Steroid Receptors of the Uterine Myometrium, Myoma, Adenomyosis and Ovarian Endometriosis in the Human Subject

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This study characterized steroid receptors in uterine myometrium, myoma, adenomyosis, and ovarian endometriosis, finding that lower progesterone receptor levels in adenomyosis and endometriosis reduce their responsiveness to progestogens compared to normal endometrium.

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This 1978 study characterized steroid receptors in human uterine myometrium, leiomyomas, adenomyosis, and ovarian endometriosis using cytosol homogenates and Scatchard plot analysis. The researchers found that while estrogen and androgen receptors were present in all adenomyosis cases, progesterone receptor levels were often absent or low, correlating with a histological delay and reduced progestogen responsiveness in the aberrant tissue. Similarly, endometriotic lesions exhibited significantly lower progesterone receptor concentrations compared to normal endometrium, suggesting a diminished response to progestogens despite the presence of other steroid receptors. Relevance to endometriosis: This paper is centrally about endometriosis — specifically characterizing its steroid receptor profile and comparing it to adenomyosis and normal endometrium.

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Abstract

Steroid receptors in benign human uterine tumors and disorders were characterized and investigated to clarify their clinical significance.A 248,800x g supernatant of tissue homogenates was used for the cytosol, where the steroid receptor was characterized and determined by a Scatchard plot. In the myo-metrial cytosol, the estrogen receptor (=ER) was sedimented to the 7S, 5S and 4S regions, and the estradiol-17β (=E2) -ER complex demonstrated the dissociation constant (=Kd) = 4.5×10110M (at 4°C, by dextran coated charcoal=DCC). The progesterone receptor (=PR) was sedimented to the 7S and 4S regions, and the Kd of the progesterone-PR complex was 1.5x 10-9M (at 4°C by DCC). The androgen receptor (=AR) was sedimented to the 7-6S and 5S regions, and the dihydrotestosterone (=DHT) -AR complex demonstrated Kd=4.0x 10-10M (at 4°C by DCC). All of these steroid-7S bindings were easily degraded during sucrose gradient centrifugation. A ligand specificity study characterized the specificity of the receptors.There was no relation between the steroid receptor level in the myometrium and the corresponding myoma. The steroid receptor level was determined during the menstrual cycle and did not show a constant tendency.In adenomyosis, the histological dating showed a delay in the aberrant endometrium of adenomyosis when compared with the dating of a normal endometrium. This indicates that the steroid is less responsive to the aberrant endometrium in adenomyosis than to the corresponding normal endometrium. ER and AR were detected in all cases, but PR was not detected in some of them. Thus it would seem that the lower responsiveness of adenomyosis tissue to progestogen is derived from the lower content of PR.In most cases of endometriosis the steroid receptor was detected; however, the level of PR in endometriosis was much lower than that of a corresponding normal endometrium. This indicates that most cases of endometriosis respond to steroids, but to a lesser extent than to progestogen.
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ヒト子宮筋, 子宮筋腫, 子宮腺筋症および子宮内膜症のステロイドレセプター 1978 年 54 巻 12 号 p. 1407-1420 詳細 抄録 Steroid receptors in benign human uterine tumors and disorders were characterized and investigated to clarify their clinical significance. A 248,800x g supernatant of tissue homogenates was used for the cytosol, where the steroid receptor was characterized and determined by a Scatchard plot. In the myo-metrial cytosol, the estrogen receptor (=ER) was sedimented to the 7S, 5S and 4S regions, and the estradiol-17β (=E2) -ER complex demonstrated the dissociation constant (=Kd) = 4.5×10110M (at 4°C, by dextran coated charcoal=DCC). The progesterone receptor (=PR) was sedimented to the 7S and 4S regions, and the Kd of the progesterone-PR complex was 1.5x 10-9M (at 4°C by DCC). The androgen receptor (=AR) was sedimented to the 7-6S and 5S regions, and the dihydrotestosterone (=DHT) -AR complex demonstrated Kd=4.0x 10-10M (at 4°C by DCC). All of these steroid-7S bindings were easily degraded during sucrose gradient centrifugation. A ligand specificity study characterized the specificity of the receptors. There was no relation between the steroid receptor level in the myometrium and the corresponding myoma. The steroid receptor level was determined during the menstrual cycle and did not show a constant tendency. In adenomyosis, the histological dating showed a delay in the aberrant endometrium of adenomyosis when compared with the dating of a normal endometrium. This indicates that the steroid is less responsive to the aberrant endometrium in adenomyosis than to the corresponding normal endometrium. ER and AR were detected in all cases, but PR was not detected in some of them. Thus it would seem that the lower responsiveness of adenomyosis tissue to progestogen is derived from the lower content of PR. In most cases of endometriosis the steroid receptor was detected; however, the level of PR in endometriosis was much lower than that of a corresponding normal endometrium. This indicates that most cases of endometriosis respond to steroids, but to a lesser extent than to progestogen. A 248,800x g supernatant of tissue homogenates was used for the cytosol, where the steroid receptor was characterized and determined by a Scatchard plot. In the myo-metrial cytosol, the estrogen receptor (=ER) was sedimented to the 7S, 5S and 4S regions, and the estradiol-17β (=E2) -ER complex demonstrated the dissociation constant (=Kd) = 4.5×10110M (at 4°C, by dextran coated charcoal=DCC). The progesterone receptor (=PR) was sedimented to the 7S and 4S regions, and the Kd of the progesterone-PR complex was 1.5x 10-9M (at 4°C by DCC). The androgen receptor (=AR) was sedimented to the 7-6S and 5S regions, and the dihydrotestosterone (=DHT) -AR complex demonstrated Kd=4.0x 10-10M (at 4°C by DCC). All of these steroid-7S bindings were easily degraded during sucrose gradient centrifugation. A ligand specificity study characterized the specificity of the receptors. There was no relation between the steroid receptor level in the myometrium and the corresponding myoma. The steroid receptor level was determined during the menstrual cycle and did not show a constant tendency. In adenomyosis, the histological dating showed a delay in the aberrant endometrium of adenomyosis when compared with the dating of a normal endometrium. This indicates that the steroid is less responsive to the aberrant endometrium in adenomyosis than to the corresponding normal endometrium. ER and AR were detected in all cases, but PR was not detected in some of them. Thus it would seem that the lower responsiveness of adenomyosis tissue to progestogen is derived from the lower content of PR. In most cases of endometriosis the steroid receptor was detected; however, the level of PR in endometriosis was much lower than that of a corresponding normal endometrium. This indicates that most cases of endometriosis respond to steroids, but to a lesser extent than to progestogen. © 一般社団法人 日本内分泌学会

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Condition tags

endometriosisadenomyosis

MeSH descriptors

Endometriosis Leiomyoma Myometrium Ovarian Neoplasms Receptors, Steroid Uterine Neoplasms Uterus Adult Cytosol Cytosol Endometriosis Female Humans Leiomyoma Menstruation Middle Aged Mitotic Index Myometrium Ovarian Neoplasms Receptors, Steroid

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