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        <full_title>The Open Dentistry Journal</full_title>
        <abbrev_title>TODENTJ</abbrev_title>
        <issn media_type="print">1874-2106</issn>
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          <month>2</month>
          <day>21</day>
          <year>2008</year>
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          <title>Predictive Role of p53 Protein as a Single Marker or Associated to Ki67 Antigen in Oral Carcinogenesis </title>
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          <person_name contributor_role="author" sequence="first">
            <given_name>L.</given_name>
            <surname>Montebugnoli</surname>
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          <person_name contributor_role="author" sequence="additional">
            <given_name>L.</given_name>
            <surname>Felicetti</surname>
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          <person_name contributor_role="author" sequence="additional">
            <given_name>D.B.</given_name>
            <surname>Gissi</surname>
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          <person_name contributor_role="author" sequence="additional">
            <given_name>F.</given_name>
            <surname>Cervellati</surname>
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          <person_name contributor_role="author" sequence="additional">
            <given_name>D.</given_name>
            <surname>Servidio</surname>
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            <given_name>C.</given_name>
            <surname>Marchetti</surname>
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            <given_name>C.</given_name>
            <surname>Prati</surname>
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            <given_name>F.</given_name>
            <surname>Flamminio</surname>
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            <given_name>M.P.</given_name>
            <surname>Foschini</surname>
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                <jats:p> p53 over-expression has been proposed as a reliable marker associated to oral carcinogenesis, although only about 50% of oral carcinomas (OSCC) are associated with p53 over-expression and even p53-negative lesions can progress to OSCC. The aim of the study was to determine whether the combination of p53 over-expression and p53 low-expression associated with Ki67 over-expression (high Ki67/p53 ratio) could lead to a more sensitive parameter. Immunohistochemical expression of Ki67 and p53 was measured in 54 specimens from OSCC; 27 specimens from moderate/severe epithelial dysplasia; 32 specimens from oral leukoplakias without epithelial dysplasia, and 13 specimens with normal epithelium. p53 over-expression was found in 31 (53%) samples from OSCC, in 10 (37%) samples from severe dysplasias, and in 5 (15%) samples from non-dysplastic lesions, while the combination of high p53 values with high Ki67/p53 ratio was observed in 93% of OSCC, in 81% of dysplastic lesions, and in 50% of non-dysplastic lesions. This parameter may have a clinical implication to detect early lesions with an impairment of p53 pathway, and probably at risk of progress to OSCC.</jats:p>
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