Literature DB >> 25780006

Clinicopathologic relevance of claudin 5 expression in breast cancer.

Hitoshi Sugimoto1, Makoto Nagahara2, Yuan Bae3, Tsuyoshi Nakagawa1, Toshiaki Ishikawa4, Takanobu Sato1, Hiroyuki Uetake4, Yoshinobu Eishi3, Kenichi Sugihara1.   

Abstract

OBJECTIVES: Claudins are major adhesion molecules in tight junctions and are strongly expressed in various cancers. We thus investigated the expression of claudin 5, a member of the claudin family, in breast cancer.
METHODS: A total of 193 patients with breast cancer were identified based on their pathologic diagnosis. The expression of each claudin 5 was analyzed in the tumor by immunohistochemical staining. Parametric correlations were done between claudin 5 expression and the clinicopathologic findings.
RESULTS: Claudin 5 expression in patients with recurrent breast cancer was statistically significantly higher (P = .004). In addition, analysis of the correlation with other clinicopathologic factors showed statistically significant differences with respect to lymphatic invasion (P = .014), venous invasion (P = .048), estrogen receptor status (P = .002), and human epidermal growth factor 2 status (P = .007). Multivariate analysis revealed that claudin 5 expression was an independent predictive factor in the recurrence for relapse-free survival (RFS) (P = .020). Kaplan-Meier analysis showed that the RFS rate was significantly lower in the high claudin 5 expression group (P = .001).
CONCLUSIONS: Patients with breast cancer with high claudin 5 expression had a significantly lower RFS rate. Our findings suggest that claudin 5 may be useful as a new biomarker of a risk factor. Copyright© by the American Society for Clinical Pathology.

Entities:  

Keywords:  Breast cancer; Claudin 5; Tight junctions

Mesh:

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Year:  2015        PMID: 25780006     DOI: 10.1309/AJCPWGBZ6D0OAIVJ

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  4 in total

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Journal:  BMC Cancer       Date:  2019-06-10       Impact factor: 4.430

3.  The G Protein-Coupled Estrogen Receptor (GPER) Expression Correlates with Pro-Metastatic Pathways in ER-Negative Breast Cancer: A Bioinformatics Analysis.

Authors:  Marianna Talia; Ernestina Marianna De Francesco; Damiano Cosimo Rigiracciolo; Maria Grazia Muoio; Lucia Muglia; Antonino Belfiore; Marcello Maggiolini; Andrew H Sims; Rosamaria Lappano
Journal:  Cells       Date:  2020-03-04       Impact factor: 6.600

4.  tRNA Queuosine Modification Enzyme Modulates the Growth and Microbiome Recruitment to Breast Tumors.

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Journal:  Cancers (Basel)       Date:  2020-03-09       Impact factor: 6.639

  4 in total

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