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Non-Coding RNAs in IGF-1R Signaling Regulation: The Underlying Pathophysiological Link between Diabetes and Cancer
- Source :
- Cells
- Publication Year :
- 2019
- Publisher :
- MDPI AG, 2019.
-
Abstract
- The intricate molecular network shared between diabetes mellitus (DM) and cancer has been broadly understood. DM has been associated with several hormone-dependent malignancies, including breast, pancreatic, and colorectal cancer (CRC). Insulin resistance, hyperglycemia, and inflammation are the main pathophysiological mechanisms linking DM to cancer. Non-coding RNAs (ncRNAs), particularly microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), are widely appreciated as pervasive regulators of gene expression, governing the evolution of metabolic disorders, including DM and cancer. The ways ncRNAs affect the development of DM complicated with cancer have only started to be revealed in recent years. Insulin-like growth factor 1 receptor (IGF-1R) signaling is a master regulator of pathophysiological processes directing DM and cancer. In this review, we briefly summarize a number of well-known miRNAs and lncRNAs that regulate the IGF-1R in DM and cancer, respectively, and further discuss the potential underlying molecular pathogenesis of this disease association.
- Subjects :
- RNA, Untranslated
Colorectal cancer
lncRNAs
Inflammation
Review
Biology
Bioinformatics
Receptor, IGF Type 1
03 medical and health sciences
0302 clinical medicine
Insulin resistance
Neoplasms
Diabetes mellitus
Gene expression
microRNA
Diabetes Mellitus
medicine
Humans
cancer
Receptor
030304 developmental biology
0303 health sciences
diabetes
Cancer
General Medicine
medicine.disease
micoRNAs
3. Good health
Gene Expression Regulation, Neoplastic
MicroRNAs
030220 oncology & carcinogenesis
RNA, Long Noncoding
medicine.symptom
IGF-1R
Signal Transduction
Subjects
Details
- ISSN :
- 20734409
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Cells
- Accession number :
- edsair.doi.dedup.....4007b379c4de96d31bfa8264d3d62d8a
- Full Text :
- https://doi.org/10.3390/cells8121638