Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/130868
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Type: Journal article
Title: Targeting aquaporins in novel therapies for male and female breast and reproductive cancers
Author: Khan, S.
Ricciardelli, C.
Yool, A.J.
Citation: Cells, 2021; 10(2):1-18
Publisher: MDPI
Issue Date: 2021
ISSN: 2073-4409
2073-4409
Statement of
Responsibility: 
Sidra Khan, Carmela Ricciardelli and Andrea J. Yool
Abstract: Aquaporins are membrane channels in the broad family of major intrinsic proteins (MIPs), with 13 classes showing tissue-specific distributions in humans. As key physiological modulators of water and solute homeostasis, mutations, and dysfunctions involving aquaporins have been associated with pathologies in all major organs. Increases in aquaporin expression are associated with greater severity of many cancers, particularly in augmenting motility and invasiveness for example in colon cancers and glioblastoma. However, potential roles of altered aquaporin (AQP) function in reproductive cancers have been understudied to date. Published work reviewed here shows distinct classes aquaporin have differential roles in mediating cancer metastasis, angiogenesis, and resistance to apoptosis. Known mechanisms of action of AQPs in other tissues are proving relevant to understanding reproductive cancers. Emerging patterns show AQPs 1, 3, and 5 in particular are highly expressed in breast, endometrial, and ovarian cancers, consistent with their gene regulation by estrogen response elements, and AQPs 3 and 9 in particular are linked with prostate cancer. Continuing work is defining avenues for pharmacological targeting of aquaporins as potential therapies to reduce female and male reproductive cancer cell growth and invasiveness.
Keywords: AQPs
aquaporins
metastasis
reproductive cancer
Rights: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
DOI: 10.3390/cells10020215
Grant ID: http://purl.org/au-research/grants/arc/DP190101745
Published version: http://dx.doi.org/10.3390/cells10020215
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