Evidence map›Paper›PMID 8286195›Full record

ArticleBritish journal of cancer1994

bcl-2 in normal human breast and carcinoma, association with oestrogen receptor-positive, epidermal growth factor receptor-negative tumours and in situ cancer.

R D Leek, L Kaklamanis, F Pezzella, K C Gatter, A L Harris

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in British journal of cancer, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
15.4field-weighted citation impact, top 1% 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

69 citing papers in PubMed, 325 citations in OpenAlex.

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  7. Effects of neoadjuvant therapies on genetic regulation of targeted pathways in ER+ primary ductal breast carcinoma: A meta-analysis of microarray datasets.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2021
    Article
  8. Article
  9. Neutralization of BCL-2/XMolecular cancer therapeutics · 2019
    Article
  10. Article
  11. Bcl-2 antigen expression in luminal A and triple-negative breast cancer.Medical oncology (Northwood, London, England) · 2017
    Article
  12. Article
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  14. Deregulation of miR-93 and miR-143 in human esophageal cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
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  19. Lactate dehydrogenase B: a metabolic marker of response to neoadjuvant chemotherapy in breast cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  20. The role of estrogen receptor alpha in mediating chemoresistance in breast cancer cells.Journal of experimental & clinical cancer research : CR · 2012
    Article

9 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

R D LeekImperial Cancer Research Fund, University of Oxford, John Radcliffe Hospital, UK.
L Kaklamanis
F Pezzella
K C Gatter
A L Harris
John Radcliffe Hospital · GBInstitute of Molecular Medicine · INMolecular Oncology (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of bcl-2 expression in solid tumours is as yet undefined. It was, therefore, the purpose of this study to investigate expression of bcl-2 protein in 111 human breast carcinomas using immunohistochemistry and the monoclonal antibody bcl-2 124. Expression was then compared with the established indicators of prognosis and biological behaviour in malignant breast disease. No relationship could be observed between bcl-2 and node status, tumour size, differentiation, type or age at excision. However, a strong positive relationship was seen between bcl-2 and oestrogen receptor (ER), with 70 of 88 (80%) bcl-2-positive tumours being ER positive also, compared with seven of 23 (30%) bcl-2-negative tumours being ER positive (P < 0.0001). The converse was found when bcl-2 was compared with epidermal growth factor receptor (EGFR). A strong negative relationship was observed, with 26 of 88 (30%) bcl-2-positive tumours being EGFR positive, compared with 16 of 23 (70%) bcl-2-negative tumours being EGFR positive (P = 0.001), raising the possibility that bcl-2 is an ER-regulated gene. An inverse relationship was also found between bcl-2 and the oncogenes c-erbB-2 and p53. Thus, loss of bcl-2 expression in breast cancer is associated with a range of molecular markers of poor prognosis and may define part of an ER-negative, EGFR-positive phenotype.

Indexed as

BreastBreast NeoplasmsCarcinoma in SituErbB ReceptorsHumansImmunohistochemistryLymphatic MetastasisNeoplasms, Hormone-DependentProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Receptors, EstrogenTissue DistributionTumor Suppressor Protein p53ErbB ReceptorsProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Receptors, EstrogenTumor Suppressor Protein p53

Identifiers

PMID8286195
PMCPMC1968762
OpenAlexW1994039691

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.