Comprehensive review of uterine fibroids: developmental origin, pathogenesis, and treatment

Q Yang, M Ciebiera, MV Bariani, M Ali… - Endocrine …, 2022 - academic.oup.com
Uterine fibroids are benign monoclonal neoplasms of the myometrium, representing the
most common tumors in women worldwide. To date, no long-term or noninvasive treatment …

Frequency of MED12 mutation in relation to tumor and patient's clinical characteristics: a meta-analysis

C He, W Nelson, H Li, YD Xu, XJ Dai, YX Wang… - Reproductive …, 2022 - Springer
Abstract Mediator complex subunit 12 (MED12) is the most frequently mutated gene in
uterine leiomyomas (ULs)—with a frequency of up to 85%—suggesting that it plays key roles …

[HTML][HTML] Leiomyoma with bizarre nuclei: a morphological, immunohistochemical and molecular analysis of 31 cases

JA Bennett, B Weigelt, S Chiang, P Selenica, YB Chen… - Modern Pathology, 2017 - Elsevier
Leiomyomas associated with hereditary leiomyomatosis and renal cell carcinoma syndrome
and leiomyomas with bizarre nuclei often show overlapping morphological features, in …

The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review

ILS Amendola, M Spann, J Segars, B Singh - Reproductive Sciences, 2024 - Springer
Uterine leiomyomas are the most common tumor of reproductive-age women worldwide.
Although benign, uterine fibroids cause significant morbidity and adversely impact the …

Mediator Kinase Disruption in MED12-Mutant Uterine Fibroids From Hispanic Women of South Texas

MJ Park, H Shen, NH Kim, F Gao… - The Journal of …, 2018 - academic.oup.com
Context Mutations in the gene encoding Mediator complex subunit MED12 are dominant
drivers of uterine fibroids (UFs) in women of diverse racial and ethnic origins. Previously, we …

[HTML][HTML] Prevalence and clinical significance of mediator complex subunit 12 mutations in 362 Han Chinese samples with uterine leiomyoma

J Wu, Y Zou, Y Luo, JB Guo, FY Liu… - Oncology …, 2017 - spandidos-publications.com
Uterine leiomyomas (ULs) are the most common gynecological benign tumors originating
from the myometrium. Prevalent mutations in the mediator complex subunit 12 (MED12) …

Understanding Obesity as a Risk Factor for Uterine Tumors Using Drosophila

X Li, M Liu, JY Ji - The Drosophila Model in Cancer, 2019 - Springer
Multiple large-scale epidemiological studies have identified obesity as an important risk
factor for a variety of human cancers, particularly cancers of the uterus, gallbladder, kidney …

Identification of Differentially Expressed K-Ras Transcript Variants in Patients With Leiomyoma

N Zolfaghari, S Shahbazi, M Torfeh… - Reproductive …, 2017 - journals.sagepub.com
Purpose: Molecular studies have demonstrated a wide range of gene expression variations
in uterine leiomyoma. The rat sarcoma virus/rapidly accelerated fibrosarcoma/mitogen …

Q192R variant in paraoxonase 1 gene confers susceptibility to leiomyoma

S Shahbazi, S Zarei, M Torfeh… - Journal of Cancer …, 2020 - journals.lww.com
Objective: Paraoxonase 1 (PON1) plays a defensive role against oxidative stress by
destroying oxidized lipids. Q192R single nucleotide polymorphism of PON1 gene alters the …

Expression study of CYP19A1 gene in a cohort of Iranian leiomyoma patients

L Emrahi, J Behroozi, S Shahbazi - Egyptian Journal of Medical Human …, 2018 - ajol.info
Background: CYP19A1 gene encodes aromatase, a microsomal key enzyme that catalyzes
the synthesis of estrogens from androgens. Accumulating evidence has revealed that …