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Open AccessJournal ArticleDOI

Risk genes in head and neck cancer: A systematic review and meta-analysis of last 5 years

TLDR
The aim of this work was to identify risk genes related to the development and progression of squamous cell carcinoma head and neck (SCCHN) and do a meta-analysis of available estimates, showing no significant association between different allelic variants of Arg72Pro rs1042522 and SCCHN risk.
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This article is published in Oral Oncology.The article was published on 2014-03-01 and is currently open access. It has received 48 citations till now. The article focuses on the topics: Odds ratio.

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Journal ArticleDOI

Head and neck cancer management and cancer stem cells implication

TL;DR: There is a newly proposed theory based on the activity of cancer stem cells (CSCs) as the model for carcinogenesis, which may explain the high mortality rate, low response to treatments, and tendency to develop multiple tumors for HNSCC patients.
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Mutation and Transcriptional Profiling of Formalin-Fixed Paraffin Embedded Specimens as Companion Methods to Immunohistochemistry for Determining Therapeutic Targets in Oropharyngeal Squamous Cell Carcinoma (OPSCC): A Pilot of Proof of Principle

TL;DR: These preliminary experiments are among the earliest to combine both mutational and gene expression profiles using Ion Torrent and NanoString technologies and show the utility of these methods with routine FFPE clinical specimens to identify potential therapeutic targets which could be readily applied in a clinical trial setting.
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Knocking down of p53 triggers apoptosis and autophagy, concomitantly with inhibition of migration on SSC-4 oral squamous carcinoma cells.

TL;DR: An in vitro RNA interference experiment provides a proof that a direct connection between p53 knockdown and OSCC cell death can be established, therefore opening new potential directions in OSCC molecular therapeutics and management.
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Anomalous altered expressions of downstream gene-targets in TP53-miRNA pathways in head and neck cancer

TL;DR: Meta-analyses of microarray and RNA-Seq data followed by qRT-PCR validation unravel these new ones in HNSCC and establish systems-level functional and mechanistic insights into the etiology of H NSCC.
References
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Journal ArticleDOI

Signaling to NF-kappaB.

TL;DR: An overview of established NF-kappaB signaling pathways is provided with focus on the current state of research into the mechanisms that regulate IKK activation and NF- kappaB transcriptional activity.
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Human DNA Repair Genes

TL;DR: Modulation of DNA repair should lead to clinical applications including improvement of radiotherapy and treatment with anticancer drugs and an advanced understanding of the cellular aging process.
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MicroRNA: Biogenesis, Function and Role in Cancer.

TL;DR: The P-body model outlines microRNA sorting and shuttling between specialized P- body compartments that house enzymes required for slicer –dependent and –independent silencing, addressing the reversibility of these silencing mechanisms.
Journal ArticleDOI

The codon 72 polymorphic variants of p53 have markedly different apoptotic potential.

TL;DR: It is found that in cell lines containing inducible versions of alleles encoding the Pro72 and Arg72 variants, and in cells with endogenous p53, the Arg72 variant induces apoptosis markedly better than does the Pro 72 variant.
Related Papers (5)
Frequently Asked Questions (14)
Q1. What are the contributions mentioned in the paper "Risk genes in head and neck cancer: a systematic review and meta-analysis of last 5 years" ?

The case-control studies guidelines of the Scottish Intercollegiate Guidelines Network and MOOSE are followed. Two members of the team ( AB, AMZ ) evaluated complete articles independently and double-blinded, to establish their quality. The papers were encoded and delivered independently to each reviewer. 

It is known that the p53 suppressor tumor gene has a key role in stress cellular response, to preserve genome stability, and it is universally recognized as a human cancer marker when it is mutated. 

Overexpression of the DEC1 Protein InducesSenescence In Vitro and Is Related to Better Survival in Esophageal Squamous Cell Carcinoma. 

59 The AA genotype of the ADH1B R48H gene encodes an enzyme that is about 40 times more active than the enzyme encoded by AG and GG genotypes. 

The evaluation of diagnostic markers such as symptoms and genetic tests helps to increase the sensitivity or specificity of the determination of the presence/absence of malignancy. 

Authors such as Piva et al. 48 have observed inflammatory infiltrate in epithelial dysplasia with overexpression of NFKB and TNF-α, establishing a connection between the cancer and inflammation. 

61,62 Research by Su et al. 62 showed that allele G of CRYAB C-802G is correlated to breast cancer risk, and could be useful as a clinical marker for its early detection. 

the model proposed in this paper could fit models 1, 2, and 3 because it considers such epigenetic events as inflammation, mutational compounds such as tobacco and alcohol, and genomic stability and the cell cycle regulation process. 

The authors conducted a systematic review and meta-analysis of case-control studies from the MEDLINE, Scopus, Cochrane, and CancerLit databases between January 2007 and January 2013. 

3,29 Cancer is a complex pathology, and its incidence and survival index are closely related to social, cultural and socio-economic determinants of health. 

Pradhan S, Nagashri MN, Gopinath KS, Kumar A.Expression profiling of CYP1B1 in oral squamous cell carcinoma: counter intuitive down regulation in tumors. 

This gene encodes glutathioneStransferase Mu 1, which is critical to detoxification and the removal of electrophilic carcinogens. 

The identification of a predictive model of risk polymorphisms could help in early diagnosis, and in understanding disease recurrence and/or progression in the subset of patients. 

A search was made of combined electronic databases, and the bibliographies of all selected papers were searched to identify grey literature.