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MicroRNAs, TGF-ß signaling, and the inflammatory microenvironment in cancer.
Guo, Lingling; Zhang, Yongsheng; Zhang, Lifeng; Huang, Fengbo; Li, Jinfan; Wang, Shouli.
Afiliação
  • Guo L; Department of Pathology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, 215123, China.
  • Zhang Y; Department of Pathology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, China.
  • Zhang L; Department of Surgery, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
  • Huang F; Department of Pathology, The Second Affiliated Hospital of Zhejiang University, Hangzhou, 310009, China.
  • Li J; Department of Pathology, The Second Affiliated Hospital of Zhejiang University, Hangzhou, 310009, China.
  • Wang S; Department of Pathology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, 215123, China. wangsoly112@hotmail.com.
Tumour Biol ; 37(1): 115-25, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26563372
Inflammatory cells and mediators form a major part of the tumor microenvironment and play important roles in the regulation of cancer initiation, tumor cell proliferation, and metastasis. MicroRNAs (miRNAs) play important roles in several physiological and pathological processes, including the regulation of the inflammatory microenvironment in cancer. Transforming growth factor-ß (TGF-ß) is an inflammation-related cytokine that functions in both tumor suppression and promotion; however, its underlying molecular mechanisms remain unclear. Recent evidence indicates an association between miRNAs and TGF-ß signaling, providing new insight into the nature of the inflammatory microenvironment in cancer. The present review is an overview of the interaction between miRNAs and inflammatory cytokines, with emphasis on the cross talk between TGF-ß signaling and miRNAs and their influence on cancer cell behavior. The emerging roles of miRNAs in cancer-related inflammation and the potential to target miRNA signaling pathways for cancer therapy are also discussed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Fator de Crescimento Transformador beta / MicroRNAs / Microambiente Tumoral / Neoplasias Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Fator de Crescimento Transformador beta / MicroRNAs / Microambiente Tumoral / Neoplasias Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China