dc.contributorTorres-Reyes, L.A., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Alvarado-Ruiz, L., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Piña-Sánchez, P., Laboratorio de Oncología Genómica, Unidad de Investigación Médica en Enfermedades Oncológicas, Centro Médico Nacional Siglo XXI-IMSS, Mexico; Martínez-Silva, M.G., Servicio de Patología, Centro Médico Nacional de Occidente-IMSSGuadalajara, Jalisco, Mexico; Ramos-Solano, M., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de GuadalajaraGuadalajara, Jalisco, Mexico; Olimón-Andalón, V., Escuela de Biología, Universidad Autónoma de Sinaloa. CuliacánSinaloa, Mexico; Ortiz-Lazareno, P.C., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico; Hernández-Flores, G., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico; Bravo-Cuellar, A., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico; Aguilar-Lemarroy, A., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico; Jave-Suarez, L.F., División de Inmunología, Centro de Investigación Biomédica de Occidente (CIBO), Instituto Mexicano del Seguro Social (IMSS)Guadalajara, Jalisco, Mexico
dc.creatorTorres-Reyes, L.A.
dc.creatorAlvarado-Ruiz, L.
dc.creatorPina-Sanchez, P.
dc.creatorMartinez-Silva, M.G.
dc.creatorRamos-Solano, M.
dc.creatorOlimon-Andalon, V.
dc.creatorOrtiz-Lazareno, P.C.
dc.creatorHernandez-Flores, G.
dc.creatorBravo-Cuellar, A.
dc.creatorAguilar-Lemarroy, A.
dc.creatorJave-Suarez, L.F.
dc.date.accessioned2015-11-19T18:49:45Z
dc.date.accessioned2022-11-02T17:06:34Z
dc.date.available2015-11-19T18:49:45Z
dc.date.available2022-11-02T17:06:34Z
dc.date.created2015-11-19T18:49:45Z
dc.date.issued2014
dc.identifierhttp://hdl.handle.net/20.500.12104/64785
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84919493948&partnerID=40&md5=897fc80c9537b8653fa8c8e500ce464f
dc.identifierhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=prem&AN=25550776
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5024762
dc.description.abstractThe transcription factor grainyhead-like 2 (GRHL2) is evolutionarily conserved in many different species, and is involved in morphogenesis, epithelial differentiation, and the control of the epithelial-mesenchymal transition. It has also recently been implicated in carcinogenesis, but its role in this remains controversial. Expression of GRHL2 has not previously been reported in cervical cancer, so the present study aimed to characterize GRHL2 expression in cervical cancer-derived cell lines (CCCLs) and cervical tissues with different grades of lesions. Microarray analysis found that the expression of 58 genes was down-regulated in CCCLs compared to HaCaT cells (non-tumorigenic human epithelial cell line). The expression of eight of these genes was validated by quantitative real-time PCR (qPCR), and GRHL2 was found to be the most down-regulated. Western blot assays corroborated that GRHL2 protein levels were strongly down-regulated in CCCLs. Cervical cells from women without cervical lesions were shown to express GRHL2, while immunohistochemistry found that positivity to GRHL2 decreased in cervical cancer tissues. In conclusion, a loss or strong reduction in GRHL2 expression appears to be a characteristic of cervical cancer, suggesting that GRHL2 down-regulation is a necessary step during cervical carcinogenesis. However, further studies are needed to delineate the role of GRHL2 in cervical cancer and during malignant progression.
dc.relationInternational Journal of Clinical and Experimental Pathology
dc.relation7
dc.relation11
dc.relation7409
dc.relation7418
dc.relationScopus
dc.relationMEDLINE
dc.relationWOS
dc.titleExpression of transcription factor grainyhead-like 2 is diminished in cervical cancer
dc.typeArticle


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