Causes of Clonal Hematopoiesis: a Review.
LiJin JooCatherine C BradleySteven H LinPaul A ScheetKevin T NeadPublished in: Current oncology reports (2023)
Studies have identified multiple potential causes of CH mutations including smoking, cancer therapies, cardiometabolic disease, inflammation, and germline risk factors. Additionally, large-scale studies have facilitated the identification of gene-specific effects of CH mutation risk factors that may have unique downstream health implications. For example, cancer therapies and sources of environmental radiation appear to cause CH through their impact on DNA damage repair genes. There is a growing body of evidence defining risk factors for CH mutations. Standardization in the identification of CH mutations may have important implications for future research. Additional studies in underrepresented populations and their diverse environmental exposures are needed to facilitate broad public health impact of the study of CH mutations.
Keyphrases
- room temperature
- risk factors
- public health
- dna damage
- papillary thyroid
- oxidative stress
- human health
- case control
- genome wide
- bioinformatics analysis
- healthcare
- squamous cell
- mental health
- squamous cell carcinoma
- gene expression
- risk assessment
- drinking water
- genome wide identification
- transcription factor
- radiation induced
- current status
- genetic diversity