Literature DB >> 25862839

Clinical significance of kallikrein-related peptidase-4 in oral cancer.

Petros Papagerakis1, Giuseppe Pannone2, L I Zheng3, Maria Athanassiou-Papaefthymiou3, Yashuo Yamakoshi4, Howard Stan McGuff5, Omar Shkeir6, Konstantinos Ghirtis3, Silvana Papagerakis7.   

Abstract

Kallikrein-related-peptidase-4 (KLK4), a serine protease originally discovered in developing tooth with broad target sequence specificity, serves vital functions in dental enamel formation. KLK4 is involved in degradation of extracellular matrix proteins and it is thought that this proteolytic activity could also promote tumor invasion and metastasis. Recent studies have associated KLK4 expression with tumor progression and clinical outcome, particularly in prostate and ovarian cancer. Very little is known in regard KLK4 involvement in oral squamous cell carcinomas (OSCCs). Our objective was to investigate KLK4 expression in OSCC pathogenesis and disease progression. KLK4 expression was evaluated by immunohistochemistry, western blots and zymograms in OSCC lines. Invasion assays using high versus low/undetectable KLK4-expressing OSCC cell lines were performed jointly with KLK4 siRNA inhibition. A large collection of OSCC specimens was evaluated for KLK4 expression and correlation with patients' characteristics and outcomes were determined. Our data indicate that KLK4 is differentially expressed in oral carcinomas. OSCC cell lines with high invasive and metastatic potential have the highest levels of KLK4 expression. KLK4 mRNA and protein expression correlated with enzyme activity detected by zymograms. Inhibition of KLK4 expression results in diminished invasive potential in OSCC cell lines. Consistently, KLK4 expression is stronger in primary tumors that later either recurred or developed metastases, suggesting that its preferential expression in OSCC might contribute to individual tumor biology. Therefore, this study provides supportive evidence in favor of a prognostic value for KLK4 in OSCC and suggests that KLK4 could serve as a potential therapeutic target in patients with oral cancer. Copyright
© 2015 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.

Entities:  

Keywords:  Kallikrein-related-peptidase-4 (KLK4); Oral squamous cell carcinoma (OSCC); cell lines; clinical outcome; invasion; metastasis

Mesh:

Substances:

Year:  2015        PMID: 25862839      PMCID: PMC4577232     

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  34 in total

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Authors:  Hong Zhao; Ying Dong; Jingjing Quan; Robert Smith; Alfred Lam; Stephen Weinstein; Judith Clements; Newell W Johnson; Jin Gao
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Journal:  Head Neck       Date:  2013-01-16       Impact factor: 3.147

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10.  The role of E-cadherin down-regulation in oral cancer: CDH1 gene expression and epigenetic blockage.

Authors:  G Pannone; A Santoro; A Feola; P Bufo; P Papagerakis; L Lo Muzio; S Staibano; F Ionna; F Longo; R Franco; G Aquino; M Contaldo; S De Maria; R Serpico; A De Rosa; C Rubini; S Papagerakis; A Giovane; V Tombolini; A Giordano; M Caraglia; M Di Domenico
Journal:  Curr Cancer Drug Targets       Date:  2014       Impact factor: 3.428

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  8 in total

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4.  Effects of DSPP and MMP20 Silencing on Adhesion, Metastasis, Angiogenesis, and Epithelial-Mesenchymal Transition Proteins in Oral Squamous Cell Carcinoma Cells.

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5.  Characterization of kallikrein-related peptidase 4 (KLK4) mRNA expression in tumor tissue of advanced high-grade serous ovarian cancer patients.

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6.  Study of Gene Expression Profiles of Breast Cancers in Indian Women.

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7.  Kallikrein 13 serves as a priming protease during infection by the human coronavirus HKU1.

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8.  Identification of methylation sites and signature genes with prognostic value for luminal breast cancer.

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  8 in total

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