Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/30385
Title: S6K2 promises an important therapeutic potential for cancer
Authors: Sever, Nurettin İlter
Cengiz Şahin, Sevilay
Keywords: cancer cell survival
cancer therapy
S6 kinase 2
B Raf kinase
fibroblast growth factor 2
initiation factor 4E binding protein 1
mammalian target of rapamycin
mitogen activated protein kinase
pf 4708671
protein bcl xl
protein kinase B
protein kinase inhibitor
Raf protein
Ras protein
S6 kinase
unclassified drug
X linked inhibitor of apoptosis
ribosomal protein S6 kinase, 70kD, polypeptide 2
Akt/mTOR signaling
apoptosis
breast cancer
cancer cell
cancer prognosis
cell growth
cell proliferation
cell survival
complex formation
correlation analysis
drug targeting
enzyme activation
enzyme structure
HEK293 cell line
human
malignant neoplasm
MCF-7 cell line
non small cell lung cancer
priority journal
protein expression
protein family
protein function
protein localization
Review
sequence homology
signal transduction
upregulation
chemistry
enzymology
metabolism
molecularly targeted therapy
neoplasm
pathology
procedures
Cell Proliferation
Humans
Molecular Targeted Therapy
Neoplasms
Ribosomal Protein S6 Kinases, 70-kDa
Publisher: Future Medicine Ltd.
Abstract: S6K2, the newer member of S6 Kinase family, is a crucial modulator of Akt/mTOR signaling pathway and is a member of AGC kinase family that regulates cellular growth and survival. S6K1 and S6K2 share high sequence similarity; therefore, S6K2 had been underestimated. However, recent studies displayed distinct functions of S6K2. Activated by both Akt/mTOR and Ras/Raf/Mek/Erk signaling pathways, S6K2 regulates cancer cell survival via different routes. Complexation with antiapoptotic proteins BRAF and PKC? avoids non-small-cell lung cancer cells from apoptosis upon FGF-2 stimulation. Indirect upregulation of the translation of antiapoptotic proteins Bcl-XL and XIAP in HEK293T cells and interference with TNF-induced apoptosis in MCF-7 cells are other routes of cancer cell survival. The aforementioned studies on S6K2 necessitate the development of therapies targeting only on S6K2. Studies targeting S6K2 may help to build important roads for cancer therapy. © 2018 Future Medicine Ltd.
URI: https://hdl.handle.net/11499/30385
https://doi.org/10.2217/fon-2018-0332
ISSN: 1479-6694
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

Show full item record



CORE Recommender

SCOPUSTM   
Citations

4
checked on Nov 16, 2024

WEB OF SCIENCETM
Citations

5
checked on Nov 21, 2024

Page view(s)

36
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.