Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions.

Standard

Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions. / Schostak, Martin; Miller, Kurt; Krause, Hans; Schrader, Mark; Kempkensteffen, Carsten; Köllermann, Jens.

In: CANCER DETECT PREV, Vol. 30, No. 5, 5, 2006, p. 449-454.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Schostak, M, Miller, K, Krause, H, Schrader, M, Kempkensteffen, C & Köllermann, J 2006, 'Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions.', CANCER DETECT PREV, vol. 30, no. 5, 5, pp. 449-454. <http://www.ncbi.nlm.nih.gov/pubmed/17067752?dopt=Citation>

APA

Schostak, M., Miller, K., Krause, H., Schrader, M., Kempkensteffen, C., & Köllermann, J. (2006). Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions. CANCER DETECT PREV, 30(5), 449-454. [5]. http://www.ncbi.nlm.nih.gov/pubmed/17067752?dopt=Citation

Vancouver

Schostak M, Miller K, Krause H, Schrader M, Kempkensteffen C, Köllermann J. Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions. CANCER DETECT PREV. 2006;30(5):449-454. 5.

Bibtex

@article{80f5a1b8ba1243bf928193f667704978,
title = "Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions.",
abstract = "BACKGROUND: High-throughput gene expression profiling has recently shown that the mRNA for alpha-methylacyl CoA racemase (AMACR or P504S) is overexpressed in prostate carcinomas (PCa). Several immunohistochemical studies have reported the usefulness of anti-AMACR/P504S for detecting prostate cancer over the full range of prostate specimens encountered in surgical pathology. We tested real-time reverse transcriptase-polymerase chain reaction (RT-PCR) for specific and sensitive detection of AMACR transcripts as a supplementary measure for discriminating between malignant and benign lesions in prostatic tissues. METHODS: Total RNA was isolated from snap-frozen chips in 55 cases of benign prostatic hyperplasia (BPH) and from frozen sections in 57 prostatectomy cases. The latter were analyzed by an uropathologist (J.K.) and found to contain at least 50% malignant epithelia. Relative quantification of AMACR transcripts was performed by RT-PCR using hybridization probes for detection and PBGD for normalization. RESULTS: Normalized AMACR transcript levels showed an average 3.75-fold increase in 57 prostate carcinomas cases when compared to 55 cases of BPH (p",
author = "Martin Schostak and Kurt Miller and Hans Krause and Mark Schrader and Carsten Kempkensteffen and Jens K{\"o}llermann",
year = "2006",
language = "Deutsch",
volume = "30",
pages = "449--454",
number = "5",

}

RIS

TY - JOUR

T1 - Kinetic fluorescence reverse transcriptase-polymerase chain reaction for alpha-methylacyl CoA racemase distinguishes prostate cancer from benign lesions.

AU - Schostak, Martin

AU - Miller, Kurt

AU - Krause, Hans

AU - Schrader, Mark

AU - Kempkensteffen, Carsten

AU - Köllermann, Jens

PY - 2006

Y1 - 2006

N2 - BACKGROUND: High-throughput gene expression profiling has recently shown that the mRNA for alpha-methylacyl CoA racemase (AMACR or P504S) is overexpressed in prostate carcinomas (PCa). Several immunohistochemical studies have reported the usefulness of anti-AMACR/P504S for detecting prostate cancer over the full range of prostate specimens encountered in surgical pathology. We tested real-time reverse transcriptase-polymerase chain reaction (RT-PCR) for specific and sensitive detection of AMACR transcripts as a supplementary measure for discriminating between malignant and benign lesions in prostatic tissues. METHODS: Total RNA was isolated from snap-frozen chips in 55 cases of benign prostatic hyperplasia (BPH) and from frozen sections in 57 prostatectomy cases. The latter were analyzed by an uropathologist (J.K.) and found to contain at least 50% malignant epithelia. Relative quantification of AMACR transcripts was performed by RT-PCR using hybridization probes for detection and PBGD for normalization. RESULTS: Normalized AMACR transcript levels showed an average 3.75-fold increase in 57 prostate carcinomas cases when compared to 55 cases of BPH (p

AB - BACKGROUND: High-throughput gene expression profiling has recently shown that the mRNA for alpha-methylacyl CoA racemase (AMACR or P504S) is overexpressed in prostate carcinomas (PCa). Several immunohistochemical studies have reported the usefulness of anti-AMACR/P504S for detecting prostate cancer over the full range of prostate specimens encountered in surgical pathology. We tested real-time reverse transcriptase-polymerase chain reaction (RT-PCR) for specific and sensitive detection of AMACR transcripts as a supplementary measure for discriminating between malignant and benign lesions in prostatic tissues. METHODS: Total RNA was isolated from snap-frozen chips in 55 cases of benign prostatic hyperplasia (BPH) and from frozen sections in 57 prostatectomy cases. The latter were analyzed by an uropathologist (J.K.) and found to contain at least 50% malignant epithelia. Relative quantification of AMACR transcripts was performed by RT-PCR using hybridization probes for detection and PBGD for normalization. RESULTS: Normalized AMACR transcript levels showed an average 3.75-fold increase in 57 prostate carcinomas cases when compared to 55 cases of BPH (p

M3 - SCORING: Zeitschriftenaufsatz

VL - 30

SP - 449

EP - 454

IS - 5

M1 - 5

ER -