| Literature DB >> 32516590 |
Ying Shen1, Xiaohong Wang2, Junyan Lu3, Martin Salfenmoser4, Naita Maren Wirsik4, Nikolai Schleussner4, Andrea Imle5, Aida Freire Valls6, Praveen Radhakrishnan4, Jie Liang7, Guoliang Wang4, Thomas Muley8, Martin Schneider4, Carmen Ruiz de Almodovar9, Alba Diz-Muñoz10, Thomas Schmidt11.
Abstract
Tumors are influenced by the mechanical properties of their microenvironment. Using patient samples and atomic force microscopy, we found that tissue stiffness is higher in liver metastases than in primary colorectal tumors. Highly activated metastasis-associated fibroblasts increase tissue stiffness, which enhances angiogenesis and anti-angiogenic therapy resistance. Drugs targeting the renin-angiotensin system, normally prescribed to treat hypertension, inhibit fibroblast contraction and extracellular matrix deposition, thereby reducing liver metastases stiffening and increasing the anti-angiogenic effects of bevacizumab. Patients treated with bevacizumab showed prolonged survival when concomitantly treated with renin-angiotensin inhibitors, highlighting the importance of modulating the mechanical microenvironment for therapeutic regimens.Entities:
Keywords: CAFs; MAFs; RAS signaling; anti-angiogenic therapy; atomic force microscopy; bevacizumab; fibroblasts; metastatic colorectal cancer; tissue stiffness
Year: 2020 PMID: 32516590 DOI: 10.1016/j.ccell.2020.05.005
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743