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Roles of SHARP1 in thyroid cancer.
Zhou, Zun-Hai; Wang, Bo; Cheng, Xiao-Bing; Zhang, Xuan-E; Tang, Jian; Tang, Wen-Jia; Gu, Lei.
Afiliação
  • Zhou ZH; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
  • Wang B; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
  • Cheng XB; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
  • Zhang XE; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
  • Tang J; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
  • Tang WJ; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
  • Gu L; Department of Endocrinology, Yangpu Hospital, Shanghai Tongji University School of Medicine, Shanghai 200090, P.R. China.
Mol Med Rep ; 13(6): 5365-71, 2016 Jun.
Article em En | MEDLINE | ID: mdl-27121679
SHARP1 is a basic helix­loop­helix transcription factor involved in various cellular processes, including proliferation and differentiation. The present study assessed the role of SHARP1 in the progression and invasion of thyroid cancer. PCR and western blot analysis demonstrated that in thyroid cancer tissues, SHARP1 was significantly downregulated at the mRNA and protein level compared with that in normal tissues. Furthermore, SHARP1 was downregulated in the TT and TPC­1 thyroid cancer cell lines compared with a normal thyroid cell line, while it was upregulated in other thyroid cancer cell lines. Overexpression of SHARP1 in TT and TPC­1 cells significantly inhibited the cell viability, migration and invasion in vitro. Furthermore, the protein and mRNA levels of HIF­1α were found to be decreased in TT and TPC­1 cells following forced overexpression of SHARP1. In addition, silencing of HIF­1α reduced the viability, migration and invasion of TT and TPC-1 cells. In conclusion, the present study indicated that SHARP1 acts as a tumor suppressor in thyroid cancer and that its downregulation may contribute to the proliferation, migration and invasion of thyroid cancer cells through mechanisms possibly involving HIF­1α, suggesting that SHARP1 may be an important therapeutic target for the treatment of thyroid cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide / Movimento Celular / Proteínas Supressoras de Tumor / Fatores de Transcrição Hélice-Alça-Hélice Básicos Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Med Rep Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Glândula Tireoide / Movimento Celular / Proteínas Supressoras de Tumor / Fatores de Transcrição Hélice-Alça-Hélice Básicos Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Med Rep Ano de publicação: 2016 Tipo de documento: Article