Clinicopathological significance of concurrent ErbB receptor expression in human meningioma
- PMID: 37719042
- PMCID: PMC10502797
- DOI: 10.3892/mco.2023.2675
Clinicopathological significance of concurrent ErbB receptor expression in human meningioma
Abstract
In general, human meningiomas grow slowly and have a favourable prognosis; however, some are prone to recur despite their benign histology. Therefore, knowledge of their tumour biology is essential to determine objective biomarkers that can identify cases with an increased risk for recurrence and to generate effective treatment options. Thus, studies on the epidermal growth factor receptor (EGFR) family, comprising ErbB1/EGFR, ErbB2/HER2, ErbB3/HER3 and ErbB4/HER4, are important. We have recently published papers on the expression of each of these receptor proteins in human meningiomas. The present study aimed to assess the clinicopathological significance of their concurrent expression. A total of 185 grade 1 and 2 meningiomas with robust clinical data underwent immunohistochemical analyses with antibodies against the aforementioned receptors. All meningiomas exhibited upregulation of these receptor proteins relative to normal meninges. In addition, the expression of phosphorylated/activated ErbB1/EGFR1 and phosphorylated/activated ErbB2/HER2 was significantly associated with histological malignancy grade and prognosis, respectively. The concurrent upregulation of ErbB receptors in human meningioma supports their fundamental role in the tumourigenesis of these tumours, and they could thus be exploited in diagnostics, prognosis, and ultimately, in targeted clinical interventions.
Keywords: EGFR; HER; brain tumours; diagnosis; growth factor receptors; immunohistochemistry; prognosis; survival.
Copyright: © Torp et al.
Conflict of interest statement
The authors declare that they have no competing interests.
Figures
Similar articles
-
Epidermal growth factor receptor family (EGFR, ErbB2-4) in gliomas and meningiomas.Acta Neuropathol. 2004 Aug;108(2):135-42. doi: 10.1007/s00401-004-0875-6. Epub 2004 May 18. Acta Neuropathol. 2004. PMID: 15148612
-
Localization of phosphorylated ErbB1-4 and heregulin in colorectal cancer.BMC Cancer. 2014 Nov 22;14:863. doi: 10.1186/1471-2407-14-863. BMC Cancer. 2014. PMID: 25416285 Free PMC article.
-
ERBB1/2/3 Expression, Prognosis, and Immune Infiltration in Cutaneous Melanoma.Front Genet. 2021 Mar 1;12:602160. doi: 10.3389/fgene.2021.602160. eCollection 2021. Front Genet. 2021. PMID: 33732282 Free PMC article.
-
Targeting of ErbB1, ErbB2, and their Dual Targeting Using Small Molecules and Natural Peptides: Blocking EGFR Cell Signaling Pathways in Cancer: A Mini-Review.Mini Rev Med Chem. 2022 Oct 21;22(22):2831-2846. doi: 10.2174/1389557522666220512152448. Mini Rev Med Chem. 2022. PMID: 35549881 Review.
-
ErbB Receptors and Cancer.Methods Mol Biol. 2017;1652:3-35. doi: 10.1007/978-1-4939-7219-7_1. Methods Mol Biol. 2017. PMID: 28791631 Review.
References
-
- Ostrom QT, Price M, Ryan K, Edelson J, Neff C, Cioffi G, Waite KA, Kruchko C, Barnholtz-Sloan JS. CBTRUS statistical report: Pediatric brain tumor foundation childhood and adolescent primary brain and other central nervous system tumors diagnosed in the United States in 2014-2018. Neuro Oncol. 2022;24(Suppl 3):iii1–iii38. doi: 10.1093/neuonc/noac161. - DOI - PMC - PubMed
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous