Evidence map›Paper›PMID 28475402›Full record

ArticleCancer biology & therapy2017

DNA repair genes PAXIP1 and TP53BP1 expression is associated with breast cancer prognosis.

Giuliana De Gregoriis, Juliene Antonio Ramos, Priscila Valverde Fernandes, Giselle Maria Vignal, Rafael Canfield Brianese, Dirce Maria Carraro, Alvaro N Monteiro, Claudio José Struchiner, Guilherme Suarez-Kurtz, Rosane Vianna-Jorge and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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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

11 authors at 6 institutions in 2 countries.

Giuliana De Gregoriisa Programa de Pesquisa Clínica , Coordenação de Pesquisa, Instituto Nacional de Câncer , Rio de Janeiro , RJ , Brazil.ORCID 0000-0002-7857-0658
Juliene Antonio Ramosb Instituto Federal do Rio de Janeiro , Rio de Janeiro , RJ , Brazil.ORCID 0000-0002-1419-5721
Priscila Valverde Fernandesc Divisão de Patologia , Instituto Nacional de Câncer , Rio de Janeiro , RJ , Brazil.
Giselle Maria Vignalc Divisão de Patologia , Instituto Nacional de Câncer , Rio de Janeiro , RJ , Brazil.ORCID 0000-0001-9891-0077
Rafael Canfield Brianesed International Research Center, A. C. Camargo Cancer Center , São Paulo , SP , Brazil.ORCID 0000-0003-1724-9024
Dirce Maria Carrarod International Research Center, A. C. Camargo Cancer Center , São Paulo , SP , Brazil.ORCID 0000-0001-5667-1418
Alvaro N Monteiroe Cancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute , Tampa , FL , USA.ORCID 0000-0002-8448-4801
Claudio José Struchinerf Programa de Computação Científica, Fundação Oswaldo Cruz , Rio de Janeiro , RJ , Brazil.ORCID 0000-0003-2114-847X
Guilherme Suarez-Kurtza Programa de Pesquisa Clínica , Coordenação de Pesquisa, Instituto Nacional de Câncer , Rio de Janeiro , RJ , Brazil.ORCID 0000-0002-1115-8319
Rosane Vianna-Jorgea Programa de Pesquisa Clínica , Coordenação de Pesquisa, Instituto Nacional de Câncer , Rio de Janeiro , RJ , Brazil.ORCID 0000-0001-5407-4695
Marcelo Alex de Carvalhoa Programa de Pesquisa Clínica , Coordenação de Pesquisa, Instituto Nacional de Câncer , Rio de Janeiro , RJ , Brazil.ORCID 0000-0002-7053-0053
Instituto Nacional de Câncer - INCA · BRAC Camargo Hospital · BRInstituto Federal do Rio de Janeiro · BRFundação Oswaldo Cruz · BRMoffitt Cancer Center · USUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite remarkable advances in diagnosis, prognosis and treatment, advanced or recurrent breast tumors have limited therapeutic approaches. Many treatment strategies try to explore the limitations of DNA damage response (DDR) in tumor cells to selectively eliminate them. BRCT (BRCA1 C-terminal) domains are present in a superfamily of proteins involved in cell cycle checkpoints and the DDR. Tandem BRCT domains (tBRCT) represent a distinct class of these domains. We investigated the expression profile of 7 tBRCT genes (BARD1, BRCA1, LIG4, ECT2, MDC1, PAXIP1/PTIP and TP53BP1) in breast cancer specimens and observed a high correlation between PAXIP1 and TP53BP1 gene expression in tumor samples. Tumors with worse prognosis (tumor grade 3 and triple negative) showed reduced expression of tBRCT genes, notably, PAXIP1 and TP53BP1. Survival analyses data indicated that tumor status of both genes may impact prognosis. PAXIP1 and 53BP1 protein levels followed gene expression results, i.e., are intrinsically correlated, and also reduced in more advanced tumors. Evaluation of both genes in triple negative breast tumor samples which were characterized for their BRCA1 status showed that PAXIP1 is overexpressed in BRCA1 mutant tumors. Taken together our findings indicate that PAXIP1 status correlates with breast cancer staging, in a manner similar to what has been characterized for TP53BP1.

Indexed as

Biomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastCarrier ProteinsDisease-Free SurvivalDNA-Binding ProteinsDNA RepairFemaleGene ExpressionHumansKaplan-Meier EstimateMultivariate AnalysisNuclear ProteinsPrognosisTumor Suppressor p53-Binding Protein 1Biomarkers, TumorCarrier ProteinsDNA-Binding ProteinsNuclear ProteinsPAXIP1 protein, humanTP53BP1 protein, humanTumor Suppressor p53-Binding Protein 1BRCTbreast cancerDNA repairPAXIP1TP53BP1

Identifiers

PMID28475402
PMCPMC5536937
OpenAlexW2611754112

What OpenQuestion holds

Textmetadata
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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.