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MicroRNA and ER stress in cancer
- Source :
- Seminars in cancer biology. 75
- Publication Year :
- 2020
-
Abstract
- The development of biological technologies in genomics, proteomics, and bioinformatics has led to the identification and characterization of the complete set of coding genes and their roles in various cellular pathways in cancer. Nevertheless, the cellular pathways have not been fully figured out like a jigsaw puzzle with missing pieces. The discovery of noncoding RNAs including microRNAs (miRNAs) has provided the missing pieces of the cellular pathways. Likewise, miRNAs have settled many questions of inexplicable patches in the endoplasmic reticulum (ER) stress pathways. The ER stress-caused pathways typified by the unfolded protein response (UPR) are pivotal processes for cellular homeostasis and survival, rectifying uncontrolled proteostasis and determining the cell fate. Although various factors and pathways have been studied and characterized, the understanding of the ER stress requires more wedges to fill the cracks of knowledge about the ER stress pathways. Moreover, the roles of the ER stress and UPR are still controversial in cancer despite their strong potential to promote cancer. The noncoding RNAs, in particular, miRNAs aid in a better understanding of the ER stress and its role in cancer. In this review, miRNAs that are the more-investigated subtype of noncoding RNAs are focused on the interpretation of the ER stress in cancer, following the introduction of miRNA and ER stress.
- Subjects :
- 0301 basic medicine
Cancer Research
Endoplasmic reticulum
Cancer
Cellular homeostasis
Computational biology
Biology
Cell fate determination
Proteomics
medicine.disease
Endoplasmic Reticulum Stress
Gene Expression Regulation, Neoplastic
03 medical and health sciences
MicroRNAs
030104 developmental biology
0302 clinical medicine
Proteostasis
030220 oncology & carcinogenesis
Neoplasms
microRNA
Unfolded protein response
medicine
Unfolded Protein Response
Animals
Humans
Subjects
Details
- ISSN :
- 10963650
- Volume :
- 75
- Database :
- OpenAIRE
- Journal :
- Seminars in cancer biology
- Accession number :
- edsair.doi.dedup.....c5bef89b2bd9391ce1842e3f3e71699c