<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1870-199X</journal-id>
<journal-title><![CDATA[Revista odontológica mexicana]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Odont. Mex]]></abbrev-journal-title>
<issn>1870-199X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional Autónoma de México, Facultad de Odontología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1870-199X2026000100024</article-id>
<article-id pub-id-type="doi">10.22201/fo.1870199xp.2026.30.1.94334</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Biomarcadores y carcinoma oral de células escamosas. Una actualización]]></article-title>
<article-title xml:lang="en"><![CDATA[Biomarkers and Oral Squamous Cell Carcinoma. An Update]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gaitán-Salvatella]]></surname>
<given-names><![CDATA[Íñigo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rivera-Reza]]></surname>
<given-names><![CDATA[Diana Ivette]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gaitán-Cepeda]]></surname>
<given-names><![CDATA[Luis Alberto]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Cardenal Herrera-CEU Escuela de Ciencias de la Salud Departmento de Farmacia]]></institution>
<addr-line><![CDATA[Valencia ]]></addr-line>
<country>Spain</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Nacional Autónoma de México División de Estudios de Posgrado e Investigación. Facultad de Odontología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad Nacional Autónoma de México Facultad de Odontología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2026</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2026</year>
</pub-date>
<volume>30</volume>
<numero>1</numero>
<fpage>24</fpage>
<lpage>34</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1870-199X2026000100024&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1870-199X2026000100024&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1870-199X2026000100024&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El carcinoma oral de células escamosas (COCE) es un problema de salud pública, constituye la neoplasia maligna predominante de la cavidad oral. El cáncer oral se asocia con altas tasas de mortalidad y una morbilidad considerable, lo que afecta profundamente la calidad de vida de los pacientes. La identificación y el uso de biomarcadores fiables, como &#945;-SMA, E-cadherina, N-cadherina, CEA, EGF, CK19 o p53, se han vuelto cruciales para la detección precoz, el diagnóstico preciso y la vigilancia eficaz de la progresión y la recurrencia de la enfermedad. Por lo tanto, la presente revisión tiene como objetivo proporcionar un análisis exhaustivo de los biomarcadores utilizados en el diagnóstico del COCE, abarcando sus diversas aplicaciones, tipos, mecanismos de acción y su uso en la investigación relacionada con el COCE. Se realizó una búsqueda sistemática en bases de datos electrónicas MEDLINE (PubMed), y Web of Science abarcando el periodo del 1 de enero de 2015 al 30 de diciembre de 2024. La estrategia de investigación fue la siguiente (&#945;-SMA) AND ((epidermoid carcinoma) OR ((Oral cancer) AND (oral squamous cell carcinoma))); para cada uno de los biomarcadores seleccionados (actina alfa del músculo liso, E-cadherina, N-cadherina, antígeno carcinoembrionario, receptor del factor de crecimiento epidérmico, citoqueratina 19, p53, Ki-67). El uso simultáneo de múltiples biomarcadores podría proporcionar una comprensión más completa de la enfermedad, lo que permitiría un diagnóstico, un pronóstico y un tratamiento más precisos y específicos, mejorando, en última instancia, los resultados de los pacientes y el manejo clínico del COCE. Este enfoque puede ayudar a los médicos e investigadores a comprender mejor la complejidad del COCE, lo que les permitirá desarrollar estrategias más eficaces para la detección precoz, la monitorización de la enfermedad y las intervenciones terapéuticas personalizadas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Oral squamous cell carcinoma (OSCC) is a public health problem and the most common malignant neoplasm of the oral cavity. Oral cancer is associated with high mortality rates and considerable morbidity, which profoundly affects patients&#8217; quality of life. The identification and use of reliable biomarkers, such as &#945;-SMA, E-cadherin, N-cadherin, CEA, EGF, CK19, or p53, have become crucial for early detection, accurate diagnosis, and effective monitoring of disease progression and recurrence. Therefore, the present review aims to provide a comprehensive analysis of biomarkers used in the diagnosis of OSCC, covering their various applications, types, mechanisms of action, and use in OSCC-related research. A systematic search was performed in the MEDLINE (PubMed) and Web of Science electronic databases covering from January 1, 2015, to December 30, 2024. The search strategy was as follows: (&#945;-SMA) AND ((epidermoid carcinoma) OR ((oral cancer) AND (oral squamous cell carcinoma))); for each of the selected biomarkers (alpha smooth muscle actin, E-cadherin, N-cadherin, carcinoembryonic antigen, epidermal growth factor receptor, cytokeratin 19, p53, Ki-67). The simultaneous use of multiple biomarkers could provide a more comprehensive understanding of the disease, enabling more accurate and specific diagnosis, prognosis, and treatment, ultimately improving patient outcomes and the clinical management of OSCC. This approach may help clinicians and researchers better understand the complexity of OSCC, enabling them to develop more effective strategies for early detection, disease monitoring, and personalized therapeutic interventions.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Biomarcadores]]></kwd>
<kwd lng="es"><![CDATA[Cáncer oral]]></kwd>
<kwd lng="es"><![CDATA[Carcinoma oral de células escamosas]]></kwd>
<kwd lng="es"><![CDATA[&#945;-SMA]]></kwd>
<kwd lng="es"><![CDATA[E-cadherina]]></kwd>
<kwd lng="es"><![CDATA[N-cadherina]]></kwd>
<kwd lng="es"><![CDATA[antígeno carcinoembrionario]]></kwd>
<kwd lng="es"><![CDATA[receptor del factor de crecimiento epidérmico]]></kwd>
<kwd lng="es"><![CDATA[citoqueratina 19]]></kwd>
<kwd lng="es"><![CDATA[p53]]></kwd>
<kwd lng="es"><![CDATA[Ki-67]]></kwd>
<kwd lng="en"><![CDATA[Biomarkers]]></kwd>
<kwd lng="en"><![CDATA[Oral cancer]]></kwd>
<kwd lng="en"><![CDATA[Oral squamous cell Carcinoma]]></kwd>
<kwd lng="en"><![CDATA[&#945;-SMA]]></kwd>
<kwd lng="en"><![CDATA[E-cadherina]]></kwd>
<kwd lng="en"><![CDATA[N-cadherina]]></kwd>
<kwd lng="en"><![CDATA[carcinoembryonic antigen]]></kwd>
<kwd lng="en"><![CDATA[epidermal growth factor receptor]]></kwd>
<kwd lng="en"><![CDATA[Citokeratin 19]]></kwd>
<kwd lng="en"><![CDATA[p53]]></kwd>
<kwd lng="en"><![CDATA[Ki-67.]]></kwd>
</kwd-group>
</article-meta>
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