Department of Breast Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Institute of Chemistry, Romanian Academy, Timisoara, Romania.
Front Endocrinol (Lausanne). 2022 Mar 10;13:869562. doi: 10.3389/fendo.2022.869562. eCollection 2022.
Antiestrogen therapy of breast cancer has been a "gold standard" of treatment of estrogen receptor (ER)-positive breast cancer for decades. Resistance to antiestrogen therapy may develop, however, a vulnerability in long-term estrogen deprived (LTED) breast cancer cells was discovered. LTED breast cancer cells may undergo estrogen-induced apoptosis within a week of treatment with estrogen . This phenomenon has been also validated and in the clinic. The molecular ER-mediated mechanism of action of estrogen-induced apoptosis was deciphered, however, the relationship between the structure of estrogenic ligands and the activity of the ER in LTED breast cancer cells remained a mystery until recently. In this review we provide an overview of the structure-activity relationship of various estrogens with different chemical structures and the modulation of estrogen-induced apoptosis in LTED breast cancer cells resistant to antihormone therapy. We provide analysis of evidence gathered over more than a decade of structure-activity relationship studies by our group on the role of the change in the conformation of the estrogen receptor and the biological activities of different classes of estrogens and the receptor as well in LTED breast cancer.
抗雌激素疗法治疗乳腺癌数十年来一直是雌激素受体(ER)阳性乳腺癌的“金标准”治疗方法。然而,抗雌激素治疗可能会产生耐药性,因此发现长期去雌激素剥夺(LTED)的乳腺癌细胞存在脆弱性。LTED 乳腺癌细胞在接受雌激素治疗一周内可能会发生雌激素诱导的细胞凋亡。这一现象已经得到了验证,并在临床上得到了应用。雌激素诱导的细胞凋亡的分子 ER 介导的作用机制已经被揭示,然而,直到最近,雌激素配体的结构与 LTED 乳腺癌细胞中 ER 的活性之间的关系仍然是一个谜。在这篇综述中,我们概述了具有不同化学结构的各种雌激素的结构-活性关系,以及它们对激素治疗耐药的 LTED 乳腺癌细胞中雌激素诱导的细胞凋亡的调节作用。我们分析了我们小组十多年来在 LTED 乳腺癌中关于雌激素受体构象变化以及不同类别的雌激素和受体的生物学活性的作用的结构-活性关系研究中积累的证据。