Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder

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Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder. / Kaczmarek, Krystian; Plage, Henning; Furlano, Kira; Hofbauer, Sebastian; Weinberger, Sarah; Ralla, Bernhard; Franz, Antonia; Fendler, Annika; de Martino, Michela; Roßner, Florian; Schallenberg, Simon; Elezkurtaj, Sefer; Kluth, Martina; Lennartz, Maximilian; Blessin, Niclas C.; Marx, Andreas H.; Samtleben, Henrik; Fisch, Margit; Rink, Michael; Slojewski, Marcin; Ecke, Thorsten; Hallmann, Steffen; Koch, Stefan; Adamini, Nico; Minner, Sarah; Simon, Ronald; Sauter, Guido; Weischenfeldt, Joachim; Klatte, Tobias; Schlomm, Thorsten; Horst, David; Zecha, Henrik.

In: International Urology and Nephrology, Vol. 56, 2024, p. 499-508.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kaczmarek, K, Plage, H, Furlano, K, Hofbauer, S, Weinberger, S, Ralla, B, Franz, A, Fendler, A, de Martino, M, Roßner, F, Schallenberg, S, Elezkurtaj, S, Kluth, M, Lennartz, M, Blessin, NC, Marx, AH, Samtleben, H, Fisch, M, Rink, M, Slojewski, M, Ecke, T, Hallmann, S, Koch, S, Adamini, N, Minner, S, Simon, R, Sauter, G, Weischenfeldt, J, Klatte, T, Schlomm, T, Horst, D & Zecha, H 2024, 'Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder', International Urology and Nephrology, vol. 56, pp. 499-508. https://doi.org/10.1007/s11255-023-03800-0

APA

Kaczmarek, K., Plage, H., Furlano, K., Hofbauer, S., Weinberger, S., Ralla, B., Franz, A., Fendler, A., de Martino, M., Roßner, F., Schallenberg, S., Elezkurtaj, S., Kluth, M., Lennartz, M., Blessin, N. C., Marx, A. H., Samtleben, H., Fisch, M., Rink, M., ... Zecha, H. (2024). Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder. International Urology and Nephrology, 56, 499-508. https://doi.org/10.1007/s11255-023-03800-0

Vancouver

Kaczmarek K, Plage H, Furlano K, Hofbauer S, Weinberger S, Ralla B et al. Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder. International Urology and Nephrology. 2024;56:499-508. https://doi.org/10.1007/s11255-023-03800-0

Author

Kaczmarek, Krystian ; Plage, Henning ; Furlano, Kira ; Hofbauer, Sebastian ; Weinberger, Sarah ; Ralla, Bernhard ; Franz, Antonia ; Fendler, Annika ; de Martino, Michela ; Roßner, Florian ; Schallenberg, Simon ; Elezkurtaj, Sefer ; Kluth, Martina ; Lennartz, Maximilian ; Blessin, Niclas C. ; Marx, Andreas H. ; Samtleben, Henrik ; Fisch, Margit ; Rink, Michael ; Slojewski, Marcin ; Ecke, Thorsten ; Hallmann, Steffen ; Koch, Stefan ; Adamini, Nico ; Minner, Sarah ; Simon, Ronald ; Sauter, Guido ; Weischenfeldt, Joachim ; Klatte, Tobias ; Schlomm, Thorsten ; Horst, David ; Zecha, Henrik. / Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder. In: International Urology and Nephrology. 2024 ; Vol. 56. pp. 499-508.

