| Literature DB >> 33207247 |
Danna M Breen1, Hanna Kim2, Donald Bennett3, Roberto A Calle2, Susie Collins4, Ryan M Esquejo2, Tao He5, Stephanie Joaquim2, Alison Joyce6, Matthew Lambert5, Laura Lin5, Betty Pettersen7, Shuxi Qiao2, Michelle Rossulek2, Gregory Weber5, Zhidan Wu2, Bei B Zhang2, Morris J Birnbaum2.
Abstract
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.Entities:
Keywords: chemotherapy; cisplatin; emesis; growth differentiation factor 15; survival; weight loss
Year: 2020 PMID: 33207247 DOI: 10.1016/j.cmet.2020.10.023
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287