Whole Exome Sequencing Reveals Novel Variants in Unexplained Erythrocytosis.
Harshit KhuranaBabylakshmi MuthusamyUday YanamandraKishore GarapatiHarikrishnan PremdeepShankar SubramanianAkhilesh PandeyPublished in: Omics : a journal of integrative biology (2023)
Erythrocytosis is characterized by an increase in red cells in peripheral blood. Polycythemia vera, the commonest primary erythrocytosis, results from pathogenic variants in JAK2 in ∼98% of cases. Although some variants have been reported in JAK2 -negative polycythemia, the causal genetic variants remain unidentified in ∼80% of cases. To discover genetic variants in unexplained erythrocytosis, we performed whole exome sequencing in 27 patients with JAK2 -negative polycythemia after excluding the presence of any mutations in genes previously associated with erythrocytosis ( EPOR , VHL , PHD2 , EPAS1 , HBA , and HBB ). We found that the majority of patients (25/27) had variants in genes involved in epigenetic processes, including TET2 and ASXL1 or in genes related to hematopoietic signaling such as MPL and GFIB . Based on computational analysis, we believe that variants identified in 11 patients in this study could be pathogenic although functional studies will be required for confirmation. To our knowledge, this is the largest study reporting novel variants in individuals with unexplained erythrocytosis. Our results suggest that genes involved in epigenetic processes and hematopoietic signaling pathways are likely associated with unexplained erythrocytosis in individuals lacking JAK2 mutations. With very few previous studies targeting JAK2 -negative polycythemia patients to identify underlying variants, this study opens a new avenue in evaluating and managing JAK2 -negative polycythemia.
Keyphrases
- end stage renal disease
- copy number
- chronic kidney disease
- newly diagnosed
- ejection fraction
- peritoneal dialysis
- gene expression
- peripheral blood
- healthcare
- prognostic factors
- bone marrow
- dna methylation
- drug delivery
- cell proliferation
- cancer therapy
- oxidative stress
- endoplasmic reticulum stress
- cell cycle arrest
- adverse drug
- genome wide identification