The association of E2F1 and E2F2 single nucleotide polymorphisms with laryngeal squamous cell carcinoma pathomorphological features
- PMID: 38360622
- PMCID: PMC10870611
- DOI: 10.1186/s12885-024-11953-z
The association of E2F1 and E2F2 single nucleotide polymorphisms with laryngeal squamous cell carcinoma pathomorphological features
Abstract
Background: Laryngeal squamous cell carcinoma (LSCC) is one of the most common types of cancer in the upper respiratory tract. It is well-known that it has a high mortality rate and poor prognosis in advanced stages. There are well-known risk factors for LSCC, though new specific and prognostic blood-based markers for LSCC development and prognosis are essential. The current study aimed to evaluate the impact of four different single nucleotide polymorphisms (SNPs), E2F1 (rs3213183 and rs3213180) and E2F2 (rs2075993 and rs3820028), on LSCC development, morphological features, and patient 5-year survival rate.
Methods: A total of 200 LSCC patients and 200 controls were included in this study; both groups were matched by age and sex. In the present study, we analyzed four single nucleotide polymorphisms (SNPs) in the genes E2F1 (rs3213183 and rs3213180) and E2F2 (rs2075993 and rs3820028) and evaluated their associations with the risk of LSCC development, its clinical and morphological manifestation, and patients 5-year survival rate. Genotyping was carried out using RT-PCR.
Results: None of the analyzed SNPs showed a direct association with LSCC development. E2F2 rs2075993 G allele carriers (OR = 4.589, 95% CI 1.050-20.051, p = 0.043) and rs3820028 A allele carriers (OR = 4.750, 95% CI 1.088-20.736, p = 0.038) had a statistically significantly higher risk for poor differentiated or undifferentiated LSCC than non-carriers. E2F1 rs3213180 GC heterozygotes were found to have a 3.7-fold increased risk for lymph node involvement (OR = 3.710, 95% CI 1.452-9.479, p = 0.006). There was no statistically significant association between investigated SNPs and patient 5-year survival rate.
Conclusions: The present study indicates that E2F2 rs2075993 and rs3820028 impact LSCC differentiation, whereas E2F1 rs3213180 - on lymph node involvement.
Keywords: E2F1; E2F2; Laryngeal squamous cell carcinoma; SNP.
© 2024. The Author(s).
Conflict of interest statement
The authors declare that they have no competing interests.
Similar articles
-
The Association of TP53, BCL2, BAX and NOXA SNPs and Laryngeal Squamous Cell Carcinoma Development.Int J Mol Sci. 2024 Nov 4;25(21):11849. doi: 10.3390/ijms252111849. Int J Mol Sci. 2024. PMID: 39519400 Free PMC article.
-
Combined effects of E2F1 and E2F2 polymorphisms on risk and early onset of squamous cell carcinoma of the head and neck.Mol Carcinog. 2012 Oct;51 Suppl 1(Suppl 1):E132-41. doi: 10.1002/mc.21882. Epub 2012 Feb 17. Mol Carcinog. 2012. PMID: 22344756 Free PMC article.
-
Genetic variants of cell cycle pathway genes are associated with head and neck squamous cell carcinoma in the Chinese population.Carcinogenesis. 2021 Nov 12;42(11):1337-1346. doi: 10.1093/carcin/bgab094. Carcinogenesis. 2021. PMID: 34643214
-
Impact of IL-10 Promoter Polymorphisms and IL-10 Serum Levels on Advanced Laryngeal Squamous Cell Carcinoma and Survival Rate.Cancer Genomics Proteomics. 2021 Jan-Feb;18(1):53-65. doi: 10.21873/cgp.20241. Cancer Genomics Proteomics. 2021. PMID: 33419896 Free PMC article.
-
Dysbiosis Patterns in Glottic and Laryngeal Cancers: A Systematic Review of Microbiome Alterations.J Voice. 2025 Mar 10:S0892-1997(25)00083-9. doi: 10.1016/j.jvoice.2025.02.036. Online ahead of print. J Voice. 2025. PMID: 40069023 Review.
References
-
- World Health Organization. Cancer Tomorrow. 2020 [cited 2023 Feb 23]. Available from: https://gco.iarc.fr/today/data/factsheets/cancers/14-Larynx-fact-sheet.pdf.
-
- World Health Organization, International Agency for Research on Cancer. Estimated number of deaths from 2020 to 2040, both sexes, age (0–85+), 2020. [cited 2023 Feb 20]. Available from: https://gco.iarc.fr/tomorrow/en/dataviz/bubbles?sexes=0&mode=population&group_populations=0&multiple_cancers=1&cancers=39_14&group_cancers=1.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases
Miscellaneous