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Development of long-lasting stapled peptides targeting BIG3-PHB2 interaction in breast cancer cells
- In: Poster Presentation
- At: Stockholm (Sweden) (2017)
- Type: Poster
- Poster code: P-A-033-Tuesday
- By: OTAKA, Akira (Insutitute of Biomedical Sciences, Tokushima University, Japan, Tokushima, Japan)
- Co-author(s): Akira Otaka: Insutitute of Biomedical Sciences, Tokushima University, Tokushima, Japan
Keisuke Aihara: Insutitute of Biomedical Sciences, Tokushima University, Tokushima, Japan
Tetsuro Yoshimaru: Institute for Genome Research, Tokushima University, Tokushima, Japan
Akira Shigenaga: Insutitute of Biomedical Sciences, Tokushima University, Tokushima, Japan
Toyomasa Katagiri: Institute for Genome Research, Tokushima University, Tokushima, Japan - Abstract:
Backgrounds
A novel estrogen signaling regulator: brefeldin A-inhibited guanine nucleotide-exchange protein 3 (BIG3), which is overexpressed in a majority of breast cancers. BIG3 captures prohibitin 2 (PHB2) in the cytoplasm of cancer cells and inhibits the suppression of ERα signaling pathways. Based on these findings, ERα activity-regulator.. The access to the whole abstract and if available the presentation file is available to FIP members and to congress participants of that specific congress.
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Last update 4 September 2025