| Literature DB >> 31187975 |
John D Martin1, Myrofora Panagi2, Chenyu Wang3, Thahomina T Khan1, Margaret R Martin1, Chrysovalantis Voutouri2, Kazuko Toh4, Panagiotis Papageorgis2,5, Fotios Mpekris2, Christiana Polydorou2, Genichiro Ishii6, Shinichiro Takahashi7, Naoto Gotohda7, Toshiyuki Suzuki7, Matthew E Wilhelm3, Vinicio Alejandro Melo4, Sabina Quader4, Jumpei Norimatsu1, Ryan M Lanning8, Motohiro Kojima6, Matthew David Stuber3, Triantafyllos Stylianopoulos2, Kazunori Kataoka4,9, Horacio Cabral1.
Abstract
Dexamethasone is a glucocorticoid steroid with anti-inflammatory properties used to treat many diseases, including cancer, in which it helps manage various side effects of chemo-, radio-, and immunotherapies. Here, we investigate the tumor microenvironment (TME)-normalizing effects of dexamethasone in metastatic murine breast cancer (BC). Dexamethasone normalizes vessels and the extracellular matrix, thereby reducing interstitial fluid pressure, tissue stiffness, and solid stress. In turn, the penetration of 13 and 32 nm dextrans, which represent nanocarriers (NCs), is increased. A mechanistic model of fluid and macromolecule transport in tumors predicts that dexamethasone increases NC penetration by increasing interstitial hydraulic conductivity without significantly reducing the effective pore diameter of the vessel wall. Also, dexamethasone increases the tumor accumulation and efficacy of ∼30 nm polymeric micelles containing cisplatin (CDDP/m) against murine models of primary BC and spontaneous BC lung metastasis, which also feature a TME with abnormal mechanical properties. These results suggest that pretreatment with dexamethasone before NC administration could increase efficacy against primary tumors and metastases.Entities:
Keywords: metastasis; normalization; penetration; polymeric micelle; tumor microenvironment
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Year: 2019 PMID: 31187975 DOI: 10.1021/acsnano.8b07865
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881