Evidence map›Paper›PMID 11322170›Full record

ArticleMolecular pathology : MP2001

Disparate E-cadherin mutations in LCIS and associated invasive breast carcinomas.

K M Rieger-Christ, J A Pezza, J M Dugan, J W Braasch, K S Hughes, I C Summerhayes

Open access · bronzeAbstract read
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Article in Molecular pathology : MP, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Molecular drivers of lobular carcinoma in situ.Breast cancer research : BCR · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Non-operative breast pathology: lobular neoplasia.Journal of clinical pathology · 2007
    Review
  11. Review
  12. Article
  13. 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

6 authors at 1 institution in 1 country.

K M Rieger-ChristCell and Molecular Biology Laboratory, Robert E Wise Research and Education Institute, Burlington, MA 01805, USA. Kimberly.R.Christ@lahey.org
J A Pezza
J M Dugan
J W Braasch
K S Hughes
I C Summerhayes
Lahey Hospital and Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe relation between lobular carcinoma in situ (LCIS) and invasive breast cancer is unresolved. In an attempt to establish whether LCIS is a precursor of invasive cancer the mutational status and the expression of E-cadherin was analysed in LCIS and associated invasive breast carcinoma in 23 patients.

methodsFoci of LCIS and associated invasive carcinoma were individually microdissected from tissue from 23 patients. Exons 4-16 of the E-cadherin gene were analysed using single strand conformation polymorphism (SSCP); protein expression and the localisation of E-cadherin and beta-catenin were assessed with the use of immunohistochemistry.

resultsImmunohistochemistry revealed a lack of expression of E-cadherin and beta-catenin in most LCIS samples and invasive foci. In all but four cases, the staining pattern was identical in the LCIS and associated invasive areas. When E-cadherin was absent, beta-catenin was also undetected, suggesting a lack of expression of alternative classic cadherin members in these lesions. Coincident E-cadherin mutations in LCIS and associated invasive carcinoma were not identified in this series of patients. However, mutational analysis of E-cadherin in multiple foci of carcinoma in situ surrounding an invasive lesion provided evidence to support ductal carcinoma in situ as a precursor of invasive ductal carcinoma.

conclusionThese data support the hypothesis that LCIS is not a precursor of invasive breast carcinoma but a marker of increased risk of developing invasive disease.

Indexed as

MutationTrans-Activatorsbeta CateninBreast NeoplasmsCadherinsCarcinoma in SituCarcinoma, LobularCytoskeletal ProteinsDisease ProgressionFemaleHumansNeoplasm InvasivenessNeoplasm ProteinsPolymorphism, Single-Stranded Conformationalbeta CateninCadherinsCTNNB1 protein, humanCytoskeletal ProteinsNeoplasm ProteinsTrans-Activators

Identifiers

PMID11322170
PMCPMC1187009
OpenAlexW2170535706

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.