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Effect of EI24 expression on the tumorigenesis of ApcMin/+ colorectal cancer mouse model.
Nam, Tae Wook; Park, Song Yi; Lee, Jae Hoon; Roh, Jae Il; Lee, Han-Woong.
  • Nam TW; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
  • Park SY; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
  • Lee JH; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
  • Roh JI; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
  • Lee HW; Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea. Electronic address: hwl@yonsei.ac.kr.
Biochem Biophys Res Commun ; 514(4): 1087-1092, 2019 07 05.
Article en En | MEDLINE | ID: mdl-31097220
Etoposide-induced 2.4 kb transcript (EI24, also known as PIG8) is a p53 target gene involved in cell growth suppression and apoptosis and known to be frequently altered in human cancers. Although EI24 expression is decreased in various cancers and is associated with colorectal cancer progression and metastasis, the physiological function of EI24 in colorectal cancer is yet unclear. We generated an Ei24 conditional transgenic (Tg) mouse to study the therapeutic effects of Ei24 in vivo and evaluated whether Ei24 plays a role of a tumor suppressor using Ei24 Tg mouse crossed with ApcMin/+ mouse, which develops multiple intestinal adenomas. The overexpression of Ei24 failed to cause any notable difference in the number of polyps, lengths of the intestine and spleen, and survival rate between ApcMin/+ and ApcMin/+Ei24 Tg mice. Ei24 plays no significant role in colon cancer caused by the substitutional mutation of Apc in mice. Therefore, our result dismisses the hypothesized direct link between ApcMin/+ mutation and Ei24 expression in colorectal cancer model.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Nucleares / Neoplasias Colorrectales / Proteína de la Poliposis Adenomatosa del Colon / Modelos Animales de Enfermedad / Proteínas Reguladoras de la Apoptosis Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Nucleares / Neoplasias Colorrectales / Proteína de la Poliposis Adenomatosa del Colon / Modelos Animales de Enfermedad / Proteínas Reguladoras de la Apoptosis Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Año: 2019 Tipo del documento: Article