Evidence map›Paper›PMID 35805051›Full record

ArticleCancers2022

Triple-Negative Breast Cancer circRNAome Reveals Hsa_circ_0072309 as a Potential Risk Biomarker.

Leandro Magalhães, André M Ribeiro-Dos-Santos, Rebecca L Cruz, Kivvi Duarte de Mello Nakamura, Rafael Brianese, Rommel Burbano, Sâmio Pimentel Ferreira, Ewaldo Lúcio Foro de Oliveira, Ana Karyssa Mendes Anaissi, Márcia Cristina de Sousa Nahúm and 4 more

Abstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. 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

14 authors.

Leandro MagalhãesLaboratory of Human and Medical Genetics, Postgraduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.
André M Ribeiro-Dos-SantosLaboratory of Human and Medical Genetics, Postgraduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.
Rebecca L CruzLaboratory of Human and Medical Genetics, Postgraduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0001-7931-2434
Kivvi Duarte de Mello NakamuraGenomic and Molecular Biology Group, International Research Center/CIPE, A.C. Camargo Center, São Paulo 01508-010, Brazil.
Rafael BrianeseGenomic and Molecular Biology Group, International Research Center/CIPE, A.C. Camargo Center, São Paulo 01508-010, Brazil.
Rommel BurbanoMolecular Biology Laboratory, Ophir Loyola Hospital, Belém 66063-240, Brazil.ORCID 0000-0002-4872-234X
Sâmio Pimentel FerreiraDepartment of Clinical Oncology, Ser Clínica Oncológica, Belém 66035-265, Brazil.
Ewaldo Lúcio Foro de OliveiraDepartment of Clinical Oncology, Ser Clínica Oncológica, Belém 66035-265, Brazil.
Ana Karyssa Mendes AnaissiPostgraduate Program of Oncology and Medical Sciences, Center of Oncology Research, Federal University of Pará, Belém 66073-000, Brazil.
Márcia Cristina de Sousa NahúmPostgraduate Program of Oncology and Medical Sciences, Center of Oncology Research, Federal University of Pará, Belém 66073-000, Brazil.
Samia DemachkiPostgraduate Program of Oncology and Medical Sciences, Center of Oncology Research, Federal University of Pará, Belém 66073-000, Brazil.
Amanda F VidalLaboratory of Human and Medical Genetics, Postgraduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.
Dirce Maria CarraroGenomic and Molecular Biology Group, International Research Center/CIPE, A.C. Camargo Center, São Paulo 01508-010, Brazil.
Ândrea Ribeiro-Dos-SantosLaboratory of Human and Medical Genetics, Postgraduate Program of Genetics and Molecular Biology, Institute of Biological Sciences, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0001-7001-1483

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior CAPES/Biologia Computacional: No. 3381/2013/CAPESNational Council for Scientific and Technological Development 304413/2015-1Pró-Reitoria de Pesquisa e Pós-Graduação da Universidade Federal do Pará - PROPESP/UFPA PAPQ
6 · The paper itself

Abstract

Circular RNAs (circRNAs) are a class of long non-coding RNAs that have the ability to sponge RNA-Binding Proteins (RBPs). Triple-negative breast cancer (TNBC) has very aggressive behavior and poor prognosis for the patient. Here, we aimed to characterize the global expression profile of circRNAs in TNBC, in order to identify potential risk biomarkers. For that, we obtained RNA-Seq data from TNBC and control samples and performed validation experiments using FFPE and frozen tissues of TNBC patients and controls, followed by in silico analyses to explore circRNA-RBP interactions. We found 16 differentially expressed circRNAs between TNBC patients and controls. Next, we mapped the RBPs that interact with the top five downregulated circRNAs (hsa_circ_0072309, circ_0004365, circ_0006677, circ_0008599, and circ_0009043) and hsa_circ_0000479, resulting in a total of 16 RBPs, most of them being enriched to pathways related to cancer and gene regulation (e.g., AGO1/2, EIF4A3, ELAVL1, and PTBP1). Among the six circRNAs, hsa_circ_0072309 was the one that presented the most confidence results, being able to distinguish TNBC patients from controls with an AUC of 0.78 and 0.81, respectively. This circRNA may be interacting with some RBPs involved in important cancer-related pathways and is a novel potential risk biomarker of TNBC.

Indexed as

biomarkerscircular RNAsgene regulationtriple-negative breast cancer

Identifiers

PMID35805051
PMCPMC9265318

What Socratic 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 Socratic graph.