CD133 Role in Oral Carcinogenesis
to investigate CD133 immunoexpression, cancer stem cells marker, in oral epithelial dysplasias (OEDs) and oral squamous cells carcinomas (OSCCs) and understandits possible involvement in the malignant transformation process of these lesions and to better elucidate their biological behavior. Tissue s...
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Veröffentlicht in: | Asian Pacific Journal of Cancer Prevention 2020-09, Vol.21 (9), p.2501-2506 |
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container_title | Asian Pacific Journal of Cancer Prevention |
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creator | Luna, Ealber Carvalho Macedo Bezerra, Thâmara Manoela Marinho Barros Silva, Paulo Goberlânio De Cavalcante, Roberta Barroso Costa, Fábio Wildson Gurgel Alves, Ana Paula Negreiros Nunes Chaves, Filipe Nobre Pereira, Karuza Maria Alves |
description | to investigate CD133 immunoexpression, cancer stem cells marker, in oral epithelial dysplasias (OEDs) and oral squamous cells carcinomas (OSCCs) and understandits possible involvement in the malignant transformation process of these lesions and to better elucidate their biological behavior.
Tissue samples of 15 cases of OSCCs and 15 OEDs were subjected to CD133 antibody immunohistochemistry reactions. The analysis used quantitative parameters (number of immunostained cells regardless of immunostaining sublocations).
All samples of OSCCs and OEDs showed positive immunostaining, with no significant difference between these groups (p = 0.283). We did not observe statistical difference between the degree of dysplasia and the amount of CD133+ cells (p = 0.899). CD133 immunoexpression showed no association with the OEDs and OSCCs sites. It was observed that nuclear and cytoplasmic immunostaining was more evident with the progression of the malignant process.
It is suggested that the CD133 cellular localization together with the histopathological criteria of OEDs classification can contribute to provide more concrete indications about the oral carcinogenesis process. |
doi_str_mv | 10.31557/APJCP.2020.21.9.2501 |
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Tissue samples of 15 cases of OSCCs and 15 OEDs were subjected to CD133 antibody immunohistochemistry reactions. The analysis used quantitative parameters (number of immunostained cells regardless of immunostaining sublocations).
All samples of OSCCs and OEDs showed positive immunostaining, with no significant difference between these groups (p = 0.283). We did not observe statistical difference between the degree of dysplasia and the amount of CD133+ cells (p = 0.899). CD133 immunoexpression showed no association with the OEDs and OSCCs sites. It was observed that nuclear and cytoplasmic immunostaining was more evident with the progression of the malignant process.
It is suggested that the CD133 cellular localization together with the histopathological criteria of OEDs classification can contribute to provide more concrete indications about the oral carcinogenesis process.</description><identifier>ISSN: 2476-762X</identifier><identifier>ISSN: 1513-7368</identifier><identifier>EISSN: 2476-762X</identifier><identifier>DOI: 10.31557/APJCP.2020.21.9.2501</identifier><identifier>PMID: 32986345</identifier><language>eng</language><publisher>Thailand: West Asia Organization for Cancer Prevention</publisher><ispartof>Asian Pacific Journal of Cancer Prevention, 2020-09, Vol.21 (9), p.2501-2506</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3261-ff32e5883150d73392842b338bb569e0001dbb80912d43e80869c0c805f69ad73</citedby><orcidid>0000-0002-3262-3347 ; 0000-0002-2880-6466 ; 0000-0002-2435-7106 ; 0000-0001-6345-8156 ; 0000-0002-1513-9027</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779460/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7779460/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32986345$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luna, Ealber Carvalho Macedo</creatorcontrib><creatorcontrib>Bezerra, Thâmara Manoela Marinho</creatorcontrib><creatorcontrib>Barros Silva, Paulo Goberlânio De</creatorcontrib><creatorcontrib>Cavalcante, Roberta Barroso</creatorcontrib><creatorcontrib>Costa, Fábio Wildson Gurgel</creatorcontrib><creatorcontrib>Alves, Ana Paula Negreiros Nunes</creatorcontrib><creatorcontrib>Chaves, Filipe Nobre</creatorcontrib><creatorcontrib>Pereira, Karuza Maria Alves</creatorcontrib><title>CD133 Role in Oral Carcinogenesis</title><title>Asian Pacific Journal of Cancer Prevention</title><addtitle>Asian Pac J Cancer Prev</addtitle><description>to investigate CD133 immunoexpression, cancer stem cells marker, in oral epithelial dysplasias (OEDs) and oral squamous cells carcinomas (OSCCs) and understandits possible involvement in the malignant transformation process of these lesions and to better elucidate their biological behavior.
Tissue samples of 15 cases of OSCCs and 15 OEDs were subjected to CD133 antibody immunohistochemistry reactions. The analysis used quantitative parameters (number of immunostained cells regardless of immunostaining sublocations).
All samples of OSCCs and OEDs showed positive immunostaining, with no significant difference between these groups (p = 0.283). We did not observe statistical difference between the degree of dysplasia and the amount of CD133+ cells (p = 0.899). CD133 immunoexpression showed no association with the OEDs and OSCCs sites. It was observed that nuclear and cytoplasmic immunostaining was more evident with the progression of the malignant process.
