Pregled bibliografske jedinice broj: 1164663
Nuclear EGFR strong expression in laryngeal squamous cell carcinoma affects a more aggressive biological behaviour
Nuclear EGFR strong expression in laryngeal squamous cell carcinoma affects a more aggressive biological behaviour // Libri Oncologici : Croatian Journal of Oncology, Vol. 49 No. Supplement 1, 2021. / Vrdoljak, Eduard ; Jazvić, Marijana (ur.).
Zagreb: University Hospital for Tumors, Zagreb, Croatia, 2021. str. 114-115 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1164663 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Nuclear EGFR strong expression in laryngeal
squamous cell carcinoma affects a more aggressive
biological behaviour
Autori
Marijić, Blažen ; Tudor, Filip ; Braut, Tamara ; Babarović, Emina ; Maržić, Diana ; Avirović, Manuela ; Kujundžić, Milodar ; Velepič, Marko ; Hadžisejdić, Ita
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Libri Oncologici : Croatian Journal of Oncology, Vol. 49 No. Supplement 1, 2021.
/ Vrdoljak, Eduard ; Jazvić, Marijana - Zagreb : University Hospital for Tumors, Zagreb, Croatia, 2021, 114-115
Skup
14th Croatian oncology congress
Mjesto i datum
Online, 22.04.2021. - 25.04.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
Immunohistochemistry ; Epidermal Growth Factor Receptor ; Laryngeal Cancer ; Carcinogenesis.
Sažetak
Aim of the study: Membrane EGFR (mEGFR) protein overexpression is frequently found in the head and neck squamous cell carcinoma (HNSCC). It has been found that mEGFR upon stimulation translocates to nucleus and its nuclear localisation is associated with poor prognosis in many cancers. The main focus of this study is to asses if nuclear EGFR (nEGFR) expression affects biologically more aggressive tumor behaviour in comparison to mEGFR expression in laryngeal SCC. Material and Methods: We examined 42 laryngeal squamous cell carcinomas (SCC) for nEGFR and mEGFR expression as well as cell cycle proliferative markers Ki-67, p53, cyclin D1 using immunohistochemistry. Results: In our study group, we found in 28.57% (12/42) SCC cases a strong (3+) nEGFR expression, 64.28% (27/42) SCC had weak to moderate (1+/2+) nEGFR expression while 7.14% (3/42) cases were negative for nEGFR. The majority of patients with SCC had strong (3+) mEGFR (52.38% or 22/42) expression and 45.23% (19/42) had weak to moderate (1+/2+) mEGFR expression and one case (1/42) was negative for mEGFR. The mean values ± standard deviation (%) of Ki-67, p53 and cyclin D1 expression in our study group were 39.04 ± 18.08, 38.88 ± 32.22 and 43.82 ± 18.34, respectively. When assessing the association of nEGFR with mEGFR and cell cycle proliferation markers there was statistically significant negative correlation between nEGFR and mEGFR expression (τ = -0.389 ; P = 0.002) and statistically significant negative correlation between nEGFR and cyclin D1 (τ = -0.274 ; P = 0.032). In the analysis of mEGFR correlations with the examined cell proliferation markers there were no statistically significant associations. We also observed that higher number of patients with strong nEGFR expression and concomitant negative/weak to moderate mEGFR expression died (70% or 7/10 patients) in comparison to number of patients with strong mEGFR expression and negative/weak to moderate nEGFR expression (40% or 8/20 patients). Moreover, univariate statistical analysis showed a statistically significant correlation between strong nEGFR protein expression with worse overall survival in laryngeal SCC, alone or in co-expression with strong cyclin D1 and high Ki-67 (P=0.025, P=0.046, P=0.043, respectively). However, there was no statistically significant difference in the overall survival, when we analyzed strong mEGFR expression, alone or in co- expression with cyclin D1 and Ki-67 cell cycle proteins (P=0.953, P=0.731, P=0.647, respectively). Conclusion: Our data indicate that nuclear EGFR cellular localization with strong expression might influence the more aggressive biological behaviour of laryngeal SCC carcinoma with poor patient survival.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
--uniri-biomed-18-121 - Molekularni biomarkeri kancerogeneze u skvamoznim epitelnim lezijama grkljana (Braut, Tamara) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka
Profili:
Manuela Avirović
(autor)
Diana Maržić
(autor)
Milodar Kujundžić
(autor)
Ita Hadžisejdić
(autor)
Emina Babarović
(autor)
Blažen Marijić
(autor)
Marko Velepič
(autor)
Tamara Braut
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus