Evidence map›Paper›PMID 29025585›Full record

ArticleCancer genetics2017

Genetic Gastric Cancer Susceptibility in the International Clinical Cancer Genomics Community Research Network.

Thomas Slavin, Susan L Neuhausen, Christina Rybak, Ilana Solomon, Bita Nehoray, Kathleen Blazer, Mariana Niell-Swiller, Aaron W Adamson, Yate-Ching Yuan, Kai Yang and 11 more

Open access · greenAbstract read
In one paragraph

Article in Cancer genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Exome sequencing points to pathogenic ATM variants in gastric cancer.European journal of human genetics : EJHG · 2026
    Article
  3. Article
  4. Observational
  5. ATR-CHK1 Axis Inhibitors in Gastric Cancer Treatment.International journal of molecular sciences · 2025
    Review
  6. Article
  7. Frequency ofCancers · 2023
    Article
  8. Review
  9. Review
  10. Clonal Hematopoiesis and Mosaicism Revealed by a Multi-Tissue Analysis of Constitutional TP53 Status.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. A Novel, Likely PathogenicJournal of the Endocrine Society · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Genes · 2020
    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

21 authors at 3 institutions in 2 countries.

Thomas SlavinDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010; Department of Medical Oncology & Therapeutics Research, City of Hope National Medical Center, Duarte, CA 91010. Electronic address: tslavin@coh.org.
Susan L NeuhausenDepartment of Population Sciences, Beckman Research Institute of City of Hope, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010.
Christina RybakDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Ilana SolomonDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Bita NehorayDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Kathleen BlazerDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Mariana Niell-SwillerDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Aaron W AdamsonDepartment of Population Sciences, Beckman Research Institute of City of Hope, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010.
Yate-Ching YuanDepartment of Molecular Medicine, Beckman Research Institute of City of Hope, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010.
Kai YangDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Sharon SandDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Danielle CastilloDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Josef HerzogDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Xiwei WuDepartment of Molecular Medicine, Beckman Research Institute of City of Hope, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010.
Shu TaoDepartment of Molecular Medicine, Beckman Research Institute of City of Hope, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010.
Tanya ChavezDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010.
Yanghee WooDivision of Surgical, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010.
Joseph ChaoDepartment of Medical Oncology & Therapeutics Research, City of Hope National Medical Center, Duarte, CA 91010.
Pamela MoraInstituto Nacional de Enfermedades Neoplásticas, Av. Angamos Este 2520, Surquillo 15038, Peru.
Darling HorcasitasNew Mexico Cancer Center, 4901 Lang Avenue NE, Albuquerque, NM 87109.
Jeffrey WeitzelDivision of Clinical Cancer Genomics, City of Hope National Medical Center, 1500 E. Duarte Rd., Bldg 173, Duarte, CA 91010; Department of Medical Oncology & Therapeutics Research, City of Hope National Medical Center, Duarte, CA 91010.
City Of Hope National Medical Center · USInstituto Nacional de Enfermedades Neoplásicas · PENew Mexico Cancer Center · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Discovery and Characterization of Mutations in Breast and Ovarian CancersR50CA211280 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ADAMSON, AARON · 2016 to 2020
$1.1M
Community Cancer Genetics and Research Training (Revision)R25CA112486 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI WEITZEL, JEFFREY N · 2005 to 2009
$1.0M
Clinical Cancer Genetics Community Network: A Sustainable Research PartnershipRC4CA153828 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WEITZEL, JEFFREY N · 2010 to 2010
$1.0M
NCI NIH HHS P30 CA033572NCI NIH HHS R25 CA112486NCI NIH HHS R50 CA211280NCI NIH HHS RC4 CA153828
6 · The paper itself

Abstract

Few susceptibility genes for gastric cancer have been identified. We sought to identify germline susceptibility genes from participants with gastric cancer from an international hereditary cancer research network. Adults with gastric cancer of any histology, and with a germline DNA sample (n = 51), were retrospectively selected. For those without previously identified germline mutations (n = 43), sequencing was performed for 706 candidate genes. Twenty pathogenic or likely pathogenic variants were identified among 18 participants. Eight of the 18 participants had previous positive clinical testing, including six with CDH1 pathogenic or likely pathogenic variants, and two with pathogenic MSH2 and TP53 variants. Of the remaining 10, six were in BRCA1 DNA damage response pathway genes (ATM, ATR, BRCA2, BRIP1, FANCC, TP53), other variants were identified in CTNNA1, FLCN, SBDS, and GNAS. Participants identified with pathogenic or likely pathogenic variants were younger at gastric cancer diagnosis than those without, 39.1 versus 48.0 years, and over 50% had a close family member with gastric cancer (p-values < 0.0001). In conclusion, many participants were identified with mutations in clinically-actionable genes. Age of onset and family history of gastric cancer were mutation status predictors. Our findings support multigene panels in identifying gastric cancer predisposition.

Indexed as

Biomedical ResearchGenetic Predisposition to DiseaseGenomicsInternationalityAdolescentAdultAgedAged, 80 and overFemaleGenetic Association StudiesGenetic TestingGerm-Line MutationHumansMaleMiddle AgedSequence Analysis, DNAfamilygastric cancergeneticsStomach Neoplasms

Identifiers

PMID29025585
PMCPMC5659836
OpenAlexW2749262613

What OpenQuestion holds

Textmetadata
LicenceTDM
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.