Bibtex

@article{a94534ff76f644b38368430b778e9965,
title = "Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder",
abstract = "Background: Uroplakin-1a (Upk1a) and uroplakin-1b (Upk1b) have recently been identified as diagnostic markers for the distinction of urothelial carcinomas from other solid tumor entities. Both proteins play an important role in the stabilization and strengthening of epithelial cells that line the bladder. Methods: To evaluate the prognostic role of uroplakin expression in urothelial carcinomas, more than 2700 urothelial neoplasms were analyzed in a tissue microarray format by immunohistochemistry. To further assess the diagnostic role of uroplakin immunohistochemistry, results were compared with preexisting GATA3 data. Result: The fraction of Upk1a/Upk1b positive cases decreased slightly from pTaG2 low-grade (88% positive for Upk1a/87% positive for Upk1b) and pTaG2 high-grade (92%/89%) to pTaG3 (83%/88%; p > 0.05) and was lower in muscle-invasive (pT2-4) carcinomas (42%/64%; p < 0.0001/p < 0.0001 for pTa vs. pT2-4). Within pT2-4 carcinomas, high expression of Upk1a and Upk1b was linked to nodal metastasis and lymphatic vessel infiltration (p < 0.05) but unrelated to patient outcome. There were significant associations between Upk1a, Upk1b and GATA3 immunostaining (p < 0.0001 each), but 11% of GATA3 negative cancers were Upk1a/b positive and 8% of Upk1a/b negative cancers were GATA3 positive. Absence of GATA3/Upk1a/b staining was significantly linked to poor patient survival in the subgroup of 126 pT4 carcinomas (p = 0.0004) but not in pT2 and pT3 cancers. Conclusions: In summary, the results of our study demonstrate that Upk1a and/or Upk1b immunohistochemistry can complement GATA3 for the distinction of urothelial carcinomas. Furthermore, a progressive loss of Upk1a/b expression during stage progression and a prognostic role of the combination GATA3/Upk1a/Upk1b in pT4 carcinomas is evident.",
keywords = "Diagnostic marker, Immunohistochemistry, Tissue microarray, Upk1a, Upk1b, Urothelial carcinoma",
author = "Krystian Kaczmarek and Henning Plage and Kira Furlano and Sebastian Hofbauer and Sarah Weinberger and Bernhard Ralla and Antonia Franz and Annika Fendler and {de Martino}, Michela and Florian Ro{\ss}ner and Simon Schallenberg and Sefer Elezkurtaj and Martina Kluth and Maximilian Lennartz and Blessin, {Niclas C.} and Marx, {Andreas H.} and Henrik Samtleben and Margit Fisch and Michael Rink and Marcin Slojewski and Thorsten Ecke and Steffen Hallmann and Stefan Koch and Nico Adamini and Sarah Minner and Ronald Simon and Guido Sauter and Joachim Weischenfeldt and Tobias Klatte and Thorsten Schlomm and David Horst and Henrik Zecha",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2024",
doi = "10.1007/s11255-023-03800-0",
language = "English",
volume = "56",
pages = "499--508",
journal = "International Urology and Nephrology",
issn = "0301-1623",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - Loss of Upk1a and Upk1b expression is linked to stage progression in urothelial carcinoma of the bladder

AU - Kaczmarek, Krystian

AU - Plage, Henning

AU - Furlano, Kira

AU - Hofbauer, Sebastian

AU - Weinberger, Sarah

AU - Ralla, Bernhard

AU - Franz, Antonia

AU - Fendler, Annika

AU - de Martino, Michela

AU - Roßner, Florian

AU - Schallenberg, Simon

AU - Elezkurtaj, Sefer

AU - Kluth, Martina

AU - Lennartz, Maximilian

AU - Blessin, Niclas C.

AU - Marx, Andreas H.

AU - Samtleben, Henrik

AU - Fisch, Margit

AU - Rink, Michael

AU - Slojewski, Marcin

AU - Ecke, Thorsten

AU - Hallmann, Steffen

AU - Koch, Stefan

AU - Adamini, Nico

AU - Minner, Sarah

AU - Simon, Ronald

AU - Sauter, Guido

AU - Weischenfeldt, Joachim

AU - Klatte, Tobias

AU - Schlomm, Thorsten

AU - Horst, David

AU - Zecha, Henrik

N1 - Publisher Copyright: © 2023, The Author(s).

