Literature DB >> 19190825

Expression analysis and study of KLK4 in benign and malignant breast tumours.

Georgia Papachristopoulou1, Margaritis Avgeris, Andreas Scorilas.   

Abstract

The steroid hormone-regulated gene KLK4 (kallikrein 4) is a new member of the human kallikrein-related peptidase gene family. Up to date, studies report that KLK4 is differentially expressed in many tumours. The purpose of this study was the expression analysis and study of KLK4 in benign and malignant breast tumours. Total RNA was isolated from 16 benign and 45 malignant breast tissue specimens. After testing RNA quality, cDNA was prepared by reverse transcription. Highly sensitive quantitative real-time PCR method for KLK4 mRNA quantification was developed using the SYBR Green chemistry. GAPDH served as a housekeeping gene. Relative quantification analysis was performed using the comparative C(T) method 2(-DeltaDeltaC)(T) KLK4 expression was found to vary in both patients' cohorts; however, a statistically significant elevation of the KLK4 mRNA levels was observed in malignant compared to benign tumour patients. Low KLK4 expression levels were found in well-differentiated tumours (p = 0.011) as well as in stage I (p = 0.024) patients. Moreover, a statistically significant (r(s) = -0.318, p = 0.035) negative correlation between the KLK4 expression and progesterone receptor staining was observed. ROC and logistic regression analysis recommended that KLK4 gene expression may be used as a new potential biomarker in breast cancer.

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Year:  2009        PMID: 19190825

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  7 in total

1.  Protease-activated receptors mediate crosstalk between coagulation and fibrinolysis.

Authors:  Troy A McEachron; Rafal Pawlinski; Kristy L Richards; Frank C Church; Nigel Mackman
Journal:  Blood       Date:  2010-08-24       Impact factor: 22.113

2.  Elevated levels of both microRNA 378 (miR-378) and kallikrein-related peptidase 4 (KLK4) mRNA are associated with an unfavorable prognosis in triple-negative breast cancer.

Authors:  Weiwei Gong; Caixia Zhu; Yueyang Liu; Alexander Muckenhuber; Holger Bronger; Andreas Scorilas; Marion Kiechle; Julia Dorn; Viktor Magdolen; Tobias Dreyer
Journal:  Am J Transl Res       Date:  2021-03-15       Impact factor: 4.060

3.  Aberrant KLK4 gene promoter hypomethylation in pediatric hepatoblastomas.

Authors:  Baihui Liu; Ximao Cui; Shan Zheng; Kuiran Dong; Rui Dong
Journal:  Oncol Lett       Date:  2017-01-02       Impact factor: 2.967

4.  Significant alterations in the expression pattern of kallikrein-related peptidase genes KLK4, KLK5 and KLK14 after treatment of breast cancer cells with the chemotherapeutic agents epirubicin, docetaxel and methotrexate.

Authors:  Georgia Papachristopoulou; Maroulio Talieri; Andreas Scorilas
Journal:  Tumour Biol       Date:  2012-10-20

5.  Down-regulation of kallikrein-related peptidase 5 (KLK5) expression in breast cancer patients: a biomarker for the differential diagnosis of breast lesions.

Authors:  Margaritis Avgeris; Georgia Papachristopoulou; Athanasios Polychronis; Andreas Scorilas
Journal:  Clin Proteomics       Date:  2011-05-31       Impact factor: 3.988

6.  Kallikrein 4 and matrix metalloproteinase-20 immunoexpression in malignant, benign and infiltrative odontogenic tumors.

Authors:  Marcelo Macedo Crivelini; Denise Tostes Oliveira; Ricardo Alves de Mesquita; Suzana Cantanhede Orsini Machado de Sousa; Adriano Motta Loyola
Journal:  J Oral Maxillofac Pathol       Date:  2016 May-Aug

7.  Diagnostic and prognostic biomarker potential of kallikrein family genes in different cancer types.

Authors:  Prashant D Tailor; Sai Karthik Kodeboyina; Shan Bai; Nikhil Patel; Shruti Sharma; Akshay Ratnani; John A Copland; Jin-Xiong She; Ashok Sharma
Journal:  Oncotarget       Date:  2018-04-03
  7 in total

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