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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

Targeting hypoxia regulated sodium driven bicarbonate transporters reduces triple negative breast cancer metastasis Thumbnail


Authors

Adrian L. Harris

Philip A. Clarke

Christopher Paul Carroll

Hannah Bolland

Eric Vancauwenberghe

Pamela Collier

Alison A. Ritchie

ANNA GRABOWSKA ANNA.GRABOWSKA@NOTTINGHAM.AC.UK
Professor of Cancer Microenvironment



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., …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 BV
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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