Differential expression of SKALP/Elafin in human epidermal tumors

Recently we described a new epidermal serine proteinase inhibitor, skin-derived antileukoproteinase (SKALP), also known as elafin. SKALP/elafin was found to be absent in normal human epidermis, but can be induced in vitro and in vivo under hyperproliferative conditions. Here we studied the expressio...

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Veröffentlicht in:The American journal of pathology 1993-12, Vol.143 (6), p.1679-1687
Hauptverfasser: Alkemade, HA, Molhuizen, HO, van Vlijmen-Willems, IM, van Haelst, UJ, Schalkwijk, J
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container_end_page 1687
container_issue 6
container_start_page 1679
container_title The American journal of pathology
container_volume 143
creator Alkemade, HA
Molhuizen, HO
van Vlijmen-Willems, IM
van Haelst, UJ
Schalkwijk, J
description Recently we described a new epidermal serine proteinase inhibitor, skin-derived antileukoproteinase (SKALP), also known as elafin. SKALP/elafin was found to be absent in normal human epidermis, but can be induced in vitro and in vivo under hyperproliferative conditions. Here we studied the expression of SKALP/elafin in several types of epidermal tumors (basal cell carcinoma, squamous cell carcinoma, Bowen's disease, actinic keratosis, and keratoacanthoma). Using immunohistochemical staining SKALP/elafin appeared to be differentially expressed in these tumors. Functional measurements of anti-proteinase activity, and Western blotting of tumor extracts confirmed our findings at the histological level. In well differentiated squamous cell carcinoma, SKALP/elafin messenger RNA was demonstrated by non-radioactive in situ hybridization. We conclude that SKALP/elafin is a marker for abnormal or disturbed squamous differentiation. A possible role of SKALP/elafin in the control of tumor cell invasion is discussed.
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SKALP/elafin was found to be absent in normal human epidermis, but can be induced in vitro and in vivo under hyperproliferative conditions. Here we studied the expression of SKALP/elafin in several types of epidermal tumors (basal cell carcinoma, squamous cell carcinoma, Bowen's disease, actinic keratosis, and keratoacanthoma). Using immunohistochemical staining SKALP/elafin appeared to be differentially expressed in these tumors. Functional measurements of anti-proteinase activity, and Western blotting of tumor extracts confirmed our findings at the histological level. In well differentiated squamous cell carcinoma, SKALP/elafin messenger RNA was demonstrated by non-radioactive in situ hybridization. We conclude that SKALP/elafin is a marker for abnormal or disturbed squamous differentiation. 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A possible role of SKALP/elafin in the control of tumor cell invasion is discussed.</description><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Bowen's Disease - chemistry</subject><subject>Bowen's Disease - pathology</subject><subject>Carcinoma, Basal Cell - chemistry</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Carcinoma, Basal Cell - physiopathology</subject><subject>Carcinoma, Squamous Cell - chemistry</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - physiopathology</subject><subject>Dermatology</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Keratoacanthoma - metabolism</subject><subject>Keratoacanthoma - pathology</subject><subject>Medical sciences</subject><subject>Proteinase Inhibitory Proteins, Secretory</subject><subject>Proteins</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - genetics</subject><subject>Serine Proteinase Inhibitors - analysis</subject><subject>Serine Proteinase Inhibitors - genetics</subject><subject>Serine Proteinase Inhibitors - metabolism</subject><subject>Skin - chemistry</subject><subject>Skin - metabolism</subject><subject>Skin - pathology</subject><subject>Skin Diseases - metabolism</subject><subject>Skin Diseases - pathology</subject><subject>Skin Neoplasms - chemistry</subject><subject>Skin Neoplasms - pathology</subject><subject>Skin Neoplasms - physiopathology</subject><subject>Tumors of the skin and soft tissue. 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Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alkemade, HA</creatorcontrib><creatorcontrib>Molhuizen, HO</creatorcontrib><creatorcontrib>van Vlijmen-Willems, IM</creatorcontrib><creatorcontrib>van Haelst, UJ</creatorcontrib><creatorcontrib>Schalkwijk, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alkemade, HA</au><au>Molhuizen, HO</au><au>van Vlijmen-Willems, IM</au><au>van Haelst, UJ</au><au>Schalkwijk, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of SKALP/Elafin in human epidermal tumors</atitle><jtitle>The American journal of pathology</jtitle><addtitle>Am J Pathol</addtitle><date>1993-12-01</date><risdate>1993</risdate><volume>143</volume><issue>6</issue><spage>1679</spage><epage>1687</epage><pages>1679-1687</pages><issn>0002-9440</issn><eissn>1525-2191</eissn><coden>AJPAA4</coden><abstract>Recently we described a new epidermal serine proteinase inhibitor, skin-derived antileukoproteinase (SKALP), also known as elafin. SKALP/elafin was found to be absent in normal human epidermis, but can be induced in vitro and in vivo under hyperproliferative conditions. Here we studied the expression of SKALP/elafin in several types of epidermal tumors (basal cell carcinoma, squamous cell carcinoma, Bowen's disease, actinic keratosis, and keratoacanthoma). Using immunohistochemical staining SKALP/elafin appeared to be differentially expressed in these tumors. Functional measurements of anti-proteinase activity, and Western blotting of tumor extracts confirmed our findings at the histological level. In well differentiated squamous cell carcinoma, SKALP/elafin messenger RNA was demonstrated by non-radioactive in situ hybridization. We conclude that SKALP/elafin is a marker for abnormal or disturbed squamous differentiation. A possible role of SKALP/elafin in the control of tumor cell invasion is discussed.</abstract><cop>Bethesda, MD</cop><pub>ASIP</pub><pmid>8256855</pmid><tpages>9</tpages></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Biological and medical sciences
Blotting, Western
Bowen's Disease - chemistry
Bowen's Disease - pathology
Carcinoma, Basal Cell - chemistry
Carcinoma, Basal Cell - pathology
Carcinoma, Basal Cell - physiopathology
Carcinoma, Squamous Cell - chemistry
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - physiopathology
Dermatology
Electrophoresis, Polyacrylamide Gel
Humans
Immunohistochemistry
In Situ Hybridization
Keratoacanthoma - metabolism
Keratoacanthoma - pathology
Medical sciences
Proteinase Inhibitory Proteins, Secretory
Proteins
RNA, Messenger - analysis
RNA, Messenger - genetics
Serine Proteinase Inhibitors - analysis
Serine Proteinase Inhibitors - genetics
Serine Proteinase Inhibitors - metabolism
Skin - chemistry
Skin - metabolism
Skin - pathology
Skin Diseases - metabolism
Skin Diseases - pathology
Skin Neoplasms - chemistry
Skin Neoplasms - pathology
Skin Neoplasms - physiopathology
Tumors of the skin and soft tissue. Premalignant lesions
title Differential expression of SKALP/Elafin in human epidermal tumors
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