AMACR expression in colorectal cancer is associated with left-sided tumor localization.

Standard

AMACR expression in colorectal cancer is associated with left-sided tumor localization. / Marx, Andreas; Simon, Philipp; Simon, Ronald; Mirlacher, Martina; Izbicki, Jakob R.; Yekebas, Emre F.; Kaifi, Jussuf; Terracciano, Luigi; Sauter, Guido.

in: VIRCHOWS ARCH, Jahrgang 453, Nr. 3, 3, 2008, S. 243-248.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Marx, A, Simon, P, Simon, R, Mirlacher, M, Izbicki, JR, Yekebas, EF, Kaifi, J, Terracciano, L & Sauter, G 2008, 'AMACR expression in colorectal cancer is associated with left-sided tumor localization.', VIRCHOWS ARCH, Jg. 453, Nr. 3, 3, S. 243-248. <http://www.ncbi.nlm.nih.gov/pubmed/18712414?dopt=Citation>

APA

Marx, A., Simon, P., Simon, R., Mirlacher, M., Izbicki, J. R., Yekebas, E. F., Kaifi, J., Terracciano, L., & Sauter, G. (2008). AMACR expression in colorectal cancer is associated with left-sided tumor localization. VIRCHOWS ARCH, 453(3), 243-248. [3]. http://www.ncbi.nlm.nih.gov/pubmed/18712414?dopt=Citation

Vancouver

Marx A, Simon P, Simon R, Mirlacher M, Izbicki JR, Yekebas EF et al. AMACR expression in colorectal cancer is associated with left-sided tumor localization. VIRCHOWS ARCH. 2008;453(3):243-248. 3.

Bibtex

@article{d0502203f7614c85a360816031a54581,
title = "AMACR expression in colorectal cancer is associated with left-sided tumor localization.",
abstract = "Alpha-methylacyl-CoA racemase (AMACR) is an enzyme playing an important role in the beta-oxidation of branched-chain fatty acids and fatty acid derivatives. Altered expression levels of AMACR have been described in various cancers including colorectal cancer (CRC). To determine the potential prognostic impact of AMACR expression, we analyzed 1,315 CRC on a tissue microarray (TMA) by immunohistochemistry (IHC). Clinical follow-up data were available from all cancer patients. Positive AMACR staining was observed in 1,074 (81.7%) of the 1,315 cases including 276 cancers with weak (21.0%) and 798 cancers with strong staining (60.7%). AMACR IHC was significantly associated with tumor grade, stage, non-mucinous phenotype, and left-sided tumor localization (p <0.0001 each). AMACR positivity was observed in 65.8% of cancers from the right-sided colon, in 73.2% of cancers from the colon transversum, in 81.1% of cancers from the colon descendens, and in 88.9% of the distal left-sided cancers (sigma and rectum; p <0.0001). However, AMACR staining results were unrelated to clinical outcome. It is concluded that AMACR cannot serve as a prognostic marker in CRC. We hypothesize that the association of AMACR expression with tumor localization may be related to differences in the metabolism/exposure to fatty acids occurring along the colon.",
author = "Andreas Marx and Philipp Simon and Ronald Simon and Martina Mirlacher and Izbicki, {Jakob R.} and Yekebas, {Emre F.} and Jussuf Kaifi and Luigi Terracciano and Guido Sauter",
year = "2008",
language = "Deutsch",
volume = "453",
pages = "243--248",
journal = "VIRCHOWS ARCH",
issn = "0945-6317",
publisher = "Springer",
number = "3",

}

RIS

TY - JOUR

T1 - AMACR expression in colorectal cancer is associated with left-sided tumor localization.

AU - Marx, Andreas

AU - Simon, Philipp

AU - Simon, Ronald

AU - Mirlacher, Martina

AU - Izbicki, Jakob R.

AU - Yekebas, Emre F.

AU - Kaifi, Jussuf

AU - Terracciano, Luigi

AU - Sauter, Guido

PY - 2008

Y1 - 2008

N2 - Alpha-methylacyl-CoA racemase (AMACR) is an enzyme playing an important role in the beta-oxidation of branched-chain fatty acids and fatty acid derivatives. Altered expression levels of AMACR have been described in various cancers including colorectal cancer (CRC). To determine the potential prognostic impact of AMACR expression, we analyzed 1,315 CRC on a tissue microarray (TMA) by immunohistochemistry (IHC). Clinical follow-up data were available from all cancer patients. Positive AMACR staining was observed in 1,074 (81.7%) of the 1,315 cases including 276 cancers with weak (21.0%) and 798 cancers with strong staining (60.7%). AMACR IHC was significantly associated with tumor grade, stage, non-mucinous phenotype, and left-sided tumor localization (p <0.0001 each). AMACR positivity was observed in 65.8% of cancers from the right-sided colon, in 73.2% of cancers from the colon transversum, in 81.1% of cancers from the colon descendens, and in 88.9% of the distal left-sided cancers (sigma and rectum; p <0.0001). However, AMACR staining results were unrelated to clinical outcome. It is concluded that AMACR cannot serve as a prognostic marker in CRC. We hypothesize that the association of AMACR expression with tumor localization may be related to differences in the metabolism/exposure to fatty acids occurring along the colon.

AB - Alpha-methylacyl-CoA racemase (AMACR) is an enzyme playing an important role in the beta-oxidation of branched-chain fatty acids and fatty acid derivatives. Altered expression levels of AMACR have been described in various cancers including colorectal cancer (CRC). To determine the potential prognostic impact of AMACR expression, we analyzed 1,315 CRC on a tissue microarray (TMA) by immunohistochemistry (IHC). Clinical follow-up data were available from all cancer patients. Positive AMACR staining was observed in 1,074 (81.7%) of the 1,315 cases including 276 cancers with weak (21.0%) and 798 cancers with strong staining (60.7%). AMACR IHC was significantly associated with tumor grade, stage, non-mucinous phenotype, and left-sided tumor localization (p <0.0001 each). AMACR positivity was observed in 65.8% of cancers from the right-sided colon, in 73.2% of cancers from the colon transversum, in 81.1% of cancers from the colon descendens, and in 88.9% of the distal left-sided cancers (sigma and rectum; p <0.0001). However, AMACR staining results were unrelated to clinical outcome. It is concluded that AMACR cannot serve as a prognostic marker in CRC. We hypothesize that the association of AMACR expression with tumor localization may be related to differences in the metabolism/exposure to fatty acids occurring along the colon.

M3 - SCORING: Zeitschriftenaufsatz

VL - 453

SP - 243

EP - 248

JO - VIRCHOWS ARCH

JF - VIRCHOWS ARCH

SN - 0945-6317

IS - 3

M1 - 3

ER -