Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy
MUC1, the transmembrane glycoprotein Mucin 1, is usually found to be overexpressed in a variety of epithelial cancers playing an important role in disease progression. MUC1 isoforms such as MUC1/Y, which lacks the entire variable number of tandem repeat region, are involved in oncogenic processes by...
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doaj-1692a653d37c475cbd96b20bd2ea2e5a2021-08-26T14:13:09ZengMDPI AGPharmaceutics1999-49232021-08-01131239123910.3390/pharmaceutics13081239Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer TherapyHuma Khan0Vaidehi Makwana1Sofia Nascimento dos Santos2Carlos Eduardo Bonacossa de Almeida3Ralph Santos-Oliveira4Sotiris Missailidis5Department of Life, Health and Chemical Sciences, Faculty of Science, The Open University, Walton Hall, Milton Keynes MK7 6AA, UKDepartment of Life, Health and Chemical Sciences, Faculty of Science, The Open University, Walton Hall, Milton Keynes MK7 6AA, UKRadiopharmacy Department, Nuclear Energy Research Institute, São Paulo 05508-000, BrazilDivision of Medical Physics, Radiation Protection and Dosimetry Institute, Brazilian Nuclear Energy Commission, Rio de Janeiro 22783-127, BrazilNuclear Engineering Institute, Brazilian Nuclear Energy Commission, Rio de Janeiro 21941-972, BrazilBio-Manguinhos Institute of Technology in Immunobiologics, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, BrazilMUC1, the transmembrane glycoprotein Mucin 1, is usually found to be overexpressed in a variety of epithelial cancers playing an important role in disease progression. MUC1 isoforms such as MUC1/Y, which lacks the entire variable number of tandem repeat region, are involved in oncogenic processes by enhancing tumour initiation. MUC1/Y is therefore considered a promising target for the identification and treatment of epithelial cancers; but so far, the precise role of MUC1/Y remains to be elucidated. In this work, we developed and identified a DNA aptamer that specifically recognizes the splice variant MUC1/Y for the first time. The DNA aptamer could bind to a wide variety of human cancer cells, and treatment of MUC1/Y positive cells resulted in reduced growth in vitro. Moreover, MUC1/Y aptamer inhibited the tumour growth of breast cancer cells in vivo. The present study highlights the importance of targeting MUC1/Y for cancer treatment and unravels the suitability of a DNA aptamer to act as a new therapeutic tool.https://www.mdpi.com/1999-4923/13/8/1239canceraptamertherapyMUC1/Ypharmacokinetics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Huma Khan Vaidehi Makwana Sofia Nascimento dos Santos Carlos Eduardo Bonacossa de Almeida Ralph Santos-Oliveira Sotiris Missailidis |
spellingShingle |
Huma Khan Vaidehi Makwana Sofia Nascimento dos Santos Carlos Eduardo Bonacossa de Almeida Ralph Santos-Oliveira Sotiris Missailidis Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy Pharmaceutics cancer aptamer therapy MUC1/Y pharmacokinetics |
author_facet |
Huma Khan Vaidehi Makwana Sofia Nascimento dos Santos Carlos Eduardo Bonacossa de Almeida Ralph Santos-Oliveira Sotiris Missailidis |
author_sort |
Huma Khan |
title |
Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy |
title_short |
Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy |
title_full |
Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy |
title_fullStr |
Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy |
title_full_unstemmed |
Development, Characterization, and In Vivo Evaluation of a Novel Aptamer (Anti-MUC1/Y) for Breast Cancer Therapy |
title_sort |
development, characterization, and in vivo evaluation of a novel aptamer (anti-muc1/y) for breast cancer therapy |
publisher |
MDPI AG |
series |
Pharmaceutics |
issn |
1999-4923 |
publishDate |
2021-08-01 |
description |
MUC1, the transmembrane glycoprotein Mucin 1, is usually found to be overexpressed in a variety of epithelial cancers playing an important role in disease progression. MUC1 isoforms such as MUC1/Y, which lacks the entire variable number of tandem repeat region, are involved in oncogenic processes by enhancing tumour initiation. MUC1/Y is therefore considered a promising target for the identification and treatment of epithelial cancers; but so far, the precise role of MUC1/Y remains to be elucidated. In this work, we developed and identified a DNA aptamer that specifically recognizes the splice variant MUC1/Y for the first time. The DNA aptamer could bind to a wide variety of human cancer cells, and treatment of MUC1/Y positive cells resulted in reduced growth in vitro. Moreover, MUC1/Y aptamer inhibited the tumour growth of breast cancer cells in vivo. The present study highlights the importance of targeting MUC1/Y for cancer treatment and unravels the suitability of a DNA aptamer to act as a new therapeutic tool. |
topic |
cancer aptamer therapy MUC1/Y pharmacokinetics |
url |
https://www.mdpi.com/1999-4923/13/8/1239 |
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