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Fat Wasting Is Damaging: Role of Adipose Tissue in Cancer-Associated Cachexia.
Sun, Xiaoting; Feng, Xiaogang; Wu, Xiaojing; Lu, Yongtian; Chen, Kaihong; Ye, Ying.
Afiliação
  • Sun X; Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
  • Feng X; Institute of Physiology, University of Zurich, Zurich, Switzerland.
  • Wu X; Department of Cardiology, Shenzhen University General Hospital, Shenzhen, China.
  • Lu Y; Department of ENT, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, China.
  • Chen K; Department of Cardiology, The Affiliated Longyan First Hospital of Fujian Medical University, Longyan, China.
  • Ye Y; Department of Oral Implantology, School and Hospital of Stomatology, Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai, China.
Front Cell Dev Biol ; 8: 33, 2020.
Article em En | MEDLINE | ID: mdl-32117967
ABSTRACT
Loss of body weight, especially loss of adipose tissue and skeletal muscle weight, characterizes cancer-associated cachexia (CAC). Clinically, therapeutic options for CAC are limited due to the complicated signaling between cancer and other organs. Recent research advances show that adipose tissues play a critical role during thermogenesis, glucose homeostasis, insulin sensitivity, and lipid metabolism. Understanding the adipocyte lipolysis, the formation of beige adipocytes, and the activation of brown adipocytes is vital for novel therapies for metabolic syndromes like CAC. The system-level crosstalk between adipose tissue and other organs involves adipocyte lipolysis, white adipose tissue browning, and secreted factors and metabolites. Novel CAC animal models and accumulating molecular signaling knowledge have provided mechanisms that may ultimately be translated into future therapeutic possibilities that benefit CAC patients. This mini review discusses the role of adipose tissue in CAC development, mechanism, and therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China