Evidence map›Paper›PMID 18752049›Full record

ArticlePathology oncology research : POR2009

Expression of tight junction protein claudin-4 in basal-like breast carcinomas.

Janina Kulka, Attila Marcell Szász, Zsuzsanna Németh, Lilla Madaras, Zsuzsa Schaff, István Arthur Molnár, Anna-Mária Tokés

Abstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.8field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 63 citations in OpenAlex.

  1. CK8/18 and Claudin Profile of Female Breast Cancers from Botswana.Breast cancer : basic and clinical research · 2026
    Article
  2. Article
  3. Article
  4. Claudins as biomarkers of differential diagnosis and prognosis of tumors.Journal of cancer research and clinical oncology · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Claudins in cancer: bench to bedside.Pflugers Archiv : European journal of physiology · 2017
    Review
  16. Article
  17. Mechanisms involved in breast cancer liver metastasis.Journal of translational medicine · 2015
    Review
  18. Article
  19. Emerging roles of claudins in human cancer.International journal of molecular sciences · 2013
    Review
  20. Claudin expression in high-grade invasive ductal carcinoma of the breast: correlation with the molecular subtype.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2013
    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

7 authors at 1 institution in 1 country.

Janina Kulka2nd Department of Pathology, Semmelweis University, 93 Ulloi út, 1091, Budapest, Hungary. kj@korb2.sote.hu
Attila Marcell Szász
Zsuzsanna Németh
Lilla Madaras
Zsuzsa Schaff
István Arthur Molnár
Anna-Mária Tokés
Semmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Claudins (CLDN) are tight junction proteins which contribute to the paracellular transport and ionic permeability of various epithelia. In recent years they came into focus for their suggested role in carcinogenesis and possible role in cancer therapy. According to our previous studies, in breast tissue CLDN4 is also related to the level of cellular differentiation. Thirty-eight estrogen (ER) and progesterone receptor (PgR) negative, HER2/neu negative, but cytokeratin 5/6 positive basal-like-mainly grade 3-breast carcinomas were compared with twenty-one grade 1, twenty-five grade 2 and twenty grade 3 non-basal-like invasive breast carcinomas, in respect to their CLDN4 expression. The immunohistochemical reactions were evaluated both semiquantitatively and by morphometrical analysis. Statistically significant difference (p = 0.001) was observable regarding CLDN4 expression in the basal-like group as compared to grade 1 and 2 cancers. Further, CLDN4 expression was significantly higher (p = 0.017) in the basal-like compared with the non-basal-like grade 3 carcinomas. Our results suggest that basal-like carcinomas are a subset of breast cancer with high level of CLDN4 protein expression. The finding is in accordance with our former observation that CLDN4 is indeed related to cellular differentiation. This observation may be seen as a further proof that basal-like carcinomas represent a separable group amongst grade 3 breast carcinomas.

Indexed as

Basal Cell CarcinomaBreast NeoplasmsCarcinoma, AdenosquamousCarcinoma, LobularClaudin-4Erb-b2 Receptor Tyrosine KinasesFemaleHumansImmunoenzyme TechniquesIn Situ Hybridization, FluorescenceMembrane ProteinsMiddle AgedPrognosisReceptors, EstrogenReceptors, ProgesteroneTissue Array AnalysisClaudin-4CLDN4 protein, humanErb-b2 Receptor Tyrosine KinasesMembrane ProteinsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID18752049
OpenAlexW2001096226

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.