Coriell Institute for Medical Research, 403 Haddon Ave, Camden, NJ, 08103, USA.
Coriell Institute for Medical Research, 403 Haddon Ave, Camden, NJ, 08103, USA; MD Anderson Cancer Center at Cooper, Cooper University Hospital, 2 Cooper Plaza, Camden, NJ, 08103, USA; Departments of Surgery and Biomedical Sciences, Cooper Medical School of Rowan University, 401 Broadway, Camden, NJ, 08103, USA.
Cancer Lett. 2024 Nov 1;604:217244. doi: 10.1016/j.canlet.2024.217244. Epub 2024 Sep 10.
Cancer-associated fibroblasts (CAFs) are activated fibroblasts that play a role in numerous malignant phenotypes, including hyperproliferation, invasion, and metastasis. These phenotypes correlate with activity of the Hippo pathway oncoprotein, Yes-associated protein-1 (YAP1), and its paralog, transcriptional coactivator with PDZ-binding motif (TAZ). YAP1/TAZ are normally involved in organ growth, under the regulation of various kinases and upon phosphorylation, are retained in the cytoplasm by chaperone proteins, leading to their proteasomal degradation. In CAFs and tumor cells, however, a lack of YAP1 phosphorylation results in its translocation to the nucleus, binding to TEAD transcription factors, and activation of mitogenic pathways. In this review we summarize the literature discussing the central role of YAP1 in CAF activation, the upstream cues that promote YAP1-mediated CAF activation and extracellular matrix remodeling, and how CAFs mediate tumor-stroma crosstalk to support progression, invasion and metastasis in various cancer models. We further highlight YAP1CAFs functions in modulating an immunosuppressive tumor microenvironment and propose evaluation of several YAP1 targets regarding their role in regulating intra-tumoral immune landscapes. Finally, we propose that co-administration of YAP1- targeted therapies with immune checkpoint inhibitors can improve therapeutic outcomes in patients with advanced tumors.
癌症相关成纤维细胞 (CAFs) 是一种激活的成纤维细胞,在多种恶性表型中发挥作用,包括过度增殖、侵袭和转移。这些表型与 Hippo 通路致癌蛋白 Yes 相关蛋白-1 (YAP1) 及其同源物转录共激活因子 PDZ 结合基序 (TAZ) 的活性相关。YAP1/TAZ 通常参与器官生长,受多种激酶的调节,磷酸化后,伴侣蛋白将其保留在细胞质中,导致其被蛋白酶体降解。然而,在 CAFs 和肿瘤细胞中,YAP1 磷酸化的缺乏导致其易位到细胞核,与 TEAD 转录因子结合,并激活有丝分裂途径。在这篇综述中,我们总结了文献中讨论的 YAP1 在 CAF 激活中的核心作用、促进 YAP1 介导的 CAF 激活和细胞外基质重塑的上游信号,以及 CAFs 如何介导肿瘤-基质相互作用,以支持各种癌症模型中的进展、侵袭和转移。我们进一步强调了 YAP1CAFs 在调节免疫抑制性肿瘤微环境中的功能,并提出了评估几个 YAP1 靶点在调节肿瘤内免疫景观中的作用。最后,我们提出联合使用 YAP1 靶向治疗与免疫检查点抑制剂可以改善晚期肿瘤患者的治疗效果。