Evidence map›Paper›PMID 33081152›Full record

ArticleInternational journal of molecular sciences2020

Global Analyses of Expressed Piwi-Interacting RNAs in Gastric Cancer.

Tatiana Vinasco-Sandoval, Fabiano Cordeiro Moreira, Amanda F Vidal, Pablo Pinto, André M Ribeiro-Dos-Santos, Rebecca L S Cruz, Gleyce Fonseca Cabral, Ana K M Anaissi, Katia de Paiva Lopes, Arthur Ribeiro-Dos-Santos and 4 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  10. Non-Coding RNA in Penile Cancer.Frontiers in oncology · 2022
    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

14 authors at 1 institution in 1 country.

Tatiana Vinasco-SandovalGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.ORCID 0000-0002-0189-0573
Fabiano Cordeiro MoreiraGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.ORCID 0000-0002-2799-3546
Amanda F VidalGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.ORCID 0000-0003-4180-9925
Pablo PintoGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
André M Ribeiro-Dos-SantosGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
Rebecca L S CruzGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
Gleyce Fonseca CabralGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.ORCID 0000-0002-6213-5037
Ana K M AnaissiGraduate Program in Oncology and Medical Sciences, Center of Oncology Research, Federal University of Pará, Belém, Pará 66063-023, Brazil.
Katia de Paiva LopesGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
Arthur Ribeiro-Dos-SantosGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
Samia DemachkiGraduate Program in Oncology and Medical Sciences, Center of Oncology Research, Federal University of Pará, Belém, Pará 66063-023, Brazil.
Paulo Pimentel de AssumpçãoGraduate Program in Oncology and Medical Sciences, Center of Oncology Research, Federal University of Pará, Belém, Pará 66063-023, Brazil.
Ândrea Ribeiro-Dos-SantosGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
Sidney SantosGraduate Program in Genetics and Molecular Biology, Laboratory of Human and Medical Genetics, Federal University of Pará, Belém, Pará 66075-110, Brazil.
Universidade Federal do Pará · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico CNPQ 304413/2015-1Conselho Nacional de Desenvolvimento Científico e Tecnológico CNPQ 305258/2013-3Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 3381/2013 CAPES BioComputacional
6 · The paper itself

Abstract

Gastric cancer (GC) represents a notable amount of morbidity and mortality worldwide. Understanding the molecular basis of CG will offer insight into its pathogenesis in an attempt to identify new molecular biomarkers to early diagnose this disease. Therefore, studies involving small non-coding RNAs have been widely explored. Among these, PIWI-interacting RNAs (piRNAs) are an emergent class that can play important roles in carcinogenesis. In this study, small-RNA sequencing was used to identify the global piRNAs expression profile (piRNome) of gastric cancer patients. We found 698 piRNAs in gastric tissues, 14 of which were differentially expressed (DE) between gastric cancer (GC), adjacent to gastric cancer (ADJ), and non-cancer tissues (NC). Moreover, three of these DE piRNAs (piR-48966*, piR-49145, piR-31335*) were differently expressed in both GC and ADJ samples in comparison to NC samples, indicating that the tumor-adjacent tissue was molecularly altered and should not be considered as a normal control. These three piRNAs are potential risk biomarkers for GC, especially piR-48966* and piR-31335*. Furthermore, an in-silico search for mRNAs targeted by the differentially expressed piRNAs revealed that these piRNAs may regulate genes that participate in cancer-related pathways, suggesting that these small non-coding RNAs may be directly and indirectly involved in gastric carcinogenesis.

Indexed as

TranscriptomeBiomarkers, TumorGene Regulatory NetworksHumansNeoplasm MetastasisRNA, Small InterferingStomach NeoplasmsBiomarkers, TumorRNA, Small Interferingcancer biomarkersfield cancerizationfield-effectgastric cancermetastasisnon-coding RNApiRNAs expression profile (piRNome)PIWI-interacting RNA (piRNA)

Identifiers

PMID33081152
PMCPMC7593925
OpenAlexW3093250315

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.