Evidence map›Paper›PMID 28127413›Full record

ReviewHereditary cancer in clinical practice2017

Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.

Marcia Cruz-Correa, Julyann Pérez-Mayoral, Julie Dutil, Miguel Echenique, Rafael Mosquera, Keila Rivera-Román, Sharee Umpierre, Segundo Rodriguez-Quilichini, Maria Gonzalez-Pons, Myrta I Olivera and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Hereditary cancer in clinical practice, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Role of microRNA in colorectal carcinoma (CRC): a narrative review.Annals of medicine and surgery (2012) · 2024
    Review
  6. Article
  7. Article
  8. Identification of a novel CNV at theFrontiers in molecular biosciences · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. Identification of Eleven NovelFrontiers in oncology · 2021
    Article
  13. Breast Cancer Health Disparities in Hispanics/Latinas.Current breast cancer reports · 2020
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

12 authors at 4 institutions in 1 country.

Marcia Cruz-CorreaDepartment of Cancer Biology, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR USA ; University of Puerto Rico Medical Sciences Campus, School of Medicine, San Juan, PR USA ; University of Puerto Rico Comprehensive Cancer Center, PMB711 Ave. De Diego 89 Ste. 105, San Juan, PR 00927-6346 USA.
Julyann Pérez-MayoralDepartment of Cancer Biology, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR USA ; University of Puerto Rico Medical Sciences Campus, School of Medicine, San Juan, PR USA.
Julie DutilPonce Health Sciences University, Ponce Research Institute, Ponce, PR USA.
Miguel EcheniqueCancer Center, Auxilio Mutuo Hospital, San Juan, PR USA.
Rafael MosqueraPuerto Rico Gastroenterology Association, San Juan, PR USA.
Keila Rivera-RománDepartment of Pediatrics, University of Puerto Rico School of Medicine, San Juan, PR USA.
Sharee UmpierreDepartment of Cancer Biology, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR USA.
Segundo Rodriguez-QuilichiniDepartment of Cancer Biology, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR USA.
Maria Gonzalez-PonsDepartment of Cancer Biology, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR USA ; University of Puerto Rico Medical Sciences Campus, School of Medicine, San Juan, PR USA.
Myrta I OliveraDepartment of Cancer Biology, University of Puerto Rico Comprehensive Cancer Center, San Juan, PR USA ; University of Puerto Rico Medical Sciences Campus, School of Medicine, San Juan, PR USA.
Sherly PardoDepartment of Pathology, University of Puerto Rico School of Medicine, San Juan, PR USA.
Puerto Rico Clinical Cancer Genetics Consortia
University of Puerto Rico System · PRUniversity of Puerto Rico, Medical Sciences Campus · PRAuxilio Mutuo Hospital · PRPonce Health Sciences University · PR

Funding

UPR/MDACC Partnership for Excellence in Cancer Research(Parent Grant U54 CA096297)U54CA096297 · NCI · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI SHARON Hermes GIORDANO, REYNOLD Eugenio LOPEZ-ENRIQUEZ · 2002 to 2026
$36.9M
TECHNOLOGIES AND RESOURCES FOR CORE LABORATORIESU54MD007587 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI LUCIANO, CARLOS A., WOJNA, VALERIE · 2012 to 2018
$23.2M
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
FUNCTIONAL ANALYSIS OF BRCA1 MUTANTSR01CA092309 · NCI · STRANG CANCER PREVENTION CENTER · PI MONTEIRO, ALVARO N · 2002 to 2006
$1.3M
NCI NIH HHS R01 CA092309NCI NIH HHS U54 CA096297NCI NIH HHS U54 CA163068NCI NIH HHS U54 CA163071NIMHD NIH HHS U54 MD007587
6 · The paper itself

Abstract

Hereditary cancer predisposition syndromes comprise approximately 10% of diagnosed cancers; however, familial forms are believed to account for up to 30% of some cancers. In Hispanics, the most commonly diagnosed hereditary cancers include colorectal cancer syndromes such as, Lynch Syndrome, Familial Adenomatous Polyposis, and hereditary breast and ovarian cancer syndromes. Although the incidence of hereditary cancers is low, patients diagnosed with hereditary cancer syndromes are at high-risk for developing secondary cancers. Furthermore, the productivity loss that occurs after cancer diagnosis in these high-risk patients has a negative socio-economic impact. This review summarizes the genetic basis, phenotype characteristics, and the National Comprehensive Cancer Network's screening, testing, and surveillance guidelines for the leading hereditary cancer syndromes. The aim of this review is to promote a better understanding of cancer genetics and genetic testing in Hispanic patients.

Indexed as

Genetic counselingGenetic testingGermline mutationsHereditary cancerHispanics

Identifiers

PMID28127413
PMCPMC5251307
OpenAlexW2575311144

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.