Radioresistant head and neck squamous cell carcinoma cells: Intracellular signaling, putative biomarkers for tumor recurrences and possible therapeutic targets

被引:52
作者
Skvortsov, Sergej [1 ]
Jimenez, Connie R. [3 ]
Knol, Jaco C. [3 ]
Eichberger, Paul [1 ]
Schiestl, Bernhard [1 ]
Debbage, Paul [2 ]
Skvortsova, Ira [1 ]
Lukas, Peter [1 ]
机构
[1] Innsbruck Med Univ, Dept Therapeut Radiol & Oncol, A-6020 Innsbruck, Austria
[2] Innsbruck Med Univ, Dept Anat Histol & Embryol, A-6020 Innsbruck, Austria
[3] VUmc Canc Ctr Amsterdam, Dept Med Oncol, Amsterdam, Netherlands
关键词
Head and neck squamous cell carcinoma; Radiation resistance; Rac1; Cell migration; Metastasis; Proteomics; DOWN-REGULATION; CANCER; METASTASIS; EXPRESSION; CHEMOTHERAPY; RADIOTHERAPY; ONCOLOGY; RAC1;
D O I
10.1016/j.radonc.2011.05.067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Treatment of local and distant head and neck cancer recurrences after radiotherapy remains an unsolved problem. In order to identify potential targets for use in effective therapy of recurrent tumors, we have investigated protein patterns in radioresistant (FaDu-IRR and SCC25-IRR, "IRR cells") as compared to parental (FaDu and SCC25) head and neck carcinoma cells. Methods and materials: Radiation resistant IRR cells were derived from parental cells after repeated exposure to ionizing radiation 10 times every two weeks at a single dose of 10 Gy, resulting in a total dose of 100 Gy. Protein profiling in parental and IRR cells was carried out using two-dimensional differential gel electrophoresis (2D-DIGE) followed by MALDI-TOF/TOF mass spectrometry. Cell viability, cell migration assays and Western blot analysis were used to confirm results obtained using the proteome approach. Results: Forty-five proteins that were similarly modulated in FaDu-IRR and SCC25-IRR cells compared to parental cells were selected to analyze their common targets. It was found that these either up- or down-regulated proteins are closely related to the enhancement of cell migration which is regulated by Rac1 protein. Further investigations confirmed that Rac1 is up-regulated in IRR cells, and inhibiting its action reduces the migratory abilities of these cells. Additionally, the Rac1 inhibitor exerts cytostatic effects in HNSCC cells, mostly in migratory cells. Conclusions: Based on these results, we conclude that radioresistant HNSCC cells possess enhanced metastatic abilities that are regulated by a network of migration-related proteins. Rac1 protein may be considered as a putative biomarker of HNSCC radiation resistance, and as a potential therapeutic target for treating local and distant HNSCC recurrences. (C) 2011 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 101 (2011) 177-182
引用
收藏
页码:177 / 182
页数:6
相关论文
共 26 条
[1]   Moesin-dependent cytoskeleton remodelling is associated with an anaplastic phenotype of pancreatic cancer [J].
Abiatari, Ivane ;
Esposito, Irene ;
De Oliveira, Tiago ;
Felix, Klaus ;
Xin, Hong ;
Penzel, Roland ;
Giese, Thomas ;
Friess, Helmut ;
Kleeff, Joerg .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2010, 14 (05) :1166-1179
[2]   Prognostic factors and long-term survivorship in patients with recurrent or metastatic carcinoma of the head and neck - An analysis of two Eastern Cooperative Oncology Group randomized trials [J].
Argiris, A ;
Li, Y ;
Forastiere, A .
CANCER, 2004, 101 (10) :2222-2229
[3]   Evidence-based radiation oncology in head and neck squamous cell carcinoma [J].
Corvo, Renzo .
RADIOTHERAPY AND ONCOLOGY, 2007, 85 (01) :156-170
[4]   Interaction of the tumor metastasis suppressor nonmetastatic protein 23 homologue h1 and estrogen receptor α alters estrogen-responsive gene expression [J].
Curtis, Carol D. ;
Likhite, Varsha S. ;
McLeod, Ian X. ;
Yates, John R. ;
Nardulli, Ann M. .
CANCER RESEARCH, 2007, 67 (21) :10600-10607
[5]   Intensity-modulated radiotherapy for recurrent and second primary head and neck cancer in previously irradiated territory [J].
Duprez, Frederic ;
Madani, Indira ;
Bonte, Katrien ;
Boterberg, Tom ;
Vakaet, Luc ;
Derie, Cristina ;
De Gersem, Werner ;
De Neve, Wilfried .
RADIOTHERAPY AND ONCOLOGY, 2009, 93 (03) :563-569
[6]   Moesin orchestrates cortical polarity of melanoma tumour cells to initiate 3D invasion [J].
Estecha, Ana ;
Sanchez-Martin, Lorena ;
Puig-Kroeger, Amaya ;
Bartolome, Ruben A. ;
Teixido, Joaquin ;
Samaniego, Rafael ;
Sanchez-Mateos, Paloma .
JOURNAL OF CELL SCIENCE, 2009, 122 (19) :3492-3501
[7]   Targeted Therapies in Squamous Cell Carcinoma of the Head and Neck [J].
Gold, Kathryn A. ;
Lee, Ho-Young ;
Kim, Edward S. .
CANCER, 2009, 115 (05) :922-935
[8]  
Hernández E, 2010, P R HEALTH SCI J, V29, P348
[9]   Metastasis suppression: The evolving role of metastasis suppressor genes for regulating cancer cell growth at the secondary site [J].
Kauffman, EC ;
Robinson, VL ;
Stadler, WM ;
Sokoloff, MH ;
Rinker-Schaeffer, CW .
JOURNAL OF UROLOGY, 2003, 169 (03) :1122-1133
[10]   Down-regulation of survivin by oxaliplatin diminishes radioresistance of head and neck squamous carcinoma cells [J].
Khan, Zakir ;
Khan, Noor ;
Tiwari, Ram P. ;
Patro, Ishan K. ;
Prasad, G. B. K. S. ;
Bisen, Prakash S. .
RADIOTHERAPY AND ONCOLOGY, 2010, 96 (02) :267-273