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ADAMTS8 Inhibits Progression of Esophageal Squamous Cell Carcinoma.
Wu, Zhonglin; Shi, Yanjun; Ren, Shuguang; Ju, Yingchao; Hu, Yueyang; Wu, Jianhua.
Afiliação
  • Wu Z; Department of Radiology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
  • Shi Y; Department of Out-patient, The Fourth Hospital of Hengshui, Hengshui, People's Republic of China.
  • Ren S; Animal Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
  • Ju Y; Animal Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
  • Hu Y; Animal Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
  • Wu J; Animal Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
DNA Cell Biol ; 2020 Oct 15.
Article em En | MEDLINE | ID: mdl-33054388
ABSTRACT
A disintegrin and metallopeptidase with thrombospondin motifs (ADAMTSs), which is frequently dysregulated in cancers and is involved in carcinogenesis and cancer progression. The present study identified that ADAMTS8 expression is downregulated in esophageal squamous cell carcinoma (ESCC) tissues when compared with nontumor tissue. The expression of ADAMTS8 is closely associated with clinical stage and lymph node metastasis in patients with ESCC. Furthermore, functional studies have shown that ADAMTS8 overexpression could reduce abilities of proliferation, migration, and invasion and promote apoptosis of ESCC cells. Meanwhile, monocyte chemotactic protein-1 and interleukin-6 are markedly deregulated by ADAMTS8 overexpression. Consistently, in vivo data showed that ADAMTS8 overexpression led to a reduction in tumor growth. These results indicate that altering ADAMTS8 expression could modify the outcomes of ESCC by inhibiting cell proliferation and invasion, while promoting the apoptosis of ECSS cells. Thus, ADAMTS8 represents a potential therapeutic target for ESCC therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: DNA Cell Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: DNA Cell Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article