Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer

Known as a key effector in breast cancer (BC) progression, calcium (Ca<sup>2+</sup>) is tightly regulated to maintain the desired concentration to fine-tune cell functions. Ca<sup>2+</sup> channels are the main actors among Ca<sup>2+</sup> transporters that contro...

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Main Authors: Mohamed Chamlali, Lise Rodat-Despoix, Halima Ouadid-Ahidouch
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/12/7/994
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author Mohamed Chamlali
Lise Rodat-Despoix
Halima Ouadid-Ahidouch
author_facet Mohamed Chamlali
Lise Rodat-Despoix
Halima Ouadid-Ahidouch
author_sort Mohamed Chamlali
collection DOAJ
description Known as a key effector in breast cancer (BC) progression, calcium (Ca<sup>2+</sup>) is tightly regulated to maintain the desired concentration to fine-tune cell functions. Ca<sup>2+</sup> channels are the main actors among Ca<sup>2+</sup> transporters that control the intracellular Ca<sup>2+</sup> concentration in cells. It is well known that the basal Ca<sup>2+</sup> concentration is regulated by both store-dependent and independent Ca<sup>2+</sup> channels in BC development and progression. However, most of the literature has reported the role of store-dependent Ca<sup>2+</sup> entry, and only a few studies are focusing on store-independent Ca<sup>2+</sup> entry (SICE). In this review, we aim to summarize all findings on SICE in the BC progression field.
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spelling doaj.art-7bcd198a097c40479197e76964d59bd42023-12-03T13:15:47ZengMDPI AGGenes2073-44252021-06-0112799410.3390/genes12070994Store-Independent Calcium Entry and Related Signaling Pathways in Breast CancerMohamed Chamlali0Lise Rodat-Despoix1Halima Ouadid-Ahidouch2Laboratory of Cellular and Molecular Physiology, UR-UPJV 4667, University of Picardie Jules Verne, 80000 Amiens, FranceLaboratory of Cellular and Molecular Physiology, UR-UPJV 4667, University of Picardie Jules Verne, 80000 Amiens, FranceLaboratory of Cellular and Molecular Physiology, UR-UPJV 4667, University of Picardie Jules Verne, 80000 Amiens, FranceKnown as a key effector in breast cancer (BC) progression, calcium (Ca<sup>2+</sup>) is tightly regulated to maintain the desired concentration to fine-tune cell functions. Ca<sup>2+</sup> channels are the main actors among Ca<sup>2+</sup> transporters that control the intracellular Ca<sup>2+</sup> concentration in cells. It is well known that the basal Ca<sup>2+</sup> concentration is regulated by both store-dependent and independent Ca<sup>2+</sup> channels in BC development and progression. However, most of the literature has reported the role of store-dependent Ca<sup>2+</sup> entry, and only a few studies are focusing on store-independent Ca<sup>2+</sup> entry (SICE). In this review, we aim to summarize all findings on SICE in the BC progression field.https://www.mdpi.com/2073-4425/12/7/994calcium channelsbasal calcium entryOrai-K<sup>+</sup> channel complextransient receptor potential channelsvoltage-gated calcium channelsbreast cancer
spellingShingle Mohamed Chamlali
Lise Rodat-Despoix
Halima Ouadid-Ahidouch
Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer
Genes
calcium channels
basal calcium entry
Orai-K<sup>+</sup> channel complex
transient receptor potential channels
voltage-gated calcium channels
breast cancer
title Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer
title_full Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer
title_fullStr Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer
title_full_unstemmed Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer
title_short Store-Independent Calcium Entry and Related Signaling Pathways in Breast Cancer
title_sort store independent calcium entry and related signaling pathways in breast cancer
topic calcium channels
basal calcium entry
Orai-K<sup>+</sup> channel complex
transient receptor potential channels
voltage-gated calcium channels
breast cancer
url https://www.mdpi.com/2073-4425/12/7/994
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