Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells

Cryopreservation represents an efficient way to preserve human mesenchymal stem cells (hMSCs) at early culture/passage, and allows pooling of cells to achieve sufficient cells required for off-the-shelf use in clinical applications, e.g. cell-based therapies and regenerative medicine. To fully apply...

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Main Authors: Yong, K.W., Wan Kamarul Zaman, Wan Safwani, Xu, F., Zhang, X., Choi, J.R., Wan Abas, Wan Abu Bakar, Omar, Siti Zawiah, Noor Azmi, Mat Adenan, Chua, K.H., Pingguan-Murphy, Belinda
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Published: Wiley 2016
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Online Access:http://eprints.um.edu.my/18903/
http://dx.doi.org/10.1002/term.2120
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spelling my.um.eprints.189032019-12-16T03:35:26Z http://eprints.um.edu.my/18903/ Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells Yong, K.W. Wan Kamarul Zaman, Wan Safwani Xu, F. Zhang, X. Choi, J.R. Wan Abas, Wan Abu Bakar Omar, Siti Zawiah Noor Azmi, Mat Adenan Chua, K.H. Pingguan-Murphy, Belinda R Medicine Cryopreservation represents an efficient way to preserve human mesenchymal stem cells (hMSCs) at early culture/passage, and allows pooling of cells to achieve sufficient cells required for off-the-shelf use in clinical applications, e.g. cell-based therapies and regenerative medicine. To fully apply cryopreserved hMSCs in a clinical setting, it is necessary to evaluate their biosafety, e.g. chromosomal abnormality and tumourigenic potential. To date, many studies have demonstrated that cryopreserved hMSCs display no chromosomal abnormalities. However, the tumourigenic potential of cryopreserved hMSCs has not yet been evaluated. In the present study, we cryopreserved human adipose-derived mesenchymal stem cells (hASCs) for 3 months, using a slow freezing method with various cryoprotective agents (CPAs), followed by assessment of the tumourigenic potential of the cryopreserved hASCs after thawing and subculture. We found that long-term cryopreserved hASCs maintained normal levels of the tumour suppressor markers p53, p21, p16 and pRb, hTERT, telomerase activity and telomere length. Further, we did not observe significant DNA damage or signs of p53 mutation in cryopreserved hASCs. Our findings suggest that long-term cryopreserved hASCs are at low risk of tumourigenesis. These findings aid in establishing the biosafety profile of cryopreserved hASCs, and thus establishing low hazardous risk perception with the use of long-term cryopreserved hASCs for future clinical applications. Wiley 2016 Article PeerReviewed Yong, K.W. and Wan Kamarul Zaman, Wan Safwani and Xu, F. and Zhang, X. and Choi, J.R. and Wan Abas, Wan Abu Bakar and Omar, Siti Zawiah and Noor Azmi, Mat Adenan and Chua, K.H. and Pingguan-Murphy, Belinda (2016) Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells. Journal of Tissue Engineering and Regenerative Medicine, 11 (8). pp. 2217-2226. ISSN 1932-6254 http://dx.doi.org/10.1002/term.2120 doi:10.1002/term.2120
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic R Medicine
spellingShingle R Medicine
Yong, K.W.
Wan Kamarul Zaman, Wan Safwani
Xu, F.
Zhang, X.
Choi, J.R.
Wan Abas, Wan Abu Bakar
Omar, Siti Zawiah
Noor Azmi, Mat Adenan
Chua, K.H.
Pingguan-Murphy, Belinda
Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
description Cryopreservation represents an efficient way to preserve human mesenchymal stem cells (hMSCs) at early culture/passage, and allows pooling of cells to achieve sufficient cells required for off-the-shelf use in clinical applications, e.g. cell-based therapies and regenerative medicine. To fully apply cryopreserved hMSCs in a clinical setting, it is necessary to evaluate their biosafety, e.g. chromosomal abnormality and tumourigenic potential. To date, many studies have demonstrated that cryopreserved hMSCs display no chromosomal abnormalities. However, the tumourigenic potential of cryopreserved hMSCs has not yet been evaluated. In the present study, we cryopreserved human adipose-derived mesenchymal stem cells (hASCs) for 3 months, using a slow freezing method with various cryoprotective agents (CPAs), followed by assessment of the tumourigenic potential of the cryopreserved hASCs after thawing and subculture. We found that long-term cryopreserved hASCs maintained normal levels of the tumour suppressor markers p53, p21, p16 and pRb, hTERT, telomerase activity and telomere length. Further, we did not observe significant DNA damage or signs of p53 mutation in cryopreserved hASCs. Our findings suggest that long-term cryopreserved hASCs are at low risk of tumourigenesis. These findings aid in establishing the biosafety profile of cryopreserved hASCs, and thus establishing low hazardous risk perception with the use of long-term cryopreserved hASCs for future clinical applications.
format Article
author Yong, K.W.
Wan Kamarul Zaman, Wan Safwani
Xu, F.
Zhang, X.
Choi, J.R.
Wan Abas, Wan Abu Bakar
Omar, Siti Zawiah
Noor Azmi, Mat Adenan
Chua, K.H.
Pingguan-Murphy, Belinda
author_facet Yong, K.W.
Wan Kamarul Zaman, Wan Safwani
Xu, F.
Zhang, X.
Choi, J.R.
Wan Abas, Wan Abu Bakar
Omar, Siti Zawiah
Noor Azmi, Mat Adenan
Chua, K.H.
Pingguan-Murphy, Belinda
author_sort Yong, K.W.
title Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
title_short Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
title_full Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
title_fullStr Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
title_full_unstemmed Assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
title_sort assessment of tumourigenic potential in long-term cryopreserved human adipose-derived stem cells
publisher Wiley
publishDate 2016
url http://eprints.um.edu.my/18903/
http://dx.doi.org/10.1002/term.2120
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