Evidence map›Paper›PMID 31113927›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Adenomatous Polyposis Coli Gene Mutations in 22 Chinese Pedigrees with Familial Adenomatous Polyposis.

Dan Wang, Zhao Zhang, Yuwei Li, Chen Xu, Yongjun Yu, Mingsen Li, Chao Chen, Xipeng Zhang

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Update on Surgical Management of FAP.Clinics in colon and rectal surgery · 2023
    Review
  3. Review
  4. Genes · 2021
    Article
  5. A rare missense variant inHereditary cancer in clinical practice · 2020
    Article
  6. Article
  7. 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

8 authors at 2 institutions in 1 country.

Dan WangDepartment of Pathology, Tianjin Medical University General Hospital, Tianjin, China (mainland).
Zhao ZhangDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Yuwei LiDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Chen XuDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Yongjun YuDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Mingsen LiDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Chao ChenDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Xipeng ZhangDepartment of Colorectal Surgery, Tianjin Union Medical Center, Tianjin, China (mainland).
Tianjin People's Hospital · CNTianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Familial adenomatous polyposis (FAP), which has a very high tendency of progression to colorectal cancer, is mainly caused by mutations of the adenomatous polyposis coli (APC) gene. This study systematically screened the APC mutations and observed the correlation of APC mutations with clinical manifestations of FAP. MATERIAL AND METHODS Eighty subjects (probands and their family members of 22 FAP pedigrees) were enrolled, underwent abdominal ultrasound, computed tomography, and colonoscopic examinations, and were assessed for APC mutations between January 2010 and June 2015 at Tianjin Union Medical Center. Peripheral blood was collected from subjects, and DNA was extracted and screened for APC mutations using multiplex ligation-dependent probe amplification for large-fragment deletions or PCR-denaturing high-performance liquid chromatography with DNA sequencing for micromutations. RESULTS Nineteen of 22 FAP pedigrees were found to have mutations of APC, and 17 types APC mutations were identified. All the mutations were heterozygosity with autosomal dominant inheritance. APC mutations included 8 caused by frameshift, 3 by aberrant splicing, 2 by missense mutation, 2 by nonsense mutation, and 2 by large-fragment deletion. Frameshift mutation was the most common type of APC mutation, and Coding DNA Sequence 15 was the most common mutation site. Five novel APC mutations, including 1 with large-fragment deletion, were identified. CONCLUSIONS We systematically screened 17 mutations of APC from 22 Chinese pedigrees with FAP. This study will broaden the spectrum of known APC germline mutations and help understand the types and distribution of APC mutations among Chinese patients with FAP.

Indexed as

Adenomatous Polyposis ColiAdolescentAdultAgedAsian PeopleBase SequenceChinaColonoscopyColorectal NeoplasmsExonsFemaleGenes, APCGenetic Predisposition to DiseaseGerm-Line MutationHeterozygoteHumans

Identifiers

PMID31113927
PMCPMC6542301
OpenAlexW2946158458

What OpenQuestion holds

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Registered trials

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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.