Significant association between functional microRNA polymorphisms and head and neck cancer susceptibility: a

Yu-Ming Niu1, Xin-Ya Du2, Ming-Yi Lu3

  • 11] Department of Stomatology and Center for Evidence-Based Medicine and Clinical Research, Taihe Hospital, Hubei University of Medicine, 32 South Renmin Road, Shiyan 442000, China [2] Department of Neurosurgery and Evidence-Based Medicine Center, Taihe Hospital, Hubei University of Medicine, 32 South Renmin Road, Shiyan 442000, China.

Scientific Reports
|August 18, 2015
PubMed

Insights

This meta-analysis reveals specific microRNA polymorphisms are linked to head and neck cancer (HNC) risk. Findings highlight ethnicity-specific associations for microRNA-146a and microRNA-196a2, contributing to understanding HNC development.

Area of Science:

  • Genetics
  • Oncology
  • Molecular Epidemiology

Background:

  • MicroRNA (miRNA) polymorphisms have been investigated for their association with head and neck cancer (HNC) risk.
  • Previous molecular epidemiological studies yielded inconsistent results regarding these associations.

Purpose of the Study:

  • To conduct a comprehensive meta-analysis clarifying the relationship between specific miRNA polymorphisms and HNC risk.
  • To evaluate the influence of ethnicity on these potential associations.

Main Methods:

  • A systematic search of four electronic databases (PubMed, Embase, CNKI, Wanfang) was performed.
  • Meta-analysis included 11 studies with 16,100 subjects, calculating odds ratios (ORs) and 95% confidence intervals (CIs).
  • Polymorphisms analyzed included miR-146a rs2910164 G>C, miR-196a2 rs11614913 C>T, miR-149 rs2292832 C>T, and miR-499 rs3746444 A>G.

Main Results:

  • A significantly increased HNC risk was associated with the miR-146a rs2910164 G>C polymorphism in Caucasian populations.
  • The miR-196a2 rs11614913 C>T polymorphism showed a significantly increased HNC risk in Asian populations.
  • No significant associations were found for miR-149 rs2292832 C>T and miR-499 rs3746444 A>G polymorphisms with HNC risk.

Conclusions:

  • MicroRNA polymorphisms are associated with the development of head and neck cancer.
  • Ethnicity plays a crucial role in the association between specific miRNA polymorphisms and HNC risk, particularly for miR-146a and miR-196a2.

Related Concept Videos

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...
4.3K
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...
24.7K
MicroRNAs01:22

MicroRNAs

12.1K
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...
10.2K
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
19.9K
Loss of Tumor Suppressor Gene Functions01:12

Loss of Tumor Suppressor Gene Functions

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
6.3K