Evidence map›Paper›PMID 31780696›Full record

ArticleScientific reports2019

Germline variants in cancer genes in high-risk non-BRCA patients from Puerto Rico.

Julie Dutil, Jamie K Teer, Volha Golubeva, Sean Yoder, Wei Lue Tong, Nelly Arroyo, Rachid Karam, Miguel Echenique, Jaime L Matta, Alvaro N Monteiro

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Summary ofGenes · 2020
    Pooled it
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  12. A RecurrentCancers · 2018
    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

10 authors at 5 institutions in 2 countries.

Julie DutilCancer Biology Division, Ponce Research Institute, Ponce Health Sciences University, Ponce, PR, USA. jdutil@psm.edu.
Jamie K TeerDepartment of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID http://orcid.org/0000-0003-4513-0282
Volha GolubevaCancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Sean YoderMolecular Genomics Core, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Wei Lue TongUniversity of South Florida Morsani College of Medicine, Tampa, FL, USA.
Nelly ArroyoCancer Biology Division, Ponce Research Institute, Ponce Health Sciences University, Ponce, PR, USA.
Rachid KaramAmbry Genetics, Aliso Viejo, CA, USA.ORCID http://orcid.org/0000-0002-5645-498X
Miguel EcheniqueAuxilio Cancer Center, Auxilio Mutuo Hospital, San Juan, PR, USA.
Jaime L MattaCancer Biology Division, Ponce Research Institute, Ponce Health Sciences University, Ponce, PR, USA.
Alvaro N MonteiroCancer Epidemiology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID http://orcid.org/0000-0002-8448-4801
Moffitt Cancer Center · USPonce Health Sciences University · PRAmbry Genetics (United States) · USAuxilio Mutuo Hospital · PRUniversity of South Florida · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI Christine O'Connell · 1998 to 2026
$93.5M
The Role of Midbrain to Prelimbic Cortex Glutamatergic projections in Stress-induced Drug SeekingU54MD007579 · NIMHD · PONCE SCHOOL OF MEDICINE · PI Emmanuel Antonio Cruz, Kenira J Thompson · 2019 to 2026
$35.9M
Using MC1R genotype to impact skin cancer risk behaviors in Hispanics/LatinosU54CA163068 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI Shannon Marie Christy · 2012 to 2026
$23.1M
Using MC1R genotype to impact skin cancer risk behaviors in Hispanics/LatinosU54CA163071 · NCI · PONCE SCHOOL OF MEDICINE · PI Harold I Saavedra · 2012 to 2026
$23.0M
VIRAL SEQUENCES IN PEDIATRIC HIV INFECTION IN PRG12MD007579 · NIMHD · PONCE SCHOOL OF MEDICINE · PI TORRES-RUIZ, JOSE A · 2012 to 2018
$15.9M
FUNCTIONAL ANALYSIS OF BRCA1 MUTANTSR01CA092309 · NCI · STRANG CANCER PREVENTION CENTER · PI MONTEIRO, ALVARO N · 2002 to 2006
$1.3M
Inherited genetic factors in breast cancer predisposition and tumor presentationSC1CA182845 · NCI · PONCE SCHOOL OF MEDICINE · PI DUTIL, JULIE · 2013 to 2016
$1.3M
NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA092309NCI NIH HHS SC1 CA182845NCI NIH HHS U54 CA163068NCI NIH HHS U54 CA163071NIMHD NIH HHS G12 MD007579NIMHD NIH HHS U54 MD007579U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) 1SC1CA182845U.S. Department of Health & Human Services | NIH | National Institute on Minority Health and Health Disparities (NIMHD) MD007579
6 · The paper itself

Abstract

Inherited pathogenic variants in genes that confer moderate to high risk of breast cancer may explain up to 50% of familial breast cancer. This study aimed at identifying inherited pathogenic variants in breast cancer cases from Puerto Rico that were not linked to BRCA1 or BRCA2. Forty-eight breast cancer patients that met the clinical criteria for BRCA testing but had received a negative BRCA1/2 result were recruited. Fifty-three genes previously implicated in hereditary cancer predisposition were captured using the BROCA Agilent cancer risk panel followed by massively parallel sequencing. Missense variants of uncertain clinical significance in CHEK2 were evaluated using an in vitro kinase assays to determine their impact on function. Pathogenic variants were identified in CHEK2, MUTYH, and RAD51B in four breast cancer patients, which represented 8.3% of the cohort. We identified three rare missense variants of uncertain significance in CHEK2 and two variants (p.Pro484Leu and p.Glu239Lys) showed markedly decreased kinase activity in vitro comparable to a known pathogenic variant. Interestingly, the local ancestry at the RAD51B locus in the carrier of p.Arg47* was predicted to be of African origin. In this cohort, 12.5% of the BRCA-negative breast cancer patients were found to carry a known pathogenic variant or a variant affecting protein activity. This study reveals an unmet clinical need of genetic testing that could benefit a significant proportion of at-risk Latinas. It also highlights the complexity of Hispanic populations as pathogenic factors may originate from any of the ancestral populations that make up their genetic backgrounds.

Indexed as

OncogenesBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCheckpoint Kinase 2DNA-Binding ProteinsDNA GlycosylasesFemaleGenetic Predisposition to DiseaseGerm-Line MutationHumansModels, MolecularMutation, MissensePoint MutationPuerto RicoBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanCheckpoint Kinase 2CHEK2 protein, humanDNA-Binding ProteinsDNA GlycosylasesmutY adenine glycosylaseRAD51B protein, human

Identifiers

PMID31780696
PMCPMC6882826
OpenAlexW2989769386

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.