厌食症
化疗
减肥
内科学
癌症
医学
内分泌学
肿瘤科
免疫学
肥胖
作者
Danna M. Breen,Hanna Kim,Donald Bennett,Roberto A. Calle,Susie M. Collins,Ryan M. Esquejo,Tao He,Stephanie Joaquim,Alison Joyce,Matthew Lambert,Laura Lin,Betty Pettersen,Shuxi Qiao,Michelle I. Rossulek,Gregory L. Weber,Zhidan Wu,Bei B. Zhang,Morris J. Birnbaum
出处
期刊:Cell Metabolism
[Elsevier]
日期:2020-11-17
卷期号:32 (6): 938-950.e6
被引量:117
标识
DOI:10.1016/j.cmet.2020.10.023
摘要
Platinum-based cancer therapy is restricted by dose-limiting side effects and is associated with elevation of growth differentiation factor 15 (GDF-15). But whether this elevation contributes to such side effects has been unclear. Here, we explored the effects of GDF-15 blockade on platinum-based chemotherapy-induced emesis, anorexia, and weight loss in mice and/or nonhuman primate models. We found that circulating GDF-15 is higher in subjects with cancer receiving platinum-based chemotherapy and is positively associated with weight loss in colorectal cancer (NCT00609622). Further, chemotherapy agents associated with high clinical emetic score induce circulating GDF-15 and weight loss in mice. Platinum-based treatment-induced anorexia and weight loss are attenuated in GDF-15 knockout mice, while GDF-15 neutralization with the monoclonal antibody mAB1 improves survival. In nonhuman primates, mAB1 treatment attenuates anorexia and emesis. These results suggest that GDF-15 neutralization is a potential therapeutic approach to alleviate chemotherapy-induced side effects and improve the quality of life.
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