Objectives: microRNAs (miRNAs), are non-coding RNAs that regulate gene expression, and are involved in tumour development. The aim of this study was to investigate microRNA-497 (miR-497) expression and its role in development of colorectal cancer (CRC).

Materials And Methods: RT-PCR was performed to detect expression of miR-497 in CRC cell lines (HCT8, LOVO, Ls-174, HCT116 and HT29) and in clinical cancer specimens. To further understand its role, we restored expression of miR-497 in the HCT116 cell line by transfection with miR-497 mimics or inhibitors. Effects of miR-497 on cell proliferation, migration and invasion of targets were also determined both in vitro and in vivo.

Results: miR-497 expression decreased in 34 CRC tissues compared to non-tumour tissues and in tumour cell lines. Overexpression of miR-497 did not inhibit cancer cell growth but suppressed metastasis and invasion both in vitro and in vivo. Vascular endothelial growth factor-A (VEGF-A) was confirmed to be a target of miR-497. Furthermore, we found overexpression of miR-497 altered expression of key molecules of the VEGF-A/ERK/MMP-9 signalling pathway.

Conclusions: Thus our results provide evidence that miR-497 might function as a metastasis suppressor in CRC. Targeting miR-497 may provide a strategy for blocking its metastasis.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495881PMC
http://dx.doi.org/10.1111/cpr.12237DOI Listing

Publication Analysis

Top Keywords

mir-497
11
colorectal cancer
8
vascular endothelial
8
endothelial growth
8
growth factor-a
8
mir-497 expression
8
expression mir-497
8
cell lines
8
overexpression mir-497
8
expression
6

Similar Publications

Fibroblasts play a crucial role in diabetic wound healing, and their senescence is the cause of delayed wound repair. It was reported that fibroblasts can secrete exosomes that can mediate a vital role in diabetic complications. Our purpose is to examine the biological function of high glucose (HG)-induced senescent fibroblasts from the perspective of exosomes and reveal the mechanism at cellular and animal levels.

View Article and Find Full Text PDF

Objectives: Electroconvulsive therapy (ECT) is one of the most effective treatments for treatment-resistant depression (TRD), even though the molecular mechanisms underlying its efficacy remain largely unclear. This study aimed, for the first time, to analyze plasma levels of miRNAs, key regulators of gene expression, in TRD patients undergoing ECT to investigate potential changes during treatment and their associations with symptom improvement.

Methods: The study involved 27 TRD patients who underwent ECT.

View Article and Find Full Text PDF

Objective: To evaluate the characteristics of the circulating microRNA expression profiles in patients with osteoporosis.

Methods: A systematic literature search was performed using the Web of Science, PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure (CNKI), VIP, and WANFANG databases from inception until 1 March 2024. The search strategy employed keywords, encompassing "osteoporosis", "bone loss", or "osteopenia" and "miRNA" or "microRNA".

View Article and Find Full Text PDF
Article Synopsis
  • Bone marrow mesenchymal stem cells (BMSCs) show promise for treating spinal cord injuries (SCI) due to their ability to release exosomes (BMSC-Exos) that aid in repair processes.
  • In a rat model of SCI, the study demonstrated that BMSC-Exos led to improved motor function, reduced inflammation, and decreased oxidative stress, indicating effective healing mechanisms.
  • The mechanism involves the microRNA miR-497-5p, which enhances the protective effects of BMSC-Exos by regulating the TXNIP/NLRP3 pathway, potentially offering a target for SCI treatment strategies.
View Article and Find Full Text PDF
Article Synopsis
  • Preeclampsia (PE) is a significant topic in obstetrics research, yet its mechanisms are not fully understood, prompting the analysis of several gene expression datasets to identify differences between PE and control groups.
  • Researchers established a competitive endogenous RNA (ceRNA) network, identifying five hub genes (DAXX, EFNB1, NCOR2, RBBP4, and SOCS1) linked to PE and predicted potential drugs that could interact with these genes.
  • The study's findings highlight AGAP2-AS1's role in a regulatory network involving 41 mRNAs and two miRNAs, aiming to deepen the understanding of the molecular connections in PE and create a basis for future scientific exploration.
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!