Evidence map›Paper›PMID 28808484›Full record

ArticleOncology letters2017

ERα and ERβ co-expression: An indicator of aggressive tumors and hormonal sensitivity.

Mohamed Oueslati, Ilhem Bittaieb, Nadia Sassi, Awatef Ben Jemaa, Amor Gamoudi, Khaled Rahal, Ridha Oueslati

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. PeerJ · 2022
    Article
  9. Article
  10. Review
  11. Review
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

7 authors at 3 institutions in 1 country.

Mohamed OueslatiUnit of Immunology, Environmental Microbiology and Carcinogenesis, Faculty of Sciences of Bizerte, University of Carthage, Zarzouna 7021, Tunisia.
Ilhem BittaiebPathological Anatomy Service, Saleh Azeiz Oncology Institute, Beb Saadoun, Tunis 1006, Tunisia.
Nadia SassiImmuno-Rheumatology Research laboratory, Rheumatology Department, La Rabta Hospital, Tunis 1007, Tunisia.
Awatef Ben JemaaUnit of Immunology, Environmental Microbiology and Carcinogenesis, Faculty of Sciences of Bizerte, University of Carthage, Zarzouna 7021, Tunisia.
Amor GamoudiPathological Anatomy Service, Saleh Azeiz Oncology Institute, Beb Saadoun, Tunis 1006, Tunisia.
Khaled RahalCancer Surgery Service, Saleh Azeiz Oncology Institute, Beb Saadoun, Tunis 1006, Tunisia.
Ridha OueslatiUnit of Immunology, Environmental Microbiology and Carcinogenesis, Faculty of Sciences of Bizerte, University of Carthage, Zarzouna 7021, Tunisia.
Institut Salah-Azaïz · TNUniversity of Carthage · TNHôpital La Rabta · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The estrogen receptors (ERs) ERα and ERβ are important factors in breast cancer progression. Nevertheless, the molecular interplay between ERα and ERβ and its clinical significance in breast cancer is controversial. The establishment of a clear association is required; therefore, the current study analyzed the expression patterns of ERα and ERβ in 32 breast tumor tissues using reverse transcription-quantitative polymerase chain reaction. Furthermore, human epidermal growth factor receptor 2 (HER2) and the Ki-67 status were detected by immunohistochemistry. The results revealed that the ERα and ERβ expression rates recorded were 68 and 65%, respectively. The ERα:ERβ ratio exhibited a decline along with disease progression. ERα and ERβ were found to be negatively correlated with HER2 status but positively correlated with Ki-67. Co-expression of ERα and ERβ was associated with breast cancer aggressiveness, including higher histological grade and positive nodal status, which commonly occur following the menopause. In addition, in cases where ERβ was coexpressed with ERα, HER2 expression was frequently found to be negative, whereas the Ki-67 index was upregulated. These data suggest that ERα and ERβ co-expression may be an indicator of tumor aggressiveness and the sensitivity of hormonal therapy via the downregulation of HER2.

Indexed as

breast cancerestrogen receptor αestrogen receptor βhuman epidermal growth factor receptor 2Ki-67

Identifiers

PMID28808484
PMCPMC5542036
OpenAlexW2623458441

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.