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Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells
BACKGROUND: It is becoming increasingly recognised that opioids are responsible for tumour growth. However, the effects of opioids on tumour growth have been controversial. METHODS: The effects of κ-opioid receptor (KOR) agonist on the growth of non-small cell lung cancer (NSCLC) cells were assessed...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304401/ https://www.ncbi.nlm.nih.gov/pubmed/22343623 http://dx.doi.org/10.1038/bjc.2011.574 |
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author | Kuzumaki, N Suzuki, A Narita, M Hosoya, T Nagasawa, A Imai, S Yamamizu, K Morita, H Nagase, H Okada, Y Okano, H J Yamashita, J K Okano, H Suzuki, T Narita, M |
author_facet | Kuzumaki, N Suzuki, A Narita, M Hosoya, T Nagasawa, A Imai, S Yamamizu, K Morita, H Nagase, H Okada, Y Okano, H J Yamashita, J K Okano, H Suzuki, T Narita, M |
author_sort | Kuzumaki, N |
collection | PubMed |
description | BACKGROUND: It is becoming increasingly recognised that opioids are responsible for tumour growth. However, the effects of opioids on tumour growth have been controversial. METHODS: The effects of κ-opioid receptor (KOR) agonist on the growth of non-small cell lung cancer (NSCLC) cells were assessed by a cell proliferation assay. Western blotting was performed to ascertain the mechanism by which treatment with KOR agonist suppresses tumour growth. RESULTS: Addition of the selective KOR agonist U50,488H to gefitinib-sensitive (HCC827) and gefitinib-resistant (H1975) NSCLC cells produced a concentration-dependent decrease in their growth. These effects were abolished by co-treatment with the selective KOR antagonist nor-BNI. Furthermore, the growth-inhibitory effect of gefitinib in HCC827 cells was further enhanced by co-treatment with U50,488H. With regard to the inhibition of tumour growth, the addition of U50, 488H to H1975 cells produced a concentration-dependent decrease in phosphorylated-glycogen synthase kinase 3β (p-GSK3β). CONCLUSION: The present results showed that stimulation of KOR reduces the growth of gefitinib-resistant NSCLC cells through the activation of GSK3β. |
format | Online Article Text |
id | pubmed-3304401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33044012013-03-13 Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells Kuzumaki, N Suzuki, A Narita, M Hosoya, T Nagasawa, A Imai, S Yamamizu, K Morita, H Nagase, H Okada, Y Okano, H J Yamashita, J K Okano, H Suzuki, T Narita, M Br J Cancer Short Communication BACKGROUND: It is becoming increasingly recognised that opioids are responsible for tumour growth. However, the effects of opioids on tumour growth have been controversial. METHODS: The effects of κ-opioid receptor (KOR) agonist on the growth of non-small cell lung cancer (NSCLC) cells were assessed by a cell proliferation assay. Western blotting was performed to ascertain the mechanism by which treatment with KOR agonist suppresses tumour growth. RESULTS: Addition of the selective KOR agonist U50,488H to gefitinib-sensitive (HCC827) and gefitinib-resistant (H1975) NSCLC cells produced a concentration-dependent decrease in their growth. These effects were abolished by co-treatment with the selective KOR antagonist nor-BNI. Furthermore, the growth-inhibitory effect of gefitinib in HCC827 cells was further enhanced by co-treatment with U50,488H. With regard to the inhibition of tumour growth, the addition of U50, 488H to H1975 cells produced a concentration-dependent decrease in phosphorylated-glycogen synthase kinase 3β (p-GSK3β). CONCLUSION: The present results showed that stimulation of KOR reduces the growth of gefitinib-resistant NSCLC cells through the activation of GSK3β. Nature Publishing Group 2012-03-13 2012-02-16 /pmc/articles/PMC3304401/ /pubmed/22343623 http://dx.doi.org/10.1038/bjc.2011.574 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Short Communication Kuzumaki, N Suzuki, A Narita, M Hosoya, T Nagasawa, A Imai, S Yamamizu, K Morita, H Nagase, H Okada, Y Okano, H J Yamashita, J K Okano, H Suzuki, T Narita, M Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells |
title | Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells |
title_full | Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells |
title_fullStr | Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells |
title_full_unstemmed | Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells |
title_short | Effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (NSCLC) cells |
title_sort | effect of κ-opioid receptor agonist on the growth of non-small cell lung cancer (nsclc) cells |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304401/ https://www.ncbi.nlm.nih.gov/pubmed/22343623 http://dx.doi.org/10.1038/bjc.2011.574 |
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