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大麻素与激素受体阳性乳腺癌治疗

Cannabinoids and Hormone Receptor-Positive Breast Cancer Treatment.

作者信息

Dobovišek Luka, Krstanović Fran, Borštnar Simona, Debeljak Nataša

机构信息

Institute of Oncology Ljubljana, Zaloška cesta 2, SI-1000 Ljubljana, Slovenia.

Medical Centre for Molecular Biology, Institute of Biochemistry, Faculty of Medicine, University of Ljubljana, SI-1000 Ljubljana, Slovenia.

出版信息

Cancers (Basel). 2020 Feb 25;12(3):525. doi: 10.3390/cancers12030525.

Abstract

Breast cancer (BC) is the most common cancer in women worldwide. Approximately 70-80% of BCs express estrogen receptors (ER), which predict the response to endocrine therapy (ET), and are therefore hormone receptor-positive (HR+). Endogenous cannabinoids together with cannabinoid receptor 1 and 2 (CB1, CB2) constitute the basis of the endocannabinoid system. Interactions of cannabinoids with hypothalamic-pituitary-gonadal axis hormones are well documented, and two studies found a positive correlation between peak plasma endogenous cannabinoid anandamide with peak plasma 17β-estradiol, luteinizing hormone and follicle-stimulating hormone levels at ovulation in healthy premenopausal women. Do cannabinoids have an effect on HR+ BC? In this paper we review known and possible interactions between cannabinoids and specific HR+ BC treatments. In preclinical studies, CB1 and CB2 agonists (i.e., anandamide, THC) have been shown to inhibit the proliferation of ER positive BC cell lines. There is less evidence for antitumor cannabinoid action in HR+ BC in animal models and there are no clinical trials exploring the effects of cannabinoids on HR+ BC treatment outcomes. Two studies have shown that tamoxifen and several other selective estrogen receptor modulators (SERM) can act as inverse agonists on CB1 and CB2, an interaction with possible clinical consequences. In addition, cannabinoid action could interact with other commonly used endocrine and targeted therapies used in the treatment of HR+ BC.

摘要

乳腺癌(BC)是全球女性中最常见的癌症。大约70-80%的乳腺癌表达雌激素受体(ER),这可预测对内分泌治疗(ET)的反应,因此是激素受体阳性(HR+)。内源性大麻素与大麻素受体1和2(CB1、CB2)共同构成内源性大麻素系统的基础。大麻素与下丘脑-垂体-性腺轴激素之间的相互作用已有充分记录,两项研究发现,健康绝经前女性排卵时血浆内源性大麻素花生四烯乙醇胺峰值与血浆17β-雌二醇、促黄体生成素和促卵泡生成素水平峰值之间呈正相关。大麻素对HR+乳腺癌有影响吗?在本文中,我们综述了大麻素与特定HR+乳腺癌治疗之间已知的和可能的相互作用。在临床前研究中,CB1和CB2激动剂(即花生四烯乙醇胺、四氢大麻酚)已被证明可抑制ER阳性乳腺癌细胞系的增殖。在动物模型中,关于大麻素在HR+乳腺癌中的抗肿瘤作用的证据较少,并且没有临床试验探索大麻素对HR+乳腺癌治疗结果的影响。两项研究表明,他莫昔芬和其他几种选择性雌激素受体调节剂(SERM)可作为CB1和CB2的反向激动剂,这种相互作用可能具有临床意义。此外,大麻素的作用可能与用于治疗HR+乳腺癌的其他常用内分泌和靶向治疗相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9d1/7139952/ef2f3db48d0f/cancers-12-00525-g001.jpg

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