Racial Disparity in Uterine Leiomyoma: New Insights of Genetic and Environmental Burden in Myometrial Cells.
Nazeer H KhanRoss McNallyJ Julie KimJian-Jun WeiPublished in: Molecular human reproduction (2024)
Uterine leiomyoma (LM), also known as uterine fibroids, are common gynecological tumors and can reach a prevalence of 70% among women by the age of 50. Notably, the LM burden is much higher in Black women with earlier onset, a greater tumor number, size and severity compared to White women. Published knowledge shows that there are genetic, environmental and lifestyle-based risk factors associated with racial disparity for LM. Significant strides have been made on genomic, epigenomic, and transcriptomic data levels in Black and White women to elucidate the underlying pathomolecular reasons of racial disparity in LM development. However, racial disparity of LM remains a major area of concern in gynecological research. This review highlights risk factors of LM and their role in different races. Furthermore, we discuss the genetics and uterine myometrial microenvironment in LM development. Comparative findings revealed that a major racial difference in the disease is linked to myometrial oxidative burden and altered ROS pathways which is relevant to the oxidized guanine in genomic DNA and MED12 mutations that drive the LM genesis. Considering the burden and morbidity of LM, we anticipate that this review on genetic risk and myometrial microenvironment will strengthen understanding and propel the growth of research to address the racial disparity of LM burden.
Keyphrases
- risk factors
- african american
- copy number
- stem cells
- healthcare
- genome wide
- pregnancy outcomes
- induced apoptosis
- metabolic syndrome
- type diabetes
- randomized controlled trial
- gene expression
- single cell
- dna damage
- weight loss
- dna methylation
- electronic health record
- cervical cancer screening
- deep learning
- cell proliferation
- oxidative stress
- human health
- signaling pathway
- insulin resistance
- cell cycle arrest
- rna seq