Prognostic value of alpha-methyl CoA racemase (AMACR) expression in renal cell carcinoma.

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Prognostic value of alpha-methyl CoA racemase (AMACR) expression in renal cell carcinoma. / Eichelberg, Christian; Minner, Sarah; Isbarn, Hendrik; Burandt, Eike; Terracciano, Luigi; Moch, Holger; Kell, Alexandra; Heuer, Roman; Chun, Felix K; Sauter, Guido; Fisch, Margit; Tennstedt, Pierre.

in: WORLD J UROL, Jahrgang 31, Nr. 4, 2013, S. 847-53.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Eichelberg, C, Minner, S, Isbarn, H, Burandt, E, Terracciano, L, Moch, H, Kell, A, Heuer, R, Chun, FK, Sauter, G, Fisch, M & Tennstedt, P 2013, 'Prognostic value of alpha-methyl CoA racemase (AMACR) expression in renal cell carcinoma.', WORLD J UROL, Jg. 31, Nr. 4, S. 847-53. https://doi.org/10.1007/s00345-011-0783-z

APA

Eichelberg, C., Minner, S., Isbarn, H., Burandt, E., Terracciano, L., Moch, H., Kell, A., Heuer, R., Chun, F. K., Sauter, G., Fisch, M., & Tennstedt, P. (2013). Prognostic value of alpha-methyl CoA racemase (AMACR) expression in renal cell carcinoma. WORLD J UROL, 31(4), 847-53. https://doi.org/10.1007/s00345-011-0783-z

Vancouver

Bibtex

@article{70a63d9ad1c14d078ea9636809b25ad5,
title = "Prognostic value of alpha-methyl CoA racemase (AMACR) expression in renal cell carcinoma.",
abstract = "PURPOSE: Alpha-methyl CoA racemase (AMACR) is used as an immunohistochemical marker for renal cell carcinoma (RCC) subtyping to distinguish papillary (pap) RCC. Expression of AMACR in other renal tumor subtypes is inhomogeneous, and the clinical and prognostic value of AMACR is unknown. The aim of this study was to asses AMACR protein expression in different RCC subtypes and to investigate its prognostic significance.METHODS: Protein expression of AMACR was analyzed in 1,088 renal tumor samples, among them 809 clear cell RCC and 151 papRCC, by immunohistochemistry using tissue microarry (TMA) technique. Results were correlated with clinicopathological data and to follow-up data [overall (OS)/cancer-specific survival (CSS)].RESULTS: Frequency of AMACR expression was significantly higher in papRCC compared to other tumor subtypes (83% vs. 15-35%, p < 0.0001). Presence of AMACR did not correlate with stage or nodal metastases in papRCC. In a dichotomized scoring (negative vs. positive expression), an inverse correlation between higher grade (p = 0.03) and presence of distant metastasis (p = 0.014) was observed in papRCC. AMACR expression correlated with the presence of nodal metastasis in ccRCC (p = 0.02). Both in ccRCC and in papRCC, OS and CSS did not correlate with the AMACR expression status.CONCLUSIONS: The high expression in papRCC confirms AMACR to be a marker for subtype differentiation in RCC, while a missing expression in this subtype seems to be associated with negative pathological features. However, in contrast to other tumor entities, AMACR expression seems to have a limited prognostic impact in renal carcinoma, especially with regard to survival.",
keywords = "Carcinoma, Renal Cell, Cohort Studies, Follow-Up Studies, Gene Expression Regulation, Neoplastic, Humans, Kaplan-Meier Estimate, Kidney Neoplasms, Neoplasm Staging, Predictive Value of Tests, Prognosis, Racemases and Epimerases, Retrospective Studies, Survival Rate, Tumor Markers, Biological",
author = "Christian Eichelberg and Sarah Minner and Hendrik Isbarn and Eike Burandt and Luigi Terracciano and Holger Moch and Alexandra Kell and Roman Heuer and Chun, {Felix K} and Guido Sauter and Margit Fisch and Pierre Tennstedt",
year = "2013",
doi = "10.1007/s00345-011-0783-z",
language = "English",
volume = "31",
pages = "847--53",
journal = "WORLD J UROL",
issn = "0724-4983",
publisher = "Springer",
number = "4",

}

RIS

TY - JOUR

T1 - Prognostic value of alpha-methyl CoA racemase (AMACR) expression in renal cell carcinoma.

