Discordant expression of desmoglein 2 and 3 at the mRNA and protein levels in nodular and superficial basal cell carcinoma revealed by immunohistochemistry and fluorescent in situ hybridization. (July 2014)
- Record Type:
- Journal Article
- Title:
- Discordant expression of desmoglein 2 and 3 at the mRNA and protein levels in nodular and superficial basal cell carcinoma revealed by immunohistochemistry and fluorescent in situ hybridization. (July 2014)
- Main Title:
- Discordant expression of desmoglein 2 and 3 at the mRNA and protein levels in nodular and superficial basal cell carcinoma revealed by immunohistochemistry and fluorescent in situ hybridization
- Authors:
- Pietkiewicz, P.
Gornowicz‐Porowska, J.
Bowszyc‐Dmochowska, M.
Jagielska, J.
Helak‐Łapaj, C.
Kaczmarek, E.
Dmochowski, M. - Abstract:
- <abstract abstract-type="main" id="ced12355-abs-0001"> <title>Summary</title> <sec id="ced12355-sec-0001" sec-type="section"> <title>Background</title> <p>Basal cell carcinoma (BCC) is the most common human cancer. It is thought that skewed expression of desmogleins (Dsgs) in BCC may promote tumourigenesis.</p> </sec> <sec id="ced12355-sec-0002" sec-type="section"> <title>Aim</title> <p>To comparatively examine expression of Dsg2/Dsg3, using fluorescent <italic>in situ</italic> hybridization (FISH) and immunohistochemistry (IHC) in BCC subtypes.</p> </sec> <sec id="ced12355-sec-0003" sec-type="section"> <title>Methods</title> <p>In total, 84 frozen sections from patients with various clinical or histological subtypes of BCC were analyzed. Expressions of Dsg2/Dsg3 protein and <italic>Dsg2</italic>/<italic>Dsg3</italic> mRNA were evaluated using IHC and FISH, respectively, in BCC nests and BCC‐free epidermis, and then quantitatively measured.</p> </sec> <sec id="ced12355-sec-0004" sec-type="section"> <title>Results</title> <p>There was loss of correlation between Dsg2 and Dsg3 (IHC) in nodular and superficial BCC (nBCC, sBCC), and significant correlation between <italic>Dsg2</italic> and <italic>Dsg3</italic> (FISH) in BCC, but not nBCC and sBCC.</p> </sec> <sec id="ced12355-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Because more prominent aberrations of Dsg2/Dsg3 expression were seen at the protein than at the mRNA level in BCC, these comparative observations<abstract abstract-type="main" id="ced12355-abs-0001"> <title>Summary</title> <sec id="ced12355-sec-0001" sec-type="section"> <title>Background</title> <p>Basal cell carcinoma (BCC) is the most common human cancer. It is thought that skewed expression of desmogleins (Dsgs) in BCC may promote tumourigenesis.</p> </sec> <sec id="ced12355-sec-0002" sec-type="section"> <title>Aim</title> <p>To comparatively examine expression of Dsg2/Dsg3, using fluorescent <italic>in situ</italic> hybridization (FISH) and immunohistochemistry (IHC) in BCC subtypes.</p> </sec> <sec id="ced12355-sec-0003" sec-type="section"> <title>Methods</title> <p>In total, 84 frozen sections from patients with various clinical or histological subtypes of BCC were analyzed. Expressions of Dsg2/Dsg3 protein and <italic>Dsg2</italic>/<italic>Dsg3</italic> mRNA were evaluated using IHC and FISH, respectively, in BCC nests and BCC‐free epidermis, and then quantitatively measured.</p> </sec> <sec id="ced12355-sec-0004" sec-type="section"> <title>Results</title> <p>There was loss of correlation between Dsg2 and Dsg3 (IHC) in nodular and superficial BCC (nBCC, sBCC), and significant correlation between <italic>Dsg2</italic> and <italic>Dsg3</italic> (FISH) in BCC, but not nBCC and sBCC.</p> </sec> <sec id="ced12355-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Because more prominent aberrations of Dsg2/Dsg3 expression were seen at the protein than at the mRNA level in BCC, these comparative observations indicate greater importance of events at the proteome level than those at the genome level in tumour functional compartments. Different Dsg2/Dsg3 expression in sBCC and nBCC might corroborate the possibility that sBCC and nBCC are separate conditions. These results may contribute to better understanding of the biological behaviour of BCC.</p> </sec> </abstract> … (more)
- Is Part Of:
- Clinical and experimental dermatology. Volume 39:Number 5(2014)
- Journal:
- Clinical and experimental dermatology
- Issue:
- Volume 39:Number 5(2014)
- Issue Display:
- Volume 39, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 39
- Issue:
- 5
- Issue Sort Value:
- 2014-0039-0005-0000
- Page Start:
- 628
- Page End:
- 635
- Publication Date:
- 2014-07
- Subjects:
- Skin -- Diseases -- Periodicals
616.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2230 ↗
https://academic.oup.com/ced/issue ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ced.12355 ↗
- Languages:
- English
- ISSNs:
- 0307-6938
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.250000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3473.xml