agency: NIH (R21CA103486)
    PI: John J. Bissler, MD
    Dates/Effort: 07/01/03-06/30/06 (30%)
    Total Direct Costs: $445,000
    Goal: To assess the role of rapamycin in the treatment of renal angiomyolipomas.
  3. Utility of Rapamycin for the Treatment of Renal Angiomyolipomas
    Agency: TS Alliance
    PI: John Bissler, MD
    Dates/Effort: 7/1/03-6/30/06 (0%)
    Total costs: $100,000
    Goal: To assess the role of rapamycin in the treatment of renal angiomyolipomas.
  4. RAD001 Therapy of Angiomyolipomata in Patients with Tuberous Sclerosis Complex and Sporadic Lymphangioleiomyomatosis
    Agency: Novartis
    PI: John Bissler, MD
    Dates/Effort: 10/1/04-9/30/06 (30%)
    Total costs: $622,248
    Goal: To assess the role of everlimus in the treatment of renal angiomyolipomata.
  5. Natural History of Tuberous Sclerosis: Renal Disease
    Agency: Department of Defense
    PI: John Bissler, MD
    Dates: 06/01/05-05/31/08
    Total costs: $1,000,000
    Goal: To assess the natural history of the renal lesions in tuberous sclerosis complex.