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人乳腺、子宫内膜及卵巢恶性肿瘤中的瘤内芳香化酶

Intratumoral aromatase in human breast, endometrial, and ovarian malignancies.

作者信息

Sasano H, Harada N

机构信息

Department of Pathology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Endocr Rev. 1998 Oct;19(5):593-607. doi: 10.1210/edrv.19.5.0342.

Abstract

In human estrogen-dependent neoplasms such as breast, endometrioid endometrial, and surface epithelial-stromal ovarian carcinomas, intratumoral aromatase is considered to play important roles in converting circulating androgens derived from adrenal cortex and/or ovary to estrogens, possibly in association with 17 beta-HSD type 1 and estrogen sulfatase. Analysis of intratumoral aromatase in these estrogen-dependent neoplasms is important not only in understanding the development and biological behavior of these tumors, but also in the clinical management of these patients, because suppression of intratumoral aromatase by newly developed aromatase inhibitors may provide new potentials in endocrine therapy of these patients.

摘要

在人类雌激素依赖性肿瘤中,如乳腺癌、子宫内膜样子宫内膜癌和表面上皮-间质卵巢癌,肿瘤内芳香化酶被认为在将源自肾上腺皮质和/或卵巢的循环雄激素转化为雌激素的过程中发挥重要作用,这可能与1型17β-羟类固醇脱氢酶和雌激素硫酸酯酶有关。分析这些雌激素依赖性肿瘤中的肿瘤内芳香化酶不仅对于理解这些肿瘤的发生发展和生物学行为很重要,而且对于这些患者的临床管理也很重要,因为新开发的芳香化酶抑制剂对肿瘤内芳香化酶的抑制作用可能为这些患者的内分泌治疗提供新的潜力。

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