Evidence map›Paper›PMID 17154657›Full record

ArticleMolecular diagnosis & therapy2006

Detection of alpha-methylacyl-coenzyme-A racemase transcripts in blood and urine samples of prostate cancer patients.

Barbara K Zehentner, Heather Secrist, XinQun Zhang, Dawn C Hayes, Richard Ostenson, Gary Goodman, Jiangchun Xu, Mark Kiviat, Nancy Kiviat, David H Persing and 1 more

Abstract read
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In one paragraph

Article in Molecular diagnosis & therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Approaches to urinary detection of prostate cancer.Prostate cancer and prostatic diseases · 2019
    Review
  4. High frequency of the SDK1:AMACR fusion transcript in Chinese prostate cancer.International journal of clinical and experimental medicine · 2015
    Article
  5. The present and future of prostate cancer urine biomarkers.International journal of molecular sciences · 2013
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Urine biomarkers in prostate cancer.Nature reviews. Urology · 2010
    Review
  12. Article
  13. Article
  14. Beyond prostate-specific antigen: alternate serum markers.Prostate cancer and prostatic diseases · 2008
    Review
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Barbara K ZehentnerHematoLogics Inc., Seattle, Washington 98109, USA. barbara@hematologics.com
Heather Secrist
XinQun Zhang
Dawn C Hayes
Richard Ostenson
Gary Goodman
Jiangchun Xu
Mark Kiviat
Nancy Kiviat
David H Persing
Raymond L Houghton
Harborview Medical Center · USAmgen (United States) · USInBios International (United States) · USMultiCare Good Samaritan Hospital · USSwedish Medical Center · US

Funding

NOVEL MARKERS FOR PROSTATE CANCER DIAGNOSIS/PROGNOSISR44CA080518 · NCI · CORIXA CORPORATION · PI PERSING, DAVID H · 2001 to 2002
$669k
NCI NIH HHS R44 CA-80518
6 · The paper itself

Abstract

backgroundAlpha-methylacyl-coenzyme-A racemase (AMACR) has been shown to be a highly specific marker for prostate cancer cells, even in the earliest stages of malignant progression. It is expressed at much higher levels than prostate-specific antigen (PSA) in malignant tissues, and is not expressed at appreciable levels in normal prostatic epithelium. In this study, we demonstrate the quantitative detection of AMACR transcripts in peripheral blood of prostate cancer patients using real-time RT-PCR. In addition, we have undertaken a pilot study to demonstrate the potential application of this technique for the detection of prostate tumor cells in urine samples from patients with prostate cancer.

methodsA real-time RT-PCR assay was developed for detection of the expression of AMACR in prostate cancer patients. Blood samples from 163 patients were tested at various stages of disease progression, with or without therapy. Blood specimens from patients with benign prostate disorders and other types of cancer were also evaluated.

resultsIn 28 of 58 samples from patients with known metastatic disease who were undergoing treatment, an AMACR expression signal above the cut-off value was detected, consistent with the presence of circulating tumor cells. In 39 of 88 patients with presumptive organ-confined disease, there was evidence of low levels of circulating tumor cells. Comparison of AMACR RT-PCR with known serum PSA values indicated that a combination of these parameters significantly increased the sensitivity for detection of progressive disease. In a pilot study analyzing urine samples from seven prostate cancer patients, elevated AMACR expression levels were detected in the urine sediments of four of six stage-T1 prostate cancer patients and in the one patient with stage-T2 prostate cancer.

conclusionThe data presented in this study indicates that AMACR real-time RT-PCR may aid in the detection and staging of prostate cancer.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorHumansMaleMiddle AgedNeoplasm StagingProstate-Specific AntigenProstatic NeoplasmsRacemases and EpimerasesReverse Transcriptase Polymerase Chain ReactionRNA, NeoplasmSensitivity and Specificityalpha-methylacyl-CoA racemaseBiomarkers, TumorProstate-Specific AntigenRacemases and EpimerasesRNA, Neoplasm

Identifiers

PMID17154657
OpenAlexW2065758985

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.