The water channels Aquaporin-1 and Aquaporin-3 interact with and affect the cell polarity protein Scribble in 3D in vitro models of breast cancer.

Aquaporin Breast cancer Polarity Scribble

Journal

American journal of physiology. Cell physiology
ISSN: 1522-1563
Titre abrégé: Am J Physiol Cell Physiol
Pays: United States
ID NLM: 100901225

Informations de publication

Date de publication:
16 Sep 2024
Historique:
medline: 16 9 2024
pubmed: 16 9 2024
entrez: 16 9 2024
Statut: aheadofprint

Résumé

Cellular changes in carcinomas include alterations in cell proliferation, cell migration, cell-cell adhesion and cellular polarity. In vitro studies have revealed that the water channels, aquaporin-1 (AQP1) and AQP3 can influence cell migration and cell-cell adhesion. Of note, we previously showed that AQP1 overexpression reduced levels of cell-cell adhesion proteins, whereas AQP3 increased levels when overexpressed in normal epithelial cells. Expression of AQP1 and AQP3 in breast carcinoma is associated with lymph node metastasis, recurrence, and poor survival of breast cancer patients. In this study, we investigated if AQP1 and AQP3 affected cell polarity in breast cancer by studying the relationship between the major polarity protein Scribble and AQP1 and AQP3. In breast cancer tissue samples, the protein expression of AQP1, AQP3 and Scribble did not show an obvious correlation. However, in a GST pull-down assay, AQP1 and AQP3 interacted with Scribble. AQP1 overexpression reduced the size of 3D spheroids as well as reduced Scribble levels at cell-cell contacts, whereas AQP3 overexpression showed no significant change in spheroid size compared to control, AQP3 overexpression also reduced Scribble levels at cell-cell contacts. Of note, AQP1 overexpression increased cell migration and induced cell detachment and dissemination from migrating breast cancer cell sheets, whereas AQP3 overexpression did not. Thus, AQP1 and AQP3 differentially affect 3D grown breast cancer spheroids and especially AQP1 may contribute to cancer development and spread via negatively affecting cellular junctions and cell polarity proteins as well as increasing cell migration and cell detachment.

Identifiants

pubmed: 39279492
doi: 10.1152/ajpcell.00094.2024
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NEYE Foundation
ID : NA
Organisme : The Graduate School of Health AU
ID : NA
Organisme : A.P. Møller Fonden | Fonden til Lægevidenskabens Fremme (A.P. Møller Fonden til Lægevidenskabens Fremme)
ID : NA
Organisme : Fabrikant Einar Willumsens Mindelegat (Manufacturer Einar Willumsens Minelegat)
ID : NA
Organisme : Dagmar Marshalls Fond (Dagmar Marshalls Fund)
ID : NA
Organisme : Else og Mogens Wedell Wedellsborgs Fond (Else and Mogens Wedell Wedellsborgs Fund)
ID : NA

Auteurs

Sarannya Edamana (S)

Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.

Frédéric H Login (FH)

Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.

Andreas Riishede (A)

Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.

Vibeke S Dam (VS)

Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.

Teresa Kirkegaard (T)

Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.

Lene N Nejsum (LN)

Department of Clinical Medicine, Aarhus University, Aarhus N, Denmark.

Classifications MeSH