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Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer
Patients with medullary thyroid cancer (MTC) are often diagnosed with spread tumour disease and the development of better systemic treatment options for these patients is important. Treatment with the radiolabelled somatostatin analogue (177)Lu-octreotate is already a promising option but can be opt...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855663/ https://www.ncbi.nlm.nih.gov/pubmed/31725814 http://dx.doi.org/10.1371/journal.pone.0225260 |
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author | Sandblom, Viktor Spetz, Johan Shubbar, Emman Montelius, Mikael Ståhl, Ingun Swanpalmer, John Nilsson, Ola Forssell-Aronsson, Eva |
author_facet | Sandblom, Viktor Spetz, Johan Shubbar, Emman Montelius, Mikael Ståhl, Ingun Swanpalmer, John Nilsson, Ola Forssell-Aronsson, Eva |
author_sort | Sandblom, Viktor |
collection | PubMed |
description | Patients with medullary thyroid cancer (MTC) are often diagnosed with spread tumour disease and the development of better systemic treatment options for these patients is important. Treatment with the radiolabelled somatostatin analogue (177)Lu-octreotate is already a promising option but can be optimised. For example, combination treatment with another substance could increase the effect on tumour tissue. Gemcitabine is a nucleoside analogue that has been shown to sensitise tumour cells to radiation. The aim of this study was to investigate potentially additive or synergistic effects of combining radiation with gemcitabine for treatment of MTC. Nude mice transplanted with patient-derived MTC tumours (GOT2) were divided into groups and treated with radiation and/or gemcitabine. Radiation treatment was given as (177)Lu-octreotate or external beam radiotherapy (EBRT). The volume of treated and untreated tumours was followed. The absorbed dose and amount of gemcitabine were chosen to give moderate tumour volume reduction when given as monotherapy to enable detection of increased effects from combination treatment. After follow-up, the mice were killed and tumours were immunohistochemically (IHC) analysed. Overall, the animals that received a combination of EBRT and gemcitabine showed the largest reduction in tumour volume. Monotherapy with EBRT or gemcitabine also resulted in a clear detrimental effect on tumour volume, while the animals that received (177)Lu-octreotate monotherapy showed similar response as the untreated animals. The GOT2 tumour was confirmed in the IHC analyses by markers for MTC. The IHC analyses also revealed that the proliferative activity of tumour cells was similar in all tumours, but indicated that fibrotic tissue was more common after EBRT and/or gemcitabine treatment. The results indicate that an additive, or even synergistic, effect may be achieved by combining radiation with gemcitabine for treatment of MTC. Future studies should be performed to evaluate the full potential of combining (177)Lu-octreotate with gemcitabine in patients. |
format | Online Article Text |
id | pubmed-6855663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68556632019-12-06 Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer Sandblom, Viktor Spetz, Johan Shubbar, Emman Montelius, Mikael Ståhl, Ingun Swanpalmer, John Nilsson, Ola Forssell-Aronsson, Eva PLoS One Research Article Patients with medullary thyroid cancer (MTC) are often diagnosed with spread tumour disease and the development of better systemic treatment options for these patients is important. Treatment with the radiolabelled somatostatin analogue (177)Lu-octreotate is already a promising option but can be optimised. For example, combination treatment with another substance could increase the effect on tumour tissue. Gemcitabine is a nucleoside analogue that has been shown to sensitise tumour cells to radiation. The aim of this study was to investigate potentially additive or synergistic effects of combining radiation with gemcitabine for treatment of MTC. Nude mice transplanted with patient-derived MTC tumours (GOT2) were divided into groups and treated with radiation and/or gemcitabine. Radiation treatment was given as (177)Lu-octreotate or external beam radiotherapy (EBRT). The volume of treated and untreated tumours was followed. The absorbed dose and amount of gemcitabine were chosen to give moderate tumour volume reduction when given as monotherapy to enable detection of increased effects from combination treatment. After follow-up, the mice were killed and tumours were immunohistochemically (IHC) analysed. Overall, the animals that received a combination of EBRT and gemcitabine showed the largest reduction in tumour volume. Monotherapy with EBRT or gemcitabine also resulted in a clear detrimental effect on tumour volume, while the animals that received (177)Lu-octreotate monotherapy showed similar response as the untreated animals. The GOT2 tumour was confirmed in the IHC analyses by markers for MTC. The IHC analyses also revealed that the proliferative activity of tumour cells was similar in all tumours, but indicated that fibrotic tissue was more common after EBRT and/or gemcitabine treatment. The results indicate that an additive, or even synergistic, effect may be achieved by combining radiation with gemcitabine for treatment of MTC. Future studies should be performed to evaluate the full potential of combining (177)Lu-octreotate with gemcitabine in patients. Public Library of Science 2019-11-14 /pmc/articles/PMC6855663/ /pubmed/31725814 http://dx.doi.org/10.1371/journal.pone.0225260 Text en © 2019 Sandblom et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Sandblom, Viktor Spetz, Johan Shubbar, Emman Montelius, Mikael Ståhl, Ingun Swanpalmer, John Nilsson, Ola Forssell-Aronsson, Eva Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
title | Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
title_full | Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
title_fullStr | Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
title_full_unstemmed | Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
title_short | Gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
title_sort | gemcitabine potentiates the anti-tumour effect of radiation on medullary thyroid cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855663/ https://www.ncbi.nlm.nih.gov/pubmed/31725814 http://dx.doi.org/10.1371/journal.pone.0225260 |
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