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理解转移性进展背景下的恶病质。

Understanding cachexia in the context of metastatic progression.

机构信息

Institute for Cancer Genetics, Department of Pathology and Cell Biology, Columbia University, New York, NY, USA.

Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.

出版信息

Nat Rev Cancer. 2020 May;20(5):274-284. doi: 10.1038/s41568-020-0251-4. Epub 2020 Mar 31.

Abstract

Tumours reprogram host physiology, metabolism and immune responses during cancer progression. The release of soluble factors, exosomes and metabolites from tumours leads to systemic changes in distant organs, where cancer cells metastasize and grow. These tumour-derived circulating factors also profoundly impact tissues that are rarely inhabited by metastatic cancer cells such as skeletal muscle and adipose tissue. In fact, the majority of patients with metastatic cancer develop a debilitating muscle-wasting syndrome, known as cachexia, that is associated with decreased tolerance to antineoplastic therapy, poor prognosis and accelerated death, with no approved treatments. In this Perspective, we discuss the development of cachexia in the context of metastatic progression. We briefly discuss how circulating factors either directly or indirectly promote cachexia development and examine how signals from the metastatic process can trigger and amplify this process. Finally, we highlight promising therapeutic opportunities for targeting cachexia in the context of metastatic cancers.

摘要

肿瘤在癌症进展过程中重新编程宿主的生理、代谢和免疫反应。肿瘤释放的可溶性因子、外泌体和代谢物导致远处器官发生系统性变化,癌细胞在这些器官转移和生长。这些源自肿瘤的循环因子也会深刻影响转移性癌细胞很少存在的组织,如骨骼肌和脂肪组织。事实上,大多数转移性癌症患者都会患上一种使人虚弱的肌肉消耗综合征,即恶病质,这与对抗肿瘤治疗的耐受性降低、预后不良和加速死亡有关,目前尚无批准的治疗方法。在本观点中,我们将讨论转移性进展背景下恶病质的发生。我们简要讨论了循环因子如何直接或间接地促进恶病质的发生,并研究了转移性过程中的信号如何引发和放大这一过程。最后,我们强调了针对转移性癌症恶病质的有前景的治疗机会。

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