Cited by 30Endometriosis Research and TreatmentOvarian cancer diagnosis and treatmentGynecological conditions and treatments

Molecular analysis of clonality in ovarian endometrial cysts

Yano, Tetsu, Jimbo, Haruko, Yoshikawa, Hiroyuki, Tsutsumi, Osamu, Taketani, Yuji·1999·Gynecologic and Obstetric Investigation

Abstract

Ovarian endometrial cysts, one of the typical manifestations of endometriosis, are classified as tumor-like lesions rather than as neoplasms. Clonality analysis provides important information on the histogenesis and progression of neoplastic diseases. It is generally accepted that most neoplasms are monoclonal in origin, while the clonality of endometrial cysts remains uncertain. In our study, the clonality of endometrial cysts was analyzed by means of polymerase chain reaction (PCR) based on restriction fragment length polymorphism of the X chromosome-linked human androgen receptor gene (HUMARA) and on random inactivation of the gene by methylation. We separated 21 fresh epithelial cell samples from 11 endometrial cysts and found that all were monoclonal in the methylation pattern of the human androgen receptor alleles. Moreover, in each of the five cysts where epithelial cells were sampled from multiple areas, the methylation patterns of all samples from a single cyst were identical. These data indicate that endometrial cysts are monoclonal in origin and suggest their neoplastic potential.

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Crossref · 10.1159/000052858

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Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Endometriosis lesions are clonal, as demonstrated for typical, deep, and cystic ovarian endometriosis.

    “Endometriosis lesions are clonal, as demonstrated for typical (149), deep (150), and cystic ovarian (151-153) endometriosis.”

    From Pathogenesis of endometriosis: The genetic/epigenetic theory (2019) · cites this paper as [152]

  • Deep and cystic ovarian endometriosis are consistently found to be clonal in origin.

    “A strong argument is that deep (174, 175) and cystic (176-178) ovarian endometriosis are consistently found to be clonal in origin.”

    From Pathogenesis of deep endometriosis (2017) · cites this paper as [177]

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References 24 · Cited by 30

Authors
Yano, T., Jimbo, H., Yoshikawa, H., Tsutsumi, O., & Taketani, Y.
Affiliations
The University of Tokyo (JP)
Venue
Gynecologic and Obstetric Investigation
Publisher
S. Karger AG
Published
1999
Volume
47
Issue
Suppl. 1
Pages
41-46
ISSN
  • 0378-7346 (ISSN-L)
  • 1423-002X
OpenAlex
W2000562460
Cited by
30
References
24
Citations by year
2023: 1 · 2022: 1 · 2021: 1 · 2020: 2 · 2019: 1 · 2018: 1 · 2017: 3 · 2016: 1 · 2012: 3
FWCI
2.06
Type
journal article
Language
en
Open access
closed
Locations
  • Gynecologic and Obstetric Investigation (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Reproductive Medicine › Endometriosis Research and Treatment
  • Health Sciences › Medicine › Reproductive Medicine › Ovarian cancer diagnosis and treatment
  • Health Sciences › Medicine › Obstetrics and Gynecology › Gynecological conditions and treatments
Keywords
endometrioma, endometriotic cysts, clonality, monoclonal origin, androgen receptor gene, HUMARA, DNA methylation, X chromosome inactivation, tumor-like lesions, neoplastic potential
MeSH terms
Adult, Alleles, Cell Separation, Clone Cells, DNA, Dosage Compensation, Genetic, Endometriosis, Endometrium, Epithelial Cells, Female, Humans, Middle Aged, Ovarian Cysts, Receptors, Androgen, Polymorphism, Restriction Fragment Length, Polymerase Chain Reaction, Trinucleotide Repeats

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