4.7 Review

Mg2+ Transporters in Digestive Cancers

Journal

NUTRIENTS
Volume 13, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/nu13010210

Keywords

magnesium transporters; digestive cancers; TCGA; overall survival

Funding

  1. Ministere de l'Enseignement Superieur de la Recherche et de l'Innovation
  2. Universite de Picardie Jules Verne (UPJV)
  3. Universite de Lille
  4. le CHU Amiens-Picardie
  5. Institut National de la Sante et de la Recherche Medicale (Inserm)
  6. Centre National de la Recherche Scientifique (CNRS)
  7. La Ligue Nationale contre le Cancer (comite Septentrion)
  8. l'Agence Nationale de Securite Sanitaire, de l'Alimentation, de l'Environnement et du Travail

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This study investigates the expression of Mg2+ transporters in digestive cancers and their impact on patient survival. The findings suggest that these Mg2+ transporters may affect various cancer cell characteristics and play a crucial role in regulating cancer cell fates and oncogenic signaling pathways.
Despite magnesium (Mg2+) representing the second most abundant cation in the cell, its role in cellular physiology and pathology is far from being elucidated. Mg2+ homeostasis is regulated by Mg2+ transporters including Mitochondrial RNA Splicing Protein 2 (MRS2), Transient Receptor Potential Cation Channel Subfamily M, Member 6/7 (TRPM6/7), Magnesium Transporter 1 (MAGT1), Solute Carrier Family 41 Member 1 (SCL41A1), and Cyclin and CBS Domain Divalent Metal Cation Transport Mediator (CNNM) proteins. Recent data show that Mg2+ transporters may regulate several cancer cell hallmarks. In this review, we describe the expression of Mg2+ transporters in digestive cancers, the most common and deadliest malignancies worldwide. Moreover, Mg2+ transporters' expression, correlation and impact on patient overall and disease-free survival is analyzed using Genotype Tissue Expression (GTEx) and The Cancer Genome Atlas (TCGA) datasets. Finally, we discuss the role of these Mg2+ transporters in the regulation of cancer cell fates and oncogenic signaling pathways.

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