Cited by 239Uterine Myomas and TreatmentsReproductive System and PregnancyGynecological conditions and treatments

Submucosal uterine leiomyomas have a global effect on molecular determinants of endometrial receptivity

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Rackow, Beth W., Taylor, Hugh S.·2010·Fertility and Sterility

Abstract

Objective To evaluate the effect of uterine leiomyomas on the endometrium using molecular markers of endometrial receptivity: HOXA10, HOXA11, LIF, and BTEB1.Design Case-control study.Setting University medical center.Patient(s) Thirty reproductive-aged women with submucosal, intramural, or no uterine myomas who underwent hysteroscopy or hysterectomy.Intervention(s) Proliferative phase endometrial sampling was performed at the time of surgery. In uteri with a submucosal myoma, directed endometrial biopsies were obtained over the myoma and over normal myometrium.Main outcome measure(s) Endometrial HOXA10 expression was evaluated as a primary endpoint using quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemistry. HOXA11, BTEB1, and LIF were evaluated using real-time RT-PCR.Result(s) Endometrial HOXA10 and HOXA11 messenger RNA (mRNA) expression were significantly decreased in uteri with submucosal myomas compared with controls and with uteri with intramural myomas. A similar trend was seen in BTEB1 mRNA expression; however, no difference was found in LIF mRNA expression. Immunohistochemistry localized the decrease in endometrial HOXA10 protein expression to stroma. In the presence of a submucosal myoma, there were no regional differences in gene expression.Conclusion(s) The molecular mechanism by which submucosal myomas adversely affect reproduction includes a global decrease in endometrial HOX gene expression, not simply a focal change over the myoma. This may explain the reproductive dysfunction observed with submucosal myomas.

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Crossref · 10.1016/j.fertnstert.2008.03.029

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  • HOXA10 expression is lower in the endometrium of women with endometriosis and is abnormally methylated.

    “We have previously shown that HOXA10 expression is lower in the endometrium of women with endometriosis and is abnormally methylated.44,53,54”

    From Altered genome-wide methylation in endometriosis (2014) · cites this paper as [53]

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References 65 · Cited by 239

Research works printed but not linked: 1

  1. Du H, Sarno JL, Taylor HS. Basic transcription element binding protein (BTEB1) is regulated by HOXA10 in endometrial cells. J Soc Gynecol Investig 2006;13:71A-2.

Authors
Rackow, B. W., & Taylor, H. S.
Affiliations
Yale University (US)
Corresponding author
Rackow, Beth W.
Venue
Fertility and Sterility
Publisher
Elsevier BV
Published
2010-04
Volume
93
Issue
6
Pages
2027-2034
ISSN
0015-0282 (ISSN-L)
OpenAlex
W2073456100
Cited by
239
References
65
Citations by year
2026: 10 · 2025: 9 · 2024: 8 · 2023: 19 · 2022: 14 · 2021: 18 · 2020: 15 · 2019: 9 · 2018: 14 · 2017: 20 · 2016: 16 · 2015: 16 · 2014: 16 · 2013: 16 · 2012: 11
FWCI
10.71
Type
journal article
Language
en
Open access
Locations
  • Fertility and Sterility (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
Eunice Kennedy Shriver National Institute of Child Health and Human Development (R29HD036887, HD36887, U54HD052668, R01HD036887)
Topics
  • Health Sciences › Medicine › Obstetrics and Gynecology › Uterine Myomas and Treatments
  • Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
  • Health Sciences › Medicine › Obstetrics and Gynecology › Gynecological conditions and treatments
Keywords
endometrial receptivity, endometrium, HOXA10, HOXA11, LiF, Hox genes, endometrial gene expression, endometrial stroma, reproductive disorders, intramural myoma
MeSH terms
Homeobox A10 Proteins, Adult, Endometrium, Female, Humans, Infertility, Female, Leiomyoma, Middle Aged, Mucous Membrane, Embryo Implantation, Prognosis, Biomarkers, Tumor, Uterine Neoplasms, Gene Expression Regulation, Neoplastic, Case-Control Studies, Homeodomain Proteins, Kruppel-Like Transcription Factors, Leukemia Inhibitory Factor

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