PY - 2024

Y1 - 2024

N2 - Background: Uroplakin-1a (Upk1a) and uroplakin-1b (Upk1b) have recently been identified as diagnostic markers for the distinction of urothelial carcinomas from other solid tumor entities. Both proteins play an important role in the stabilization and strengthening of epithelial cells that line the bladder. Methods: To evaluate the prognostic role of uroplakin expression in urothelial carcinomas, more than 2700 urothelial neoplasms were analyzed in a tissue microarray format by immunohistochemistry. To further assess the diagnostic role of uroplakin immunohistochemistry, results were compared with preexisting GATA3 data. Result: The fraction of Upk1a/Upk1b positive cases decreased slightly from pTaG2 low-grade (88% positive for Upk1a/87% positive for Upk1b) and pTaG2 high-grade (92%/89%) to pTaG3 (83%/88%; p > 0.05) and was lower in muscle-invasive (pT2-4) carcinomas (42%/64%; p < 0.0001/p < 0.0001 for pTa vs. pT2-4). Within pT2-4 carcinomas, high expression of Upk1a and Upk1b was linked to nodal metastasis and lymphatic vessel infiltration (p < 0.05) but unrelated to patient outcome. There were significant associations between Upk1a, Upk1b and GATA3 immunostaining (p < 0.0001 each), but 11% of GATA3 negative cancers were Upk1a/b positive and 8% of Upk1a/b negative cancers were GATA3 positive. Absence of GATA3/Upk1a/b staining was significantly linked to poor patient survival in the subgroup of 126 pT4 carcinomas (p = 0.0004) but not in pT2 and pT3 cancers. Conclusions: In summary, the results of our study demonstrate that Upk1a and/or Upk1b immunohistochemistry can complement GATA3 for the distinction of urothelial carcinomas. Furthermore, a progressive loss of Upk1a/b expression during stage progression and a prognostic role of the combination GATA3/Upk1a/Upk1b in pT4 carcinomas is evident.

AB - Background: Uroplakin-1a (Upk1a) and uroplakin-1b (Upk1b) have recently been identified as diagnostic markers for the distinction of urothelial carcinomas from other solid tumor entities. Both proteins play an important role in the stabilization and strengthening of epithelial cells that line the bladder. Methods: To evaluate the prognostic role of uroplakin expression in urothelial carcinomas, more than 2700 urothelial neoplasms were analyzed in a tissue microarray format by immunohistochemistry. To further assess the diagnostic role of uroplakin immunohistochemistry, results were compared with preexisting GATA3 data. Result: The fraction of Upk1a/Upk1b positive cases decreased slightly from pTaG2 low-grade (88% positive for Upk1a/87% positive for Upk1b) and pTaG2 high-grade (92%/89%) to pTaG3 (83%/88%; p > 0.05) and was lower in muscle-invasive (pT2-4) carcinomas (42%/64%; p < 0.0001/p < 0.0001 for pTa vs. pT2-4). Within pT2-4 carcinomas, high expression of Upk1a and Upk1b was linked to nodal metastasis and lymphatic vessel infiltration (p < 0.05) but unrelated to patient outcome. There were significant associations between Upk1a, Upk1b and GATA3 immunostaining (p < 0.0001 each), but 11% of GATA3 negative cancers were Upk1a/b positive and 8% of Upk1a/b negative cancers were GATA3 positive. Absence of GATA3/Upk1a/b staining was significantly linked to poor patient survival in the subgroup of 126 pT4 carcinomas (p = 0.0004) but not in pT2 and pT3 cancers. Conclusions: In summary, the results of our study demonstrate that Upk1a and/or Upk1b immunohistochemistry can complement GATA3 for the distinction of urothelial carcinomas. Furthermore, a progressive loss of Upk1a/b expression during stage progression and a prognostic role of the combination GATA3/Upk1a/Upk1b in pT4 carcinomas is evident.

KW - Diagnostic marker

KW - Immunohistochemistry

KW - Tissue microarray

KW - Upk1a

KW - Upk1b

KW - Urothelial carcinoma

U2 - 10.1007/s11255-023-03800-0

DO - 10.1007/s11255-023-03800-0

M3 - Journal article

C2 - 37777995

AN - SCOPUS:85173044422

VL - 56

SP - 499

EP - 508

JO - International Urology and Nephrology

JF - International Urology and Nephrology

SN - 0301-1623

ER -

ID: 369924579