Combined inhibition of c-Src and epidermal growth factor receptor abrogates growth and invasion of head and neck squamous cell carcinoma

被引:87
作者
Koppikar, Priya [1 ]
Choi, Seung-Ho [1 ,4 ]
Egloff, Ann Marie [1 ]
Cai, Quan [1 ]
Suzuki, Shinsuke [1 ]
Freilino, Maria [1 ]
Nozawa, Hiroshi [1 ]
Thomas, Sufi M. [1 ]
Gooding, William E. [3 ]
Siegfried, Jill M. [2 ]
Grandis, Jennifer R. [1 ,2 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Otolaryngol, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15261 USA
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Otolaryngol, Seoul, South Korea
关键词
D O I
10.1158/1078-0432.CCR-07-5226
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Increased expression and/or activation of epidermal growth factor receptor (EGFR) is associated with tumor progression and poor prognosis in many cancers, including head and neck squamous cell carcinoma (HNSCC). Src family kinases, including c-Src, mediate a variety of intracellular or extracellular signals that contribute to tumor formation and progression. This study was undertaken to elucidate the role of c-Src in the growth and invasion of HNSCC and to determine the effects of combined targeting of EGFR and Src kinases in HNSCC cell lines. Experimental Design: HNSCC cells were engineered to stably express a dominant-active form of c-Src and investigated in cell growth and invasion assays. The biochemical effects of combined treatment with the Src inhibitor AZD0530, a potent, orally active Src inhibitor with Bcr/Abl activity, and the EGFR kinase inhibitor gefitinib were examined, as well as the consequences of dual Src/EGFR targeting on the growth and invasion of a panel of HNSCC cell lines. Results: HNSCC cells expressing dominant-active c-Src showed increased growth and invasion compared with vector-transfected controls. Combined treatment with AZD0530 and gefitinib resulted in greater inhibition of HNSCC cell growth and invasion compared with either agent alone. Conclusions: These results suggest that increased expression and activation of c-Src promotes HNSCC progression where combined targeting of EGFR and c-Src may be an efficacious treatment approach.
引用
收藏
页码:4284 / 4291
页数:8
相关论文
共 69 条
  • [1] Ang KK, 2002, CANCER RES, V62, P7350
  • [2] The specificities of protein kinase inhibitors: an update
    Bain, J
    McLauchlan, H
    Elliott, M
    Cohen, P
    [J]. BIOCHEMICAL JOURNAL, 2003, 371 : 199 - 204
  • [3] Src promotes destruction of c-Cbl: Implications for oncogenic synergy between Src and growth factor receptors
    Bao, J
    Gur, G
    Yarden, Y
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (05) : 2438 - 2443
  • [4] LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE
    BEHRENS, J
    VAKAET, L
    FRIIS, R
    WINTERHAGER, E
    VANROY, F
    MAREEL, MM
    BIRCHMEIER, W
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 120 (03) : 757 - 766
  • [5] Deregulation of the cytoplasmic tyrosine kinase cSrc in the absence of a truncating mutation at codon 531 in human bladder carcinoma
    Bénistant, C
    Chapuis, H
    Mottet, N
    Noletti, J
    Crapez, E
    Bali, JP
    Roche, S
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (02) : 425 - 430
  • [6] Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck
    Bonner, JA
    Harari, PM
    Giralt, J
    Azarnia, N
    Shin, DM
    Cohen, RB
    Jones, CU
    Sur, R
    Raben, D
    Jassem, J
    Ove, R
    Kies, MS
    Baselga, J
    Youssoufian, H
    Amellal, N
    Rowinsky, EK
    Ang, KK
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) : 567 - 578
  • [7] CD44 interaction with c-Src kinase promotes cortactin-mediated cytoskeleton function and hyaluronic acid-dependent ovarian tumor cell migration
    Bourguignon, LYW
    Zhu, HB
    Shao, LJ
    Chen, YW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (10) : 7327 - 7336
  • [8] The interplay between Src family kinases and receptor tyrosine kinases
    Bromann, PA
    Korkaya, H
    Courtneidge, SA
    [J]. ONCOGENE, 2004, 23 (48) : 7957 - 7968
  • [9] A role for epidermal growth factor receptor, c-Src and focal adhesion kinase in an in vitro model for the progression of colon cancer
    Brunton, VG
    Ozanne, BW
    Paraskeva, C
    Frame, MC
    [J]. ONCOGENE, 1997, 14 (03) : 283 - 293
  • [10] CARPENTER G, 1990, J BIOL CHEM, V265, P7709