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The potential role of microRNA-31 expression in early colorectal cancer.
Tateishi, Yoko; Okudela, Koji; Mitsui, Hideaki; Umeda, Shigeaki; Suzuki, Takehisa; Kojima, Yoko; Watanabe, Kazuteru; Kawano, Naomi; Endo, Itaru; Ohashi, Kenichi.
Afiliación
  • Tateishi Y; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Okudela K; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Mitsui H; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Umeda S; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Suzuki T; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Kojima Y; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Watanabe K; Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Kawano N; Department of Pathology, Yokohama Minami Kyousai Hospital, Yokohama, Japan.
  • Endo I; Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Ohashi K; Department of Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Pathol Int ; 65(10): 513-8, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26173758
The expression of microRNA-31 (miR-31) has been implicated in the progression of some human malignancies including colorectal cancer. However, the clinical significance of the expression of miR-31 in submucosally invasive (T1) colorectal cancer remains unclear. The aim of the present study was to delineate the relationship between clinicopathological features and the oncogenic modulator miR-31 in submucosally invasive colorectal cancer. We investigated the expression of miR-31 in 50 submucosally invasive colorectal cancer specimens, along with the corresponding non-tumoral mucosa specimens, using a real-time quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The relationships between miR-31 expression levels and clinicopathological characteristics were assessed. The miR-31 host gene locus was investigated using fluorescence in situ hybridization. qRT-PCR revealed that the expression of miR-31 was higher in colorectal cancer tissue than in non-tumoral tissue (P = 0.0002). The up-regulated expression of miR-31 may play an oncogenic role in the early stage of carcinogenesis in colorectal cancers.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Regulación Neoplásica de la Expresión Génica / MicroARNs Tipo de estudio: Diagnostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Pathol Int Asunto de la revista: PATOLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Regulación Neoplásica de la Expresión Génica / MicroARNs Tipo de estudio: Diagnostic_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Pathol Int Asunto de la revista: PATOLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Japón