IP Receptor Biology and Endoplasmic Reticulum Calcium Dynamics in Cancer.

Prog Mol Subcell Biol

Laboratory for Molecular and Cellular Signaling, Department of Cellular and Molecular Medicine & Leuven Cancer Institute, KU Leuven, Leuven, Belgium.

Published: August 2021

AI Article Synopsis

  • The IPR (inositol 1,4,5-trisphosphate receptor) is a special channel in cells that helps control calcium signals, which are important for many cell functions.
  • There are three types of IPR (IPR1, IPR2, and IPR3), and their balance is crucial because problems with them can be linked to diseases like cancer.
  • This review talks about how the IPR influences cancer by affecting processes like cell death, growth, and movement, and it suggests that understanding how IPR is regulated could lead to new cancer treatments.

Article Abstract

Intracellular Ca signaling regulates a plethora of cellular functions. A central role in these processes is reserved for the inositol 1,4,5-trisphosphate receptor (IPR), a ubiquitously expressed Ca-release channel, mainly located in the endoplasmic reticulum (ER). Three IPR isoforms (IPR1, IPR2 and IPR3) exist, encoded respectively by ITPR1, ITPR2 and ITPR3. The proteins encoded by these genes are each about 2700 amino acids long and assemble into large tetrameric channels, which form the target of many regulatory proteins, including several tumor suppressors and oncogenes. Due to the important role of the IPRs in cell function, their dysregulation is linked to multiple pathologies. In this review, we highlight the complex role of the IPR in cancer, as it participates in most of the so-called "hallmarks of cancer". In particular, the IPR directly controls cell death and cell survival decisions via regulation of autophagy and apoptosis. Moreover, the IPR impacts cellular proliferation, migration and invasion. Typical examples of the role of the IPRs in these various processes are discussed. The relative levels of the IPR isoforms expressed and their subcellular localization, e.g. at the ER-mitochondrial interface, is hereby important. Finally, evidence is provided about how the knowledge of the regulation of the IPR by tumor suppressors and oncogenes can be exploited to develop novel therapeutic approaches to fight cancer.

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Source
http://dx.doi.org/10.1007/978-3-030-67696-4_11DOI Listing

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