Evidence map›Paper›PMID 28850092›Full record

ArticleInternational journal of molecular sciences2017

Measurement of Telomere Length in Colorectal Cancers for Improved Molecular Diagnosis.

Eric Le Balc'h, Nathalie Grandin, Marie-Véronique Demattei, Serge Guyétant, Anne Tallet, Jean-Christophe Pagès, Mehdi Ouaissi, Thierry Lecomte, Michel Charbonneau

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Role of telomere length in human carcinogenesis (Review).International journal of oncology · 2023
    Review
  3. Article
  4. Review
  5. Article
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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

9 authors at 2 institutions in 1 country.

Eric Le Balc'hCHRU Hôpital de Tours Trousseau, avenue de la République, 37170 Chambray-lès-Tours, France. ericlebalch85@gmail.com.
Nathalie GrandinUMR CNRS 7292, UFR Pharmacy, University of Tours, Parc Grandmont, 31 avenue Monge, 37200 Tours, France. nathalie.grandin@uca.fr.
Marie-Véronique DematteiUMR CNRS 7292, UFR Pharmacy, University of Tours, Parc Grandmont, 31 avenue Monge, 37200 Tours, France. baud@univ-tours.fr.
Serge GuyétantCHRU Hôpital de Tours Trousseau, avenue de la République, 37170 Chambray-lès-Tours, France. guyetant@univ-tours.fr.
Anne TalletCHRU Hôpital de Tours Trousseau, avenue de la République, 37170 Chambray-lès-Tours, France. anne.tallet@univ-tours.fr.
Jean-Christophe PagèsCHRU Hôpital de Tours Trousseau, avenue de la République, 37170 Chambray-lès-Tours, France. jean.pages@univ-tours.fr.
Mehdi OuaissiCHRU Hôpital de Tours Trousseau, avenue de la République, 37170 Chambray-lès-Tours, France. mehdi.ouaissi@univ-tours.fr.
Thierry LecomteCHRU Hôpital de Tours Trousseau, avenue de la République, 37170 Chambray-lès-Tours, France. thierry.lecomte@univ-tours.fr.
Michel CharbonneauUMR CNRS 7292, UFR Pharmacy, University of Tours, Parc Grandmont, 31 avenue Monge, 37200 Tours, France. michel.charbonneau@uca.fr.
Centre Hospitalier Universitaire de Tours · FRUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All tumors have in common to reactivate a telomere maintenance mechanism to allow for unlimited proliferation. On the other hand, genetic instability found in some tumors can result from the loss of telomeres. Here, we measured telomere length in colorectal cancers (CRCs) using TRF (Telomere Restriction Fragment) analysis. Telomeric DNA content was also quantified as the ratio of total telomeric (TTAGGG) sequences over that of the invariable Alu sequences. In most of the 125 CRCs analyzed, there was a significant diminution in telomere length compared with that in control healthy tissue. Only 34 tumors exhibited no telomere erosion and, in some cases, a slight telomere lengthening. Telomere length did not correlate with age, gender, tumor stage, tumor localization or stage of tumor differentiation. In addition, while telomere length did not correlate with the presence of a mutation in BRAF (V-raf murine sarcoma viral oncogene homolog B), PIK3CA (phosphatidylinositol 3-kinase catalytic subunit), or MSI status, it was significantly associated with the occurrence of a mutation in KRAS. Interestingly, we found that the shorter the telomeres in healthy tissue of a patient, the larger an increase in telomere length in the tumor. Our study points to the existence of two types of CRCs based on telomere length and reveals that telomere length in healthy tissue might influence telomere maintenance mechanisms in the tumor.

Indexed as

Biomarkers, TumorClass I Phosphatidylinositol 3-KinasesColorectal NeoplasmsFemaleHumansMaleMicrosatellite InstabilityMutationPathology, MolecularProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)TelomereTelomere HomeostasisBiomarkers, TumorBRAF protein, humanClass I Phosphatidylinositol 3-KinasesKRAS protein, humanPIK3CA protein, humanProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)colorectal cancerKRAS mutationstelomere lengthtelomere restriction fragment analysis

Identifiers

PMID28850092
PMCPMC5618520
OpenAlexW2752933713

What OpenQuestion holds

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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.