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Khan, Huma; Makwana, Vaidehi; Nascimento dos Santos, Sofia; Bonacossa de Almeida, Carlos Eduardo; Santos-Oliveira, Ralph and Missailidis, Sotiris
(2021).
DOI: https://doi.org/10.3390/pharmaceutics13081239
Abstract
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.
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About
- Item ORO ID
- 78559
- Item Type
- Journal Item
- ISSN
- 1999-4923
- Keywords
- cancer; aptamer; therapy; MUC1/Y; pharmacokinetics
- Academic Unit or School
-
Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM) - Copyright Holders
- © 2021 Huma Khan, © 2021 Vaidehi Makwana, © 2021 Sofia Nascimento dos Santos, © 2021 Carlos Eduardo Bonacossa de Almeida, © 2021 Ralph Santos-Oliveira, © 2021 Sotiris Missailidis
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