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Altered desmoplakin expression at transcriptional and protein levels provides prognostic information in human oropharyngeal cancer

Summary Desmoplakin, a desmosomal component, is a key protein involved in cell-cell adhesion. Down-regulation of desmosomal proteins is associated with the invasive and metastatic ability of tumor cells. We examined 37 cases of human primary oropharyngeal squamous cell carcinomas lacking overt dista...

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Published in:Human pathology 2009-09, Vol.40 (9), p.1320-1329
Main Authors: Papagerakis, Silvana, MD, MS, PhD, Shabana, Al-Hassan, BDS, PhD, Pollock, Brad H., MPH, PhD, Papagerakis, Petros, BDS, MS, PhD, Depondt, Joël, MD, PhD, Berdal, Ariane, BDS, MS, PhD
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cited_by cdi_FETCH-LOGICAL-c542t-905c880d0404510a1ccd40e179efb1d20c1e429bc0707374c20076fa43c0ecd33
cites cdi_FETCH-LOGICAL-c542t-905c880d0404510a1ccd40e179efb1d20c1e429bc0707374c20076fa43c0ecd33
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creator Papagerakis, Silvana, MD, MS, PhD
Shabana, Al-Hassan, BDS, PhD
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Depondt, Joël, MD, PhD
Berdal, Ariane, BDS, MS, PhD
description Summary Desmoplakin, a desmosomal component, is a key protein involved in cell-cell adhesion. Down-regulation of desmosomal proteins is associated with the invasive and metastatic ability of tumor cells. We examined 37 cases of human primary oropharyngeal squamous cell carcinomas lacking overt distant metastases to gain further insights on the potential role of desmoplakin in oral cancer. Desmoplakin expression was evaluated using reverse transcriptase–polymerase chain reaction and immunohistochemistry on frozen unfixed sections. Western blotting was performed to characterize the relative expression levels for each of the 2 desmoplakin protein isoforms, I and II. Desmoplakin expression was compared with histopathological grade, clinical stage, and patient outcome. Desmoplakin expression was prominent in highly differentiated tumors and reduced or absent in poorly differentiated tumors that developed distant metastases within the 3 years of follow-up period. Desmoplakin mRNA levels tracked with protein levels, suggesting that lack of desmoplakin protein expression is due to down-regulation of mRNA expression at the transcription level. Western blot analysis demonstrated that the 2 desmoplakin isoforms displayed different patterns of subcellular distribution in tumors, with the desmoplakin II detected only in patients in which desmoplakin immunoreactivity displayed an abnormal cytoplasmic localization. Our findings suggest that down-regulation of desmoplakin expression may represent a useful marker for evaluating the risk of distant metastasis formation in oropharyngeal squamous cell carcinomas. Interestingly, desmoplakin II was detected only in tumors associated with a poor clinical outcome, suggesting a potential specific function for this isoform in oral carcinogenesis. Characterizing DSP expression may improve evaluation risk of distant metastasis formation in oral cancer patients.
doi_str_mv 10.1016/j.humpath.2009.02.002
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Down-regulation of desmosomal proteins is associated with the invasive and metastatic ability of tumor cells. We examined 37 cases of human primary oropharyngeal squamous cell carcinomas lacking overt distant metastases to gain further insights on the potential role of desmoplakin in oral cancer. Desmoplakin expression was evaluated using reverse transcriptase–polymerase chain reaction and immunohistochemistry on frozen unfixed sections. Western blotting was performed to characterize the relative expression levels for each of the 2 desmoplakin protein isoforms, I and II. Desmoplakin expression was compared with histopathological grade, clinical stage, and patient outcome. Desmoplakin expression was prominent in highly differentiated tumors and reduced or absent in poorly differentiated tumors that developed distant metastases within the 3 years of follow-up period. Desmoplakin mRNA levels tracked with protein levels, suggesting that lack of desmoplakin protein expression is due to down-regulation of mRNA expression at the transcription level. Western blot analysis demonstrated that the 2 desmoplakin isoforms displayed different patterns of subcellular distribution in tumors, with the desmoplakin II detected only in patients in which desmoplakin immunoreactivity displayed an abnormal cytoplasmic localization. Our findings suggest that down-regulation of desmoplakin expression may represent a useful marker for evaluating the risk of distant metastasis formation in oropharyngeal squamous cell carcinomas. Interestingly, desmoplakin II was detected only in tumors associated with a poor clinical outcome, suggesting a potential specific function for this isoform in oral carcinogenesis. Characterizing DSP expression may improve evaluation risk of distant metastasis formation in oral cancer patients.