白细胞介素-6 家族细胞因子在癌症恶病质中的作用

Samet Agca, Serkan Kir
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摘要

恶病质是一种消耗性综合征,半数以上的癌症患者都会出现这种症状。癌症相关恶病质对患者的生存和生活质量有负面影响。癌症相关恶病质的特征是脂肪和骨骼肌组织的快速流失,而这部分是由炎性细胞因子介导的。在此,我们探究了白细胞介素-6(IL-6)家族细胞因子(包括 IL-6、白血病抑制因子和 oncostatin M)在癌症恶病质发展过程中的关键作用。研究表明,这些细胞因子会促进脂肪和肌肉组织的消耗,激活促进脂肪分解和蛋白质分解的机制,从而加剧恶病质。IL-6 家族细胞因子的重叠效应依赖于破伤风激酶/信号转导和转录激活因子 3 信号转导。我们认为,单独阻断这些细胞因子通路可能会因冗余而失败,未来的治疗方法应针对共同的下游元素,以产生有效的临床效果。
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The role of interleukin-6 family cytokines in cancer cachexia

Cachexia is a wasting syndrome that manifests in more than half of all cancer patients. Cancer-associated cachexia negatively influences the survival of patients and their quality of life. It is characterized by a rapid loss of adipose and skeletal muscle tissues, which is partly mediated by inflammatory cytokines. Here, we explored the crucial roles of interleukin-6 (IL-6) family cytokines, including IL-6, leukemia inhibitory factor, and oncostatin M, in the development of cancer cachexia. These cytokines have been shown to exacerbate cachexia by promoting the wasting of adipose and muscle tissues, activating mechanisms that enhance lipolysis and proteolysis. Overlapping effects of the IL-6 family cytokines depend on janus kinase/signal transducer and activator of transcription 3 signaling. We argue that the blockade of these cytokine pathways individually may fail due to redundancy and future therapeutic approaches should target common downstream elements to yield effective clinical outcomes.

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