Evidence map›Paper›PMID 25337278›Full record

ArticleInternational journal of clinical and experimental pathology2014

Prevalence of BRCA1 gene mutation in breast cancer patients in Guangxi, China.

Liping Sun, Junjie Liu, Sida Wang, Yuanyuan Chen, Zhixian Li

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

4 citing papers in PubMed.

  1. SNHG1 Long Noncoding RNA is Potentially Up-Regulated in Colorectal Adenocarcinoma.Asian Pacific journal of cancer prevention : APJCP · 2020
    Article
  2. A Review of the Epidemiology of Breast Cancer in Asia: Focus on Risk Factors.Asian Pacific journal of cancer prevention : APJCP · 2020
    Review
  3. Article
  4. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Liping SunDepartment of Diagnostic Ultrasound, The First Affiliated Hospital of Guangxi Medical University Nanning, Guangxi, China.
Junjie LiuDepartment of Diagnostic Ultrasound, The First Affiliated Hospital of Guangxi Medical University Nanning, Guangxi, China.
Sida WangDepartment of Diagnostic Ultrasound, The First Affiliated Hospital of Guangxi Medical University Nanning, Guangxi, China.
Yuanyuan ChenDepartment of Diagnostic Ultrasound, The First Affiliated Hospital of Guangxi Medical University Nanning, Guangxi, China.
Zhixian LiDepartment of Diagnostic Ultrasound, The First Affiliated Hospital of Guangxi Medical University Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe prevalence of breast cancer susceptibility gene 1 mutation in breast cancer patients of south China has not been well revealed. This study was to invest the prevalence of BRCA1 gene mutation in breast cancer patients in Guangxi, China, and to try reflecting its relevance in genetic counseling of breast cancer.

methodsIn this study, 463 breast cancer patients and 30 healthy women (control group) were involved. Entire sequence and splicing sites of BRCA1 genes were detected by PCR-DNA sequencing.

resultsAbout 8.9% (41/463) patients were with 22 BRCA1 mutations (all in exon 10). The average hospitalized age of BRCA1-associated breast cancer cases was significantly younger (t = -2.965, P = 0.003). The nuclear grade (U = 2321.0, P = 0.030), ER (U = 4343.5, P = 0.041) and CerbB-2 (U = 3894.0, P = 0.038) expression levels, and triple negative breast cancer diagnosing rate (χ(2) = 4.719, P = 0.03) were disclosed more in BRCA1-associated patients.

conclusionsThe four most frequent BRCA1 mutation (2798 T > C, 3971 G > A, 3971 G > A and 624 C > T) found in female breast cancer cases in Guangxi are all located in exon 10. BRCA1-associated breast cancer cases have earlier onset age, higher nuclear grade and negative ER and CerbB-2 expression.

Indexed as

MutationAdolescentAdultAgedAged, 80 and overAge of OnsetAsian PeopleBiomarkers, TumorBRCA1 ProteinBreast NeoplasmsCase-Control StudiesChinaChi-Square DistributionDNA Mutational AnalysisExonsFemaleBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanBRCA1 gene mutationBreast cancerhistopathologypathology

Identifiers

PMID25337278
PMCPMC4203249

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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.