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  4. Expression Profiles of CDKN2A, MDM2, E2F2 and LTF Genes in Oral Squamous Cell Carcinoma
 
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Expression Profiles of CDKN2A, MDM2, E2F2 and LTF Genes in Oral Squamous Cell Carcinoma

Type
Journal article
Language
English
Date issued
2022
Author
Gołąbek, Karolina
Rączka, Grzegorz 
Gaździcka, Jadwiga
Miśkiewicz-Orczyk, Katarzyna
Zięba, Natalia
Krakowczyk, Łukasz
Misiołek, Maciej
Strzelczyk, Joanna Katarzyna
Faculty
Wydział Leśny i Technologii Drewna
Journal
Biomedicines
ISSN
2227-9059
DOI
10.3390/biomedicines10123011
Web address
https://www.mdpi.com/2227-9059/10/12/3011
Volume
10
Number
12
Pages from-to
art. 3011
Abstract (EN)
Background: Oral squamous cell carcinoma (OSCC) is one of the most commonly detected neoplasms worldwide. Not all mechanisms associated with cell cycle disturbances are known in OSCC. Examples of genes involved in the control of the cell cycle are CDKN2A, MDM2, E2F2 and LTF. The aim of this study was to examine the possible association between CDKN2A, MDM2, E2F2 and LTF mRNA expression and influence on clinical variables. Methods: The study group consisted of 88 Polish patients. The gene expression levels were assessed by quantitative reverse transcription PCR. Results: We found no statistically significant differences in the expression level of CDKN2A, MDM2, E2F2 and LTF genes in tumour samples compared to margin samples. No association was found between the gene expression levels and clinical parameters, except E2F2. The patients with G2 tumours had a significantly higher gene expression level of E2F2 than patients with low-grade G1 tumours. Conclusions: We have not demonstrated that a change in expression profiles of genes has a significant impact on the pathogenesis of OSCC. It may also be useful to conduct further studies on the use of E2F2 expression profile changes as a factor to describe the invasiveness and dynamics of OSCC development.
Keywords (EN)
  • CDKN2A

  • MDM2

  • E2F2

  • LTF

  • oral squamous cell carcinoma

  • gene expression

  • cancer

License
cc-bycc-by CC-BY - Attribution
Open access date
November 23, 2022
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