Journal of International Oncology ›› 2017, Vol. 44 ›› Issue (4): 241-245.doi: 10.3760/cma.j.issn.1673422X.2017.04.001

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Effects of interleukin-17 on human laryngeal carcinoma Hep-2 cells

Feng Shu, Wang Junfu, Chen Xuemei, Luan Junwen, Su Qinghong, Luan Meng, Xu Xiaoqun   

  1. School of Medicine and Life Sciences, University of Ji′nanShandong Academy of Medical Sciences, Ji′nan 250062, China
  • Online:2017-04-08 Published:2017-05-09
  • Contact: Xu Xiaoqun E-mail:xuxiaoqunsd@163.com
  • Supported by:

    Natural Science Foundation of Shandong Province of China (ZR2013HL028, ZR2014HQ030, ZR2014HM085, ZR2015PC018); Special Research Foundation of Large Scientific Instruments on Upgrading and Technological Transformation of Shandong Province of China (2013SJGZ09); Innovation Project of Shandong Academy of Medical Sciences; Project of Medical and Health Technology Development Program of Shandong Province of China (2015-326)

Abstract: Objective To investigate the effects of interleukin-17 (IL-17) on the cell proliferation, apoptosis and migration of human laryngeal carcinoma Hep-2 cells. Methods IL-17 was transiently transfected into Hep-2 cells, and at the same time empty vector group (pEGFP-N1) and normal control group were set up. The efficiency of transfection was evaluated by fluorescence microscope, and the mRNA and protein expressions of IL-17 were detected by reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting. The proliferation of cells was detected by methyl thiazolyl tetrazolium (MTT) method, and the apoptosis was detected by flow cytometry. The migration ability was detected by woundhealing assay and Transwell assay. Results  Hep-2 cells transfected with empty vector pEGFP-N1 and IL-17 showed green fluorescence under the fluorescence microscope. Hep-2 cells expressed IL-17 at both mRNA and protein levels after transfection with IL-17. Compared with the normal control group, the proliferation of IL-17 transfected Hep-2 cells was significantly inhibited after 48 h transfection (0.34±0.03 vs. 0.46±0.04, P=0.006). The apoptotic rate of IL-17 transfected cells was higher than that of normal control group (26.80%±0.80% vs. 2.90%±0.31%, P=0.000). According to the woundhealing assay, compared with the normal control group, the scratch width of IL-17 transfected cells was significantly greater (1.59±0.01 vs. 1.36±0.01, P=0.000). Transwell migration experiment showed that the migration of  IL-17 transfected cells was significantly lower than that of the normal control group (26.33±2.08 vs. 49.33±1.53, P=0.000). Conclusion IL-17 can inhibit the proliferation of human laryngeal carcinoma Hep-2 cells, reduce their migration ability and enhance their apoptosis ability. Therefore, IL-17 may inhibit the occurrence and development of laryngeal carcinoma through a variety of mechanisms.

Key words: Interleukin-17, Laryngeal neoplasms, Cell proliferation, Apoptosis, Cell movement