Evidence map›Paper›PMID 31126249›Full record

ArticleBMC cancer2019

Association of newly identified genetic variant rs2853677 of TERT with non-small cell lung cancer and leukemia in population of Jammu and Kashmir, India.

Gh Rasool Bhat, Amrita Bhat, Sonali Verma, Itty Sethi, Ruchi Shah, Varun Sharma, Khursheed A Dar, Deepak Abrol, Subiya Kaneez, Sandeep Kaul and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. 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
1.0field-weighted citation impact, top 23% 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, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Can TERT rs2853669 polymorphysm indicate fibrosis in sarcoidosis?Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2023
    Article
  6. Article
  7. Article
  8. Parent-of-Origin inference for biobanks.Nature communications · 2022
    Article
  9. Article
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

12 authors at 4 institutions in 2 countries.

Gh Rasool BhatCancer Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.
Amrita BhatCancer Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.
Sonali VermaCancer Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.
Itty SethiHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.
Ruchi ShahHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.
Varun SharmaHuman Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India.
Khursheed A DarChest Disease Hospital, Government Medical College, Srinagar, India.
Deepak AbrolDepartment of Radiotherapy, Government Medical College, Jammu, India.
Subiya KaneezDepartment of Radiotherapy, Government Medical College, Srinagar, India.
Sandeep KaulDepartment of surgical Oncology, Shri Mata Vaishno Devi Narayana Super speciality hospital, kata, India.
Ramesh GanjuDepartment of Pathology, College of Medicine, The OHIO State University, Columbus, USA.
Rakesh KumarCancer Genetics Research Group, School of Biotechnology, Shri Mata Vaishno Devi University, Katra, India. kumar.rakesh@smvdu.ac.in.
Shri Mata Vaishno Devi University · INGovernment Medical College · INGovernment Medical College · INThe Ohio State University · US

Funding

Department of Science and Technology, Ministry of Science and Technology (IN) DST/SSTP/J&K/459
6 · The paper itself

Abstract

backgroundTelomere genetics has recently been emerged as an important field in molecular oncology. Various genome-wide association studies in different population groups have revealed that polymorphisms in Telomere maintenance gene (TERT) gene located on 5p15.33 is associated with susceptibility to leukemia and lung cancer risk. However, association of TERT with leukemia and lung cancer risk in north Indian population groups is still unknown. This study observed the association between genetic variant rs2853677 of TERT and leukemia and lung cancer in the state of Jammu and Kashmir, India.

methodsA total of 781 subjects, out of which 381 cases (203 leukemic patients and 178 non-small cell lung cancer patients NSCLC) and 400 healthy controls were recruited for the study. Genetic variant rs2853677of TERT was detected using the real-time and Taqman Chemistry. Hardy-Weinberg Equilibrium was assessed using the chi square test. The allele and genotype- specific risks were estimated as odds ratio with 95% confidence interval.

resultsWe observed that variant rs2853677 was strongly associated with lung cancer and leukemia risk with an odds ratio (OR) =1.8 (1.03-3.2 at 95% CI); p value (adjusted) = 0.03; odds ratio (OR) =2.9 (1.4-5.5.at 95% CI); p value (adjusted) = 0.002, respectively.

conclusionThe results of this study suggested that rs2853677 of TERT signifies association in multiple cancers and suggests that it can become potential marker for diagnosis of non-small cell lung cancer and leukemia. The study will provide an insight in understanding the genetic etiology and highlights the role of telomere-associated pathways in non-small cell lung cancer and leukemia. However, it would be quite interesting to explore the contribution of this variant in other cancers as well.

Indexed as

AdultAgedBiomarkers, TumorCarcinoma, Non-Small-Cell LungCase-Control StudiesChi-Square DistributionFemaleGene FrequencyGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansIndiaLeukemiaLung NeoplasmsMaleBiomarkers, TumorTelomeraseTERT protein, humanJammu and KashmirLeukemiaNon-small cell lung cancerTelomerase reverse transcriptase (TERT)

Identifiers

PMID31126249
PMCPMC6533689
OpenAlexW2947319088

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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.