Contemporary Oncology
eISSN: 1897-4309
ISSN: 1428-2526
Contemporary Oncology/Współczesna Onkologia
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SCImago Journal & Country Rank
3/2025
vol. 29
 
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abstract:
Original paper

High expression of the eukaryotic initiation factors eIF4a and eIF4e in retinoblastoma

Nora Fischer
1
,
Antje Schinlauer
1
,
Piotr Czapiewski
1, 2
,
Yvonne Garbers
3
,
Christoph Garbers
4

  1. Department of Pathology, Otto-von-Guericke-University Magdeburg, 39120 Magdeburg, Germany
  2. Department of Pathology, Staedtisches Klinikum Dessau, Brandenburg Medical School Theodor Fontane and Faculty of Health Sciences Brandenburg, Dessau, Germany
  3. Faculty of Management, Culture and Technology (Lingen campus), Osnabrück University of Applied Sciences, 49809 Lingen, Germany
  4. Institute of Clinical Biochemistry, Hannover Medical School, 30625 Hannover, Germany
Contemp Oncol (Pozn) 2025; 29 (3): 257–266
Online publish date: 2025/09/17
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Introduction:
Retinoblastoma is a malignant, intraocular tumor which deve­lops within the first three years of life and has a variable prognosis. Aberrant expression of eukaryotic initiation factors (eIFs) has been reported in a variety of tumor entities, but there is a lack of data regarding eIF expression in retinoblastoma.

Material and methods:
We analyzed the expression of eIF4a and eIF4e in 30 retinoblastomas and samples of other ocular diseases via immunohisto­chemistry. Via western blot, we determined the expression of eIF4a and eIF4e in the two retinoblastoma cell lines WERI-Rb1 and Y79. Furthermore, we evaluated the influence of the eIF inhibitor 4EGI-1 on the cell viabi­lity of both cancer cell lines.

Results:
In this study, we observed increased expression of eIF4a and eIF4e in retinoblastoma samples compared to other ocular diseases. We also found that both proteins are expressed in the retinoblastoma cell lines WERI-Rb1 and Y79 and that their expression is independent of treatment with the eIF inhibitor 4EGI-1. However, inhibition of eIF function via 4EGI-1 reduced the cell viability of both cell lines in a dose- and time-dependent manner.

Conclusions:
We provide evidence that eIF4a and eIF4e are overexpressed in retinoblastoma and that their inhibition might represent a therapeutic target for the therapy of retinoblastoma.

keywords:

eIFs, 4EGI-1, retinoblastoma cells

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