•  Home
  • Library
  • DRO home
Submit research Contact DRO

DRO

Openly accessible

Bumetanide-derived aquaporin 1 inhibitors, AqB013 and AqB050 inhibit tube formation of endothelial cells through induction of apoptosis and impaired migration in vitro

Tomita, Y, Palethorpe, HM, Smith, E, Nakhjavani, Maryam, Townsend, AR, Price, TJ, Yool, AJ and Hardingham, JE 2019, Bumetanide-derived aquaporin 1 inhibitors, AqB013 and AqB050 inhibit tube formation of endothelial cells through induction of apoptosis and impaired migration in vitro, International Journal of Molecular Sciences, vol. 20, no. 8, pp. 1-11, doi: 10.3390/ijms20081818.

Attached Files
Name Description MIMEType Size Downloads

Title Bumetanide-derived aquaporin 1 inhibitors, AqB013 and AqB050 inhibit tube formation of endothelial cells through induction of apoptosis and impaired migration in vitro
Author(s) Tomita, Y
Palethorpe, HM
Smith, E
Nakhjavani, Maryam
Townsend, AR
Price, TJ
Yool, AJ
Hardingham, JE
Journal name International Journal of Molecular Sciences
Volume number 20
Issue number 8
Article ID 1818
Start page 1
End page 11
Total pages 11
Publisher MDPI
Place of publication Basel, Switzerland
Publication date 2019-04
ISSN 1661-6596
1422-0067
Keyword(s) angiogenesis
apoptosis
AqB013
AqB050
AQP1
aquaporin 1 (AQP1)
Biochemistry & Molecular Biology
Chemistry
Chemistry, Multidisciplinary
endothelial cells
EXPRESSION
Life Sciences & Biomedicine
LUNG-CANCER
migration
MOUSE MODEL
PERMEABILITY
Physical Sciences
PROLIFERATION
Science & Technology
TUMOR-GROWTH
WATER
Summary AqB013 and AqB050 compounds inhibit aquaporin 1 (AQP1), a dual water and ion channel implicated in tumour angiogenesis. We tested AqB013 and AqB050 either as monotherapy or in combination on tube formation of murine endothelial cells (2H-11 and 3B-11) and human umbilical vascular endothelial cells (HUVECs). The mechanism underlying their anti-tubulogenic effect was explored by examining cell viability, induction of apoptosis and migration using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay, Annexin V/propidium iodide apoptosis assay and scratch wound assay. Tube formation of all the cell lines was inhibited by AqB013, AqB050 and the combination of the two compounds. The inhibition of 2H-11 and 3B-11 was frequently accompanied by impaired migration, whereas that of HUVEC treated with AqB050 and the combination was associated with reduced cell viability due to apoptosis. AqB013 and AqB050 exhibited an anti-tubulogenic effect through inhibition of AQP1-mediated cell migration and induction of apoptosis. Together with previously reported anti-tumour cell effect of AqB013 and AqB050, our findings support further evaluation of these compounds as potential cancer therapeutics
Language eng
DOI 10.3390/ijms20081818
Field of Research 0399 Other Chemical Sciences
0604 Genetics
0699 Other Biological Sciences
HERDC Research category C1 Refereed article in a scholarly journal
Free to Read? Yes
Persistent URL http://hdl.handle.net/10536/DRO/DU:30159023

Document type: Journal Article
Collections: Faculty of Health
School of Medicine
Open Access Collection
Related Links
Link Description
Link to full-text (open access)  
Connect to Elements publication management system
Go to link with your DU access privileges
 
Connect to link resolver
 
Unless expressly stated otherwise, the copyright for items in DRO is owned by the author, with all rights reserved.

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.

Versions
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 11 times in TR Web of Science
Scopus Citation Count Cited 13 times in Scopus Google Scholar Search Google Scholar
Access Statistics: 44 Abstract Views, 0 File Downloads  -  Detailed Statistics
Created: Mon, 22 Nov 2021, 09:36:10 EST

Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.