Evidence map›Paper›PMID 23851165›Full record

Trial reportThe Journal of steroid biochemistry and molecular biology2013

Development, validation and application of a stable isotope dilution liquid chromatography electrospray ionization/selected reaction monitoring/mass spectrometry (SID-LC/ESI/SRM/MS) method for quantification of keto-androgens in human serum.

Daniel Tamae, Michael Byrns, Brett Marck, Elahe A Mostaghel, Peter S Nelson, Paul Lange, Daniel Lin, Mary-Ellen Taplin, Steven Balk, William Ellis and 5 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The Journal of steroid biochemistry and molecular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Article
  8. Determination of Intraprostatic and Intratesticular Androgens.International journal of molecular sciences · 2021
    Review
  9. Contribution of Adrenal Glands to Intratumor Androgens and Growth of Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  10. Article
  11. Dehydroepiandrosterone (DHEA)-SOVitamins and hormones · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

15 authors at 4 institutions in 1 country.

Daniel TamaeCenters of Excellence in Environmental Toxicology and Cancer Pharmacology, Department of Pharmacology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Michael Byrns
Brett Marck
Elahe A Mostaghel
Peter S Nelson
Paul Lange
Daniel Lin
Mary-Ellen Taplin
Steven Balk
William Ellis
Larry True
Robert Vessella
Bruce Montgomery
Ian A Blair
Trevor M Penning
University of Washington · USUniversity of Pennsylvania · USFred Hutch Cancer Center · USHarvard University · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Robert H. Vonderheide · 1985 to 2026
$222.3M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2006 to 2026
$35.3M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PETER S NELSON · 2013 to 2026
$25.0M
Training Program in Cancer PharmacologyR25CA101871 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BLAIR, IAN ALEXANDER · 2003 to 2013
$4.3M
Human Aldo Keto Reductases and Steroid Hormone ActionR01CA090744 · NCI · UNIVERSITY OF PENNSYLVANIA · PI PENNING, TREVOR M · 2001 to 2011
$3.1M
NCI NIH HHS 5R25-CA101871NCI NIH HHS P01 CA163227NCI NIH HHS P01-CA163227-01A1NCI NIH HHS P30 CA016520NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA090744NCI NIH HHS R01-CA90744NCI NIH HHS R25 CA101871NIEHS NIH HHS P30 ES013508NIEHS NIH HHS P30-ES013508
6 · The paper itself

Abstract

Prostate cancer is the most frequently diagnosed form of cancer in males in the United States. The disease is androgen driven and the use of orchiectomy or chemical castration, known as androgen deprivation therapy (ADT) has been employed for the treatment of advanced prostate cancer for over 70 years. Agents such as GnRH agonists and non-steroidal androgen receptor antagonists are routinely used in the clinic, but eventually relapse occurs due to the emergence of castration-resistant prostate cancer. With the appreciation that androgen signaling still persists in these patients and the development of new therapies such as abiraterone and enzalutamide that further suppresses androgen synthesis or signaling, there is a renewed need for sensitive and specific methods to quantify androgen precursor and metabolite levels to assess drug efficacy. We describe the development, validation and application of a stable isotope dilution liquid chromatography electrospray ionization selected reaction monitoring mass spectrometry (SID-LC/ESI/SRM/MS) method for quantification of serum keto-androgens and their sulfate and glucuronide conjugates using Girard-T oxime derivatives. The method is robust down to 0.2-4pg on column, depending on the androgen metabolite quantified, and can also quantify dehydroepiandrosterone sulfate (DHEA-S) in only 1μL of serum. The clinical utility of this method was demonstrated by analyzing serum androgens from patients enrolled in a clinical trial assessing combinations of pharmacological agents to maximally suppress gonadal and adrenal androgens (Targeted Androgen Pathway Suppression, TAPS clinical trial). The method was validated by correlating the results obtained with a hydroxylamine derivatization procedure coupled with tandem mass spectrometry using selected reaction monitoring that was conducted in an independent laboratory.

Indexed as

AndrogensChromatography, LiquidHumansMaleMass SpectrometrySpectrometry, Mass, Electrospray IonizationAndrogens5α-androstane-3,17-dione5α-dihydrotestosteroneAAdioneADTandrogen deprivation therapyAndrogen metabolomeandrosteronecastration resistant prostate cancerCD-FBScharcoal dextran stripped fetal bovine serumcoefficient of variationCRPCCVdehydroepiandrosteronedehydroepiandrosterone glucuronidedehydroepiandrosterone sulfateDHEADHEA-GDHEA-SDHTELISAenzyme-linked immunosorbent assayEpi-TepitestosteroneGnRHgonadotropin releasing hormoneHSDhydroxysteroid dehydrogenaseLCliquid chromatographyLLOQlower limit of quantificationMass spectrometrymass to charge ratiom/zNDnot detectednot significantNSProstate cancerprostate specific antigenPSAQCquality controlradioimmunoassayRIASID-LC/ESI/SRM/MSstable isotope dilution liquid chromatography electrospray ionization selected reaction monitoring mass spectrometryTTAPSTargeted Androgen Pathway Suppression clinical trialtestosteroneTFAtrifluoroacetic acidUDP glucuronosyltransferaseUGTΔ(4)-ADΔ(4)-androstene-3,17-dione

Identifiers

PMID23851165
PMCPMC3866616
OpenAlexW1996331126

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.