Related Experiment Video
Updated: May 9, 2025

11:29
miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
10.8K
Non-coding RNAs PROX1-AS1 and miR-647: Potential Interaction and Prognostic Value in Gastric Cancer
Irina V Bure1,2, Ekaterina A Vetchinkina1, Ekaterina B Kuznetsova1,3
1Laboratory of Medical Genetics, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119991, Moscow, Russia.
Current Molecular Medicine
|May 6, 2025
Summary
Gastric cancer (GC) progression is linked to specific non-coding RNAs (ncRNAs). This study found a negative correlation between PROX1-AS1 and miR-647 in GC tissues, suggesting their potential as prognostic biomarkers.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Gastric cancer (GC) is a leading cause of cancer mortality globally.
- Non-coding RNAs (ncRNAs), including microRNAs and long ncRNAs, play roles in GC pathogenesis and progression.
- ncRNAs are potential diagnostic and prognostic biomarkers for GC.
Purpose of the Study:
- To assess the expression of PROX1-AS1 (Prospero Homeobox 1 Antisense RNA 1) and miR-647 (microRNA-647) in GC.
- To investigate the interaction between PROX1-AS1 and miR-647.
- To evaluate their clinical significance and prognostic value in GC.
Main Methods:
- Quantified PROX1-AS1 and miR-647 expression in 110 GC patient tissues and 65 plasma samples using real-time polymerase chain reaction (RT-PCR).
- Included 38 normal gastric tissue and 49 healthy plasma samples as controls.
- Analyzed correlations with clinical-pathological characteristics and conducted in vitro experiments to assess their interaction.
Main Results:
- PROX1-AS1 expression was significantly decreased, while miR-647 expression was increased in GC tissues compared to controls.
- A negative correlation was observed between PROX1-AS1 and miR-647 in both tumor and adjacent non-tumor tissues.
- Expression levels were associated with clinical-pathological characteristics, including primary tumor size.
Conclusions:
- A negative correlation exists between PROX1-AS1 and miR-647 in GC tissues and cell lines.
- These ncRNAs, particularly their association with tumor size, indicate potential prognostic value for GC.
- Further research into PROX1-AS1 and miR-647 could lead to novel GC biomarkers.
Keywords:
Non-coding RNAsbiomarkercancer cell linesepigeneticsgastric cancerlong noncoding RNAmicroRNAMore Related Videos
Related Concept Videos
MicroRNAs
2.9K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
2.9K
lncRNA - Long Non-coding RNAs
8.4K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
8.4K
mTOR Signaling and Cancer Progression
3.6K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
The mTOR pathway or the...
3.6K

