Not exact matches
A study in this week's Neuron provides
key evidence that DNA methylation — also known to occur as cancerous cells divide, when tumor suppressor
genes are
silenced — occurs in adult brains and can be triggered by environmental cues.
Hypermethylation of DNA is a
key epigenetic mechanism for the
silencing of many
genes, including those for cell cycle regulation, receptors, DNA repair, and apoptosis (5, 6, 7, 8).
We are focusing on a few
key molecular pathways including; 1) Polycomb - mediated epigenetic
gene silencing in the tumor initiation, maintenance, and invasion, 2) c - Met (receptor tyrosine kinase) signal transduction pathways in stemness and migration of these tumor cells, 3) Novel mitogenic signaling pathways that are specific to GSCs, and 4) Identification of radio - and chemo - sensitizing pathway to maximize therapeutic efficacy.
These two histones thus have a
key role of epigenetic
silencing of tumor suppressor
genes in breast cancer (and likely other cancers), suggesting that they may represent new therapeutic targets.
Epigenetics Dream Team leaders have identified an epigenetic process, known as DNA de-methylation, that inactivates or «
silences»
key genes that might otherwise correct for the «mistakes» that permit cancer to exist and flourish.
Background: Small non-coding RNAs, including miRNAs, and
gene silencing mediated by RNA interference have been described in free - living and parasitic lineages of flatworms, but only few
key factors of the small RNA pathways have been exhaustively investigated in a limited number of species.
Arognaute plays a
key role in the RNA interference (RNAi) pathway that
silences gene expression.
This complex plays a
key role in the RNA interference (RNAi) pathway that
silences gene expression.