Evidence map›Paper›PMID 30265426›Full record

ArticleGenes, chromosomes & cancer2019

Small RNA sequencing of sessile serrated polyps identifies microRNA profile associated with colon cancer.

Priyanka Kanth, Mark W Hazel, Kenneth M Boucher, Zhihong Yang, Li Wang, Mary P Bronner, Katherine E Boylan, Randall W Burt, Michelle Westover, Deborah W Neklason and 1 more

Abstract read
In one paragraph

Article in Genes, chromosomes & cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 16 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

11 authors at 3 institutions in 1 country.

Priyanka KanthDivision of Gastroenterology, Department of Internal Medicine, University of Utah, Salt Lake City, Utah.
Mark W HazelDivision of Gastroenterology, Department of Internal Medicine, University of Utah, Salt Lake City, Utah.
Kenneth M BoucherHuntsman Cancer Institute, Salt Lake City, Utah.
Zhihong YangDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.
Li WangDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut.
Mary P BronnerHuntsman Cancer Institute, Salt Lake City, Utah.
Katherine E BoylanDepartment of Pathology, University of Utah, Salt Lake City, Utah.
Randall W BurtDivision of Gastroenterology, Department of Internal Medicine, University of Utah, Salt Lake City, Utah.
Michelle WestoverHuntsman Cancer Institute, Salt Lake City, Utah.
Deborah W NeklasonHuntsman Cancer Institute, Salt Lake City, Utah.
Don A DelkerDivision of Gastroenterology, Department of Internal Medicine, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-6104-3093
University of Utah · USUniversity of Connecticut · USHuntsman Cancer Institute · US

Funding

Non-coding RNAs in serrated polyps identify patients with high colon cancer riskR21CA191507 · NCI · UNIVERSITY OF UTAH · PI DELKER, DON A, KANTH, PRIYANKA · 2015 to 2016
$371k
NCI NIH HHS R21 CA191507NIH HHS CA191507
6 · The paper itself

Abstract

Sessile serrated adenoma/polyps (SSA/Ps) of the colon account for 20-30% of all colon cancers. Small non-coding RNAs, including microRNAs (miRNAs), may function as oncogenes or tumor suppressor genes involved in cancer development. Small RNA sequencing (RNA-seq) was used to characterize miRNA profiles in SSA/Ps, hyperplastic polyps (HPs), adenomatous polyps and paired uninvolved colon. Our 108 small RNA-seq samples' results were compared to small RNA-seq data from 212 colon cancers from the Cancer Genome Atlas. Twenty-three and six miRNAs were differentially expressed in SSA/Ps compared to paired uninvolved colon and HPs, respectively. Differential expression of MIR31-5p, MIR135B-5p and MIR378A-5p was confirmed by RT-qPCR. SSA/P-specific miRNAs are similarly expressed in colon cancers containing genomic aberrations described in serrated cancers. Correlation of miRNA expression with consensus molecular subtypes suggests more than one subtype is associated with the serrated neoplasia pathway. Canonical pathway analysis suggests many of these miRNAs target growth factor signaling pathways.

Indexed as

AdenomaAgedAnimalsBiomarkers, TumorColonic NeoplasmsColonic PolypsFemaleHumansMaleMicroRNAsMiddle AgedSequence Analysis, RNAThoracicaBiomarkers, TumorMicroRNAscolon cancergene expressionhyperplastic polypsmicroRNAsRNA sequencingsessile serrated adenoma/polyps

Identifiers

PMID30265426
PMCPMC6437779
OpenAlexW2894004239

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.