Cargando…
Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo
BACKGROUND: Recent Clinical trials of administration of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in combination with standard first-line chemotherapy have failed to improve survival in patients with advanced NSCLC, However, the sequential treatment with EGFR-TKIs and c...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451286/ https://www.ncbi.nlm.nih.gov/pubmed/30953548 http://dx.doi.org/10.1186/s13046-019-1133-z |
_version_ | 1783409168651124736 |
---|---|
author | Liu, Tianze Jin, Lizi Lu, Wenjing Gan, Hairun Lin, Zhidong Chen, Miao Liu, Jiani Zhang, Fan Wang, Siyang Zhang, Hongyu Deng, Wuguo Chen, Hongtao |
author_facet | Liu, Tianze Jin, Lizi Lu, Wenjing Gan, Hairun Lin, Zhidong Chen, Miao Liu, Jiani Zhang, Fan Wang, Siyang Zhang, Hongyu Deng, Wuguo Chen, Hongtao |
author_sort | Liu, Tianze |
collection | PubMed |
description | BACKGROUND: Recent Clinical trials of administration of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in combination with standard first-line chemotherapy have failed to improve survival in patients with advanced NSCLC, However, the sequential treatment with EGFR-TKIs and chemotherapy is expected to improve survival of NSCLC. The aim of this study is to test the antiproliferative effect of pemetrexed combined with icotinib in different sequences on non-small cell lung cancer (NSCLC) cell lines to determine the optimal combination schedule, and subsequently elaborated the potential mechanisms. METHODS: Six human lung cancer cell lines with wild-type or mutant EGFR gene were exposed to pemetrexed and icotinib combined in different sequences. Cell proliferation was examined by cell counting kit-8 (CCK-8) and colony formation assay; cell cycle and apoptosis were evaluated by flow cytometry; cell migration and invasion were measured by wound healing and transwell invasion assays respectively; protein expression was by detected by Western blot. RESULTS: The growth inhibition effect of pemetrexed combined with icotinib on NSCLC cells were schedule-dependent in vitro and in vivo. Treatment with pemetrexed followed by icotinib (P-I) had significantly stronger anticancer ability than treatment with icotinib followed by pemetrexed (I-P) and concomitant treatment with pemetrexed and icotinib (P + I). Cell cycle analysis revealed that pemetrexed blocked cells in S phase, whereas icotinib arrested cells in G1 phase. We also found that icotinib markedly enhanced the pro-apoptotic activity of pemetrexed via cytochrome-C/Caspase/Bcl-2 signaling pathway. In addition, our results showed that pemetrexed alone increased the levels of p-EGFR, p-AKT and p-MAPK, which were inhibited by icotinib. Finally, we showed that the washout period of icotinib was no less than 96 h. CONCLUSIONS: Sequential treatment of NSCLC cells with pemetrexed followed by icotinib had powerful antiproliferative effect, and it could become a novel effective combination therapy for NSCLC patients. |
format | Online Article Text |
id | pubmed-6451286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64512862019-04-17 Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo Liu, Tianze Jin, Lizi Lu, Wenjing Gan, Hairun Lin, Zhidong Chen, Miao Liu, Jiani Zhang, Fan Wang, Siyang Zhang, Hongyu Deng, Wuguo Chen, Hongtao J Exp Clin Cancer Res Research BACKGROUND: Recent Clinical trials of administration of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in combination with standard first-line chemotherapy have failed to improve survival in patients with advanced NSCLC, However, the sequential treatment with EGFR-TKIs and chemotherapy is expected to improve survival of NSCLC. The aim of this study is to test the antiproliferative effect of pemetrexed combined with icotinib in different sequences on non-small cell lung cancer (NSCLC) cell lines to determine the optimal combination schedule, and subsequently elaborated the potential mechanisms. METHODS: Six human lung cancer cell lines with wild-type or mutant EGFR gene were exposed to pemetrexed and icotinib combined in different sequences. Cell proliferation was examined by cell counting kit-8 (CCK-8) and colony formation assay; cell cycle and apoptosis were evaluated by flow cytometry; cell migration and invasion were measured by wound healing and transwell invasion assays respectively; protein expression was by detected by Western blot. RESULTS: The growth inhibition effect of pemetrexed combined with icotinib on NSCLC cells were schedule-dependent in vitro and in vivo. Treatment with pemetrexed followed by icotinib (P-I) had significantly stronger anticancer ability than treatment with icotinib followed by pemetrexed (I-P) and concomitant treatment with pemetrexed and icotinib (P + I). Cell cycle analysis revealed that pemetrexed blocked cells in S phase, whereas icotinib arrested cells in G1 phase. We also found that icotinib markedly enhanced the pro-apoptotic activity of pemetrexed via cytochrome-C/Caspase/Bcl-2 signaling pathway. In addition, our results showed that pemetrexed alone increased the levels of p-EGFR, p-AKT and p-MAPK, which were inhibited by icotinib. Finally, we showed that the washout period of icotinib was no less than 96 h. CONCLUSIONS: Sequential treatment of NSCLC cells with pemetrexed followed by icotinib had powerful antiproliferative effect, and it could become a novel effective combination therapy for NSCLC patients. BioMed Central 2019-04-05 /pmc/articles/PMC6451286/ /pubmed/30953548 http://dx.doi.org/10.1186/s13046-019-1133-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Liu, Tianze Jin, Lizi Lu, Wenjing Gan, Hairun Lin, Zhidong Chen, Miao Liu, Jiani Zhang, Fan Wang, Siyang Zhang, Hongyu Deng, Wuguo Chen, Hongtao Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
title | Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
title_full | Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
title_fullStr | Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
title_full_unstemmed | Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
title_short | Sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
title_sort | sequence-dependent synergistic cytotoxicity of icotinib and pemetrexed in human lung cancer cell lines in vitro and in vivo |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451286/ https://www.ncbi.nlm.nih.gov/pubmed/30953548 http://dx.doi.org/10.1186/s13046-019-1133-z |
work_keys_str_mv | AT liutianze sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT jinlizi sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT luwenjing sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT ganhairun sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT linzhidong sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT chenmiao sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT liujiani sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT zhangfan sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT wangsiyang sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT zhanghongyu sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT dengwuguo sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo AT chenhongtao sequencedependentsynergisticcytotoxicityoficotinibandpemetrexedinhumanlungcancercelllinesinvitroandinvivo |