A View on Uterine Leiomyoma Genesis through the Prism of Genetic, Epigenetic and Cellular Heterogeneity

被引:8
|
作者
Koltsova, Alla S. S. [1 ]
Efimova, Olga A. A. [1 ]
Pendina, Anna A. A. [1 ]
机构
[1] DO Ott Res Inst Obstet Gynecol & Reproductol, St Petersburg 199034, Russia
基金
俄罗斯科学基金会;
关键词
uterine leiomyoma; intratumoral heterogeneity; MED12; HMGA2; chromosomal rearrangements; chromothripsis; epigenetic abnormalities; DNA methylation; histone modifications; non-coding RNAs; X-CHROMOSOME INACTIVATION; BENIGN METASTASIZING LEIOMYOMA; GENOME-WIDE ASSOCIATION; ESTROGEN-RECEPTOR-ALPHA; MED12; EXON-2; MUTATIONS; STEM-CELLS; SMOOTH-MUSCLE; AROMATASE EXPRESSION; AFRICAN-AMERICAN; DNA METHYLATION;
D O I
10.3390/ijms24065752
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Uterine leiomyomas (ULs), frequent benign tumours of the female reproductive tract, are associated with a range of symptoms and significant morbidity. Despite extensive research, there is no consensus on essential points of UL initiation and development. The main reason for this is a pronounced inter- and intratumoral heterogeneity resulting from diverse and complicated mechanisms underlying UL pathobiology. In this review, we comprehensively analyse risk and protective factors for UL development, UL cellular composition, hormonal and paracrine signalling, epigenetic regulation and genetic abnormalities. We conclude the need to carefully update the concept of UL genesis in light of the current data. Staying within the framework of the existing hypotheses, we introduce a possible timeline for UL development and the associated key events-from potential prerequisites to the beginning of UL formation and the onset of driver and passenger changes.
引用
收藏
页数:34
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