Evidence map›Paper›PMID 27508094›Full record

ArticleAmerican journal of cancer research2016

TMEM45A, SERPINB5 and p16INK4A transcript levels are predictive for development of high-grade cervical lesions.

Anna Manawapat-Klopfer, Louise T Thomsen, Peter Martus, Christian Munk, Rainer Russ, Hans Gmuender, Kirsten Frederiksen, Juliane Haedicke-Jarboui, Frank Stubenrauch, Susanne K Kjaer and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed, 33 citations in OpenAlex.

  1. MCell death & disease · 2026
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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 5 institutions in 4 countries.

Anna Manawapat-KlopferDivision of Experimental Virology, Institute of Medical Virology, University Hospital Tübingen Elfriede-Aulhorn Str. 6, 72076 Tübingen, Germany.
Louise T ThomsenUnit of Virus, Lifestyle and Genes, Danish Cancer Society Research Center Strandboulevarden 49, DK-2100 Copenhagen, Denmark.
Peter MartusInstitute for Clinical Epidemiology and Applied Biometry Silcherstraße 5, 72076 Tübingen, Germany.
Christian MunkUnit of Virus, Lifestyle and Genes, Danish Cancer Society Research Center Strandboulevarden 49, DK-2100 Copenhagen, Denmark.
Rainer RussGenedata AG Margarethenstrasse 38, CH-4053 Basel, Switzerland.
Hans GmuenderGenedata AG Margarethenstrasse 38, CH-4053 Basel, Switzerland.
Kirsten FrederiksenUnit of Statistics, Bioinformatics and Registry, Danish Cancer Society Research Center Strandboulevarden 49, DK-2100 Copenhagen, Denmark.
Juliane Haedicke-JarbouiDivision of Experimental Virology, Institute of Medical Virology, University Hospital Tübingen Elfriede-Aulhorn Str. 6, 72076 Tübingen, Germany.
Frank StubenrauchDivision of Experimental Virology, Institute of Medical Virology, University Hospital Tübingen Elfriede-Aulhorn Str. 6, 72076 Tübingen, Germany.
Susanne K KjaerUnit of Virus, Lifestyle and Genes, Danish Cancer Society Research CenterStrandboulevarden 49, DK-2100 Copenhagen, Denmark; Department of Obstetrics and Gynecology, Rigshospitalet, University of CopenhagenBlegdamsvej 9, DK-2100 Copenhagen, Denmark.
Thomas IftnerDivision of Experimental Virology, Institute of Medical Virology, University Hospital Tübingen Elfriede-Aulhorn Str. 6, 72076 Tübingen, Germany.
Institute of Virology of the Slovak Academy of Sciences · SKDanish Cancer Society · DKGenedata (Switzerland) · CHUniversity of Copenhagen · DKZimmer Biomet (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Women persistently infected with human papillomavirus (HPV) type 16 are at high risk for development of cervical intraepithelial neoplasia grade 3 or cervical cancer (CIN3+). We aimed to identify biomarkers for progression to CIN3+ in women with persistent HPV16 infection. In this prospective study, 11,088 women aged 20-29 years were enrolled during 1991-1993, and re-invited for a second visit two years later. Cervical cytology samples obtained at both visits were tested for HPV DNA by Hybrid Capture 2 (HC2), and HC2-positive samples were genotyped by INNO-LiPA. The cohort was followed for up to 19 years via a national pathology register. To identify markers for progression to CIN3+, we performed microarray analysis on RNA extracted from cervical swabs of 30 women with persistent HPV16-infection and 11 HPV-negative women. Six genes were selected and validated by quantitative PCR. Three genes were subsequently validated within a different and large group of women from the same cohort. Secondly, Kaplan-Meier and Cox-regression analyses were used to investigate whether expression levels of those three genes predict progression to CIN3+. We found that high transcript levels of TMEM45A, SERPINB5 and p16INK4a at baseline were associated with increased risk of CIN3+ during follow-up. The hazard ratios of CIN3+ per 10-fold increase in baseline expression level were 1.6 (95% CI: 1.1-2.3) for TMEM45A, 1.6 (95% CI: 1.1-2.5) for p16INK4a, and 1.8 (95% CI: 1.2-2.7) for SERPINB5. In conclusion, high mRNA expression levels of TMEM45A, SERPINB5 and p16INK4a were associated with increased risk of CIN3+ in persistently HPV16-infected women.

Indexed as

biomarkerCervical cancerCIN3+HPV16p16INK4ASERPINB5TMEM45A

Identifiers

PMID27508094
PMCPMC4969401
OpenAlexW2508498890

What OpenQuestion holds

Textmetadata
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.