Evidence map›Paper›PMID 24980554›Full record

ArticleCancer research2014

Cancer affects microRNA expression, release, and function in cardiac and skeletal muscle.

Daohong Chen, Chirayu P Goswami, Riesa M Burnett, Manjushree Anjanappa, Poornima Bhat-Nakshatri, William Muller, Harikrishna Nakshatri

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

35 citing papers in PubMed, 57 citations in OpenAlex.

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  9. Untoward immune effects of modern medication.Journal of biomedical research · 2023
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  17. Heparin beyond anti-coagulation.Current research in translational medicine · 2021
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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

7 authors at 2 institutions in 2 countries.

Daohong ChenDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Chirayu P GoswamiCenter for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, Indiana.
Riesa M BurnettDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Manjushree AnjanappaDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Poornima Bhat-NakshatriDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
William MullerMolecular Oncology Group, McGill University, Montreal, Canada.
Harikrishna NakshatriDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana. Center for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, Indiana. Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana. hnakshat@iupui.edu.
Indiana University – Purdue University Indianapolis · USMcGill University · CA

Funding

Persistent microRNA changes in serum of cancer-free breast cancer patientsR21CA159158 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI NAKSHATRI, HARIKRISHNA · 2011 to 2012
$368k
NCI NIH HHS R21 CA159158NCI NIH HHS R21CA159158
6 · The paper itself

Abstract

Circulating microRNAs (miRNA) are emerging as important biomarkers of various diseases, including cancer. Intriguingly, circulating levels of several miRNAs are lower in patients with cancer compared with healthy individuals. In this study, we tested the hypothesis that a circulating miRNA might serve as a surrogate of the effects of cancer on miRNA expression or release in distant organs. Here we report that circulating levels of the muscle-enriched miR486 is lower in patients with breast cancer compared with healthy individuals and that this difference is replicated faithfully in MMTV-PyMT and MMTV-Her2 transgenic mouse models of breast cancer. In tumor-bearing mice, levels of miR486 were relatively reduced in muscle, where there was elevated expression of the miR486 target genes PTEN and FOXO1A and dampened signaling through the PI3K/AKT pathway. Skeletal muscle expressed lower levels of the transcription factor MyoD, which controls miR486 expression. Conditioned media (CM) obtained from MMTV-PyMT and MMTV-Her2/Neu tumor cells cultured in vitro were sufficient to elicit reduced levels of miR486 and increased PTEN and FOXO1A expression in C2C12 murine myoblasts. Cytokine analysis implicated tumor necrosis factor α (TNFα) and four additional cytokines as mediators of miR486 expression in CM-treated cells. Because miR486 is a potent modulator of PI3K/AKT signaling and the muscle-enriched transcription factor network in cardiac/skeletal muscle, our findings implicated TNFα-dependent miRNA circuitry in muscle differentiation and survival pathways in cancer.

Indexed as

AnimalsBreast NeoplasmsCell DifferentiationFemaleHeartHumansMaleMammary Neoplasms, ExperimentalMiceMice, TransgenicMicroRNAsMuscle, SkeletalSignal TransductionMicroRNAsMIRN486 microRNA, human

Identifiers

PMID24980554
PMCPMC4134725
OpenAlexW2009773330

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.