Related Experiment Video
Updated: Nov 19, 2025

07:00
Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
Published on: February 28, 2019
6.1K
Genetics and Epigenetics of Nasal Polyposis: A Systematic Review
M J Martin1,2,3, A Garcia-Sanchez1,2,4, M Estravis1,2,4
1IBSAL, Institute of Biomedical Research of Salamanca, Salamanca, Spain.
Journal of Investigational Allergology & Clinical Immunology
|January 27, 2021
Summary
Genetic and epigenetic variations are crucial in chronic rhinosinusitis with nasal polyposis (CRSwNP). This review compiles over 150 genetic variants and 89 miRNAs, offering insights for targeted CRSwNP treatments.
Area of Science:
- Genetics and Epigenetics
- Immunology
- Otolaryngology
Background:
- Chronic rhinosinusitis with nasal polyposis (CRSwNP) is a complex inflammatory upper airway disease.
- Genetic and environmental factors are implicated in CRSwNP pathogenesis.
- Understanding these factors is key to developing effective treatments.
Purpose of the Study:
- To systematically review genetic and epigenetic variations associated with CRSwNP since 2000.
- To identify genes, genetic variants, and microRNAs (miRNAs) involved in CRSwNP.
- To explore potential gene-miRNA interactions for future research.
Main Methods:
- Systematic literature review of studies published from 2000 onwards.
- Inclusion of articles focusing on genetic and epigenetic factors in CRSwNP.
- Analysis and synthesis of identified genetic variants, genes, and miRNAs.
Main Results:
- 104 articles were reviewed, with 24 focusing on epigenetics.
- Over 150 genetic variants in 99 genes linked to CRSwNP pathogenesis were identified.
- 89 miRNAs associated with cell cycle, inflammation, and immune response were found, forming 8 gene networks.
Conclusions:
- Genetic and epigenetic factors significantly contribute to CRSwNP development.
- Identified gene variants and miRNAs provide potential therapeutic targets.
- Further research into gene-miRNA interactions could lead to personalized CRSwNP treatments.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
17.4K
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,...
17.4K
Incomplete Dominance
28.8K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
28.8K
Human Genetics
1.1K
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
The complex relationship between genetics and psychology is observable through common biological components such...
1.1K
Cystic Fibrosis: Pathogenesis
550
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
550
Genomic Imprinting and Inheritance
36.1K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
36.1K

