UM171 glues asymmetric CRL3-HDAC1/2 assembly to degrade CoREST corepressors. [PDF]
Yeo MJR+28 more
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LMK235 ameliorates inflammation and fibrosis after myocardial infarction by inhibiting LSD1-related pathway. [PDF]
Lv F, Xie L, Li L, Lin J.
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Crosstalk Between Abiotic and Biotic Stresses Responses and the Role of Chloroplast Retrograde Signaling in the Cross-Tolerance Phenomena in Plants. [PDF]
Kamran M, Burdiak P, Karpiński S.
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Emerging Insights into Sall4's Role in Cardiac Regenerative Medicine. [PDF]
Yang J.
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LSD1 inhibits the invasion and migration of breast cancer through exosomes. [PDF]
Zhang N+7 more
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Lysine and arginine methylation of transcription factors. [PDF]
Giaimo BD, Ferrante F, Borggrefe T.
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Histone lysine methylation modifiers controlled by protein stability. [PDF]
Park S, Cho JH, Kim JH, Kim JA.
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Reversible Lysine Specific Demethylase 1 (LSD1) Inhibitors: A Promising Wrench to Impair LSD1
Journal of Medicinal Chemistry, 2021As a flavin adenine dinucleotide (FAD)-dependent monoamine oxidase, lysine specific demethylase 1 (LSD1/KDM1A) functions as a transcription coactivator or corepressor to regulate the methylation of histone 3 lysine 4 and 9 (H3K4/9), and it has emerged as a promising epigenetic target for anticancer treatment. To date, numerous inhibitors targeting LSD1
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A comprehensive comparative study on LSD1 in different cancers and tumor specific LSD1 inhibitors
European Journal of Medicinal Chemistry, 2022LSD1 was significantly over-expressed in several cancer types, and its aberrant overexpression was revealed to play a crucial role in the initiation and progression of cancer. Several LSD1 inhibitors that were discovered and developed so far were found to be effective in attenuating tumor growth in both in vivo and in vitro studies.
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