Akt signalling parameters are different in oncocytomas compared to renal cell carcinoma

B. Amend, J. Hennenlotter, M. Scharpf, S. Kruck, U. Kuehs, E. Senger, A. S. Merseburger, M. A. Kuczyk, K. D. Sievert, A. Stenzl, J. Bedke*

*Corresponding author for this work
2 Citations (Scopus)


Purpose: Renal oncocytomas are assigned as benign tumours, and their detailed molecular mechanism is poorly characterised. Activation of the PKB/Akt pathway is assumed to contribute to the pathogenesis and progression of malignant disease. For oncocytomas, hardly any data are available for Akt signalling parameters. Aim of the present work was to determine the alterations of Akt parameters PTEN, phosphorylated Akt (p-Akt) and p27Kip1 in oncocytoma to better understand the dedifferentiation of renal tumours. Methods: By tissue microarray analysis 15 oncocytoma, 18 clear cell renal cell carcinoma (ccRCC) and the corresponding benign tissue were investigated. Significant expression differences between PTEN, p-Akt and p27Kip1 were determined by immunohistochemistry using One-way ANOVA with all pairs Tukey-Kramer as post hoc analyses. To investigate Akt parameter interactions in the oncocytoma, linear regression analyses were performed. Results: Expression of all proteins was significantly different between the groups and in all groups the lowest for oncocytoma: PTEN: 32.9 ± 13.0 versus 75.5 ± 8.0 versus 123.7 ± 8.8; p < 0.001 for oncocytoma, benign parenchyma and ccRCC and 2.7 ± 1.2 versus 40.8 ± 9.5 versus 143.6 ± 12.2; p < 0.001 for p27Kip1. p-Akt expression was significantly different between oncocytoma and ccRCC (67.3 ± 15.7 vs. 144.0 ± 26.6; p < 0.05). Conclusion: All three investigated parameters were the lowest in oncocytoma when compared to ccRCC. Expression of PTEN and p27Kip1 seems to be exceedingly associated with malignant conditions of ccRCC. These findings might contribute to the understanding of tumorous signalling of the PKB/Akt axis in renal tumours.

Original languageEnglish
JournalWorld Journal of Urology
Issue number3
Pages (from-to)353-359
Number of pages7
Publication statusPublished - 06.2012

Research Areas and Centers

  • Research Area: Luebeck Integrated Oncology Network (LION)


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