Evidence map›Paper›PMID 26969590›Full record

ReviewHormones & cancer2016

The Metabolism, Analysis, and Targeting of Steroid Hormones in Breast and Prostate Cancer.

Cameron P Capper, James M Rae, Richard J Auchus

Abstract readReview
In one paragraph

Review in Hormones & cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
8.1field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
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  3. Recent advances in hormone-based biopharmaceuticals for cancer therapy.Journal of the Egyptian National Cancer Institute · 2026
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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

3 authors at 1 institution in 1 country.

Cameron P CapperDivision of Hematology/Oncology, Department of Internal Medicine and Department of Pharmacology, University of Michigan, Ann Arbor, MI, 48019, USA.
James M RaeDivision of Hematology/Oncology, Department of Internal Medicine and Department of Pharmacology, University of Michigan, Ann Arbor, MI, 48019, USA.
Richard J AuchusDivision of Metabolism, Diabetes, and Endocrinology, Department of Internal Medicine and Department of Pharmacology, University of Michigan School of Medicine, Room 5560A, MSRBII, 1150 W. Medical Center Drive, Ann Arbor, MI, 48019, USA. rauchus@med.umich.edu.
University of Michigan–Ann Arbor · US

Funding

Activation of androgen biosynthesis and drug metabolism by cytochrome b5R01GM086596 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI RICHARD J. AUCHUS · 2009 to 2026
$4.8M
Cooperative steroidogenic inhibition for treatment of advanced prostate cancerR01CA168899 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI SHARIFI, NIMA · 2013 to 2017
$1.6M
Genetic Predictors of Anti-Estrogen Clinical Activity in Breast Cancer PatientsR01GM099143 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAE, JAMES MICHAEL · 2011 to 2015
$1.6M
NCI NIH HHS R01 CA168899NIGMS NIH HHS R01 GM086596NIGMS NIH HHS R01 GM099143
6 · The paper itself

Abstract

Breast and prostate cancers are malignancies in which steroid hormones drive cellular proliferation. Over the past century, this understanding has led to successful treatment strategies aimed to inhibit hormone-mediated tumor growth. Nonetheless, disease relapse and progression still pose significant clinical problems, with recurrent and metastatic tumors often exhibiting resistance to current drug therapies. The central role of androgens and estrogens in prostate and breast cancer etiology explains not only why endocrine therapies are often initially successful but also why many tumors ultimately become resistant. It is hypothesized that reducing the concentration of active hormones in the systemic circulation may be insufficient to block cancer progression, as this action selects for tumor cells that can generate active steroids from circulating precursors. This review aims to highlight the currently known differences of steroid biosynthesis in normal physiology versus hormone-dependent cancers, modern approaches to the assessment and targeting of these pathways, and priorities for future research.

Indexed as

AndrogensAnimalsAntineoplastic AgentsBreast NeoplasmsEstrogensFemaleGonadsHumansHypothalamo-Hypophyseal SystemMaleMolecular Targeted TherapyMutationPituitary-Adrenal SystemProstatic NeoplasmsReceptors, Cytoplasmic and NuclearSignal TransductionAndrogensAntineoplastic AgentsEstrogensReceptors, Cytoplasmic and NuclearSteroids

Identifiers

PMID26969590
PMCPMC4860032
OpenAlexW2294549982

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.