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Proteomic and phosphoproteomic analyses of myectomy tissue reveals difference between sarcomeric and genotype-negative hypertrophic cardiomyopathy.
Garmany, Ramin; Bos, J Martijn; Dasari, Surendra; Johnson, Kenneth L; Tester, David J; Giudicessi, John R; Dos Remedios, Cristobal; Maleszewski, Joseph J; Ommen, Steve R; Dearani, Joseph A; Ackerman, Michael J.
Afiliación
  • Garmany R; Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic Alix School of Medicine and the Mayo Clinic Medical Scientist Training Program, Rochester, MN, USA.
  • Bos JM; Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN, USA.
  • Dasari S; Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN, USA.
  • Johnson KL; Department of Cardiovascular Medicine, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN, USA.
  • Tester DJ; Department of Pediatric and Adolescent Medicine/Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN, USA.
  • Giudicessi JR; Department of Quantitative Health Sciences/Division of Computational Biology, Mayo Clinic, Rochester, MN, USA.
  • Dos Remedios C; Proteomics Core, Mayo Clinic, Rochester, MN, USA.
  • Maleszewski JJ; Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN, USA.
  • Ommen SR; Department of Cardiovascular Medicine, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN, USA.
  • Dearani JA; Mechanobiology Laboratory, Victor Chang Cardiac Research Institute, Darlinghurst, Australia.
  • Ackerman MJ; Department of Cardiovascular Medicine, Windland Smith Rice Genetic Heart Rhythm Clinic, Mayo Clinic, Rochester, MN, USA.
Sci Rep ; 13(1): 14341, 2023 09 01.
Article en En | MEDLINE | ID: mdl-37658118
ABSTRACT
Hypertrophic cardiomyopathy (HCM) is a genetically heterogenous condition with about half of cases remaining genetically elusive or non-genetic in origin. HCM patients with a positive genetic test (HCMSarc) present earlier and with more severe disease than those with a negative genetic test (HCMNeg). We hypothesized these differences may be due to and/or reflect proteomic and phosphoproteomic differences between the two groups. TMT-labeled mass spectrometry was performed on 15 HCMSarc, 8 HCMNeg, and 7 control samples. There were 243 proteins differentially expressed and 257 proteins differentially phosphorylated between HCMSarc and HCMNeg. About 90% of pathways altered between genotypes were in disease-related pathways and HCMSarc showed enhanced proteomic and phosphoproteomic alterations in these pathways. Thus, we show HCMSarc has enhanced proteomic and phosphoproteomic dysregulation observed which may contribute to the more severe disease phenotype.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cardiomiopatía Hipertrófica / Proteómica Límite: Humans Idioma: En Revista: Sci Rep Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cardiomiopatía Hipertrófica / Proteómica Límite: Humans Idioma: En Revista: Sci Rep Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos