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The journal of clinical endocrinology and metabolism, 2000-06, Vol.85 (6), p.2334-2338
2000
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Autor(en) / Beteiligte
Titel
Changes in Endometrial PTEN Expression throughout the Human Menstrual Cycle1
Ist Teil von
  • The journal of clinical endocrinology and metabolism, 2000-06, Vol.85 (6), p.2334-2338
Ort / Verlag
Endocrine Society
Erscheinungsjahr
2000
Quelle
Oxford Journals 2020 Medicine
Beschreibungen/Notizen
  • Frequent mutation of the PTEN tumor suppressor gene in endometrial adenocarcinoma has led to the prediction that its product, a phosphatase that regulates the cell cycle, apoptosis, and possibly cell adhesion, is functionally active within normal endometrial tissues. We examined PTEN expression in normal human endometrium during response to changing physiological levels of steroid hormones. PTEN ribonucleic acid levels, assessed by RT-PCR, increase severalfold in secretory compared to proliferative endometrium. This suggested that progesterone, a known antineoplastic factor for endometrial adenocarcinoma, increases PTEN levels. Immunohistochemistry with an anti-PTEN monoclonal antibody displayed a complex pattern of coordinate stromal and epithelial expression. Early in the menstrual cycle under the dominant influence of estrogens, the proliferative endometrium shows ubiquitous cytoplasmic and nuclear PTEN expression. After 3–4 days of progesterone exposure, glandular epithelium of early secretory endometrium maintains cytoplasmic PTEN protein in an apical distribution offset by expanding PTEN-free basal secretory vacuoles. By the midsecretory phase, epithelial PTEN is exhausted, but increases dramatically in the cytoplasm of stromal cells undergoing decidual change. We conclude that stromal and epithelial compartments contribute to the hormone-driven changes in endometrial PTEN expression and infer that abnormal hormonal conditions may, in turn, disrupt normal patterns of PTEN expression in this tissue.
Sprache
Englisch
Identifikatoren
ISSN: 0021-972X
eISSN: 1945-7197
DOI: 10.1210/jcem.85.6.6652
Titel-ID: cdi_endocrinepress_journals_10_1210_jcem_85_6_6652
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