VEGF, EGFR and PSMA as possible imaging targets of lymph node metastases of urothelial carcinoma of the bladder

BMC Urol. 2022 Dec 29;22(1):213. doi: 10.1186/s12894-022-01157-7.

Abstract

Background: In this study we investigated the expression of vascular endothelial growth factor (VEGF), epidermal growth factor receptor (EGFR) and prostate-specific membrane antigen (PSMA) to analyze their potency as targets for the detection of lymph node (LN) metastases of urothelial carcinoma of the bladder.

Methods: Antigen expression was determined in 40 samples with urothelial carcinoma and compared to 17 matched samples without metastases by immunohistochemistry. The total immunostaining score (TIS 0-12) was determined as the product of a proportion score (PS 0-4) and intensity score (IS 0-3).

Results: VEGF expression was high in primary tumor and LN metastases (median TIS 8 in both) and VEGF expression was also seen in LNs without metastases (median TIS 6). EGFR expression was low in primary tumor and LN metastases (median TIS 3 and 2 respectively) and absent in LNs without metastases. PSMA expression was low in samples with urothelial carcinoma (median TIS 2).

Conclusion: VEGF shows moderate to high expression levels in both primary tumors and LN metastases and could be a candidate as a target agent for imaging modalities of urothelial carcinoma. EGFR and PSMA do show low staining levels in tumor tissue with urothelial carcinoma and do not seem suitable as target agents.

Trial registration: The Medical Ethics Review Board of the University Medical Center Groningen approved this study on 14 December 2017 (METc UMCG 2017/639). Trial registration number (UMCG Research Register): 201700868.

Keywords: Antigens; Bladder cancer; Lymph nodes; Targeted imaging; Urothelial carcinoma.

MeSH terms

  • Carcinoma, Transitional Cell* / pathology
  • ErbB Receptors
  • Humans
  • Lymph Nodes / pathology
  • Lymphatic Metastasis
  • Urinary Bladder / pathology
  • Urinary Bladder Neoplasms* / pathology
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • EGFR protein, human
  • ErbB Receptors
  • Vascular Endothelial Growth Factor A
  • FOLH1 protein, human