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Regulation of Krüppel-Like Factor 4 (KLF4) expression through the transcription factor Yin-Yang 1 (YY1) in non-Hodgkin B-cell lymphoma.
Morales-Martinez, Mario; Valencia-Hipolito, Alberto; Vega, Gabriel G; Neri, Natividad; Nambo, Maria J; Alvarado, Isabel; Cuadra, Ivonne; Duran-Padilla, Marco A; Martinez-Maza, Otoniel; Huerta-Yepez, Sara; Vega, Mario I.
Afiliación
  • Morales-Martinez M; Molecular Signal Pathway in Cancer Laboratory, UIMEO, Oncology Hospital, Siglo XXI National Medical Center, IMSS, México City, México.
  • Valencia-Hipolito A; Unidad de Posgrado, Facultad de Medicina Universidad Nacional Autónoma de México, México City, México.
  • Vega GG; Molecular Signal Pathway in Cancer Laboratory, UIMEO, Oncology Hospital, Siglo XXI National Medical Center, IMSS, México City, México.
  • Neri N; Molecular Signal Pathway in Cancer Laboratory, UIMEO, Oncology Hospital, Siglo XXI National Medical Center, IMSS, México City, México.
  • Nambo MJ; Unidad de Posgrado, Facultad de Medicina Universidad Nacional Autónoma de México, México City, México.
  • Alvarado I; Department of Hematology, Oncology Hospital, National Medical Center, IMSS, México City, México.
  • Cuadra I; Department of Hematology, Oncology Hospital, National Medical Center, IMSS, México City, México.
  • Duran-Padilla MA; Servicio de Anatomía Patológica, Hospital de Oncología, Centro Médico Nacional Siglo XXI, IMSS, México City, México.
  • Martinez-Maza O; Servicio de Anatomía Patológica, Hospital de Oncología, Centro Médico Nacional Siglo XXI, IMSS, México City, México.
  • Huerta-Yepez S; Servicio de Patología, Hospital General de México "Eduardo Liceaga", Facultad de Medicina de la UNAM, México City, México.
  • Vega MI; Department of Obstetrics and Gynecology, Jonsson Comprehensive Cancer Center, UCLA AIDS Institute, David Geffen School of Medicine, University of California, Los Angeles, California, USA.
Oncotarget ; 10(22): 2173-2188, 2019 Mar 15.
Article en En | MEDLINE | ID: mdl-31040909
Krüppel-Like Factor 4 (KLF4) is a member of the KLF transcription factor family, and evidence suggests that KLF4 is either an oncogene or a tumor suppressor. The regulatory mechanism underlying KLF4 expression in cancer, and specifically in lymphoma, is still not understood. Bioinformatics analysis revealed two YY1 putative binding sites in the KLF4 promoter region (-950 bp and -105 bp). Here, the potential regulation of KLF4 by YY1 in NHL was analyzed. Mutation of the putative YY1 binding sites in a previously reported system containing the KLF4 promoter region and CHIP analysis confirmed that these binding sites are important for KLF4 regulation. B-NHL cell lines showed that both KLF4 and YY1 are co-expressed, and transfection with siRNA-YY1 resulted in significant inhibition of KLF4. The clinical implications of YY1 in the transcriptional regulation of KLF4 were investigated by IHC in a TMA with 43 samples of subtypes DLBCL and FL, and all tumor tissues expressing YY1 demonstrated a correlation with KLF4 expression, which was consistent with bioinformatics analyses in several databases. Our findings demonstrated that KLF4 can be transcriptionally regulated by YY1 in B-NHL, and a correlation between YY1 expression and KLF4 was found in clinical samples. Hence, both YY1 and KLF4 may be possible therapeutic biomarkers of NHL.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncotarget Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Oncotarget Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos