Evidence map›Paper›PMID 28878133›Full record

ArticleJCI insight2017

Exome-capture RNA sequencing of decade-old breast cancers and matched decalcified bone metastases.

Nolan Priedigkeit, Rebecca J Watters, Peter C Lucas, Ahmed Basudan, Rohit Bhargava, William Horne, Jay K Kolls, Zhou Fang, Margaret Q Rosenzweig, Adam M Brufsky and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
5.6field-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

76 citing papers in PubMed, 126 citations in OpenAlex.

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16 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 1 country.

Nolan PriedigkeitDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Rebecca J WattersWomen's Cancer Research Center, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
Peter C LucasWomen's Cancer Research Center, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
Ahmed BasudanWomen's Cancer Research Center, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
Rohit BhargavaDepartment of Pathology, and.
William HorneRichard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Jay K KollsRichard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
Zhou FangDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Margaret Q RosenzweigAcute and Tertiary Care Department, University of Pittsburgh School of Nursing, Pittsburgh, Pennsylvania, USA.
Adam M BrufskyWomen's Cancer Research Center, UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, USA.
Kurt R WeissDepartment of Orthopedic Surgery.
Steffi OesterreichDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Adrian V LeeDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
University of Pittsburgh · USChildren's Hospital of Pittsburgh · USUPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
PREDOCTORAL TRAINING IN PHARMACOLOGICAL SCIENCEST32GM008424 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PAGANO, PATRICK J · 1994 to 2019
$3.4M
Transcriptomic profiling and functional characterization of fusion genes in recurrent ovarian cancerF30CA203095 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PRIEDIGKEIT, NOLAN · 2016 to 2018
$135k
NCI NIH HHS F30 CA203095NCI NIH HHS P30 CA047904NIGMS NIH HHS T32 GM008424
6 · The paper itself

Abstract

Bone metastases (BoM) are a significant cause of morbidity in patients with estrogen receptor-positive (ER-positive) breast cancer; yet, characterizations of human specimens are limited. In this study, exome-capture RNA sequencing (ecRNA-seq) on aged (8-12 years), formalin-fixed, paraffin-embedded (FFPE), and decalcified cancer specimens was evaluated. Gene expression values and ecRNA-seq quality metrics from FFPE or decalcified tumor RNA showed minimal differences when compared with matched flash-frozen or nondecalcified tumors. ecRNA-seq was then applied on a longitudinal collection of 11 primary breast cancers and patient-matched synchronous or recurrent BoMs. Overtime, BoMs exhibited gene expression shifts to more Her2 and LumB PAM50 subtype profiles, temporally influenced expression evolution, recurrently dysregulated prognostic gene sets, and longitudinal expression alterations of clinically actionable genes, particularly in the CDK/Rb/E2F and FGFR signaling pathways. Taken together, this study demonstrates the use of ecRNA-seq on decade-old and decalcified specimens and defines recurrent longitudinal transcriptional remodeling events in estrogen-deprived breast cancers.

Indexed as

ExomeSequence Analysis, RNAAdultBone NeoplasmsBreast NeoplasmsCalcinosisCohort StudiesFemaleGenes, erbB-2HumansMiddle AgedBreast cancerGeneticsOncology

Identifiers

PMID28878133
PMCPMC5621874
OpenAlexW2753295600

What OpenQuestion holds

Textmetadata
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.