Background: New onset diabetes mellitus demonstrates a roughly correlation with pancreatic cancer (PaC), which is unique in PaC and was named as PaC-induced DM, but the inner mechanism remains unclear. Exosomes mediate intercellular communication and bearing microRNAs might be direct constituent of effect in target cells.

Methods And Results: The isolated exosomes from PaC cells were used to treat pancreatic β cells or the primary mice islets, and the glucose stimulated insulin secretions were measured. We validated the exosomal miR-19a from PaC cells to be an important mediator in the down regulation of insulin secretion by targeting Neurod1, the validated gene involved in insulin secretion, by using the quantitative real-time PCR, western blot, and promoter luciferase activity. The relative insulin, cAMP and Ca expressions were also assayed to verify the inverse correlation between cancerous miR-19a and pancreatic islets Neurod1.

Conclusions: Our study indicated that signal changes between cancer cells and β cells via exosomes might be important in the pathogenesis of PaC-induced DM and supplemented the pathogenesis of PaC-induced DM and provide a possible access of PaC screening strategy.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11033-021-06980-zDOI Listing

Publication Analysis

Top Keywords

exosomal mir-19a
8
targeting neurod1
8
pancreatic cancer
8
pac cells
8
insulin secretion
8
pathogenesis pac-induced
8
insulin
5
pac
5
cells
5
mir-19a decreases
4

Similar Publications

Liquid biopsy has an underexplored diagnostic potential in colorectal cancer (CRC). Sufficient quantity and quality of its elements (circulating cell-free DNA (ccfDNA), exosomes and exosomal RNA) are essential for accurate results. The present study aims to establish the optimal protocol for handling liquid biopsy samples.

View Article and Find Full Text PDF
Article Synopsis
  • The study aimed to explore how microRNAs (miRNAs) are expressed in Indian patients with tuberculosis (TB) and how their profiles differ between those with and without HIV coinfection.
  • Researchers analyzed serum exosomes from various groups (HIV-TB coinfected, extra-pulmonary TB, HIV-only, and pulmonary TB) using real-time PCR, identifying significant changes in miRNA levels.
  • Key findings indicated specific miRNAs were differentially expressed among the groups, which are linked to important biological pathways, highlighting their potential role as biomarkers for TB and its progression in Indian patients.*
View Article and Find Full Text PDF
Article Synopsis
  • This study explored the potential of specific microRNAs (miR-19a-3p, miR-92a-3p, miR-193a-3p, and miR-210-3p) as biomarkers for colorectal cancer (CRC) and compared them to existing markers like carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA 19-9).
  • Researchers analyzed tissue samples from 52 CRC and 76 pre-CRC patients, finding that only miR-193a-3p had a significant difference in expression when comparing pre-CRC to CRC and when analyzing CRC tissues vs. exosomes.
  • The combination of CEA and miR-193
View Article and Find Full Text PDF

Alzheimer's disease (AD) is characterized by cognitive decline stemming from the accumulation of beta-amyloid (Aβ) plaques and the propagation of tau pathology through synapses. Exosomes, crucial mediators in neuronal development, maintenance, and intercellular communication, have gained attention in AD research. Yet, the molecular mechanisms involving exosomal miRNAs in AD remain elusive.

View Article and Find Full Text PDF

Exosomes derived from neighboring v-raf murine sarcoma viral oncogene homolog B1 inhibitor (BRAFi)-resistant melanoma cells mediate the formation of resistance in melanoma cells sensitive to BRAFi. The function and molecular mechanisms of exosomal miRNA in BRAFi resistance of melanoma have not been studied. We found that the expression of miR-19a in BRAFi resistant melanoma cells was significantly higher than that in sensitive cells, and miR-19a contributes to the resistance of melanoma cells to BRAFi by targeting immunoglobulin-like domains protein 1 (LRIG1).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!