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Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma

Targeted therapeutics is used as an alternative treatment of non-small cell lung cancer (NSCLC); however, treatment effect is far from being satisfactory, and therefore identification of new targets is needed. We have previously shown that metuzumab inhibit tumor growth in vivo. The present study wa...

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Autores principales: Feng, Fei, Wang, Bin, Sun, Xiuxuan, Zhu, Yumeng, Tang, Hao, Nan, Gang, Wang, Lijuan, Wu, Bo, Huhe, Muren, Liu, Shuangshuang, Diao, Tengyue, Hou, Rong, Zhang, Yang, Zhang, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323017/
https://www.ncbi.nlm.nih.gov/pubmed/28055291
http://dx.doi.org/10.1080/15384047.2016.1276126
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author Feng, Fei
Wang, Bin
Sun, Xiuxuan
Zhu, Yumeng
Tang, Hao
Nan, Gang
Wang, Lijuan
Wu, Bo
Huhe, Muren
Liu, Shuangshuang
Diao, Tengyue
Hou, Rong
Zhang, Yang
Zhang, Zheng
author_facet Feng, Fei
Wang, Bin
Sun, Xiuxuan
Zhu, Yumeng
Tang, Hao
Nan, Gang
Wang, Lijuan
Wu, Bo
Huhe, Muren
Liu, Shuangshuang
Diao, Tengyue
Hou, Rong
Zhang, Yang
Zhang, Zheng
author_sort Feng, Fei
collection PubMed
description Targeted therapeutics is used as an alternative treatment of non-small cell lung cancer (NSCLC); however, treatment effect is far from being satisfactory, and therefore identification of new targets is needed. We have previously shown that metuzumab inhibit tumor growth in vivo. The present study was performed to investigate the anti-tumor efficacy of metuzumab combined with gemcitabine and cisplatin (GP), paclitaxel and cisplatin (TP) or navelbine and cisplatin (NP) regimens in multiple NSCLC cell lines. Our results demonstrate that, in comparison to single agent metuzumab or GP treated cells, metuzumab combined with GP display inhibitory effects on tumor growth. Furthermore, we found that metuzumab elevated the sensitivity of cell lines to gemcitabine, which was identified by MTT assay. Flow cytometric analysis showed that metuzumab combined with gemcitabine (GEM) treatment led to an obvious G1 arrest and an elevated apoptosis in A549, NCI-H460 and NCI-H520 cells. Western blot analysis also demonstrated a significantly reduced level of cyclin D1, Bcl-2, and an obviously increase level of Bax and full-length caspase-3 in A549, NCI-H460 and NCI-H520 cells treated with metuzumab/gemcitabine combination in comparison with single agent treated cells. In addition, metuzumab/gemcitabine treated A549, NCI-H460 and NCI-H520 cells also demonstrated a significantly increase in deoxycytidine kinase (dCK) protein level compared with single agent metuzumab or gemcitabine treated cells. Xenograft models also demonstrated that this metuzumab/gemcitabine combination led to upregulation of dCK. Taken together, the mechanisms of metuzumab combined with GP repress tumor growth were that the combined treatment significantly inhibited the tumor cell proliferation, apoptosis and cell cycle in vitro and in vivo and at least partially by induction of dCK expression. Our results suggested that metuzumab could significantly enhance chemosensitivity of human NSCLC cells to gemcitabine. Metuzumab/gemcitabine combination treatment may be a potentially useful therapeutic regimen for NSCLC patients.
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spelling pubmed-53230172017-03-02 Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma Feng, Fei Wang, Bin Sun, Xiuxuan Zhu, Yumeng Tang, Hao Nan, Gang Wang, Lijuan Wu, Bo Huhe, Muren Liu, Shuangshuang Diao, Tengyue Hou, Rong Zhang, Yang Zhang, Zheng Cancer Biol Ther Research Paper Targeted therapeutics is used as an alternative treatment of non-small cell lung cancer (NSCLC); however, treatment effect is far from being satisfactory, and therefore identification of new targets is needed. We have previously shown that metuzumab inhibit tumor growth in vivo. The present study was performed to investigate the anti-tumor efficacy of metuzumab combined with gemcitabine and cisplatin (GP), paclitaxel and cisplatin (TP) or navelbine and cisplatin (NP) regimens in multiple NSCLC cell lines. Our results demonstrate that, in comparison to single agent metuzumab or GP treated cells, metuzumab combined with GP display inhibitory effects on tumor growth. Furthermore, we found that metuzumab elevated the sensitivity of cell lines to gemcitabine, which was identified by MTT assay. Flow cytometric analysis showed that metuzumab combined with gemcitabine (GEM) treatment led to an obvious G1 arrest and an elevated apoptosis in A549, NCI-H460 and NCI-H520 cells. Western blot analysis also demonstrated a significantly reduced level of cyclin D1, Bcl-2, and an obviously increase level of Bax and full-length caspase-3 in A549, NCI-H460 and NCI-H520 cells treated with metuzumab/gemcitabine combination in comparison with single agent treated cells. In addition, metuzumab/gemcitabine treated A549, NCI-H460 and NCI-H520 cells also demonstrated a significantly increase in deoxycytidine kinase (dCK) protein level compared with single agent metuzumab or gemcitabine treated cells. Xenograft models also demonstrated that this metuzumab/gemcitabine combination led to upregulation of dCK. Taken together, the mechanisms of metuzumab combined with GP repress tumor growth were that the combined treatment significantly inhibited the tumor cell proliferation, apoptosis and cell cycle in vitro and in vivo and at least partially by induction of dCK expression. Our results suggested that metuzumab could significantly enhance chemosensitivity of human NSCLC cells to gemcitabine. Metuzumab/gemcitabine combination treatment may be a potentially useful therapeutic regimen for NSCLC patients. Taylor & Francis 2017-01-05 /pmc/articles/PMC5323017/ /pubmed/28055291 http://dx.doi.org/10.1080/15384047.2016.1276126 Text en © 2017 The Author(s). Published with license by Taylor & Francis Group, LLC 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. The moral rights of the named author(s) have been asserted.
spellingShingle Research Paper
Feng, Fei
Wang, Bin
Sun, Xiuxuan
Zhu, Yumeng
Tang, Hao
Nan, Gang
Wang, Lijuan
Wu, Bo
Huhe, Muren
Liu, Shuangshuang
Diao, Tengyue
Hou, Rong
Zhang, Yang
Zhang, Zheng
Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
title Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
title_full Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
title_fullStr Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
title_full_unstemmed Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
title_short Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
title_sort metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323017/
https://www.ncbi.nlm.nih.gov/pubmed/28055291
http://dx.doi.org/10.1080/15384047.2016.1276126
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