Structural and Functional Significance of the Endoplasmic Reticulum Unfolded Protein Response Transducers and Chaperones at the Mitochondria-ER Contacts: A Cancer Perspective

In the last decades, the endoplasmic reticulum (ER) has emerged as a key coordinator of cellular homeostasis, thanks to its physical interconnection to almost all intracellular organelles. In particular, an intense and mutual crosstalk between the ER and mitochondria occurs at the mitochondria-ER contacts (MERCs). MERCs ensure a fine-tuned regulation of fundamental cellular processes, involving cell fate decision, mitochondria dynamics, metabolism, and proteostasis, which plays a pivotal role in the tumorigenesis and therapeutic response of cancer cells. Intriguingly, recent studies have shown that different components of the unfolded protein response (UPR) machinery, including PERK, IRE1 alpha, and ER chaperones, localize at MERCs. These proteins appear to exhibit multifaceted roles that expand beyond protein folding and UPR transduction and are often related to the control of calcium fluxes to the mitochondria, thus acquiring relevance to cell survival and death. In this review, we highlight the novel functions played by PERK, IRE1 alpha, and ER chaperones at MERCs focusing on their impact on tumor development.

Automated summary

The ER has emerged as a key coordinator of cellular homeostasis due to its connection to almost all intracellular organelles. Intense crosstalk between the ER and mitochondria at MERCs regulates fundamental cellular processes like cell fate decision, metabolism, and proteostasis, impacting tumorigenesis and therapeutic response of cancer cells. Recent studies show that UPR machinery components at MERCs have multifaceted roles related to controlling calcium fluxes to mitochondria, influencing cell survival and death.