Evidence map›Paper›PMID 31562254›Full record

ArticleMolecular cancer research : MCR2019

Prostate Tumor Cell-Derived IL1β Induces an Inflammatory Phenotype in Bone Marrow Adipocytes and Reduces Sensitivity to Docetaxel via Lipolysis-Dependent Mechanisms.

Mackenzie K Herroon, Jonathan D Diedrich, Erandi Rajagurubandara, Carly Martin, Krishna R Maddipati, Seongho Kim, Elisabeth I Heath, James Granneman, Izabela Podgorski

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Mackenzie K Herroon *Department of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan.ORCID 0000-0001-6565-9074
Jonathan D Diedrich *Department of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan.
Erandi RajagurubandaraDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan.ORCID 0000-0001-5051-8420
Carly MartinDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan.
Krishna R MaddipatiDepartment of Pathology, Wayne State University School of Medicine, Detroit, Michigan.
Seongho KimDepartment of Oncology, Wayne State University School of Medicine, Detroit, Michigan.
Elisabeth I HeathDepartment of Oncology, Wayne State University School of Medicine, Detroit, Michigan.
James GrannemanCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan.
Izabela PodgorskiDepartment of Pharmacology, Wayne State University School of Medicine, Detroit, Michigan. ipodgors@med.wayne.edu.
Wayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Functional Role of Bone Marrow Adipocytes in Metastatic Prostate CancerR01CA181189 · NCI · WAYNE STATE UNIVERSITY · PI PODGORSKI, IZABELA · 2014 to 2018
$1.6M
Triple Quadrupole - Ion Trap Hybrid LC/MS/MS SystemS10RR027926 · NCRR · WAYNE STATE UNIVERSITY · PI MADDIPATI, KRISHNARAO · 2010 to 2010
$425k
Bone Marrow Adipocytes Alter the Metabolic Phenotype of Metastatic Prostate Cancer Cells Through the Activation of HIF-1aF31CA203036 · NCI · WAYNE STATE UNIVERSITY · PI DIEDRICH, JONATHAN · 2017 to 2017
$13k
NCI NIH HHS F31 CA203036NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA181189NCI NIH HHS T32 CA009531NCRR NIH HHS S10 RR027926
6 · The paper itself

Abstract

Adipocyte-tumor cell cross-talk is one of the critical mediators of tumor progression and an emerging facilitator of therapy evasion. Tumor cells that metastasize to adipocyte-rich bone marrow take advantage of the interplay between metabolic and inflammatory pathways to activate prosurvival mechanisms that allow them to thrive and escape therapy. Using

Indexed as

AdipocytesAnimalsBiopsyBone Marrow CellsChemokine CCL2Cyclooxygenase 2DinoprostoneDocetaxelDrug Resistance, NeoplasmHumansInflammationInterleukin-1betaLipolysisMaleMiceProstateCCL2 protein, humanChemokine CCL2Cyclooxygenase 2DinoprostoneDocetaxelIL1B protein, humanInterleukin-1betaPTGS2 protein, human

Identifiers

PMID31562254
PMCPMC6891205
OpenAlexW2975479365

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.