Increased chondroitin sulphate proteoglycan expression (B5 immunoreactivity) in metastases of uveal melanoma

Background: Metastatic uveal melanoma has a poor prognosis and limited therapeutic options. Proteoglycans are involved in tumor cell invasion and metastatic behavior. The mAbB5 stains a chondroitin sulphate proteoglycan (CSPG) on cutaneous melanoma cells. Here, we compare the B5-staining of CSPG in...

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Veröffentlicht in:Annals of oncology 2006-12, Vol.17 (12), p.1830-1834
Hauptverfasser: Kiewe, P, Bechrakis, NE, Schmittel, A, Ruf, P, Lindhofer, H, Thiel, E, Nagorsen, D
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container_end_page 1834
container_issue 12
container_start_page 1830
container_title Annals of oncology
container_volume 17
creator Kiewe, P
Bechrakis, NE
Schmittel, A
Ruf, P
Lindhofer, H
Thiel, E
Nagorsen, D
description Background: Metastatic uveal melanoma has a poor prognosis and limited therapeutic options. Proteoglycans are involved in tumor cell invasion and metastatic behavior. The mAbB5 stains a chondroitin sulphate proteoglycan (CSPG) on cutaneous melanoma cells. Here, we compare the B5-staining of CSPG in primaries and metastases of uveal melanoma. Material and methods: Immunohistopathological staining was performed in 15 cutaneous and 39 uveal melanoma samples. A score for intracellular and surface staining was established. B5 staining was compared in primaries and metastases of uveal melanoma using Student's t-test. Results: Eight of 11 (73%) uveal melanoma metastases were positive for B5-staining whereas only 5 of 28 (18%) primary uveal melanoma samples were B5-positive (P < 0.001). Nine of 15 cutaneous melanoma samples (60%) were B5-positive without significant difference between primary and metastatic lesions. Surface staining was found both on uveal melanoma metastases and cutaneous melanomas. Conclusions: CSPG was expressed significantly more often in metastases than in primaries of uveal melanoma. It potentially may be one factor associated with metastatic spread. Further studies are needed to determine its use as prognostic factor. The mAbB5 may also be a promising tool for immunotherapy due to its strong staining of CSPG on the surface of cutaneous and metastatic uveal melanoma cells.
doi_str_mv 10.1093/annonc/mdl305
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Proteoglycans are involved in tumor cell invasion and metastatic behavior. The mAbB5 stains a chondroitin sulphate proteoglycan (CSPG) on cutaneous melanoma cells. Here, we compare the B5-staining of CSPG in primaries and metastases of uveal melanoma. Material and methods: Immunohistopathological staining was performed in 15 cutaneous and 39 uveal melanoma samples. A score for intracellular and surface staining was established. B5 staining was compared in primaries and metastases of uveal melanoma using Student's t-test. Results: Eight of 11 (73%) uveal melanoma metastases were positive for B5-staining whereas only 5 of 28 (18%) primary uveal melanoma samples were B5-positive (P &lt; 0.001). Nine of 15 cutaneous melanoma samples (60%) were B5-positive without significant difference between primary and metastatic lesions. Surface staining was found both on uveal melanoma metastases and cutaneous melanomas. Conclusions: CSPG was expressed significantly more often in metastases than in primaries of uveal melanoma. It potentially may be one factor associated with metastatic spread. Further studies are needed to determine its use as prognostic factor. The mAbB5 may also be a promising tool for immunotherapy due to its strong staining of CSPG on the surface of cutaneous and metastatic uveal melanoma cells.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1093/annonc/mdl305</identifier><identifier>PMID: 16971663</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Antineoplastic agents ; Biological and medical sciences ; Chondroitin Sulfate Proteoglycans - metabolism ; chondroitin sulphate proteoglycan ; Dermatology ; Humans ; Immunohistochemistry ; immunotherapy ; Medical sciences ; Melanoma - metabolism ; Melanoma - pathology ; Neoplasm Metastasis ; ocular melanoma ; Ophthalmology ; Pharmacology. Drug treatments ; Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus ; Tumors of the skin and soft tissue. 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Proteoglycans are involved in tumor cell invasion and metastatic behavior. The mAbB5 stains a chondroitin sulphate proteoglycan (CSPG) on cutaneous melanoma cells. Here, we compare the B5-staining of CSPG in primaries and metastases of uveal melanoma. Material and methods: Immunohistopathological staining was performed in 15 cutaneous and 39 uveal melanoma samples. A score for intracellular and surface staining was established. B5 staining was compared in primaries and metastases of uveal melanoma using Student's t-test. Results: Eight of 11 (73%) uveal melanoma metastases were positive for B5-staining whereas only 5 of 28 (18%) primary uveal melanoma samples were B5-positive (P &lt; 0.001). Nine of 15 cutaneous melanoma samples (60%) were B5-positive without significant difference between primary and metastatic lesions. Surface staining was found both on uveal melanoma metastases and cutaneous melanomas. Conclusions: CSPG was expressed significantly more often in metastases than in primaries of uveal melanoma. It potentially may be one factor associated with metastatic spread. Further studies are needed to determine its use as prognostic factor. The mAbB5 may also be a promising tool for immunotherapy due to its strong staining of CSPG on the surface of cutaneous and metastatic uveal melanoma cells.</description><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Chondroitin Sulfate Proteoglycans - metabolism</subject><subject>chondroitin sulphate proteoglycan</subject><subject>Dermatology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>immunotherapy</subject><subject>Medical sciences</subject><subject>Melanoma - metabolism</subject><subject>Melanoma - pathology</subject><subject>Neoplasm Metastasis</subject><subject>ocular melanoma</subject><subject>Ophthalmology</subject><subject>Pharmacology. Drug treatments</subject><subject>Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</subject><subject>Tumors of the skin and soft tissue. 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Drug treatments</topic><topic>Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><topic>uveal melanoma</topic><topic>Uveal Neoplasms - metabolism</topic><topic>Uveal Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kiewe, P</creatorcontrib><creatorcontrib>Bechrakis, NE</creatorcontrib><creatorcontrib>Schmittel, A</creatorcontrib><creatorcontrib>Ruf, P</creatorcontrib><creatorcontrib>Lindhofer, H</creatorcontrib><creatorcontrib>Thiel, E</creatorcontrib><creatorcontrib>Nagorsen, D</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kiewe, P</au><au>Bechrakis, NE</au><au>Schmittel, A</au><au>Ruf, P</au><au>Lindhofer, H</au><au>Thiel, E</au><au>Nagorsen, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased chondroitin sulphate proteoglycan expression (B5 immunoreactivity) in metastases of uveal melanoma</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>17</volume><issue>12</issue><spage>1830</spage><epage>1834</epage><pages>1830-1834</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>Background: Metastatic uveal melanoma has a poor prognosis and limited therapeutic options. 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subjects Antineoplastic agents
Biological and medical sciences
Chondroitin Sulfate Proteoglycans - metabolism
chondroitin sulphate proteoglycan
Dermatology
Humans
Immunohistochemistry
immunotherapy
Medical sciences
Melanoma - metabolism
Melanoma - pathology
Neoplasm Metastasis
ocular melanoma
Ophthalmology
Pharmacology. Drug treatments
Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus
Tumors of the skin and soft tissue. Premalignant lesions
uveal melanoma
Uveal Neoplasms - metabolism
Uveal Neoplasms - pathology
title Increased chondroitin sulphate proteoglycan expression (B5 immunoreactivity) in metastases of uveal melanoma
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