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Nickel chloride administration prevents the growth of oral squamous cell carcinoma
The effect of NiCl(2) on oral squamous cell carcinoma-derived cell line HSC3 was examined. Incubation with 1 mM NiCl(2) significantly reduced the expression of MMPs at mRNA and protein levels. The in vivo orthotopic implantation model was established by injecting highly metastatic subcell line HSC3-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963632/ https://www.ncbi.nlm.nih.gov/pubmed/29844876 http://dx.doi.org/10.18632/oncotarget.25313 |
Sumario: | The effect of NiCl(2) on oral squamous cell carcinoma-derived cell line HSC3 was examined. Incubation with 1 mM NiCl(2) significantly reduced the expression of MMPs at mRNA and protein levels. The in vivo orthotopic implantation model was established by injecting highly metastatic subcell line HSC3-M3 to nude mouse tongue. After 1 week of injection, mice were fed with or without 1 mM NiCl(2)-containing water for two to three weeks. Immunohistochamical examination revealed that MMP9 expression was drastically reduced in NiCl2-fed mice. By CT images, cancer mass was observed as a translucent area in control mice. In NiCl(2)-fed mice, much highly translucent area was observed within the translucent area. Histologically, this area corresponded to the necrotic area in the tumor mass. Real-time PCR analysis revealed the reduced expression of angiogenic factors such as IL-8 and VEGF mRNA in NiCl(2)-fed mice. To further examine the effect of NiCl(2) on metastasis, human β-globin gene expression in regional lymphnodes was compared. The β-globin gene was totaly absent in NiCl(2)-fed mice. Moreover, various cancer metastasis-related genes were inhibited in NiCl(2)-fed mice by PCR array analysis. The results indicated that NiCl(2) might be a promising new anti-cancer therapeutics for the oral cancer treatment. |
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