Evidence map›Paper›PMID 26759166›Full record

ReviewFamilial cancer2016

CDH1 germline mutations and hereditary lobular breast cancer.

Giovanni Corso, Mattia Intra, Chiara Trentin, Paolo Veronesi, Viviana Galimberti

Abstract readReview
PubMed Publisher
In one paragraph

Review in Familial cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 125 citations in OpenAlex.

  1. Article
  2. Review
  3. bioRxiv : the preprint server for biology · 2025
    Article
  4. Review
  5. Review
  6. Observational
  7. Review
  8. Review
  9. Review
  10. Anti-Cancer Potential of Edible/Medicinal Mushrooms in Breast Cancer.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. In Silico Identification of Hub Genes as Observing Biomarkers for Gastric Cancer Metastasis.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  20. 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

5 authors at 2 institutions in 1 country.

Giovanni CorsoDivision of Senology, European Institute of Oncology, via G, Ripamonti 435, 20141, Milan, Italy. giovanni.corso@ieo.it.
Mattia IntraDivision of Senology, European Institute of Oncology, via G, Ripamonti 435, 20141, Milan, Italy.
Chiara TrentinDivision of Breast Imaging, European Institute of Oncology, via G, Ripamonti 435, 20141, Milan, Italy.
Paolo VeronesiDivision of Senology, European Institute of Oncology, via G, Ripamonti 435, 20141, Milan, Italy.
Viviana GalimbertiDivision of Senology, European Institute of Oncology, via G, Ripamonti 435, 20141, Milan, Italy.
European Institute of Oncology · ITRipamonti · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary diffuse gastric cancer is an autosomal dominant inherited disease associated of CDH1 germline mutations (that encodes for the E-cadherin protein), and lobular breast cancer is the second most frequent type of neoplasia. Recently, novel E-cadherin constitutional alterations have been identified in pedigree clustering only for lobular breast carcinoma without evidence of diffuse gastric tumors and in absence of BRCA1/2 mutations. This first evidence opens novel questions about the inherited correlation between diffuse gastric and lobular breast cancers. In this brief review we revise the literature data about the CDH1 mutation frequency affecting exclusively lobular breast cancer, providing clinical recommendation for asymptomatic mutation carriers.

Indexed as

Germ-Line MutationAntigens, CDBreast NeoplasmsCadherinsCarcinoma, LobularFemaleGenetic Predisposition to DiseaseGenetic TestingHeterozygoteHumansMutation RateAntigens, CDCadherinsCDH1 protein, humanE-cadherin germline mutationHereditary breast cancerLobular breast cancer

Identifiers

PMID26759166
OpenAlexW2265927613

What OpenQuestion holds

Textmetadata
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.