Long noncoding RNA OIP5-AS1 exhibits oncogenic activity in bladder cancer through miR-217 and MTDH

S-F Zhang1, S Pang, F-P Wang

  • 1Department of Urology Surgery, Caoxian People's Hospital, Heze, China. chichenyan9@163.com.

Abstract

Insights

Long non-coding Opa-interacting protein 5 antisense RNA 1 (OIP5-AS1) promotes bladder cancer progression. Targeting the OIP5-AS1/microRNA-217/metadherin axis inhibits cancer cell proliferation and invasion, suggesting OIP5-AS1 as a potential bladder cancer biomarker.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Bladder cancer (BCa) is a significant health concern with complex molecular underpinnings.
  • Long non-coding RNAs (lncRNAs) are increasingly recognized for their roles in cancer development and progression.

Purpose of the Study:

  • To investigate the role of OIP5-AS1 in bladder cancer.
  • To elucidate the molecular mechanism involving OIP5-AS1, microRNA-217 (miR-217), and metadherin (MTDH) in BCa progression.

Main Methods:

  • Quantitative real-time PCR (qRT-PCR) and Western blot to assess OIP5-AS1, miR-217, and MTDH expression.
  • Cell Counting Kit-8 (CCK-8) and Transwell assays to evaluate BCa cell proliferation and invasion.
  • Luciferase reporter assays and Spearman correlation analysis to determine molecular interactions.

Main Results:

  • OIP5-AS1 expression was significantly upregulated in BCa tissues and cells.
  • Knockdown of OIP5-AS1 suppressed BCa cell proliferation and invasion.
  • OIP5-AS1 directly targets miR-217, which in turn targets MTDH, forming the OIP5-AS1/miR-217/MTDH axis.

Conclusions:

  • OIP5-AS1 promotes bladder cancer cell proliferation and invasion via the miR-217/MTDH pathway.
  • OIP5-AS1 functions as an oncogene in human BCa.
  • OIP5-AS1 holds potential as a diagnostic biomarker and therapeutic target for bladder cancer.

Related Concept Videos

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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...
9.3K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

3.1K
MicroRNAs01:22

MicroRNAs

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...
3.3K
MicroRNAs01:22

MicroRNAs

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...
22.8K
Experimental RNAi02:15

Experimental RNAi

RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
6.7K
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
12.4K