Analysis of the contribution of nasopharyngeal epithelial cancer cells to the induction of a local inflammatory response - Journal of Cancer Research and Clinical Oncology
- ️Li, Guiyuan
- ️Fri Sep 30 2011
Abstract
Purpose
We investigated the local contribution of nasopharyngeal epithelial cancer cells to the inflammatory process.
Materials and methods
THP-1 monocytes were treated with phorbol 12-myristate 13-acetate to induce the production of differentiated macrophages (D-THP-1), which were subsequently activated by lipopolysaccharide (LPS) (10 ng/ml). The production of pro-inflammatory cytokines in D-THP-1 cells was detected by ELISA and qRT-PCR. The effects of conditioned media harvested from LPS-treated D-THP-1 cells were investigated with regard to cell proliferation (MTT), production of pro-inflammatory cytokines (ELISA) and activation of NF-κB and STAT3 (western blot) in the nasopharyngeal epithelial cancer cell line 5–8F.
Results
LPS induced the production of the pro-inflammatory cytokines TNF-α (875.1 ± 68.31 pg/ml), IL-6 (42.2 ± 5.32 pg/ml), IL-1β (9.6 ± 1.34 pg/ml) and IL-8 (19.3 ± 3.47 pg/ml) in D-THP-1 cells significantly (P < 0.001) with similar results detected at the mRNA level. Exposure of 5–8F cells to conditioned medium from LPS-treated D-THP-1 cells significantly induced production of TNF-α (632.3 ± 71.32 pg/ml), IL-6 (51.3 ± 3.57 pg/ml), IL-1β (7.3 ± 1.31 pg/ml) and IL-8 (20.1 ± 2.36 pg/ml) (P < 0.01) and triggered significant activation of NF-κB and STAT3, which correlated with a concomitant degradation of IκBα and an increase in JAK2 phosphorylation (P < 0.05). Moreover, the LPS-treated D-THP-1 conditioned media promoted the proliferation of 5–8F cells (P < 0.05).
Conclusions
Nasopharyngeal epithelial cancer cells may play a significant role in maintaining and amplifying the inflammation process via activation of NF-κB and STAT3 pathway and through the local production of pro-inflammatory cytokines, which recruit and activate additional immune cells in the nasopharyngeal path and promote tumour progression.
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Acknowledgments
This work is supported by funding from the National Science Foundation of China (81171930, 30871282, 30871365, 30971147, 81071644, 81172189, 81101509), the 111 project (111-2-12), the Program for New Century Excellent Talents in University (NCET-08-0562) and the Hunan Province Natural Sciences Foundation of China (10JJ7003).
Conflict of interest
The authors declare no conflict of interest.
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Authors and Affiliations
Cancer Research Institute, Central South University, 110 Xiang-Ya Road, Changsha, 410078, Hunan, People’s Republic of China
Qianjin Liao, Xiaofang Guo, Xiaoling Li, Pan Chen, Fang Liang, Hailin Tang, Min Deng, Minghua Wu, Jian Ma, Wei Xiong & Guiyuan Li
Cancer Research Institute, University of South China, 28 Changsheng West Road, Hengyang, 421001, Hunan, People’s Republic of China
Qianjin Liao, Hailin Tang & Min Deng
The Third Xiangya Hospital of Central South University, Changsha, 410078, Hunan, People’s Republic of China
Xiayu Li
Changsha Medical University, 9 Kilometres’ Stop at Leifeng Road, Changsha, 410219, Hunan, People’s Republic of China
Xiaofang Guo
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- Qianjin Liao
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- Xiaofang Guo
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- Xiaoling Li
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- Xiayu Li
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- Pan Chen
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- Fang Liang
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- Hailin Tang
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- Min Deng
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- Minghua Wu
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- Jian Ma
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- Wei Xiong
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- Guiyuan Li
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Correspondence to Wei Xiong or Guiyuan Li.
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Q. Liao and X. Guo contributed equally to this work.
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Liao, Q., Guo, X., Li, X. et al. Analysis of the contribution of nasopharyngeal epithelial cancer cells to the induction of a local inflammatory response. J Cancer Res Clin Oncol 138, 57–64 (2012). https://doi.org/10.1007/s00432-011-1066-1
Received: 05 August 2011
Accepted: 02 September 2011
Published: 30 September 2011
Issue Date: January 2012
DOI: https://doi.org/10.1007/s00432-011-1066-1