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Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models
The purpose of this study was to delineate the various factors that affect the growth characteristics of human cancer xenografts in nude mice and to reveal the relationship between the growth characteristics and radiosensitivity. We retrospectively analyzed 390 xenografts comprising nine different h...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Association for Laboratory Animal Science
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206224/ https://www.ncbi.nlm.nih.gov/pubmed/28053611 http://dx.doi.org/10.5625/lar.2016.32.4.187 |
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author | Lee, Ji Young Kim, Mi-Sook Kim, Eun Ho Chung, Namhyun Jeong, Youn Kyoung |
author_facet | Lee, Ji Young Kim, Mi-Sook Kim, Eun Ho Chung, Namhyun Jeong, Youn Kyoung |
author_sort | Lee, Ji Young |
collection | PubMed |
description | The purpose of this study was to delineate the various factors that affect the growth characteristics of human cancer xenografts in nude mice and to reveal the relationship between the growth characteristics and radiosensitivity. We retrospectively analyzed 390 xenografts comprising nine different human cancer lines grown in nude mice used in our institute between 2009 and 2015. Tumor growth rate (TGR) was calculated using exponential growth equations. The relationship between the TGR of xenografts and the proliferation of the cells in vitro was examined. Additionally, we examined the correlations between the surviving fractions of cells after 2 Gy irradiation in vitro and the response of the xenograft to radiation. The TGR of xenografts was positively related to the proliferation of the cells in vitro (r(P)=0.9714, p<0.0001), whereas it was independent of the histological type of the xenografts. Radiation-induced suppression of the growth rate (T/C%) of xenografts was positively related to the radiosensitivity of the cells in vitro (SF(2); r(P)=0.8684, p=0.0284) and TGR (r(P)=0.7623, p=0.0780). The proliferation of human cancer cells in vitro and the growth rate of xenografts were positively related. The radiosensitivity of cancer cells, as judged from the SF(2) values in vitro, and the radiation-induced suppression of xenograft growth were positively related. In conclusion, the growth rate of human xenografts was independent of histological type and origin of the cancer cells, and was positively related to the proliferation of the cancer cells in vitro. |
format | Online Article Text |
id | pubmed-5206224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52062242017-01-04 Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models Lee, Ji Young Kim, Mi-Sook Kim, Eun Ho Chung, Namhyun Jeong, Youn Kyoung Lab Anim Res Original Article The purpose of this study was to delineate the various factors that affect the growth characteristics of human cancer xenografts in nude mice and to reveal the relationship between the growth characteristics and radiosensitivity. We retrospectively analyzed 390 xenografts comprising nine different human cancer lines grown in nude mice used in our institute between 2009 and 2015. Tumor growth rate (TGR) was calculated using exponential growth equations. The relationship between the TGR of xenografts and the proliferation of the cells in vitro was examined. Additionally, we examined the correlations between the surviving fractions of cells after 2 Gy irradiation in vitro and the response of the xenograft to radiation. The TGR of xenografts was positively related to the proliferation of the cells in vitro (r(P)=0.9714, p<0.0001), whereas it was independent of the histological type of the xenografts. Radiation-induced suppression of the growth rate (T/C%) of xenografts was positively related to the radiosensitivity of the cells in vitro (SF(2); r(P)=0.8684, p=0.0284) and TGR (r(P)=0.7623, p=0.0780). The proliferation of human cancer cells in vitro and the growth rate of xenografts were positively related. The radiosensitivity of cancer cells, as judged from the SF(2) values in vitro, and the radiation-induced suppression of xenograft growth were positively related. In conclusion, the growth rate of human xenografts was independent of histological type and origin of the cancer cells, and was positively related to the proliferation of the cancer cells in vitro. Korean Association for Laboratory Animal Science 2016-12 2016-12-23 /pmc/articles/PMC5206224/ /pubmed/28053611 http://dx.doi.org/10.5625/lar.2016.32.4.187 Text en Copyright © 2016 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Ji Young Kim, Mi-Sook Kim, Eun Ho Chung, Namhyun Jeong, Youn Kyoung Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
title | Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
title_full | Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
title_fullStr | Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
title_full_unstemmed | Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
title_short | Retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
title_sort | retrospective growth kinetics and radiosensitivity analysis of various human xenograft models |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206224/ https://www.ncbi.nlm.nih.gov/pubmed/28053611 http://dx.doi.org/10.5625/lar.2016.32.4.187 |
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