AU - Eichelberg, Christian

AU - Minner, Sarah

AU - Isbarn, Hendrik

AU - Burandt, Eike

AU - Terracciano, Luigi

AU - Moch, Holger

AU - Kell, Alexandra

AU - Heuer, Roman

AU - Chun, Felix K

AU - Sauter, Guido

AU - Fisch, Margit

AU - Tennstedt, Pierre

PY - 2013

Y1 - 2013

N2 - PURPOSE: Alpha-methyl CoA racemase (AMACR) is used as an immunohistochemical marker for renal cell carcinoma (RCC) subtyping to distinguish papillary (pap) RCC. Expression of AMACR in other renal tumor subtypes is inhomogeneous, and the clinical and prognostic value of AMACR is unknown. The aim of this study was to asses AMACR protein expression in different RCC subtypes and to investigate its prognostic significance.METHODS: Protein expression of AMACR was analyzed in 1,088 renal tumor samples, among them 809 clear cell RCC and 151 papRCC, by immunohistochemistry using tissue microarry (TMA) technique. Results were correlated with clinicopathological data and to follow-up data [overall (OS)/cancer-specific survival (CSS)].RESULTS: Frequency of AMACR expression was significantly higher in papRCC compared to other tumor subtypes (83% vs. 15-35%, p < 0.0001). Presence of AMACR did not correlate with stage or nodal metastases in papRCC. In a dichotomized scoring (negative vs. positive expression), an inverse correlation between higher grade (p = 0.03) and presence of distant metastasis (p = 0.014) was observed in papRCC. AMACR expression correlated with the presence of nodal metastasis in ccRCC (p = 0.02). Both in ccRCC and in papRCC, OS and CSS did not correlate with the AMACR expression status.CONCLUSIONS: The high expression in papRCC confirms AMACR to be a marker for subtype differentiation in RCC, while a missing expression in this subtype seems to be associated with negative pathological features. However, in contrast to other tumor entities, AMACR expression seems to have a limited prognostic impact in renal carcinoma, especially with regard to survival.

AB - PURPOSE: Alpha-methyl CoA racemase (AMACR) is used as an immunohistochemical marker for renal cell carcinoma (RCC) subtyping to distinguish papillary (pap) RCC. Expression of AMACR in other renal tumor subtypes is inhomogeneous, and the clinical and prognostic value of AMACR is unknown. The aim of this study was to asses AMACR protein expression in different RCC subtypes and to investigate its prognostic significance.METHODS: Protein expression of AMACR was analyzed in 1,088 renal tumor samples, among them 809 clear cell RCC and 151 papRCC, by immunohistochemistry using tissue microarry (TMA) technique. Results were correlated with clinicopathological data and to follow-up data [overall (OS)/cancer-specific survival (CSS)].RESULTS: Frequency of AMACR expression was significantly higher in papRCC compared to other tumor subtypes (83% vs. 15-35%, p < 0.0001). Presence of AMACR did not correlate with stage or nodal metastases in papRCC. In a dichotomized scoring (negative vs. positive expression), an inverse correlation between higher grade (p = 0.03) and presence of distant metastasis (p = 0.014) was observed in papRCC. AMACR expression correlated with the presence of nodal metastasis in ccRCC (p = 0.02). Both in ccRCC and in papRCC, OS and CSS did not correlate with the AMACR expression status.CONCLUSIONS: The high expression in papRCC confirms AMACR to be a marker for subtype differentiation in RCC, while a missing expression in this subtype seems to be associated with negative pathological features. However, in contrast to other tumor entities, AMACR expression seems to have a limited prognostic impact in renal carcinoma, especially with regard to survival.

KW - Carcinoma, Renal Cell

KW - Cohort Studies

KW - Follow-Up Studies

KW - Gene Expression Regulation, Neoplastic

KW - Humans

KW - Kaplan-Meier Estimate

KW - Kidney Neoplasms

KW - Neoplasm Staging

KW - Predictive Value of Tests

KW - Prognosis

KW - Racemases and Epimerases

KW - Retrospective Studies

KW - Survival Rate

KW - Tumor Markers, Biological

U2 - 10.1007/s00345-011-0783-z

DO - 10.1007/s00345-011-0783-z

M3 - SCORING: Journal article

C2 - 22009118

VL - 31

SP - 847

EP - 853

JO - WORLD J UROL

JF - WORLD J UROL

SN - 0724-4983

IS - 4

ER -