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Healing effects of a protein scaffold loaded with adipose-derived mesenchymal stem cells on radiation-induced vaginal injury in rats
OBJECTIVES: Cervical cancer, the most common female cancer after breast cancer, is typically treated using radiotherapy. However, pelvic radiotherapy can cause irreversible damage to the vagina, seriously affecting patients’ quality of life. In this study, protein scaffolds loaded with rat adipose-d...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607296/ https://www.ncbi.nlm.nih.gov/pubmed/33115306 http://dx.doi.org/10.1177/0300060520958826 |
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author | Ye, Mingxia Yu, Ling She, Yujia Wang, Shufang Wang, Min Zhao, Qingdong Gu, Chenglei Bian, Lihua Wen, Na Gong, Jing Li, Lian Meng, Yuanguang |
author_facet | Ye, Mingxia Yu, Ling She, Yujia Wang, Shufang Wang, Min Zhao, Qingdong Gu, Chenglei Bian, Lihua Wen, Na Gong, Jing Li, Lian Meng, Yuanguang |
author_sort | Ye, Mingxia |
collection | PubMed |
description | OBJECTIVES: Cervical cancer, the most common female cancer after breast cancer, is typically treated using radiotherapy. However, pelvic radiotherapy can cause irreversible damage to the vagina, seriously affecting patients’ quality of life. In this study, protein scaffolds loaded with rat adipose-derived mesenchymal stem cells (ADSCs) were implanted into irradiated tissue to assess their healing potential. METHODS: We established a rat model of radiation-induced vaginal injury. Complexes (consisting of protein scaffolds loaded with ADSCs) were implanted into injury sites. Histological analysis were used to assess regeneration of the vaginal epithelium. RNA sequencing was used to study the therapeutic mechanism of the complexes. RESULTS: The complexes promoted vaginal epithelial cell regeneration, vaginal tissue repair and improved vaginal stenosis and contracture. Compared with rats transplanted with ADSCs, rats transplanted with complexes achieved better therapeutic effects. CONCLUSIONS: Protein scaffold-ADSC complexes had a beneficial therapeutic effect on radiation-induced vaginal injury in rats and may serve as the basis of a novel therapeutic approach for radiation dermatitis. |
format | Online Article Text |
id | pubmed-7607296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-76072962020-11-13 Healing effects of a protein scaffold loaded with adipose-derived mesenchymal stem cells on radiation-induced vaginal injury in rats Ye, Mingxia Yu, Ling She, Yujia Wang, Shufang Wang, Min Zhao, Qingdong Gu, Chenglei Bian, Lihua Wen, Na Gong, Jing Li, Lian Meng, Yuanguang J Int Med Res Pre-Clinical Research Report OBJECTIVES: Cervical cancer, the most common female cancer after breast cancer, is typically treated using radiotherapy. However, pelvic radiotherapy can cause irreversible damage to the vagina, seriously affecting patients’ quality of life. In this study, protein scaffolds loaded with rat adipose-derived mesenchymal stem cells (ADSCs) were implanted into irradiated tissue to assess their healing potential. METHODS: We established a rat model of radiation-induced vaginal injury. Complexes (consisting of protein scaffolds loaded with ADSCs) were implanted into injury sites. Histological analysis were used to assess regeneration of the vaginal epithelium. RNA sequencing was used to study the therapeutic mechanism of the complexes. RESULTS: The complexes promoted vaginal epithelial cell regeneration, vaginal tissue repair and improved vaginal stenosis and contracture. Compared with rats transplanted with ADSCs, rats transplanted with complexes achieved better therapeutic effects. CONCLUSIONS: Protein scaffold-ADSC complexes had a beneficial therapeutic effect on radiation-induced vaginal injury in rats and may serve as the basis of a novel therapeutic approach for radiation dermatitis. SAGE Publications 2020-10-28 /pmc/articles/PMC7607296/ /pubmed/33115306 http://dx.doi.org/10.1177/0300060520958826 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Pre-Clinical Research Report Ye, Mingxia Yu, Ling She, Yujia Wang, Shufang Wang, Min Zhao, Qingdong Gu, Chenglei Bian, Lihua Wen, Na Gong, Jing Li, Lian Meng, Yuanguang Healing effects of a protein scaffold loaded with adipose-derived mesenchymal stem cells on radiation-induced vaginal injury in rats |
title | Healing effects of a protein scaffold loaded with adipose-derived
mesenchymal stem cells on radiation-induced vaginal injury in
rats |
title_full | Healing effects of a protein scaffold loaded with adipose-derived
mesenchymal stem cells on radiation-induced vaginal injury in
rats |
title_fullStr | Healing effects of a protein scaffold loaded with adipose-derived
mesenchymal stem cells on radiation-induced vaginal injury in
rats |
title_full_unstemmed | Healing effects of a protein scaffold loaded with adipose-derived
mesenchymal stem cells on radiation-induced vaginal injury in
rats |
title_short | Healing effects of a protein scaffold loaded with adipose-derived
mesenchymal stem cells on radiation-induced vaginal injury in
rats |
title_sort | healing effects of a protein scaffold loaded with adipose-derived
mesenchymal stem cells on radiation-induced vaginal injury in
rats |
topic | Pre-Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607296/ https://www.ncbi.nlm.nih.gov/pubmed/33115306 http://dx.doi.org/10.1177/0300060520958826 |
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