White adipose tissue IFN-γ expression and signalling along the progression of rodent cancer cachexia

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Data

2017-01-01

Autores

Yamashita, Alex Shimura
das Neves, Rodrigo Xavier
Rosa-Neto, José Cesar
Lira, Fábio dos Santos [UNESP]
Batista, Miguel Luís
Alcantara, Paulo Sérgio
Otoch, José Pinhata
Seelaender, Marília

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Resumo

Cachexia is associated with increased morbidity and mortality in cancer. The White adipose tissue (WAT) synthesizes and releases several pro-inflammatory cytokines that play a role in cancer cachexia-related systemic inflammation. IFN-γ is a pleiotropic cytokine that regulates several immune and metabolic functions. To assess whether IFN-γ signalling in different WAT pads is modified along cancer-cachexia progression, we evaluated IFN-γ receptors expression (IFNGR1 and IFNGR2) and IFN-γ protein expression in a rodent model of cachexia (7, 10, and 14 days after tumour implantation). IFN-γ protein expression was heterogeneously modulated in WAT, with increases in the mesenteric pad and decreased levels in the retroperitoneal depot along cachexia progression. Ifngr1 was up-regulated 7 days after tumour cell injection in mesenteric and epididymal WAT, but the retroperitoneal depot showed reduced Ifngr1 gene expression. Ifngr2 gene expression was increased 7 and 14 days after tumour inoculation in mesenteric WAT. The results provide evidence that changes in IFN-γ expression and signalling may be perceived at stages preceding refractory cachexia, and therefore, might be employed as a means to assess the early stage of the syndrome.

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Palavras-chave

Cancer-cachexia, Interferon-γ signalling, White adipose tissue

Como citar

Cytokine, v. 89, p. 122-126.

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