Medicinal chemistry insights in the discovery of novel LSD1 inhibitors

被引:45
作者
Wang, Xueshun [1 ]
Huang, Boshi [1 ]
Suzuki, Takayoshi [2 ,3 ]
Liu, Xinyong [1 ]
Zhan, Peng [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Dept Med Chem, Key Lab Chem Biol,Minist Educ, Jinan 250012, Shandong, Peoples R China
[2] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Sakyo Ku, Kyoto 6060823, Japan
[3] Japan Sci & Technol Agcy JST, CREST, Kawaguchi, Saitama 3320012, Japan
基金
奥地利科学基金会; 中国国家自然科学基金; 日本学术振兴会;
关键词
drug design; epigenomics; histone modification; LSD1; medicinal chemistry; DEMETHYLASE; 1; LSD1; LYSINE-SPECIFIC DEMETHYLASE-1; DRUG DISCOVERY; CYCLOPROPYLAMINE DERIVATIVES; REVERSIBLE INHIBITORS; THERAPEUTIC STRATEGY; BIOLOGICAL-ACTIVITY; NATURAL-PRODUCTS; HDAC INHIBITORS; CANCER-CELLS;
D O I
10.2217/epi.15.86
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
LSD1 is an epigenetic modulator associated with transcriptional regulation of genes involved in a broad spectrum of key cellular processes, and its activity is often altered under pathological conditions. LSD1 inhibitors are considered to be candidates for therapy of cancer, viral diseases and neurodegeneration. Many LSD1 inhibitors with various scaffolds have been disclosed, and a few potent molecules are in different stages of clinical development. In this review, we summarize recent biological findings on the roles of LSD1 and the current understanding of the clinical significance of LSD1, and focus on the medicinal chemistry strategies used in the design and development of LSD1 inhibitors as drug-like epigenetic modulators since 2012, including a brief consideration of structure-activity relationships.
引用
收藏
页码:1379 / 1396
页数:18
相关论文
共 99 条
[1]
Abdulla Arian, 2013, J Biochem Pharmacol Res, V1, P56
[2]
Regulation of Lipogenic Gene Expression by Lysine-specific Histone Demethylase-1 (LSD1) [J].
Abdulla, Arian ;
Zhang, Yi ;
Hsu, Fu-Ning ;
Xiaoli, Alus M. ;
Zhao, Xiaoping ;
Yang, Ellen S. T. ;
Ji, Jun-Yuan ;
Yang, Fajun .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (43) :29937-29947
[3]
The histone LSD1 demethylase in stemness and cancer transcription programs [J].
Amente, Stefano ;
Lania, Luigi ;
Majello, Barbara .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2013, 1829 (10) :981-986
[4]
A dihydro-pyrido-indole potently inhibits HSV-1 infection by interfering the viral immediate early transcriptional events [J].
Bag, Paromita ;
Ojha, Durbadal ;
Mukherjee, Hemanta ;
Halder, Umesh C. ;
Mondal, Supriya ;
Biswas, Aruna ;
Sharon, Ashoke ;
Van Kaer, Luc ;
Chakrabarty, Sekhar ;
Das, Gobardhan ;
Mitra, Debashis ;
Chattopadhyay, Debprasad .
ANTIVIRAL RESEARCH, 2014, 105 :126-134
[5]
Covalent inhibitors in drug discovery: from accidental discoveries to avoided liabilities and designed therapies [J].
Bauer, Renato A. .
DRUG DISCOVERY TODAY, 2015, 20 (09) :1061-1073
[6]
Integration of ERα-PELP1-HER2 signaling by LSD1 (KDM1A/AOF2) offers combinatorial therapeutic opportunities to circumventing hormone resistance in breast cancer [J].
Bennani-Baiti, Idriss M. .
BREAST CANCER RESEARCH, 2012, 14 (05)
[7]
Lysine-Specific Demethylase 1 Has Dual Functions as a Major Regulator of Androgen Receptor Transcriptional Activity [J].
Cai, Changmeng ;
He, Housheng Hansen ;
Gao, Shuai ;
Chen, Sen ;
Yu, Ziyang ;
Gao, Yanfei ;
Chen, Shaoyong ;
Chen, Mei Wei ;
Zhang, Jesse ;
Ahmed, Musaddeque ;
Wang, Yang ;
Metzger, Eric ;
Schuele, Roland ;
Liu, X. Shirley ;
Brown, Myles ;
Balk, Steven P. .
CELL REPORTS, 2014, 9 (05) :1618-1627
[8]
Expression of Lysine-specific demethylase 1 in human epithelial ovarian cancer [J].
Chen, Cong ;
Ge, Jing ;
Lu, Qibin ;
Ping, Guoqiang ;
Yang, Chunqing ;
Fang, Xuefeng .
JOURNAL OF OVARIAN RESEARCH, 2015, 8
[9]
Chen LJ, 2014, INT J CLIN EXP PATHO, V7, P8929
[10]
Targeting the PELP1-KDM1 axis as a potential therapeutic strategy for breast cancer [J].
Cortez, Valerie ;
Mann, Monica ;
Tekmal, Seshidhar ;
Suzuki, Takayoshi ;
Miyata, Naoki ;
Rodriguez-Aguayo, Cristian ;
Lopez-Berestein, Gabriel ;
Sood, Anil K. ;
Vadlamudi, Ratna K. .
BREAST CANCER RESEARCH, 2012, 14 (04)