Evidence map›Paper›PMID 22768805›Full record

ArticleBMC gastroenterology2012

hTERT, MYC and TP53 deregulation in gastric preneoplastic lesions.

Tanielly Cristina Raiol Silva, Mariana Ferreira Leal, Danielle Queiroz Calcagno, Carolina Rosal Teixeira de Souza, André Salim Khayat, Ney Pereira Carneiro dos Santos, Raquel Carvalho Montenegro, Silvia Helena Barem Rabenhorst, Mayara Quaresma Nascimento, Paulo Pimentel Assumpção and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  8. Review
  9. Menadione reducesTherapeutic advances in gastroenterology · 2020
    Article
  10. Article
  11. Antidepressant and Antiaging Effects of Açaí (Oxidative medicine and cellular longevity · 2019
    Article
  12. Association of HER2 gene amplification and tumor progression in early gastric cancer.Virchows Archiv : an international journal of pathology · 2018
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. What gastric cancer proteomic studies show about gastric carcinogenesis?Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  18. Review
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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

12 authors at 3 institutions in 1 country.

Tanielly Cristina Raiol SilvaLaboratório de Citogenética Humana, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.
Mariana Ferreira Leal
Danielle Queiroz Calcagno
Carolina Rosal Teixeira de Souza
André Salim Khayat
Ney Pereira Carneiro dos Santos
Raquel Carvalho Montenegro
Silvia Helena Barem Rabenhorst
Mayara Quaresma Nascimento
Paulo Pimentel Assumpção
Marília de Arruda Cardoso Smith
Rommel Rodríguez Burbano
Universidade Federal do Pará · BRUniversidade Federal de São Paulo · BRUniversidade Federal do Ceará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer is a serious public health problem in Northern Brazil and in the world due to its high incidence and mortality. Despite the severity of the disease, more research is needed to better understand the molecular events involved in this intestinal-type gastric carcinogenesis process. Since precancerous lesions precede intestinal-type gastric cancer, here, we evaluated the hTERT, MYC, and TP53 mRNA and protein expression, as well as TP33 copy number, in gastric preneoplastic lesions.

methodsWe evaluated 19 superficial gastritis, 18 atrophic gastritis, and 18 intestinal metaplasia from cancer-free individuals of Northern Brazil. Quantitative reverse transcription PCR was used to analyze the mRNA expression and immunohistochemical methods were used to assess protein immunoreactivity in tissue samples. The number of TP53 gene copies was investigated in gastric diseases by quantitative PCR.

resultsWe observed hTERT, MYC, and p53 immunoreactivity only in intestinal metaplasia samples. The immunoreactivity of these proteins was strongly associated with each other. A significantly higher MYC mRNA expression was observed in intestinal metaplasia compared to gastritis samples. Loss of TP53 was also only detected in intestinal metaplasia specimens.

conclusionsWe demonstrated that hTERT, MYC, and TP53 are deregulated in intestinal metaplasia of individuals from Northern Brazil and these alterations may facilitate tumor initiation.

Indexed as

BrazilCell Transformation, NeoplasticFemaleGastritisGene DosageGene Expression Regulation, NeoplasticHumansImmunohistochemistryMaleMetaplasiaPrecancerous ConditionsProto-Oncogene Proteins c-mycStomach NeoplasmsTelomeraseTumor Suppressor Protein p53MYC protein, humanProto-Oncogene Proteins c-mycTelomeraseTERT protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID22768805
PMCPMC3482568
OpenAlexW2015575129

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.