| Literature DB >> 33673405 |
Andreas Domen1,2, Delphine Quatannens1, Sara Zanivan3,4, Christophe Deben1, Jonas Van Audenaerde1, Evelien Smits1, An Wouters1, Filip Lardon1, Geert Roeyen1,5, Yannick Verhoeven1, Annelies Janssens6, Timon Vandamme1,2, Peter van Dam1,7, Marc Peeters1,2, Hans Prenen1,2.
Abstract
Cancer arises from mutations accruing within cancer cells, but the tumor microenvironment (TME) is believed to be a major, often neglected, factor involved in therapy resistance and disease progression. Cancer-associated fibroblasts (CAFs) are prominent and key components of the TME in most types of solid tumors. Extensive research over the past decade revealed their ability to modulate cancer metastasis, angiogenesis, tumor mechanics, immunosuppression, and drug access through synthesis and remodeling of the extracellular matrix and production of growth factors. Thus, they are considered to impede the response to current clinical cancer therapies. Therefore, targeting CAFs to counteract these protumorigenic effects, and overcome the resistance to current therapeutic options, is an appealing and emerging strategy. In this review, we discuss how CAFs affect prognosis and response to clinical therapy and provide an overview of novel therapies involving CAF-targeting agents in lung and pancreatic cancer.Entities:
Keywords: cancer associated fibroblasts; lung cancer; pancreatic cancer; therapy resistance
Year: 2021 PMID: 33673405 DOI: 10.3390/cancers13050987
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639