Effectiveness of combined treatment using X-rays and a phosphoinositide 3-kinase inhibitor, ZSTK474, on proliferation of HeLa cells in vitro and in vivo

被引:8
作者
Anzai, Kazunori [2 ,3 ]
Sekine-Suzuki, Emiko [2 ]
Ueno, Megumi [2 ]
Okamura, Mutsumi [1 ]
Yoshimi, Hisashi [1 ,4 ]
Dan, Shingo [1 ]
Yaguchi, Shin-ichi [1 ,4 ]
Enami, Jumpei [4 ]
Yamori, Takao [1 ]
Okayasu, Ryuichi [2 ]
机构
[1] Japanese Fdn Canc Res, Ctr Canc Chemotherapy, Div Mol Pharmacol, Tokyo 170, Japan
[2] Natl Inst Radiol Sci, Heavy Ion Radiobiol Res Grp, Chiba 260, Japan
[3] Nihon Pharmaceut Univ, Saitama, Japan
[4] Zenyaku Kogyo Co, Cent Res Lab, Tokyo, Japan
基金
日本学术振兴会;
关键词
ANTITUMOR-ACTIVITY; CANCER-CELLS; RADIATION; KINASE; RADIORESISTANCE; GROWTH; PHOSPHORYLATION; IDENTIFICATION; IRRADIATION; ACTIVATION;
D O I
10.1111/j.1349-7006.2011.01916.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ZSTK474 is a novel orally applicable phosphoinositide 3-kinase-specific inhibitor that strongly inhibits cancer cell proliferation. To further explore the antitumor effect of ZSTK474 for future clinical usage, we studied its combined effects with radiation. The proliferation of HeLa cells was inhibited by treatment with X-rays alone or ZSTK474 alone. Combination treatment using X-rays then ZSTK474 given orally for 8 days, starting 24 h post-irradiation, significantly enhanced cell growth inhibition. The combined effect was also observed for clonogenic survival with continuous ZSTK474 treatment. Western blot analysis showed enhanced phosphorylation of Akt and GSK-3 beta by X-irradiation, whereas phosphorylation was inhibited by ZSTK474 treatment alone. Treatment with ZSTK474 after X-irradiation also inhibited phosphorylation, and remarkably inhibited xenograft tumor growth. Combined treatment with X-rays and ZSTK474 has greater therapeutic potential than radiation or drug therapy alone, both in vitro and in vivo. (Cancer Sci 2011; 102: 1176-1180).
引用
收藏
页码:1176 / 1180
页数:5
相关论文
共 24 条
[1]   Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G0/G1 arrest [J].
Dan, Shingo ;
Yoshimi, Hisashi ;
Okamura, Mutsumi ;
Mukai, Yumiko ;
Yamori, Takao .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 379 (01) :104-109
[2]   A dual phosphoinositide-3-kinase α/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma [J].
Fan, Qi-Wen ;
Cheng, Christine K. ;
Nicolaides, Theodore P. ;
Hackett, Christopher S. ;
Knight, Zachary A. ;
Shokat, Kevan M. ;
Weiss, William A. .
CANCER RESEARCH, 2007, 67 (17) :7960-7965
[3]   The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer [J].
Folkes, Adrian J. ;
Ahmadi, Khatereh ;
Alderton, Wendy K. ;
Alix, Sonia ;
Baker, Stewart J. ;
Box, Gary ;
Chuckowree, Irina S. ;
Clarke, Paul A. ;
Depledge, Paul ;
Eccles, Suzanne A. ;
Friedman, Lori S. ;
Hayes, Angela ;
Hancox, Timothy C. ;
Kugendradas, Arumugam ;
Lensun, Letitia ;
Moore, Pauline ;
Olivero, Alan G. ;
Pang, Jodie ;
Patel, Sonal ;
Pergl-Wilson, Giles H. ;
Raynaud, Florence I. ;
Robson, Anthony ;
Saghir, Nahid ;
Salphati, Laurent ;
Sohal, Sukhjit ;
Ultsch, Mark H. ;
Valenti, Melanie ;
Wallweber, Heidi J. A. ;
Wan, Nan Chi ;
Wiesmann, Christian ;
Workman, Paul ;
Zhyvoloup, Alexander ;
Zvelebil, Marketa J. ;
Shuttleworth, Stephen J. .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (18) :5522-5532
[4]   A vascular targeted pan phosphoinositide 3-kinase inhibitor prodrug, SF1126, with antitumor and antiangiogenic activity [J].
Garlich, Joseph R. ;
De, Pradip ;
Dey, Nandini ;
Su, Jing Dong ;
Peng, Xiaodong ;
Miller, Antoinette ;
Murali, Ravoori ;
Lu, Yiling ;
Mills, Gordon B. ;
Kundra, Vikas ;
Shu, H-K. ;
Peng, Qiong ;
Durden, Donald L. .
CANCER RESEARCH, 2008, 68 (01) :206-215
[5]  
Giaccia, 2006, RADIOBIOLOGY RADIOLO, VVol 6
[6]   Radiation sensitization of human cancer cells in vivo by inhibiting the activity of PI3k using LY294002 [J].
Gupta, AK ;
Cerniglia, GJ ;
Mick, R ;
Ahmed, MS ;
Bakanauskas, VJ ;
Muschel, RJ ;
McKenna, WG .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2003, 56 (03) :846-853
[7]  
Hosoi Y, 1998, INT J CANCER, V78, P642, DOI 10.1002/(SICI)1097-0215(19981123)78:5<642::AID-IJC19>3.0.CO
[8]  
2-3
[9]  
Ihle NT, 2004, MOL CANCER THER, V3, P763
[10]   ZSTK474 is an ATP-competitive inhibitor of class I phosphatidylinositol 3 kinase isoforms [J].
Kong, Dexin ;
Yamori, Takao .
CANCER SCIENCE, 2007, 98 (10) :1638-1642