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2009.02.002</identifier><identifier>PMID: 19386346</identifier><identifier>CODEN: HPCQA4</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adhesion ; Adult ; Aged ; Aged, 80 and over ; Binding sites ; Biological and medical sciences ; Cancer ; Carcinoma, Squamous Cell - genetics ; Cell Adhesion ; Cohort Studies ; Cytoskeletal Proteins - genetics ; Cytoskeletal Proteins - metabolism ; Dermatology ; Desmoplakin ; Desmoplakins - genetics ; Desmoplakins - metabolism ; Desmosomes - metabolism ; Female ; Follow-Up Studies ; Gene Expression Regulation, Neoplastic ; Hospitals ; Humans ; Immunohistochemistry ; Investigative techniques, diagnostic techniques (general aspects) ; Kaplan-Meier Estimate ; Male ; Medical sciences ; Metastasis ; Middle Aged ; Mouth Neoplasms - genetics ; Mouth Neoplasms - pathology ; Mouth Neoplasms - secondary ; Neoplasm Invasiveness ; Neoplasm Metastasis ; Oropharyngeal Neoplasms - genetics ; Oropharyngeal Neoplasms - pathology ; Oropharyngeal Neoplasms - secondary ; Oropharynx ; Otorhinolaryngology. Stomatology ; Pathology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Prognosis ; Prospective Studies ; Protein Isoforms - genetics ; Protein Isoforms - metabolism ; Proteins ; RNA, Messenger - metabolism ; RNA, Neoplasm - analysis ; Rodents ; Signal transduction ; Squamous cell carcinomas ; Studies ; Survival Analysis ; Time Factors ; Transcription, Genetic ; Tumor Burden ; Tumors ; Tumors of the skin and soft tissue. 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Down-regulation of desmosomal proteins is associated with the invasive and metastatic ability of tumor cells. We examined 37 cases of human primary oropharyngeal squamous cell carcinomas lacking overt distant metastases to gain further insights on the potential role of desmoplakin in oral cancer. Desmoplakin expression was evaluated using reverse transcriptase–polymerase chain reaction and immunohistochemistry on frozen unfixed sections. Western blotting was performed to characterize the relative expression levels for each of the 2 desmoplakin protein isoforms, I and II. Desmoplakin expression was compared with histopathological grade, clinical stage, and patient outcome. Desmoplakin expression was prominent in highly differentiated tumors and reduced or absent in poorly differentiated tumors that developed distant metastases within the 3 years of follow-up period. Desmoplakin mRNA levels tracked with protein levels, suggesting that lack of desmoplakin protein expression is due to down-regulation of mRNA expression at the transcription level. Western blot analysis demonstrated that the 2 desmoplakin isoforms displayed different patterns of subcellular distribution in tumors, with the desmoplakin II detected only in patients in which desmoplakin immunoreactivity displayed an abnormal cytoplasmic localization. Our findings suggest that down-regulation of desmoplakin expression may represent a useful marker for evaluating the risk of distant metastasis formation in oropharyngeal squamous cell carcinomas. Interestingly, desmoplakin II was detected only in tumors associated with a poor clinical outcome, suggesting a potential specific function for this isoform in oral carcinogenesis. Characterizing DSP expression may improve evaluation risk of distant metastasis formation in oral cancer patients.</description><subject>Adhesion</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Binding sites</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Cell Adhesion</subject><subject>Cohort Studies</subject><subject>Cytoskeletal Proteins - genetics</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Dermatology</subject><subject>Desmoplakin</subject><subject>Desmoplakins - genetics</subject><subject>Desmoplakins - metabolism</subject><subject>Desmosomes - metabolism</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Mouth Neoplasms - genetics</subject><subject>Mouth Neoplasms - pathology</subject><subject>Mouth Neoplasms - secondary</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Metastasis</subject><subject>Oropharyngeal Neoplasms - genetics</subject><subject>Oropharyngeal Neoplasms - pathology</subject><subject>Oropharyngeal Neoplasms - secondary</subject><subject>Oropharynx</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Pathology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Protein Isoforms - genetics</subject><subject>Protein Isoforms - metabolism</subject><subject>Proteins</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA, Neoplasm - analysis</subject><subject>Rodents</subject><subject>Signal transduction</subject><subject>Squamous cell carcinomas</subject><subject>Studies</subject><subject>Survival Analysis</subject><subject>Time Factors</subject><subject>Transcription, Genetic</subject><subject>Tumor Burden</subject><subject>Tumors</subject><subject>Tumors of the skin and soft tissue. 