Biologically driven cut-off definition of lymphocyte ratios in metastatic breast cancer and association with exosomal subpopulations and prognosis

基于生物学因素的转移性乳腺癌淋巴细胞比例临界值定义及其与外泌体亚群和预后的关系

阅读:5
作者:Lorenzo Gerratana # ,Debora Basile # ,Barbara Toffoletto ,Michela Bulfoni ,Silvia Zago ,Alessandro Magini ,Marta Lera ,Giacomo Pelizzari ,Pietro Parisse ,Loredana Casalis ,Maria Grazia Vitale ,Valentina Fanotto ,Marta Bonotto ,Federica Caponnetto ,Michele Bartoletti ,Camilla Lisanti ,Alessandro Marco Minisini ,Carla Emiliani ,Carla Di Loreto ,Gianpiero Fasola ,Francesco Curcio ,Antonio Paolo Beltrami ,Daniela Cesselli ,Fabio Puglisi

Abstract

High neutrophil to lymphocyte ratio (NLR) and monocyte to lymphocyte ratio (MLR) are respectively associated with systemic inflammation and immune suppression and have been associated with a poor outcome. Plasmatic exosomes are extracellular vesicles involved in the intercellular communication system that can exert an immunosuppressive function. Aim of this study was to investigate the interplay between the immune system and circulating exosomes in metastatic breast cancer (MBC). A threshold capable to classify patients according to MLR, NLR and PLR, was computed through a receiving operator curve analysis after propensity score matching with a series of female blood donors. Exosomes were isolated from plasma by ExoQuick solution and characterized by flow-cytometry. NLR, MLR, PLR and exosomal subpopulations potentially involved in the pre-metastatic niche were significantly different in MBC patients with respect to controls. MLR was significantly associated with number of sites at the onset of metastatic disease, while high levels of MLR and NLR were found to be associated with poor prognosis. Furthermore, exosomal subpopulations varied according to NLR, MLR, PLR and both were associated with different breast cancer subtypes and sites of distant involvement. This study highlights the nuanced role of immunity in MBC spread, progression and outcome. Moreover, they suggest potential interaction mechanisms between immunity, MBC and the metastatic niche.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。