Kessler, Carolina, von Brandenstein, Melanie ORCID: 0000-0002-1499-7644, Klümper, Niklas, Krausewitz, Philipp, Storz, Enno ORCID: 0009-0002-8250-5522, Rieger, Constantin ORCID: 0009-0000-3993-7974, Sperber, Laurenz, Paffenholz, Pia ORCID: 0000-0002-8209-7795, Tolkach, Yuri ORCID: 0000-0001-5239-2841, Wirtz, Ralph, Eckstein, Markus, Heidenreich, Axel ORCID: 0000-0002-2511-3664 and Weiten, Richard ORCID: 0009-0002-7216-1033 (2025). TROP-2 overexpression in papillary renal cell carcinoma supports its potential as a therapeutic target for antibody-drug-conjugate therapy. World Journal of Urology, 43 (1). pp. 1-8. Springer Nature. ISSN 1433-8726

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Identification Number:10.1007/s00345-025-05880-2

Abstract

[Artikel-Nr.: 522] Objective: To evaluate the expression of trophoblast cell surface antigen-2 (TROP-2), a broadly expressed antibody-drug conjugate (ADC) target, in non-clear cell renal cell carcinoma (nccRCC), and to perform a proof-of-concept analysis assessing the cytotoxic efficacy of the TROP-2-directed ADC Sacituzumab govitecan (SG) in RCC cell lines. Methods: A cohort comprising clear cell RCC (ccRCC, n = 44), papillary (pRCC, n = 22), chromophobe (chRCC, n = 22), and benign renal tumors (n = 8, including oncocytoma and angiomyolipoma) was analysed using reverse transcription quantitative PCR (RT-qPCR), immunohistochemistry (IHC) with H-score quantification, and enzyme-linked immunosorbent assay (ELISA). In RCC cell lines, TROP-2 protein levels were assessed by Western blotting and flow cytometry, and SG cytotoxicity was evaluated using MTT assays. Results: TROP-2 mRNA levels were significantly elevated in pRCC compared to ccRCC, chRCC and benign renal tumors (p < 0.001). IHC revealed moderate to strong membranous TROP-2 expression in most pRCC cases [n = 20/22 with H-score ≥ 100, median H-score 265 (IQR 202.5–290)], while TROP-2 expression was absent or weak in ccRCC and chRCC (p < 0.0001). Soluble TROP-2 was detectable in patient serum of RCC patients and strongly correlated with tissue expression (ρ = 0.78, p = 0.0001, R2 = 0.52). In vitro, TROP-2-positive Caki-1 cells exhibited significant growth inhibition after SG treatment, whereas TROP-2-negative 769-P cells showed resistance (p < 0.01). Conclusion: The selective overexpression of TROP-2 in pRCC, and its functional relevance demonstrated in vitro, provide compelling preclinical evidence supporting TROP-2 as a therapeutic target. These findings support further investigation of TROP-2-directed ADCs, such as SG, in patients with metastatic TROP-2-positive pRCC.

Item Type: Article
Creators:
Creators
Email
ORCID
ORCID Put Code
Kessler, Carolina
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
von Brandenstein, Melanie
UNSPECIFIED
UNSPECIFIED
Klümper, Niklas
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Krausewitz, Philipp
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Storz, Enno
UNSPECIFIED
UNSPECIFIED
Rieger, Constantin
UNSPECIFIED
UNSPECIFIED
Sperber, Laurenz
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Paffenholz, Pia
UNSPECIFIED
UNSPECIFIED
Tolkach, Yuri
UNSPECIFIED
UNSPECIFIED
Wirtz, Ralph
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Eckstein, Markus
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Heidenreich, Axel
UNSPECIFIED
UNSPECIFIED
Weiten, Richard
UNSPECIFIED
UNSPECIFIED
URN: urn:nbn:de:hbz:38-810912
Identification Number: 10.1007/s00345-025-05880-2
Journal or Publication Title: World Journal of Urology
Volume: 43
Number: 1
Page Range: pp. 1-8
Number of Pages: 8
Date: 1 September 2025
Publisher: Springer Nature
ISSN: 1433-8726
Language: English
Faculty: Faculty of Medicine
Divisions: Faculty of Medicine > Pathologie und Neuropathologie > Institut für Pathologie
Faculty of Medicine > Urologie > Klinik und Poliklinik für Urologie
Subjects: Medical sciences Medicine
Uncontrolled Keywords:
Keywords
Language
Antibody-drug conjugates · Renal cell carcinoma · Sacituzumab govitecan · TROP-2
English
['eprint_fieldname_oa_funders' not defined]: Publikationsfonds UzK
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/81091

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