Evidence map›Paper›PMID 28224765›Full record

ArticleAnnals of laboratory medicine2017

Dysregulation of Telomere Lengths and Telomerase Activity in Myelodysplastic Syndrome.

Hee Sue Park, Jungeun Choi, Cha Ja See, Jung Ah Kim, Si Nae Park, Kyongok Im, Sung Min Kim, Dong Soon Lee, Sang Mee Hwang

Open access · diamondAbstract read
In one paragraph

Article in Annals of laboratory medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Telomere integrated scoring system of myelodysplastic syndrome.Journal of clinical laboratory analysis · 2023
    Article
  9. Genomic landscape ofmedRxiv : the preprint server for health sciences · 2023
    Article
  10. Review
  11. New Approaches to Myelodysplastic Syndrome Treatment.Current treatment options in oncology · 2022
    Review
  12. Review
  13. Review
  14. Article
  15. Telomere Length Dynamics and the Evolution of Cancer Genome Architecture.International journal of molecular sciences · 2018
    Review
  16. Article
  17. Review
  18. Review
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 3 institutions in 1 country.

Hee Sue ParkDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Jungeun ChoiDepartment of Laboratory Medicine, Korea University Anam Hospital, Seoul, Korea.
Cha Ja SeeCytogenetics Team, Seegene Medical Foundation, Seoul, Korea.
Jung Ah KimDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Si Nae ParkCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Kyongok ImCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Sung Min KimCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Dong Soon LeeDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Sang Mee HwangDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Seoul National University · KRKorea University Medical Center · KRSeoul National University Bundang Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTelomere shortening is thought to be involved in the pathophysiology of myeloid malignancies, but telomere lengths (TL) during interphase and metaphase in hematopoietic malignancies have not been analyzed. We aimed to assess the TLs of interphase and metaphase cells of MDS and telomerase activity (TA) and to find out prognostic significances of TL and TA.

methodsThe prognostic significance of TA by quantitative PCR and TL by quantitative fluorescence in situ hybridization (QFISH) of interphase nuclei and metaphase chromosome arms of bone marrow cells from patients with MDS were evaluated.

resultsMDS patients had shorter interphase TL than normal healthy donors (P<0.001). Average interphase and metaphase TL were inversely correlated (P=0.013, p arm; P=0.029, q arm), but there was no statistically significant correlation between TA and TL (P=0.258). The progression free survival was significantly shorter in patients with high TA, but the overall survival was not different according to average TA or interphase TL groups. Multivariable Cox analysis showed that old age, higher International Prognostic Scoring System (IPSS) subtypes, transformation to AML, no history of hematopoietic stem cell transplantation and short average interphase TL (<433 TL) as independent prognostic factors for poorer survival (P=0.003, 0.001, 0.005, 0.005, and 0.013, respectively).

conclusionsThe lack of correlation between age and TL, TA, and TL, and the inverse relationship between TL and TA in MDS patients reflect the dysregulation of telomere status and proliferation. As a prognostic marker for leukemia progression, TA may be considered, and since interphase TL has the advantage of automated measurement by QFISH, it may be used as a prognostic marker for survival in MDS.

Indexed as

AdultAgedAged, 80 and overBone Marrow CellsDisease-Free SurvivalFemaleHumansIn Situ Hybridization, FluorescenceInterphaseKaplan-Meier EstimateKaryotypingMaleMetaphaseMiddle AgedMyelodysplastic SyndromesPrognosisTelomeraseInterphaseMetaphaseMyelodysplastic syndromePrognosisQuantitative fluorescence in situ hybridizationTelomerase activityTelomere length

Identifiers

PMID28224765
PMCPMC5339091
OpenAlexW2589253000

What OpenQuestion holds

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Registered trials

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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.