Cargando…
Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer
Effect of erlotinib combined with cisplatin on tumor growth, interleukin-6 (IL-6) and interleukin-12 (IL-12) in mice with Lewis lung cancer (LLC) was investigated. Forty-four pure inbred SPF C57BL/6J mice were modeled for LLC and randomized into groups A, B, C and D (n=11 each group). Mice in group...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285801/ https://www.ncbi.nlm.nih.gov/pubmed/32566018 http://dx.doi.org/10.3892/ol.2020.11632 |
_version_ | 1783544768710574080 |
---|---|
author | Zhang, Xu Chen, Jinliang Jin, Hongsong Zhao, Wei Chang, Zhibo Wu, Huijing |
author_facet | Zhang, Xu Chen, Jinliang Jin, Hongsong Zhao, Wei Chang, Zhibo Wu, Huijing |
author_sort | Zhang, Xu |
collection | PubMed |
description | Effect of erlotinib combined with cisplatin on tumor growth, interleukin-6 (IL-6) and interleukin-12 (IL-12) in mice with Lewis lung cancer (LLC) was investigated. Forty-four pure inbred SPF C57BL/6J mice were modeled for LLC and randomized into groups A, B, C and D (n=11 each group). Mice in group A were given normal saline, group B was given erlotinib, group C was given cisplatin injection and group D erlotinib combined with cisplatin. Tumor growth of the mice was observed and the tumor mass was measured. Serum IL-6 and IL-12 levels were measured by enzyme-linked immunosorbent assay (ELISA) 40 days later. At different time-points after medication, tumor volume in group D was significantly lower than that in groups A, B and C (P<0.05), and that in groups B and C was significantly lower than that in group A (P<0.05), whereas there was no significant difference between groups B and C (P>0.05). Tumor mass in groups B, C and D was significantly lower than that in group A (P<0.05), and that in group D was significantly lower than that in groups B and C (P<0.05), whereas there was no significant difference between groups B and C (P>0.05). Compared with groups B and C, mice in group D had significantly lower IL-6 level (P<0.05), but significantly higher IL-12 level (P<0.05). There was no significant difference in IL-6 and IL-12 levels between groups B and C (P>0.05). In conclusion, erlotinib combined with cisplatin can inhibit the tumor growth of mice with LLC, and inhibition of IL-6 level and upregulation of IL-12 level may be one of its therapeutic mechanisms. |
format | Online Article Text |
id | pubmed-7285801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-72858012020-06-18 Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer Zhang, Xu Chen, Jinliang Jin, Hongsong Zhao, Wei Chang, Zhibo Wu, Huijing Oncol Lett Articles Effect of erlotinib combined with cisplatin on tumor growth, interleukin-6 (IL-6) and interleukin-12 (IL-12) in mice with Lewis lung cancer (LLC) was investigated. Forty-four pure inbred SPF C57BL/6J mice were modeled for LLC and randomized into groups A, B, C and D (n=11 each group). Mice in group A were given normal saline, group B was given erlotinib, group C was given cisplatin injection and group D erlotinib combined with cisplatin. Tumor growth of the mice was observed and the tumor mass was measured. Serum IL-6 and IL-12 levels were measured by enzyme-linked immunosorbent assay (ELISA) 40 days later. At different time-points after medication, tumor volume in group D was significantly lower than that in groups A, B and C (P<0.05), and that in groups B and C was significantly lower than that in group A (P<0.05), whereas there was no significant difference between groups B and C (P>0.05). Tumor mass in groups B, C and D was significantly lower than that in group A (P<0.05), and that in group D was significantly lower than that in groups B and C (P<0.05), whereas there was no significant difference between groups B and C (P>0.05). Compared with groups B and C, mice in group D had significantly lower IL-6 level (P<0.05), but significantly higher IL-12 level (P<0.05). There was no significant difference in IL-6 and IL-12 levels between groups B and C (P>0.05). In conclusion, erlotinib combined with cisplatin can inhibit the tumor growth of mice with LLC, and inhibition of IL-6 level and upregulation of IL-12 level may be one of its therapeutic mechanisms. D.A. Spandidos 2020-07 2020-05-18 /pmc/articles/PMC7285801/ /pubmed/32566018 http://dx.doi.org/10.3892/ol.2020.11632 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Zhang, Xu Chen, Jinliang Jin, Hongsong Zhao, Wei Chang, Zhibo Wu, Huijing Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer |
title | Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer |
title_full | Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer |
title_fullStr | Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer |
title_full_unstemmed | Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer |
title_short | Effect of erlotinib combined with cisplatin on IL-6 and IL-12 in mice with Lewis lung cancer |
title_sort | effect of erlotinib combined with cisplatin on il-6 and il-12 in mice with lewis lung cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285801/ https://www.ncbi.nlm.nih.gov/pubmed/32566018 http://dx.doi.org/10.3892/ol.2020.11632 |
work_keys_str_mv | AT zhangxu effectoferlotinibcombinedwithcisplatinonil6andil12inmicewithlewislungcancer AT chenjinliang effectoferlotinibcombinedwithcisplatinonil6andil12inmicewithlewislungcancer AT jinhongsong effectoferlotinibcombinedwithcisplatinonil6andil12inmicewithlewislungcancer AT zhaowei effectoferlotinibcombinedwithcisplatinonil6andil12inmicewithlewislungcancer AT changzhibo effectoferlotinibcombinedwithcisplatinonil6andil12inmicewithlewislungcancer AT wuhuijing effectoferlotinibcombinedwithcisplatinonil6andil12inmicewithlewislungcancer |