Evidence map›Paper›PMID 25505737›Full record

ArticleFrontiers in oncology2014

Differential Gene Expression Landscape of Co-Existing Cervical Pre-Cancer Lesions Using RNA-seq.

Kathryn E Royse, Degui Zhi, Michael G Conner, Buffie Clodfelder-Miller, Vinodh Srinivasasainagendra, Laura Kelly Vaughan, Christine F Skibola, David K Crossman, Shawn Levy, Sadeep Shrestha

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  8. Amino Acid Transporter SLC6A14 (ATBFrontiers in cell and developmental biology · 2020
    Review
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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

10 authors at 2 institutions in 1 country.

Kathryn E RoyseDepartment of Epidemiology, University of Alabama at Birmingham , Birmingham, AL , USA.
Degui ZhiDepartment of Biostatistics, University of Alabama at Birmingham , Birmingham, AL , USA.
Michael G ConnerDepartment of Pathology, University of Alabama at Birmingham , Birmingham, AL , USA.
Buffie Clodfelder-MillerCellular and Molecular Neuropathology Core, University of Alabama at Birmingham , Birmingham, AL , USA.
Vinodh SrinivasasainagendraDepartment of Biostatistics, University of Alabama at Birmingham , Birmingham, AL , USA.
Laura Kelly VaughanDepartment of Biostatistics, University of Alabama at Birmingham , Birmingham, AL , USA.
Christine F SkibolaDepartment of Epidemiology, University of Alabama at Birmingham , Birmingham, AL , USA.
David K CrossmanDepartment of Genetics, University of Alabama at Birmingham , Birmingham, AL , USA.
Shawn LevyHudson Alpha Institute for Biotechnology , Huntsville, AL , USA.
Sadeep ShresthaDepartment of Epidemiology, University of Alabama at Birmingham , Birmingham, AL , USA.
University of Alabama at Birmingham · USHudsonAlpha Institute for Biotechnology · US

Funding

Treatment of HIV- and HIV+ Patients with HPV16+ CIN2/3 Using pNGLV4a-hCRTE6E7L2 DNA vaccine administered intramuscularly via electroporationP50CA098252 · NCI · JOHNS HOPKINS UNIVERSITY · PI Richard Bruce Roden · 2003 to 2026
$53.5M
Cancer Prevention & Control Training ProgramR25CA047888 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DEMARK-WAHNEFRIED, WENDY, MENESES, KAREN M · 1988 to 2016
$11.2M
Dell high performance computing cluster and associated Hitachi terabyte data storS10RR026723 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ALLISON, DAVID B · 2010 to 2010
$500k
NCI NIH HHS P50 CA098252NCI NIH HHS R25 CA047888NCRR NIH HHS S10 RR026723
6 · The paper itself

Abstract

Genetic changes occurring in different stages of pre-cancer lesions reflect causal events initiating and promoting the progression to cancer. Co-existing pre-cancerous lesions including low- and high-grade squamous intraepithelial lesion (LGSIL and HGSIL), and adjacent "normal" cervical epithelium from six formalin-fixed paraffin-embedded samples were selected. Tissues from these 18 samples were isolated using laser-capture microdissection, RNA was extracted and sequenced. RNA-sequencing generated 2.4 billion raw reads in 18 samples, of which ~50.1% mapped to known and annotated genes in the human genome. There were 40 genes up-regulated and 3 down-regulated (normal to LGSIL) in at least one-third of the sample pairs (same direction and FDR p < 0.05) including S100A7 and KLK6. Previous studies have shown that S110A7 and KLK7 are up-regulated in several other cancers, whereas CCL18, CFTR, and SLC6A14, also differentially expressed in two samples, are up-regulated specifically in cervical cancer. These differentially expressed genes in normal to LGSIL progression were enriched in pathways related to epithelial cell differentiation, keratinocyte differentiation, peptidase, and extracellular activities. In progression from LGSIL to HGSIL, two genes were up-regulated and five down-regulated in at least two samples. Further investigations using co-existing samples, which account for all internal confounders, will provide insights to better understand progression of cervical pre-cancer.

Indexed as

cervical dysplasiaco-existing lesionsgene expressionhuman genomeRNA-sequencing

Identifiers

PMID25505737
PMCPMC4244708
OpenAlexW2045259085

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.