Evidence map›Paper›PMID 29568379›Full record

ArticleOncotarget2018

Leukocyte telomere length throughout the continuum of colorectal carcinogenesis.

Cornelia Zöchmeister, Stefanie Brezina, Philipp Hofer, Andreas Baierl, Michael M Bergmann, Thomas Bachleitner-Hofmann, Judith Karner-Hanusch, Anton Stift, Armin Gerger, Gernot Leeb and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 10 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

14 authors at 7 institutions in 2 countries.

Cornelia ZöchmeisterMedical University Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria.
Stefanie BrezinaMedical University Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria.
Philipp HoferMedical University Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria.
Andreas BaierlUniversity of Vienna, Department of Statistics and Operations Research, Vienna, Austria.
Michael M BergmannMedical University Vienna, Department of Surgery, Vienna, Austria.
Thomas Bachleitner-HofmannMedical University Vienna, Department of Surgery, Vienna, Austria.
Judith Karner-HanuschMedical University Vienna, Department of Surgery, Vienna, Austria.
Anton StiftMedical University Vienna, Department of Surgery, Vienna, Austria.
Armin GergerMedical University of Graz, Division of Oncology, Department of Internal Medicine, Graz, Austria.
Gernot LeebHospital Oberpullendorf, Burgenland, Austria.
Karl MachHospital Oberpullendorf, Burgenland, Austria.
Sivaramakrishna RachakondaGerman Cancer Research Center, Division of Molecular Genetic Epidemiology, Heidelberg, Germany.
Rajiv KumarGerman Cancer Research Center, Division of Molecular Genetic Epidemiology, Heidelberg, Germany.
Andrea GsurMedical University Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria.
Comprehensive Cancer Center Vienna · ATMedical University of Vienna · ATKrankenhaus Oberndorf · ATGerman Cancer Research Center · DEHeidelberg University · DEMedical University of Graz · ATUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Considering the high prevalence of colorectal cancer (CRC) and relatively high mortality there is strong interest in identification of clinically relevant biomarkers. Telomere shortening is supposed to contribute to genomic instability and crucially involved in process of carcinogenesis. Peripheral blood leukocyte (PBL) telomere length was previously investigated in several studies as potential biomarker for CRC but with controversial results. This prompted us to investigate relative PBL telomere length in association with different histological findings throughout the continuum of colorectal carcinogenesis in order to reflect the whole spectrum of putative CRC development in a large study involving 2011 individuals. The study based on the Colorectal Cancer Study of Austria (CORSA), including 384 CRC cases as well as age- and gender-matched 544 high-risk adenomas, 537 low-risk adenoma patients and 546 colonoscopy-negative controls. Relative expression of telomeric repeats and the single copy reference gene, albumin (T/S ratio) was determined using monochrome multiplex quantitative PCR (MMQPCR). Telomeres were found to be significantly longer in CRC patients compared to control subjects (

Indexed as

adenomacancer epidemiologycolorectal cancertelomere length

Identifiers

PMID29568379
PMCPMC5862600
OpenAlexW2793909196

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.