Cargando…
The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages
The aim of this research was to investigate the value of autofluorescence imaging of oral cancer across different stages of tumor growth, to assist in detecting tumors. A xenograft mouse model was created with human oral squamous cell carcinoma cell line HSC‐3 being subcutaneously inoculated into nu...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203828/ https://www.ncbi.nlm.nih.gov/pubmed/30386639 http://dx.doi.org/10.1002/cre2.126 |
_version_ | 1783365943129276416 |
---|---|
author | Sumi, Shigeki Umemura, Naoki Adachi, Makoto Ohta, Takahisa Naganawa, Kosuke Kawaki, Harumi Takayama, Eiji Kondoh, Nobuo Sumitomo, Shinichiro |
author_facet | Sumi, Shigeki Umemura, Naoki Adachi, Makoto Ohta, Takahisa Naganawa, Kosuke Kawaki, Harumi Takayama, Eiji Kondoh, Nobuo Sumitomo, Shinichiro |
author_sort | Sumi, Shigeki |
collection | PubMed |
description | The aim of this research was to investigate the value of autofluorescence imaging of oral cancer across different stages of tumor growth, to assist in detecting tumors. A xenograft mouse model was created with human oral squamous cell carcinoma cell line HSC‐3 being subcutaneously inoculated into nude mice. Tumor imaging was performed with an autofluorescence imaging method (Illumiscan®) using the luminance ratio, which was defined as the luminance of the tumor site over the luminance of normal skin tissue normalized to a value of 1.0. This luminance ratio was continuously observed postinoculation. Tumor and normal skin tissues were harvested, and differences in the concentrations of flavin adenine dinucleotide and nicotinamide adenine dinucleotide were examined. The luminance ratio of the tumor sites was 0.85 ± 0.05, and there was no significant change in the ratio over time, even if the tumor proliferated and expanded. Furthermore, flavin adenine dinucleotide and nicotinamide adenine dinucleotide were significantly lower in tumor tissue than in normal skin tissue. A luminance ratio under 0.90 indicates a high possibility of tumor, irrespective of the tumor growth stage. However, this cutoff value was determined using a xenograft mouse model and therefore requires further validation before being used in clinical diagnosis. |
format | Online Article Text |
id | pubmed-6203828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62038282018-11-01 The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages Sumi, Shigeki Umemura, Naoki Adachi, Makoto Ohta, Takahisa Naganawa, Kosuke Kawaki, Harumi Takayama, Eiji Kondoh, Nobuo Sumitomo, Shinichiro Clin Exp Dent Res Original Articles The aim of this research was to investigate the value of autofluorescence imaging of oral cancer across different stages of tumor growth, to assist in detecting tumors. A xenograft mouse model was created with human oral squamous cell carcinoma cell line HSC‐3 being subcutaneously inoculated into nude mice. Tumor imaging was performed with an autofluorescence imaging method (Illumiscan®) using the luminance ratio, which was defined as the luminance of the tumor site over the luminance of normal skin tissue normalized to a value of 1.0. This luminance ratio was continuously observed postinoculation. Tumor and normal skin tissues were harvested, and differences in the concentrations of flavin adenine dinucleotide and nicotinamide adenine dinucleotide were examined. The luminance ratio of the tumor sites was 0.85 ± 0.05, and there was no significant change in the ratio over time, even if the tumor proliferated and expanded. Furthermore, flavin adenine dinucleotide and nicotinamide adenine dinucleotide were significantly lower in tumor tissue than in normal skin tissue. A luminance ratio under 0.90 indicates a high possibility of tumor, irrespective of the tumor growth stage. However, this cutoff value was determined using a xenograft mouse model and therefore requires further validation before being used in clinical diagnosis. John Wiley and Sons Inc. 2018-08-15 /pmc/articles/PMC6203828/ /pubmed/30386639 http://dx.doi.org/10.1002/cre2.126 Text en ©2018 The Authors. Clinical and Experimental Dental Research published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Sumi, Shigeki Umemura, Naoki Adachi, Makoto Ohta, Takahisa Naganawa, Kosuke Kawaki, Harumi Takayama, Eiji Kondoh, Nobuo Sumitomo, Shinichiro The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
title | The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
title_full | The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
title_fullStr | The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
title_full_unstemmed | The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
title_short | The luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
title_sort | luminance ratio of autofluorescence in a xenograft mouse model is stable through tumor growth stages |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6203828/ https://www.ncbi.nlm.nih.gov/pubmed/30386639 http://dx.doi.org/10.1002/cre2.126 |
work_keys_str_mv | AT sumishigeki theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT umemuranaoki theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT adachimakoto theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT ohtatakahisa theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT naganawakosuke theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT kawakiharumi theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT takayamaeiji theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT kondohnobuo theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT sumitomoshinichiro theluminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT sumishigeki luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT umemuranaoki luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT adachimakoto luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT ohtatakahisa luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT naganawakosuke luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT kawakiharumi luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT takayamaeiji luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT kondohnobuo luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages AT sumitomoshinichiro luminanceratioofautofluorescenceinaxenograftmousemodelisstablethroughtumorgrowthstages |