The Histone-Lysine N-Methyltransferase (KMT2) Family in Health and Disease. [PDF]
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Androgen receptor reactivation in castration-resistant prostate cancer: mechanisms, epigenetic adaptation, and therapeutic vulnerabilities. [PDF]
Guo J, Wu K, Ma Z, Guo S, Wang F, Lu L.
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FLI1 Expression in Invasive Breast Carcinoma: Clinicopathological Correlations and Prognostic Implications. [PDF]
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<i>N</i>'‑(1-Phenylethylidene)benzohydrazide Cytotoxicity Is Lysine-Specific Demethylase 1 Independent and Linked to Iron-Sulfur Cluster Disruption in Ewing Sarcoma. [PDF]
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Identification and expression profiling of LSD genes reveal their role in developmental and abiotic stress conditions in maize. [PDF]
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Experimental Validation of Genome-Environment Associations in Arabidopsis. [PDF]
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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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Baicalin, a natural LSD1 inhibitor
Bioorganic Chemistry, 2016Baicalin is one of the active ingredients in the skullcap, with a variety of pharmacological effects, such as blood pressure reduction, sedation, liver-protection, gallbladder-protection, anti-bacteria, and anti-inflammation. In our study, baicalin was first characterized as a LSD1 inhibitor with an IC50 of 3.01μM and showed strong LSD1 inhibitory ...
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Modeling LSD1-Mediated Tumor Stagnation
Bulletin of Mathematical Biology, 2021LSD1 (KDMA1) has gained attention in the last decade as a cancer biomarker and drug target. In particular, recent work suggests that LSD1 inhibition alone reduces tumor growth, increases T cell tumor infiltration, and complements PD1/PDL1 checkpoint inhibitor therapy.
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The histone lysine-specific demethylase 1 (LSD1) is a new and important player in the regulation of brown fat identity and function. In a recent Cell Reports article, Duteil et al. show that LSD1 exerts its effects via regulation of specific histone marks as well as through association with co-repressor complexes.
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