Fer-1 like family member 4 pseudogene

novel potential diagnostic and prognostic biomarker for cutaneous melanoma

Authors

  • Tomasz Kolenda Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland. E-mail: tomasz.kolenda@wco.pl https://orcid.org/0000-0001-5623-7398
  • Kacper Guglas Laboratory of Cancer Genetics, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Postgraduate School of Molecular Medicine, 61 Zwirki i Wigury Street, 02-091 Medical University of Warsaw, Warsaw, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland https://orcid.org/0000-0002-2296-7808
  • Maciej Stasiak Laboratory of Cancer Genetics, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland https://orcid.org/0000-0002-5724-6373
  • Paulina Poter Department of Oncologic Pathology and Prophylaxis, Poznan University of Medical Sciences, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Department of Pathology, Pomeranian Medical University, 1 Unii Lubelskiej Street, 71-242 Szczecin, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland https://orcid.org/0000-0003-1811-6901
  • Joanna Kozłowska-Masłoń Laboratory of Cancer Genetics, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland; Faculty of Biology, Institute of Human Biology and Evolution, Adam Mickiewicz University, Uniwersytetu Poznańskiego 6, 61-614 Poznań, Poland https://orcid.org/0000-0001-6914-4852
  • Piotr Białas Chair and Department of Cell Biology, Poznan University of Medical Sciences, 5D Rokietnicka, 60-806 Poznan, Poland https://orcid.org/0000-0001-9133-4177
  • Joanna Sobocińska Laboratory of Cancer Genetics, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland https://orcid.org/0000-0002-6520-6531
  • Marlena Janiczek-Polewska Department of Clinical Oncology, Greater Poland Cancer Center, 61-866 Poznan, Poland; Department of Electroradiology, Poznan University of Medical Sciences, 61-701 Poznan, Poland https://orcid.org/0000-0002-1238-5273
  • Patrycja Mantaj Greater Poland Cancer Center, Radiation Protection Department Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland https://orcid.org/0000-0001-5757-9461
  • Anna Paszkowska Laboratory of Cancer Genetics, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland; Faculty of Biology, Adam Mickiewicz University, Umultowska 89, 61-614 Poznan, Poland https://orcid.org/0009-0004-7527-5081
  • Zefiryn Cybulski Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland https://orcid.org/0000-0002-7648-1520
  • Anna Teresiak Laboratory of Cancer Genetics, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Greater Poland Cancer Center, Research and Implementation Unit, Garbary 15, 61-866 Poznan, Poland https://orcid.org/0000-0002-5327-6698
  • Urszula Kazimierczak Department of Cancer Immunology, Chair of Medical Biotechnology, Poznan University of Medical Sciences, 8 Rokietnicka Street, 60-806 Poznan, Poland; Department of Diagnostics and Cancer Immunology, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland https://orcid.org/0000-0003-3946-7399
  • Anna Przybyła Department of Cancer Immunology, Chair of Medical Biotechnology, Poznan University of Medical Sciences, 8 Rokietnicka Street, 60-806 Poznan, Poland; Department of Diagnostics and Cancer Immunology, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland https://orcid.org/0000-0002-6395-5731
  • Andrzej Mackiewicz Department of Cancer Immunology, Chair of Medical Biotechnology, Poznan University of Medical Sciences, 8 Rokietnicka Street, 60-806 Poznan, Poland; Department of Diagnostics and Cancer Immunology, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland https://orcid.org/0000-0001-5574-6609
  • Jacek Mackiewicz Department of Diagnostics and Cancer Immunology, Greater Poland Cancer Center, 15 Garbary Street, 61-866 Poznan, Poland; Department of Medical and Experimental Oncology, Institute of Oncology, Poznan University of Medical Sciences, Poznan, Poland https://orcid.org/0000-0002-0177-2972

DOI:

https://doi.org/10.17179/excli2024-7719

Keywords:

C20orf124, pseudogene, non-coding RNA, lncRNA, miRNA, miR-514a-5p, miR-330-5p, miR-128-3p, TCGA, BRAF mutation, biomarkers, FER1L4

Abstract

Cutaneous melanoma is the deadliest form of skin cancer. Despite advancements in treatment, many patients still face poor outcomes. A deeper understanding of the mechanisms involved in melanoma pathogenesis is crucial for improving diagnosis and therapy. Non-coding RNAs, with their extensive regulatory roles, show promise as diagnostic biomarkers. This study focuses on evaluating the FER1L4 pseudogene and its potential role in melanoma. FER1L4 expression was analyzed in normal melanocytes and melanoma cell lines using qRT-PCR. Additionally, TCGA data and online prediction tools were employed to correlate expression levels with clinicopathological features. The relationship between FER1L4, patient phenotypes, and immune responses was further explored using REACTOME, GSEA, and immune deconvolution analyses. In vitro analysis revealed significant upregulation of FER1L4 in melanoma cells. Its expression levels were influenced by BRAF mutations and were markedly higher in metastatic compared to primary melanomas. Higher FER1L4 expression was associated with improved patient survival. Furthermore, miR-514a-5p, miR-330-5p, and miR-128-3p were identified as interacting with FER1L4. Dysregulated genes involved in immune signaling pathways were also identified as potential miRNA targets. This is the first study to demonstrate the association of FER1L4 with melanoma. Patients with elevated FER1L4 levels exhibited distinct phenotypes, altered immunological profiles, and improved survival rates. These findings suggest that FER1L4 could serve as a potential biomarker for melanoma.

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Published

2024-11-19

How to Cite

Kolenda, T., Guglas, K., Stasiak, M., Poter, P., Kozłowska-Masłoń, J., Białas, P., … Mackiewicz, J. (2024). Fer-1 like family member 4 pseudogene: novel potential diagnostic and prognostic biomarker for cutaneous melanoma. EXCLI Journal, 23, 1375–1396. https://doi.org/10.17179/excli2024-7719

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