Cargando…
Targeting Histone Methyltransferase DOT1L by a Novel Psammaplin A Analog Inhibits Growth and Metastasis of Triple-Negative Breast Cancer
Triple-negative breast cancer (TNBC) is the most intractable cancer in women with a high risk of metastasis. While hyper-methylation of histone H3 catalyzed by disruptor of telomeric silencing 1-like (DOT1L), a specific methyltransferase for histone H3 at lysine residue 79 (H3K79), is reported as a...
Autores principales: | Byun, Woong Sub, Kim, Won Kyung, Han, Hae Ju, Chung, Hwa-Jin, Jang, Kyungkuk, Kim, Han Sun, Kim, Sunghwa, Kim, Donghwa, Bae, Eun Seo, Park, Sunghyouk, Lee, Jeeyeon, Park, Hyeung-geun, Lee, Sang Kook |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838941/ https://www.ncbi.nlm.nih.gov/pubmed/31720371 http://dx.doi.org/10.1016/j.omto.2019.09.005 |
Ejemplares similares
-
Inhibition of DOT1L by Half-Selenopsammaplin A Analogs Suppresses Tumor Growth and EMT-Mediated Metastasis in Triple-Negative Breast Cancer
por: Byun, Woong Sub, et al.
Publicado: (2020) -
Synthesis of the Marine Bromotyrosine Psammaplin F and Crystal Structure of a Psammaplin A Analogue
por: Yang, Qianjiao, et al.
Publicado: (2010) -
Cytotoxicity of psammaplin A from a two-sponge association may correlate with the inhibition of DNA replication
por: Jiang, Yahong, et al.
Publicado: (2004) -
Thioester derivatives of the natural product psammaplin A as potent histone deacetylase inhibitors
por: Baud, Matthias G J, et al.
Publicado: (2013) -
Synthesis and Preliminary Biological Evaluation of Two Fluoroolefin Analogs of Largazole Inspired by the Structural Similarity of the Side Chain Unit in Psammaplin A
por: Zhang, Bingbing, et al.
Publicado: (2019)