Aromatase inhibitors for the treatment of breast cancer: An overview (2019-2023)

被引:7
作者
Bhatia, Neha [1 ]
Thareja, Suresh [1 ]
机构
[1] Cent Univ Punjab, Sch Hlth Sci, Dept Pharmaceut Sci & Nat Prod, Bathinda 151401, Punjab, India
关键词
Aromatase; Aromatase inhibitors; Breast cancer; Estrogen; ER; -positive; CYTOCHROME-P450; GENE-EXPRESSION; ESTROGEN-RECEPTOR; POSTMENOPAUSAL PATIENTS; CYP19; EXPRESSION; EXEMESTANE; PROMOTERS; DISCOVERY; CELLS; CARDIOTOXICITY; IDENTIFICATION;
D O I
10.1016/j.bioorg.2024.107607
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aromatase inhibition is considered a legitimate approach for the treatment of ER-positive (ER+) breast cancer as it accounts for more than 70% of breast cancer cases. Aromatase inhibitor therapy has been demonstrated to be highly effective in decreasing tumour size, increasing survival rates, and lowering the chance of cancer recurrence. The present review deliberates the pathophysiology and the role of aromatase in estrogen biosynthesis. Estrogen biosynthesis, various androgens, and their function in the human body have also been discussed. The salient aspects of the aromatase active site, its mode of action, and AIs, along with their intended interactions with presently FDA-approved inhibitors, have been briefly discussed. It has been detailed how different reported AIs were designed, their SAR investigations, in silico analysis, and biological evaluations. Various AIs from multiple origins, such as synthetic and semi-synthetic, have also been discussed.
引用
收藏
页数:43
相关论文
共 180 条
[41]   Interference of endocrine disrupting chemicals with aromatase CYP19 expression or activity, and consequences for reproduction of teleost fish [J].
Cheshenko, Ksenia ;
Pakdel, Farzad ;
Segner, Helmut ;
Kah, Olivier ;
Eggen, Rik I. L. .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2008, 155 (01) :31-62
[42]  
Chumsri S, 2013, ESTROGEN ACTION, SELECTIVE ESTROGEN RECEPTOR MODULATORS AND WOMEN'S HEALTH: PROGRESS AND PROMISE, P201
[43]   Aromatase, aromatase inhibitors, and breast cancer [J].
Chumsri, Saranya ;
Howes, Timothy ;
Bao, Ting ;
Sabnis, Gauri ;
Brodie, Angela .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2011, 125 (1-2) :13-22
[44]   The ins and outs of cytochrome P450s [J].
Cojocaru, Vlad ;
Winn, Peter J. ;
Wade, Rebecca C. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2007, 1770 (03) :390-401
[45]   A PEROXIDE MODEL REACTION FOR PLACENTAL AROMATASE [J].
COLE, PA ;
ROBINSON, CH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (04) :1284-1285
[46]   Estrogen synthesis and signaling pathways during aging: from periphery to brain [J].
Cui, Jie ;
Shen, Yong ;
Li, Rena .
TRENDS IN MOLECULAR MEDICINE, 2013, 19 (03) :197-209
[47]   Chemical Constituents from Artemisia annua and Vitex agnus-castus as New Aromatase Inhibitors: In-vitro and In-silico Studies [J].
Dawood, Hend M. ;
Shawky, Eman ;
Hammoda, Hala M. ;
Metwally, Aly M. ;
Ibrahim, Reham S. .
JOURNAL OF THE MEXICAN CHEMICAL SOCIETY, 2020, 64 (04) :316-326
[48]   Ferrozoles: Ferrocenyl derivatives of letrozole with dual effects as potent aromatase inhibitors and cytostatic agents [J].
de Grenu, Borja Diaz ;
Fernandez-Aroca, Diego M. ;
Organero, Juan A. ;
Dura, Gema ;
Jalon, Felix Angel ;
Sanchez-Prieto, Ricardo ;
Ruiz-Hidalgo, M. Jose ;
Rodriguez, Ana Maria ;
Santos, Lucia ;
Albasanz, Jose L. ;
Manzano, Blanca R. .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2023, 28 (06) :531-547
[49]  
Demiraran S., 2023, J. Mol. Struct.
[50]   Novel Promoter 1.8 and Promoter Usage in the CYP19 (Aromatase) Gene [J].
Demura, Masashi ;
Reierstad, Scott ;
Innes, Joy E. ;
Bulun, Serdar E. .
REPRODUCTIVE SCIENCES, 2008, 15 (10) :1044-1053