Cargando…
Cell penetrating thiazole peptides inhibit c-MYC expression via site-specific targeting of c-MYC G-quadruplex
The structural differences among different G-quadruplexes provide an opportunity for site-specific targeting of a particular G-quadruplex structure. However, majority of G-quadruplex ligands described thus far show little selectivity among different G-quadruplexes. In this work, we delineate the des...
Autores principales: | Dutta, Debasish, Debnath, Manish, Müller, Diana, Paul, Rakesh, Das, Tania, Bessi, Irene, Schwalbe, Harald, Dash, Jyotirmayee |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009605/ https://www.ncbi.nlm.nih.gov/pubmed/29762718 http://dx.doi.org/10.1093/nar/gky385 |
Ejemplares similares
-
A Nucleus-Imaging Probe That Selectively Stabilizes a Minor Conformation of c-MYC G-quadruplex and Down-regulates c-MYC Transcription in Human Cancer Cells
por: Panda, Deepanjan, et al.
Publicado: (2015) -
Visualization of ligand-induced c-MYC duplex–quadruplex transition and direct exploration of the altered c-MYC DNA-protein interactions in cells
por: Yuan, Jia-Hao, et al.
Publicado: (2022) -
Selective recognition of c-MYC Pu22 G-quadruplex by a fluorescent probe
por: Zhai, Qianqian, et al.
Publicado: (2019) -
Site-specific amino acid substitution in dodecameric peptides determines the stability and unfolding of c-MYC quadruplex promoting apoptosis in cancer cells
por: Sengupta, Pallabi, et al.
Publicado: (2018) -
Rational design of small-molecules to recognize G-quadruplexes of c-MYC promoter and telomere and the evaluation of their in vivo antitumor activity against breast cancer
por: Long, Wei, et al.
Publicado: (2022)