2022
DOI: 10.5603/rpor.a2022.0109
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Gene polymorphisms and prognosis of head and neck squamous cell carcinoma: a systematic review

Abstract: This article has been peer reviewed and published immediately upon acceptance.It is an open access article, which means that it can be downloaded, printed, and distributed freely, provided the work is properly cited.

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Cited by 3 publications
(3 citation statements)
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“…A common genetic occurrence in the progression of HNSCCs is a mutation in the gene ARF, which causes the appearance of p14arf ( Chantre-Justino et al, 2022 ). In addition to p53 signaling pathways, secondary factors such as B-cell lymphoma 2 associated X protein (Bax) and Bcl-2 of the apoptotic regulator may be affected ( Rajabi-Moghaddam and Abbaszadeh, 2022 ). A prognostic marker for oropharyngeal HNSCCs is human papillomavirus type 16 (HPV16) ( Boza.…”
Section: Molecular Signaling Cascades Associated With Hnsccmentioning
confidence: 99%
“…A common genetic occurrence in the progression of HNSCCs is a mutation in the gene ARF, which causes the appearance of p14arf ( Chantre-Justino et al, 2022 ). In addition to p53 signaling pathways, secondary factors such as B-cell lymphoma 2 associated X protein (Bax) and Bcl-2 of the apoptotic regulator may be affected ( Rajabi-Moghaddam and Abbaszadeh, 2022 ). A prognostic marker for oropharyngeal HNSCCs is human papillomavirus type 16 (HPV16) ( Boza.…”
Section: Molecular Signaling Cascades Associated With Hnsccmentioning
confidence: 99%
“…Genetic heterogeneity results in the activation of protein-coding oncogenes, e.g., EGFR and PIK3CA, and a loss of function in tumor-suppressor genes, e.g., p53 and p16 [4]. In spite of the identification of the genes involved in the development and prognosis of HNSCC [8,9], no dramatic changes in recovery rates have been observed. However, these protein-coding transcripts constitute only about 2% of the human genome, and most of the genome consists of the non-coding genes which are responsible for regulation of cellular processes [10][11][12].…”
Section: Introductionmentioning
confidence: 99%
“…The characteristics of HNSCC are a poor response to treatment and high mortality, where only about 50–60% of patients reach the 5-year survival rate. Thus, there is an urgent need to develop novel, more effective, personalized therapies and specific prognostic biomarkers which are based on genes with protein-coding and non-coding abilities [ 3 , 4 , 5 , 6 ]. However, knowledge of the exact molecular mechanisms driving HNSCC is still limited.…”
Section: Introductionmentioning
confidence: 99%