Cancer-associated fibroblasts do not respond to combined irradiation and kinase inhibitor treatment

被引:17
作者
Affolter, Annette [1 ]
Schmidtmann, Irene [2 ]
Mann, Wolf J.
Brieger, Juergen
机构
[1] Johannes Gutenberg Univ Mainz, Dept Otorhinolaryngol Head & Neck Surg, Mol Tumor Biol Lab, Univ Med Ctr, D-55101 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Med Biostat Epidemiol & Informat, Univ Med Ctr, D-55101 Mainz, Germany
关键词
radiation resistance; cancer-associated fibroblasts; mitogen-activated protein kinase pathway; oral squamous cell carcinoma; in vitro tumor model; ACTIVATED PROTEIN-KINASE; RADIATION; STROMA; CELLS;
D O I
10.3892/or.2012.2180
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The emergence of radioresistance is a significant issue in the treatment of squamous cell carcinoma. We recently demonstrated that post-radiogenic extracellular signal-regulated kinase (ERK) signaling might decrease radiosensitivity in this cancer type. To further elucidate how tumor-organizing cell types respond to irradiation and ERK pathway inhibition, we analyzed one oral squamous cell carcinoma and one lung cancer cell line (HNSCCUM-02T, A549), fibroblasts (NIH3T3), primary normal and cancer-associated fibroblasts (CAFs) in vitro. Irradiated cells treated with mitogen-activated protein kinase (MAPK) inhibitor U0126 were screened for pERK levels. Post-radiogenic cellular responses were functionally analyzed by proliferation and colony assays. We found analogous pERK expression, proliferation and survival of tumor and normal fibroblast cells. CAFs did not show any response to treatment. We hypothesized that radiation and MAPK inhibition have no dose-limiting effect on tumor-surrounding normal tissue. As CAFs are considered to influence the radioresponse of the entire tumor, but are not affected by treatment themselves, potential CAF-mediated tumor protection should be considered in further studies.
引用
收藏
页码:785 / 790
页数:6
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