Evidence map›Paper›PMID 26522916›Full record

ArticleScientific reports2015

Heterogeneity of miR-10b expression in circulating tumor cells.

Christin Gasch, Prue N Plummer, Lidija Jovanovic, Linda M McInnes, David Wescott, Christobel M Saunders, Andreas Schneeweiss, Markus Wallwiener, Colleen Nelson, Kevin J Spring and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

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  13. Epigenetic Landscape of Liquid Biopsy in Colorectal Cancer.Frontiers in cell and developmental biology · 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

14 authors.

Christin GaschSchool of Medicine, Deakin University, Geelong, VIC, Australia.
Prue N PlummerSchool of Medicine, Deakin University, Geelong, VIC, Australia.
Lidija JovanovicAustralian Prostate Cancer Research Centre-Queensland, Queensland University of Technology, Brisbane, QLD, Australia.
Linda M McInnesSchool of Surgery, The University of Western Australia, Perth, WA, Australia.
David WescottSchool of Medicine, Deakin University, Geelong, VIC, Australia.
Christobel M SaundersSchool of Surgery, The University of Western Australia, Perth, WA, Australia.
Andreas SchneeweissNational Center for Tumor Diseases, Heidelberg, Germany.
Markus WallwienerNational Center for Tumor Diseases, Heidelberg, Germany.
Colleen NelsonAustralian Prostate Cancer Research Centre-Queensland, Queensland University of Technology, Brisbane, QLD, Australia.
Kevin J SpringIngham Institute for Applied Medical Research, Liverpool Hospital, Liverpool, NSW, Australia.
Sabine RiethdorfDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Erik W ThompsonInstitute of Health and Biomedical Innovation &School of Biomedical Sciences, Queensland University of Technology, Brisbane, QLD, Australia.
Klaus PantelDepartment of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Albert S MellickSchool of Medicine, Deakin University, Geelong, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumor cells (CTCs) in the blood of cancer patients are recognized as important potential targets for future anticancer therapies. As mediators of metastatic spread, CTCs are also promising to be used as 'liquid biopsy' to aid clinical decision-making. Recent work has revealed potentially important genotypic and phenotypic heterogeneity within CTC populations, even within the same patient. MicroRNAs (miRNAs) are key regulators of gene expression and have emerged as potentially important diagnostic markers and targets for anti-cancer therapy. Here, we describe a robust in situ hybridization (ISH) protocol, incorporating the CellSearch(®) CTC detection system, enabling clinical investigation of important miRNAs, such as miR-10b on a cell by cell basis. We also use this method to demonstrate heterogeneity of such as miR-10b on a cell-by-cell basis. We also use this method to demonstrate heterogeneity of miR-10b in individual CTCs from breast, prostate and colorectal cancer patients.

Indexed as

Biomarkers, TumorBreast NeoplasmsCell Line, TumorColorectal NeoplasmsFemaleHCT116 CellsHumansIn Situ HybridizationMCF-7 CellsMicroRNAsNeoplastic Cells, CirculatingBiomarkers, TumorMicroRNAsMIRN10 microRNA, human

Identifiers

PMID26522916
PMCPMC4629160

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Registered trials

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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.