Evidence map›Paper›PMID 28957377›Full record

ArticlePloS one2017

Androgen receptor expression on circulating tumor cells in metastatic breast cancer.

Takeo Fujii, James M Reuben, Lei Huo, Jose Rodrigo Espinosa Fernandez, Yun Gong, Rachel Krupa, Mahipal V Suraneni, Ryon P Graf, Jerry Lee, Stephanie Greene and 11 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 14% 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.

NCT04241237 unknown statusnot on this mapstarted 2020, after this paper: background citation

Concordance Between Liquid and Tissue Biopsy in Newly Diagnosed Metastatic Breast Cancer

TypeobservationalSponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph'sRan2020 to 2022Enrolled120ConditionsBreast NeoplasmsArmsBlood Draw
NCT05054010 active not recruitingnot on this mapstarted 2021, after this paper: background citation

Identification and Characterization of Commercial RUO Antibodies for the Detection of Specific Breast Cancer Tumoral Markers Expressed in Potential Circulating Tumoral Cells (CTCs)

TypeobservationalSponsorTethis S.p.A.Ran2021 to 2026Enrolled84ConditionsBreast Neoplasms
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Recent Advances in Methods for Circulating Tumor Cell Detection.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. A novel liquid biopsy assay for detection ofJournal of circulating biomarkers
    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

21 authors at 2 institutions in 1 country.

Takeo FujiiDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
James M ReubenDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Lei HuoDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Jose Rodrigo Espinosa FernandezDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Yun GongDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Rachel KrupaDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Mahipal V SuraneniDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Ryon P GrafDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Jerry LeeDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Stephanie GreeneDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Angel RodriguezDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Lyndsey DuganDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Jessica LouwDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Bora LimDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Carlos H BarcenasDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Angela N MarxDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Debu TripathyDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Yipeng WangDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Mark LandersDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Ryan DittamoreDepartment of Translational Research, Epic Sciences, La Jolla, California, United States of America.
Naoto T UenoDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.ORCID http://orcid.org/0000-0002-0166-7275
Epic Sciences (United States) · USThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

purposeAndrogen receptor (AR) is frequently detected in breast cancers, and AR-targeted therapies are showing activity in AR-positive (AR+) breast cancer. However, the role of AR in breast cancers is still not fully elucidated and the biology of AR in breast cancer remains incompletely understood. Circulating tumor cells (CTCs) can serve as prognostic and diagnostic tools, prompting us to measure AR protein expression and conduct genomic analyses on CTCs in patients with metastatic breast cancer.

methodsBlood samples from patients with metastatic breast cancer were deposited on glass slides, subjected to nuclear staining with DAPI, and reacted with fluorescent-labeled antibodies to detect CD45, cytokeratin (CK), and biomarkers of interest (AR, estrogen receptor [ER], and HER2) on all nucleated cells. The stained slides were scanned and enumerated by non-enrichment-based non-biased approach independent of cell surface epithelial cell adhesion molecule (EpCAM) using the Epic Sciences CTC platform. Data were analyzed using established digital pathology algorithms.

resultsOf 68 patients, 51 (75%) had at least 1 CTC, and 49 of these 51 (96%) had hormone-receptor-positive (HR+)/HER2-negative primary tumors. AR was expressed in CK+ CTCs in 10 patients. Of these 10 patients, 3 also had ER expression in CK+ CTCs. Single cell genomic analysis of 78 CTCs from 1 of these 3 patients identified three distinct copy number patterns. AR+ cells had a lower frequency of chromosomal changes than ER+ and HER2+ cells.

conclusionsCTC enumeration and analysis using no enrichment or selection provides a non-biased approach to detect AR expression and chromosomal aberrations in CTCs in patients with metastatic breast cancer. The heterogeneity of intrapatient AR expression in CTCs leads to the new hypothesis that patients with AR+ CTCs have heterogeneous disease with multiple drivers. Further studies are warranted to investigate the clinical applicability of AR+ CTCs and their heterogeneity.

Indexed as

AdultAgedBreast NeoplasmsDNA Copy Number VariationsErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryMiddle AgedNeoplasm MetastasisNeoplastic Cells, CirculatingPrevalenceReceptors, AndrogenReceptors, EstrogenSingle-Cell AnalysisAR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, AndrogenReceptors, Estrogen

Identifiers

PMID28957377
PMCPMC5619732
OpenAlexW2757819986

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.