Adrian L. Harris
Targeting hypoxia regulated sodium driven bicarbonate transporters reduces triple negative breast cancer metastasis
Harris, Adrian L.; Clarke, Philip A.; Carroll, Christopher Paul; Bolland, Hannah; Vancauwenberghe, Eric; Collier, Pamela; Ritchie, Alison A.; Grabowska, Anna M.; McIntyre, Alan
Authors
Philip A. Clarke
Christopher Paul Carroll
Hannah Bolland
Eric Vancauwenberghe
Pamela Collier
Alison A. Ritchie
Anna M. Grabowska
Professor Alan McIntyre ALAN.MCINTYRE@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR ONCOLOGY
Abstract
Regions of low oxygen (hypoxia) are found in >50% of breast tumours, most frequently in the more aggressive triple negative breast cancer subtype (TNBC). Metastasis is the cause of 90% of breast cancer patient deaths. Regions of tumour hypoxia tend to be more acidic and both hypoxia and acidosis increase tumour metastasis. In line with this the metastatic process is dependent on pH regulatory mechanisms. We and others have previously identified increased hypoxic expression of Na+ driven bicarbonate transporters (NDBTs) as a major mechanism of tumour pH regulation. Hypoxia induced the expression of NDBTs in TNBC, most frequently SLC4A4 and SLC4A5. NDBT inhibition (S0859) and shRNA knockdown suppressed migration (40% reduction) and invasion (70% reduction) in vitro. Tumour xenograft metastasis in vivo was significantly reduced by NDBT knockdown. To investigate the mechanism by which NDBTs support metastasis, we investigated their role in regulation of phospho-signalling, epithelial-to-mesenchymal transition (EMT) and metabolism. NDBT knockdown resulted in an attenuation in hypoxic phospho-signalling activation; most notably LYN (Y397) reduced by 75%, and LCK (Y394) by 72%. The metastatic process is associated with EMT. We showed that NDBT knockdown inhibited EMT, modulating the expression of key EMT transcription factors and ablating the expression of vimentin whilst increasing the expression of E-cadherin. NDBT knockdown also altered metabolic activity reducing overall ATP and extracellular lactate levels. These results demonstrate that targeting hypoxia-induced NDBT can be used as an approach to modulate phospho-signalling, EMT, and metabolic activity and reduce tumour migration, invasion, and metastasis in vivo.
Citation
Harris, A. L., Clarke, P. A., Carroll, C. P., Bolland, H., Vancauwenberghe, E., Collier, P., Ritchie, A. A., Grabowska, A. M., & McIntyre, A. (2022). Targeting hypoxia regulated sodium driven bicarbonate transporters reduces triple negative breast cancer metastasis. Neoplasia, 25, 41-52. https://doi.org/10.1016/j.neo.2022.01.003
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 21, 2022 |
Online Publication Date | Feb 9, 2022 |
Publication Date | Mar 1, 2022 |
Deposit Date | Jan 27, 2022 |
Publicly Available Date | Feb 14, 2022 |
Journal | Neoplasia |
Print ISSN | 1522-8002 |
Electronic ISSN | 1476-5586 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 25 |
Pages | 41-52 |
DOI | https://doi.org/10.1016/j.neo.2022.01.003 |
Keywords | Cancer Research |
Public URL | https://nottingham-repository.worktribe.com/output/7343399 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S1476558622000033?via%3Dihub |
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Targeting hypoxia regulated sodium driven bicarbonate transporters reduces triple negative breast cancer metastasis
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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