TMPRSS2:ERG fusion transcripts in urine from prostate cancer patients correlate with a less favorable prognosis.

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TMPRSS2:ERG fusion transcripts in urine from prostate cancer patients correlate with a less favorable prognosis. / Rostad, Kari; Hellwinkel, Olaf; Haukaas, Svein A; Halvorsen, Ole J; Øyan, Anne M; Haese, Alexander; Budäus, Lars; Albrecht, Heiko; Akslen, Lars A; Schlomm, Thorsten; Kalland, Karl-Henning.

In: APMIS, Vol. 117, No. 8, 8, 2009, p. 575-582.

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

Harvard

Rostad, K, Hellwinkel, O, Haukaas, SA, Halvorsen, OJ, Øyan, AM, Haese, A, Budäus, L, Albrecht, H, Akslen, LA, Schlomm, T & Kalland, K-H 2009, 'TMPRSS2:ERG fusion transcripts in urine from prostate cancer patients correlate with a less favorable prognosis.', APMIS, vol. 117, no. 8, 8, pp. 575-582. <http://www.ncbi.nlm.nih.gov/pubmed/19664128?dopt=Citation>

APA

Rostad, K., Hellwinkel, O., Haukaas, S. A., Halvorsen, O. J., Øyan, A. M., Haese, A., Budäus, L., Albrecht, H., Akslen, L. A., Schlomm, T., & Kalland, K-H. (2009). TMPRSS2:ERG fusion transcripts in urine from prostate cancer patients correlate with a less favorable prognosis. APMIS, 117(8), 575-582. [8]. http://www.ncbi.nlm.nih.gov/pubmed/19664128?dopt=Citation

Vancouver

Bibtex

@article{c3201aa2571945a98863f5a8325f3a2b,
title = "TMPRSS2:ERG fusion transcripts in urine from prostate cancer patients correlate with a less favorable prognosis.",
abstract = "The transcription factor ERG is highly upregulated in the majority of prostate cancers due to chromosomal fusion of the androgen responsive promoter of TMPRSS2 to the ERG reading frame. Our aim was to identify this gene fusion in urine samples from prostate cancer patients prior to radical treatment and to compare fusion status with clinicopathological variables. Urine fractions from 55 patients (with and without prior prostatic massage) were analyzed for the presence of TMPRSS2:ERG isoforms using real-time qPCR. Sixty-nine percent of urine samples following prostatic massage were positive for TMPRSS2:ERG isoforms a or b, five out of which were positive for both, vs 24% of samples obtained without prior massage. Isoform a seems to be most prevalent and some patients may be positive for more than one fusion variant, reflecting the multifocality of prostate cancer. Prostatic massage prior to sampling, analysis of pelleted urine material and detection of cDNA provided the highest sensitivity. Positive statistical correlations were identified between TMPRSS2:ERG fusion and high s-PSA, pathological stage and Gleason score. Our findings contribute to the increasing elucidation of the role of TMPRSS2:ERG in the development of prostate cancer.",
author = "Kari Rostad and Olaf Hellwinkel and Haukaas, {Svein A} and Halvorsen, {Ole J} and {\O}yan, {Anne M} and Alexander Haese and Lars Bud{\"a}us and Heiko Albrecht and Akslen, {Lars A} and Thorsten Schlomm and Karl-Henning Kalland",
year = "2009",
language = "Deutsch",
volume = "117",
pages = "575--582",
journal = "APMIS",
issn = "0903-4641",
publisher = "Wiley-Blackwell",
number = "8",

}

RIS

TY - JOUR

T1 - TMPRSS2:ERG fusion transcripts in urine from prostate cancer patients correlate with a less favorable prognosis.

AU - Rostad, Kari

AU - Hellwinkel, Olaf

AU - Haukaas, Svein A

AU - Halvorsen, Ole J

AU - Øyan, Anne M

AU - Haese, Alexander

AU - Budäus, Lars

AU - Albrecht, Heiko

AU - Akslen, Lars A

AU - Schlomm, Thorsten

AU - Kalland, Karl-Henning

PY - 2009

Y1 - 2009

N2 - The transcription factor ERG is highly upregulated in the majority of prostate cancers due to chromosomal fusion of the androgen responsive promoter of TMPRSS2 to the ERG reading frame. Our aim was to identify this gene fusion in urine samples from prostate cancer patients prior to radical treatment and to compare fusion status with clinicopathological variables. Urine fractions from 55 patients (with and without prior prostatic massage) were analyzed for the presence of TMPRSS2:ERG isoforms using real-time qPCR. Sixty-nine percent of urine samples following prostatic massage were positive for TMPRSS2:ERG isoforms a or b, five out of which were positive for both, vs 24% of samples obtained without prior massage. Isoform a seems to be most prevalent and some patients may be positive for more than one fusion variant, reflecting the multifocality of prostate cancer. Prostatic massage prior to sampling, analysis of pelleted urine material and detection of cDNA provided the highest sensitivity. Positive statistical correlations were identified between TMPRSS2:ERG fusion and high s-PSA, pathological stage and Gleason score. Our findings contribute to the increasing elucidation of the role of TMPRSS2:ERG in the development of prostate cancer.

AB - The transcription factor ERG is highly upregulated in the majority of prostate cancers due to chromosomal fusion of the androgen responsive promoter of TMPRSS2 to the ERG reading frame. Our aim was to identify this gene fusion in urine samples from prostate cancer patients prior to radical treatment and to compare fusion status with clinicopathological variables. Urine fractions from 55 patients (with and without prior prostatic massage) were analyzed for the presence of TMPRSS2:ERG isoforms using real-time qPCR. Sixty-nine percent of urine samples following prostatic massage were positive for TMPRSS2:ERG isoforms a or b, five out of which were positive for both, vs 24% of samples obtained without prior massage. Isoform a seems to be most prevalent and some patients may be positive for more than one fusion variant, reflecting the multifocality of prostate cancer. Prostatic massage prior to sampling, analysis of pelleted urine material and detection of cDNA provided the highest sensitivity. Positive statistical correlations were identified between TMPRSS2:ERG fusion and high s-PSA, pathological stage and Gleason score. Our findings contribute to the increasing elucidation of the role of TMPRSS2:ERG in the development of prostate cancer.

M3 - SCORING: Zeitschriftenaufsatz

VL - 117

SP - 575

EP - 582

JO - APMIS

JF - APMIS

SN - 0903-4641

IS - 8

M1 - 8

ER -