Glutamate E15 and E171 are Hotspots in p60TRP-Related Cancer
- Authors
- Kutzner, Arne; Heese, Klaus
- Issue Date
- Feb-2016
- Publisher
- Marcel Dekker Inc.
- Keywords
- Ras; Cancer; GPRASP; p60TRP; Ran; BHLHB9; GASP
- Citation
- Cancer Investigation, v.34, no.2, pp 64 - 69
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- Cancer Investigation
- Volume
- 34
- Number
- 2
- Start Page
- 64
- End Page
- 69
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/155188
- DOI
- 10.3109/07357907.2015.1088949
- ISSN
- 0735-7907
1532-4192
- Abstract
- RAS protein is a small G protein linked to multiple G protein-coupled receptor (GPCR) signaling cascades and is responsible for various types of cancer, but to this day, Ras is considered "undruggable." Multiple alternative regulators of G protein signaling (RGS) pathways have become the focus of ongoing efforts to identify new cancer therapeutics. We analyzed human cancer genome datasets and describe p60TRP, a recently identified GPCR-associated sorting protein (GPRASP), and its role in various types of cancer. We found that some regions of p60TRP were more prone to specific mutations, with two hotspots for mutations at E15 and E171.
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Collections - 서울 의생명공학전문대학원 > 서울 의생명과학과 > 1. Journal Articles
- 서울 공과대학 > 서울 정보시스템학과 > 1. Journal Articles

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