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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 |
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