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人乳腺癌中占据和未占据的II型雌激素结合位点

Occupied and unoccupied type II estrogen binding sites in human breast cancer.

作者信息

Lopes M T, Liberato M H, Widman A, Brentani M M

出版信息

J Steroid Biochem. 1987 Feb;26(2):219-26. doi: 10.1016/0022-4731(87)90075-6.

DOI:10.1016/0022-4731(87)90075-6
PMID:3560938
Abstract

Using a saturation analysis over a wide range of [3H]estradiol at two temperatures 4 and 22 degrees C we have determined unoccupied (4 degrees C) and total (22 degrees C) type II estrogen binding site (EBS) levels in individual cytosols of 100 patients with breast cancer (50 post and 50 premenopausal). Exchange was found to be complete after 18 h at 22 degrees C and receptor degradation was negligible during this treatment. Steroid specificity and affinity determined by Scatchard and Rosenthal plot analysis were not altered at 22 degrees C. Carcinomas presented a higher total type II REBS level as compared unfilled type II binding sites or the classical ER, independently of menopausal status, phase of the menstrual cycle or positivity of ER. On the other hand, unoccupied type II EBS level was strongly correlated to the concentration of type I ER, being higher on the post-menopausal group and older patients.

摘要

在4℃和22℃两个温度下,对一系列广泛浓度的[3H]雌二醇进行饱和分析,我们测定了100例乳腺癌患者(50例绝经后和50例绝经前)个体胞质溶胶中未占据(4℃)和总(22℃)II型雌激素结合位点(EBS)水平。发现在22℃下18小时后交换完全,并且在此处理过程中受体降解可忽略不计。通过Scatchard和Rosenthal作图分析确定的类固醇特异性和亲和力在22℃下未改变。无论绝经状态、月经周期阶段或ER阳性情况如何,癌组织中总II型REBS水平均高于未填充的II型结合位点或经典ER。另一方面,未占据的II型EBS水平与I型ER浓度密切相关,在绝经后组和老年患者中更高。

相似文献

1
Occupied and unoccupied type II estrogen binding sites in human breast cancer.人乳腺癌中占据和未占据的II型雌激素结合位点
J Steroid Biochem. 1987 Feb;26(2):219-26. doi: 10.1016/0022-4731(87)90075-6.
2
Occupied and unoccupied oestradiol receptor in human breast tumour cytosol.人乳腺肿瘤细胞溶质中已结合和未结合的雌二醇受体
J Steroid Biochem. 1980 Apr;13(4):405-8. doi: 10.1016/0022-4731(80)90346-5.
3
Estrogen binding sites in the nucleus of normal and malignant human tissue: characteristics of the multiple nuclear binding sites.
Cancer Res. 1982 Nov;42(11):4449-54.
4
Simultaneous measurement of estrogen and progesterone receptors in tumor cytosols with use of 125I-labeled estradiol and of 3H-R5020.
Clin Chem. 1981 May;27(5):687-91.
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Affinity of estradiol mustard for estrogen receptors and its enzymatic degradation in uterine and breast cancer cytosols.
Int J Cancer. 1976 Dec 15;18(6):750-6. doi: 10.1002/ijc.2910180605.
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Biological activity and receptor binding of a strongly interacting estrogen in human breast cancer cells.一种在人乳腺癌细胞中具有强相互作用的雌激素的生物活性及受体结合情况
Cancer Res. 1984 Jun;44(6):2302-8.
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Cytoplasmic and nuclear estradiol and progesterone receptors in human endometrium.人子宫内膜中的细胞质和细胞核雌二醇及孕酮受体
J Clin Endocrinol Metab. 1978 Apr;46(4):635-48. doi: 10.1210/jcem-46-4-635.
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Estrogen receptor. Unoccupied sites in nuclei of a breast tumor cell line.雌激素受体。乳腺肿瘤细胞系细胞核中的未占据位点。
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Unoccupied nuclear oestradiol-receptor sites in normal human endometrium.正常人类子宫内膜中未被占据的核雌激素受体位点。
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3H-estradiol and 3H-R5020 binding in cytosols of normal and neoplastic human ovarian tissue.
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引用本文的文献

1
A low-affinity estrogen-binding site in pregnant rat uteri: analysis and partial purification.妊娠大鼠子宫中的低亲和力雌激素结合位点:分析与部分纯化
Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11502-6. doi: 10.1073/pnas.91.24.11502.
2
Androgen receptor assays in specimens of prostatic tissue obtained by transurethral resection and transvesical adenomectomy.经尿道前列腺切除术和经膀胱腺瘤切除术获取的前列腺组织标本中的雄激素受体检测。
Urol Res. 1991;19(6):337-41. doi: 10.1007/BF00310146.
3
Soluble and nuclear type I and II androgen-binding sites in benign hyperplasia and cancer of the human prostate.
人前列腺良性增生和癌中可溶性及核内I型和II型雄激素结合位点
Urol Res. 1992;20(2):127-32. doi: 10.1007/BF00296524.