FABP7 Facilitates Uptake of Docosahexaenoic Acid in Glioblastoma Neural Stem-like Cells.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
30 Jul 2021
Historique:
received: 30 06 2021
revised: 26 07 2021
accepted: 29 07 2021
entrez: 27 8 2021
pubmed: 28 8 2021
medline: 5 10 2021
Statut: epublish

Résumé

Glioblastoma (GBM) is an aggressive tumor with a dismal prognosis. Neural stem-like cells contribute to GBM's poor prognosis by driving drug resistance and maintaining cellular heterogeneity. GBM neural stem-like cells express high levels of brain fatty acid-binding protein (FABP7), which binds to polyunsaturated fatty acids (PUFAs) ω-6 arachidonic acid (AA) and ω-3 docosahexaenoic acid (DHA). Similar to brain, GBM tissue is enriched in AA and DHA. However, DHA levels are considerably lower in GBM tissue compared to adult brain. Therefore, it is possible that increasing DHA content in GBM, particularly in neural stem-like cells, might have therapeutic value. Here, we examine the fatty acid composition of patient-derived GBM neural stem-like cells grown as neurosphere cultures. We also investigate the effect of AA and DHA treatment on the fatty acid profiles of GBM neural stem-like cells with or without FABP7 knockdown. We show that DHA treatment increases DHA levels and the DHA:AA ratio in GBM neural stem-like cells, with FABP7 facilitating the DHA uptake. We also found that an increased uptake of DHA inhibits the migration of GBM neural stem-like cells. Our results suggest that increasing DHA content in the GBM microenvironment may reduce the migration/infiltration of FABP7-expressing neural stem-like cancer cells.

Identifiants

pubmed: 34444824
pii: nu13082664
doi: 10.3390/nu13082664
pmc: PMC8402214
pii:
doi:

Substances chimiques

FABP7 protein, human 0
Fatty Acid-Binding Protein 7 0
Fatty Acid-Binding Proteins 0
Fatty Acids 0
Fatty Acids, Omega-3 0
Fatty Acids, Omega-6 0
Fatty Acids, Unsaturated 0
Phospholipids 0
Tumor Suppressor Proteins 0
Docosahexaenoic Acids 25167-62-8
Arachidonic Acid 27YG812J1I

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : CIHR
ID : 130314
Pays : Canada

Commentaires et corrections

Type : CommentIn

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Auteurs

Won-Shik Choi (WS)

Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.

Xia Xu (X)

Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.

Susan Goruk (S)

Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB T6G 2E1, Canada.

Yixiong Wang (Y)

Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.

Samir Patel (S)

Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.

Michael Chow (M)

Department of Surgery, University of Alberta, Edmonton, AB T6G 2B7, Canada.

Catherine J Field (CJ)

Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB T6G 2E1, Canada.

Roseline Godbout (R)

Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.

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