Evidence map›Paper›PMID 32928797›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

The Capacity of the Ovarian Cancer Tumor Microenvironment to Integrate Inflammation Signaling Conveys a Shorter Disease-free Interval.

Kimberly R Jordan, Matthew J Sikora, Jill E Slansky, Angela Minic, Jennifer K Richer, Marisa R Moroney, Junxiao Hu, Rebecca J Wolsky, Zachary L Watson, Tomomi M Yamamoto and 5 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
7.0field-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

53 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  4. Cross-assay RNA modeling reveals cancer biomarkers.bioRxiv : the preprint server for biology · 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

15 authors at 5 institutions in 1 country.

Kimberly R Jordan *Department of Immunology and Microbiology, University of Colorado, School of Medicine, Aurora, Colorado.
Matthew J Sikora *Department of Pathology, The University of Colorado Anschutz Medical Campus, Aurora, Colorado.ORCID 0000-0003-2915-7442
Jill E SlanskyDepartment of Immunology and Microbiology, University of Colorado, School of Medicine, Aurora, Colorado.ORCID 0000-0003-3820-1724
Angela MinicDepartment of Immunology and Microbiology, University of Colorado, School of Medicine, Aurora, Colorado.
Jennifer K RicherDepartment of Pathology, The University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Marisa R MoroneyDivision of Gynecologic Oncology, Department of OB/GYN, The University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Junxiao HuDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Denver, Aurora, Colorado.
Rebecca J WolskyDepartment of Pathology, The University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Zachary L WatsonUniversity of Colorado Comprehensive Cancer Center, Aurora, Colorado.
Tomomi M YamamotoDivision of Reproductive Sciences, Department of OB/GYN, The University of Colorado Anschutz Medical Campus, Aurora, Colorado.
James C CostelloUniversity of Colorado Comprehensive Cancer Center, Aurora, Colorado.ORCID 0000-0003-3158-9682
Aaron ClausetDepartment of Computer Science, The University of Colorado, Boulder, Colorado.ORCID 0000-0002-3529-8746
Kian BehbakhtUniversity of Colorado Comprehensive Cancer Center, Aurora, Colorado.
T Rajendra KumarDivision of Reproductive Sciences, Department of OB/GYN, The University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Benjamin G BitlerUniversity of Colorado Comprehensive Cancer Center, Aurora, Colorado. benjamin.bitler@cuanschutz.edu.ORCID 0000-0002-5809-5271
University of Colorado Cancer Center · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Colorado Denver · USColorado School of Public Health · USSanta Fe Institute · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Systems analysis of aggressive prostate cancer pathologyU01CA231978 · NCI · UNIVERSITY OF COLORADO DENVER · PI COSTELLO, JAMES CHRISTOPHER, CRAMER, SCOTT D · 2019 to 2023
$3.4M
Targeting Wnt signaling to overcome PARP inhibitor resistance in ovarian cancerR00CA194318 · NCI · UNIVERSITY OF COLORADO DENVER · PI BITLER, BENJAMIN G · 2017 to 2019
$745k
Functional Proteomics by Reverse Phase Protein Array in CancerR50CA221675 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LU, YILING · 2017 to 2021
$726k
WNT4 IN ENDOCRINE RESPONSE AND RESISTANCE IN INVASIVE LOBULAR CARCINOMAR00CA193734 · NCI · UNIVERSITY OF COLORADO DENVER · PI SIKORA, MATTHEW J · 2017 to 2019
$703k
Tissue Lysate Arrays for Molecular Screening (RMI)R03NS050840 · NINDS · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI LU, YILING · 2004 to 2004
$76k
NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA046934NCI NIH HHS R00 CA193734NCI NIH HHS R00 CA194318NCI NIH HHS R50 CA221675NCI NIH HHS U01 CA231978NINDS NIH HHS R03 NS050840
6 · The paper itself

Abstract

purposeOvarian cancer has one of the highest deaths to incidence ratios across all cancers. Initial chemotherapy is effective, but most patients develop chemoresistant disease. Mechanisms driving clinical chemo-response or -resistance are not well-understood. However, achieving optimal surgical cytoreduction improves survival, and cytoreduction is improved by neoadjuvant chemotherapy (NACT). NACT offers a window to profile pre- versus post-NACT tumors, which we used to identify chemotherapy-induced changes to the tumor microenvironment. EXPERIMENTAL

designWe obtained matched pre- and post-NACT archival tumor tissues from patients with high-grade serous ovarian cancer (patient,

resultsThe most upregulated gene post-NACT was

conclusionsMultiomics profiling of ovarian tumor samples pre- and post-NACT provides unique insight into chemo-induced changes to the tumor microenvironment. We identified a novel IL6/IER3 signaling axis that may drive chemoresistance and disease recurrence.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantCombined Modality TherapyCytoreduction Surgical ProceduresFemaleFollow-Up StudiesHumansInflammationNeoadjuvant TherapyOvarian NeoplasmsPrognosisSurvival RateTumor Microenvironment

Identifiers

PMID32928797
PMCPMC7923250
OpenAlexW3085901054

What OpenQuestion holds

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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.