Loss of the fructose transporter SLC2A5 inhibits cancer cell migration.

cancer cell migration invadopodia metastasis mitochondria

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2022
Historique:
received: 15 03 2022
accepted: 09 09 2022
entrez: 21 10 2022
pubmed: 22 10 2022
medline: 22 10 2022
Statut: epublish

Résumé

Metastasis is the primary cause of cancer patient death and the elevation of SLC2A5 gene expression is often observed in metastatic cancer cells. Here we evaluated the importance of SLC2A5 in cancer cell motility by silencing its gene. We discovered that CRISPR/Cas9-mediated inactivation of the SLC2A5 gene inhibited cancer cell proliferation and migration

Identifiants

pubmed: 36268513
doi: 10.3389/fcell.2022.896297
pii: 896297
pmc: PMC9578049
doi:

Types de publication

Journal Article

Langues

eng

Pagination

896297

Informations de copyright

Copyright © 2022 Groenendyk, Stoletov, Paskevicius, Li, Dai, Pujol, Busaan, Ng, Boukouris, Saleme, Haromy, Cui, Hu, Yan, Zhang, Michelakis, Chen, Lewis, Tang, Agellon and Michalak.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jody Groenendyk (J)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Konstantin Stoletov (K)

Department of Oncology, University of Alberta, Edmonton, AB, Canada.

Tautvydas Paskevicius (T)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Wenjuan Li (W)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Ning Dai (N)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Myriam Pujol (M)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Erin Busaan (E)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Hoi Hei Ng (HH)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Aristeidis E Boukouris (AE)

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

Bruno Saleme (B)

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

Alois Haromy (A)

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

Kaisa Cui (K)

Wuxi Cancer Institute, Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu, China.

Miao Hu (M)

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, China.

Yanan Yan (Y)

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, China.

Rui Zhang (R)

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, China.

Evangelos Michelakis (E)

Department of Medicine, University of Alberta, Edmonton, AB, Canada.

Xing-Zhen Chen (XZ)

Department of Physiology, University of Alberta, Edmonton, AB, Canada.

John D Lewis (JD)

Department of Oncology, University of Alberta, Edmonton, AB, Canada.

Jingfeng Tang (J)

National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan, China.

Luis B Agellon (LB)

School of Human Nutrition, McGill University, Montreal, QC, Canada.

Marek Michalak (M)

Department of Biochemistry, University of Alberta, Edmonton, AB, Canada.

Classifications MeSH