Domen Andreas, Quatannens Delphine, Zanivan Sara, Deben Christophe, Van Audenaerde Jonas, Smits Evelien, Wouters An, Lardon Filip, Roeyen Geert, Verhoeven Yannick, Janssens Annelies, Vandamme Timon, van Dam Peter, Peeters Marc, Prenen Hans
Center for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp, B2610 Antwerp, Belgium.
Department of Oncology, Antwerp University Hospital (UZA), 2650 Edegem, Belgium.
Cancers (Basel). 2021 Feb 27;13(5):987. doi: 10.3390/cancers13050987.
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.
癌症源于癌细胞内积累的突变,但肿瘤微环境(TME)被认为是参与治疗耐药性和疾病进展的一个主要且常被忽视的因素。在大多数实体瘤类型中,癌症相关成纤维细胞(CAF)是TME的突出且关键的组成部分。过去十年的广泛研究揭示了它们通过合成和重塑细胞外基质以及产生生长因子来调节癌症转移、血管生成、肿瘤力学、免疫抑制和药物可达性的能力。因此,它们被认为会阻碍对当前临床癌症治疗的反应。所以,靶向CAF以抵消这些促肿瘤作用,并克服对当前治疗方案的耐药性,是一种有吸引力的新兴策略。在这篇综述中,我们讨论了CAF如何影响预后和对临床治疗的反应,并概述了涉及靶向CAF药物的肺癌和胰腺癌新疗法。