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Stomatology</topic><topic>Pathology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Protein Isoforms - genetics</topic><topic>Protein Isoforms - metabolism</topic><topic>Proteins</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Neoplasm - analysis</topic><topic>Rodents</topic><topic>Signal transduction</topic><topic>Squamous cell carcinomas</topic><topic>Studies</topic><topic>Survival Analysis</topic><topic>Time Factors</topic><topic>Transcription, Genetic</topic><topic>Tumor Burden</topic><topic>Tumors</topic><topic>Tumors of the skin and soft tissue. 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Down-regulation of desmosomal proteins is associated with the invasive and metastatic ability of tumor cells. We examined 37 cases of human primary oropharyngeal squamous cell carcinomas lacking overt distant metastases to gain further insights on the potential role of desmoplakin in oral cancer. Desmoplakin expression was evaluated using reverse transcriptase–polymerase chain reaction and immunohistochemistry on frozen unfixed sections. Western blotting was performed to characterize the relative expression levels for each of the 2 desmoplakin protein isoforms, I and II. Desmoplakin expression was compared with histopathological grade, clinical stage, and patient outcome. Desmoplakin expression was prominent in highly differentiated tumors and reduced or absent in poorly differentiated tumors that developed distant metastases within the 3 years of follow-up period. Desmoplakin mRNA levels tracked with protein levels, suggesting that lack of desmoplakin protein expression is due to down-regulation of mRNA expression at the transcription level. Western blot analysis demonstrated that the 2 desmoplakin isoforms displayed different patterns of subcellular distribution in tumors, with the desmoplakin II detected only in patients in which desmoplakin immunoreactivity displayed an abnormal cytoplasmic localization. Our findings suggest that down-regulation of desmoplakin expression may represent a useful marker for evaluating the risk of distant metastasis formation in oropharyngeal squamous cell carcinomas. Interestingly, desmoplakin II was detected only in tumors associated with a poor clinical outcome, suggesting a potential specific function for this isoform in oral carcinogenesis. Characterizing DSP expression may improve evaluation risk of distant metastasis formation in oral cancer patients.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19386346</pmid><doi>10.1016/j.humpath.2009.02.002</doi><tpages>10</tpages></addata></record>
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subjects Adhesion
Adult
Aged
Aged, 80 and over
Binding sites
Biological and medical sciences
Cancer
Carcinoma, Squamous Cell - genetics
Cell Adhesion
Cohort Studies
Cytoskeletal Proteins - genetics
Cytoskeletal Proteins - metabolism
Dermatology
Desmoplakin
Desmoplakins - genetics
Desmoplakins - metabolism
Desmosomes - metabolism
Female
Follow-Up Studies
Gene Expression Regulation, Neoplastic
Hospitals
Humans
Immunohistochemistry
Investigative techniques, diagnostic techniques (general aspects)
Kaplan-Meier Estimate
Male
Medical sciences
Metastasis
Middle Aged
Mouth Neoplasms - genetics
Mouth Neoplasms - pathology
Mouth Neoplasms - secondary
Neoplasm Invasiveness
Neoplasm Metastasis
Oropharyngeal Neoplasms - genetics
Oropharyngeal Neoplasms - pathology
Oropharyngeal Neoplasms - secondary
Oropharynx
Otorhinolaryngology. Stomatology
Pathology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Prognosis
Prospective Studies
Protein Isoforms - genetics
Protein Isoforms - metabolism
Proteins
RNA, Messenger - metabolism
RNA, Neoplasm - analysis
Rodents
Signal transduction
Squamous cell carcinomas
Studies
Survival Analysis
Time Factors
Transcription, Genetic
Tumor Burden
Tumors
Tumors of the skin and soft tissue. Premalignant lesions
Upper respiratory tract, upper alimentary tract, paranasal sinuses, salivary glands: diseases, semeiology
title Altered desmoplakin expression at transcriptional and protein levels provides prognostic information in human oropharyngeal cancer
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