It is suggested that the CD133 cellular localization together with the histopathological criteria of OEDs classification can contribute to provide more concrete indications about the oral carcinogenesis process.</description><issn>2476-762X</issn><issn>1513-7368</issn><issn>2476-762X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVkNtKw0AQhhdRbK0-ghIfIHF2Jnu6EUrqkUKLKHi35LCpkTQpWRV8e9NWS72ageH75-dj7JxDRFwIdTWePybzCAEhQh6ZCAXwAzbEWMlQSXw93NsH7MT7d4BYaCWO2YDQaEmxGLLLZMKJgqe2dkHVBLMurYMk7fKqaReucb7yp-yoTGvvzn7niL3c3jwn9-F0dveQjKdhTih5WJaETmjdl4NCERnUMWZEOsuENA4AeJFlGgzHIianQUuTQ65BlNKkPTFi19vc1We2dEXumo--jF111TLtvm2bVvb_pane7KL9skopE0voA8Q2IO9a7ztX7lgOduPMbpzZtTOL3Bq7dtZzF_uPd9SfJPoBY5BmFQ</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Luna, Ealber Carvalho Macedo</creator><creator>Bezerra, Thâmara Manoela Marinho</creator><creator>Barros Silva, Paulo Goberlânio De</creator><creator>Cavalcante, Roberta Barroso</creator><creator>Costa, Fábio Wildson Gurgel</creator><creator>Alves, Ana Paula Negreiros Nunes</creator><creator>Chaves, Filipe Nobre</creator><creator>Pereira, Karuza Maria Alves</creator><general>West Asia Organization for Cancer Prevention</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3262-3347</orcidid><orcidid>https://orcid.org/0000-0002-2880-6466</orcidid><orcidid>https://orcid.org/0000-0002-2435-7106</orcidid><orcidid>https://orcid.org/0000-0001-6345-8156</orcidid><orcidid>https://orcid.org/0000-0002-1513-9027</orcidid></search><sort><creationdate>20200901</creationdate><title>CD133 Role in Oral Carcinogenesis</title><author>Luna, Ealber Carvalho Macedo ; Bezerra, Thâmara Manoela Marinho ; Barros Silva, Paulo Goberlânio De ; Cavalcante, Roberta Barroso ; Costa, Fábio Wildson Gurgel ; Alves, Ana Paula Negreiros Nunes ; Chaves, Filipe Nobre ; Pereira, Karuza Maria Alves</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3261-ff32e5883150d73392842b338bb569e0001dbb80912d43e80869c0c805f69ad73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luna, Ealber Carvalho Macedo</creatorcontrib><creatorcontrib>Bezerra, Thâmara Manoela Marinho</creatorcontrib><creatorcontrib>Barros Silva, Paulo Goberlânio De</creatorcontrib><creatorcontrib>Cavalcante, Roberta Barroso</creatorcontrib><creatorcontrib>Costa, Fábio Wildson Gurgel</creatorcontrib><creatorcontrib>Alves, Ana Paula Negreiros Nunes</creatorcontrib><creatorcontrib>Chaves, Filipe Nobre</creatorcontrib><creatorcontrib>Pereira, Karuza Maria Alves</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Asian Pacific Journal of Cancer Prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luna, Ealber Carvalho Macedo</au><au>Bezerra, Thâmara Manoela Marinho</au><au>Barros Silva, Paulo Goberlânio De</au><au>Cavalcante, Roberta Barroso</au><au>Costa, Fábio Wildson Gurgel</au><au>Alves, Ana Paula Negreiros Nunes</au><au>Chaves, Filipe Nobre</au><au>Pereira, Karuza Maria Alves</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD133 Role in Oral Carcinogenesis</atitle><jtitle>Asian Pacific Journal of Cancer Prevention</jtitle><addtitle>Asian Pac J Cancer Prev</addtitle><date>2020-09-01</date><risdate>2020</risdate><volume>21</volume><issue>9</issue><spage>2501</spage><epage>2506</epage><pages>2501-2506</pages><issn>2476-762X</issn><issn>1513-7368</issn><eissn>2476-762X</eissn><abstract>to investigate CD133 immunoexpression, cancer stem cells marker, in oral epithelial dysplasias (OEDs) and oral squamous cells carcinomas (OSCCs) and understandits possible involvement in the malignant transformation process of these lesions and to better elucidate their biological behavior.
Tissue samples of 15 cases of OSCCs and 15 OEDs were subjected to CD133 antibody immunohistochemistry reactions. The analysis used quantitative parameters (number of immunostained cells regardless of immunostaining sublocations).
All samples of OSCCs and OEDs showed positive immunostaining, with no significant difference between these groups (p = 0.283). We did not observe statistical difference between the degree of dysplasia and the amount of CD133+ cells (p = 0.899). CD133 immunoexpression showed no association with the OEDs and OSCCs sites. It was observed that nuclear and cytoplasmic immunostaining was more evident with the progression of the malignant process.
It is suggested that the CD133 cellular localization together with the histopathological criteria of OEDs classification can contribute to provide more concrete indications about the oral carcinogenesis process.</abstract><cop>Thailand</cop><pub>West Asia Organization for Cancer Prevention</pub><pmid>32986345</pmid><doi>10.31557/APJCP.2020.21.9.2501</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-3262-3347</orcidid><orcidid>https://orcid.org/0000-0002-2880-6466</orcidid><orcidid>https://orcid.org/0000-0002-2435-7106</orcidid><orcidid>https://orcid.org/0000-0001-6345-8156</orcidid><orcidid>https://orcid.org/0000-0002-1513-9027</orcidid><oa>free_for_read</oa></addata></record> |
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title | CD133 Role in Oral Carcinogenesis |
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