Evidence map›Paper›PMID 34477239›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2022

gp130 Cytokines Activate Novel Signaling Pathways and Alter Bone Dissemination in ER+ Breast Cancer Cells.

Tolu Omokehinde, Alec Jotte, Rachelle W Johnson

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 10 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

3 authors at 2 institutions in 1 country.

Tolu OmokehindeGraduate Program in Cancer Biology, Vanderbilt University, Nashville, TN, USA.
Alec JotteVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, USA.
Rachelle W JohnsonVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0003-2755-9851
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
CHARACTERIZATION OF BREAST CANCER DORMANCY IN BONER00CA194198 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JOHNSON, RACHELLE W · 2016 to 2018
$747k
Functional Proteomics by Reverse Phase Protein Array in CancerR50CA221675 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LU, YILING · 2017 to 2021
$726k
Howard Hughes Medical InstituteNCATS NIH HHS UL1 TR002243NCI NIH HHS P30 CA068485NCI NIH HHS R00 CA194198NCI NIH HHS R00CA194198NCI NIH HHS R50 CA221675NIH HHS P30CA068485
6 · The paper itself

Abstract

Breast cancer cells frequently home to the bone marrow, where they encounter signals that promote survival and quiescence or stimulate their proliferation. The interleukin-6 (IL-6) cytokines signal through the co-receptor glycoprotein130 (gp130) and are abundantly secreted within the bone microenvironment. Breast cancer cell expression of leukemia inhibitory factor (LIF) receptor (LIFR)/STAT3 signaling promotes tumor dormancy in the bone, but it is unclear which, if any of the cytokines that signal through LIFR, including LIF, oncostatin M (OSM), and ciliary neurotrophic factor (CNTF), promote tumor dormancy and which signaling pathways are induced. We first confirmed that LIF, OSM, and CNTF and their receptor components were expressed across a panel of breast cancer cell lines, although expression was lower in estrogen receptor-negative (ER

Indexed as

Breast NeoplasmsCytokinesCytokine Receptor gp130FemaleHumansInterleukin-6Receptors, CytokineReceptors, OSM-LIFSignal TransductionTumor MicroenvironmentCytokine Receptor gp130CytokinesIL6ST protein, humanInterleukin-6Receptors, CytokineReceptors, OSM-LIFCANCERCYTOKINES CELL/TISSUE SIGNALING-ENDOCRINE PATHWAYSOTHER CELL/TISSUE SIGNALING-PARACRINE PATHWAYSTUMOR-INDUCED BONE DISEASE

Identifiers

PMID34477239
PMCPMC8828687
OpenAlexW3196850174

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.