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Endoplasmic reticulum stress and cancer
Raj Kumar Yadav1, Soo-Wan Chae1, Hyung-Ryong Kim2
1Department of Pharmacology and Institute of Cardiovascular Research, School of Medicine, Chonbuk National University, Jeonju, Chonbuk, Korea.
The endoplasmic reticulum (ER) stress and the unfolded protein response (UPR) are linked to cancer development and therapy resistance. Understanding UPR
Area of Science:
- Cell Biology
- Molecular Biology
- Oncology
Background:
- The endoplasmic reticulum (ER) is crucial for protein folding, maturation, and cellular homeostasis.
- ER stress, triggered by various factors, activates the unfolded protein response (UPR).
- The UPR can restore homeostasis or initiate cell death.
Purpose of the Study:
- To review the role of different UPRs in tumorigenesis.
- To explore the involvement of UPR in cancer therapy resistance.
- To elucidate the UPR's function in the tumor microenvironment.
Main Methods:
- Literature review of studies on ER stress, UPR, and cancer.
- Analysis of UPR pathways in cancer development.
- Examination of UPR's role in therapeutic resistance.
Main Results:
- ER stress and UPR are implicated in cancer initiation and progression.
- UPR contributes to the unique tumor microenvironment.
- UPR acts as a resistance mechanism against cancer therapies.
Conclusions:
- The UPR plays a significant role in tumorigenesis.
- UPR pathways are key mediators of resistance to cancer therapy.
- Targeting UPR may offer novel therapeutic strategies for cancer.
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