Meerang Mayura, Bérard Karima, Felley-Bosco Emanuela, Lauk Olivia, Vrugt Bart, Boss Andreas, Kenkel David, Broggini-Tenzer Angela, Stahel Rolf A, Arni Stephan, Weder Walter, Opitz Isabelle
Division of Thoracic Surgery, University Hospital Zurich, Zurich, Switzerland.
Laboratory of Molecular Oncology, University Hospital Zurich, Zurich, Switzerland.
Mol Cancer Ther. 2016 May;15(5):1095-105. doi: 10.1158/1535-7163.MCT-15-0583. Epub 2016 Feb 2.
An autocrine-driven upregulation of the Hedgehog (Hh) signaling pathway has been described in malignant pleural mesothelioma (MPM), in which the ligand, desert Hh (DHH), was produced from tumor cells. However, our investigation revealed that the Hh pathway is activated in both tumor and stroma of MPM tumor specimens and an orthotopic immunocompetent rat MPM model. This was demonstrated by positive immunohistochemical staining of Glioma-associated oncogene 1 (GLI1) and Patched1 (PTCH1) in both tumor and stromal fractions. DHH was predominantly expressed in the tumor fractions. To further investigate the role of the Hh pathway in MPM stroma, we antagonized Hh signaling in the rat model of MPM using a Hh antagonist, vismodegib, (100 mg/kg orally). Daily treatment with vismodegib efficiently downregulated Hh target genes Gli1, Hedgehog Interacting Protein (Hhip), and Ptch1, and caused a significant reduction of tumor volume and tumor growth delay. Immunohistochemical analyses revealed that vismodegib treatment primarily downregulated GLI1 and HHIP in the stromal compartment along with a reduced expression of previously described fibroblast Hh-responsive genes such as Fibronectin (Fn1) and Vegfa Primary cells isolated from the rat model cultured in 3% O2 continued to express Dhh but did not respond to vismodegib in vitro However, culture supernatant from these cells stimulated Gli1, Ptch1, and Fn1 expression in mouse embryonic fibroblasts, which was suppressed by vismodegib. Our study provides new evidence regarding the role of Hh signaling in MPM stroma in the maintenance of tumor growth, emphasizing Hh signaling as a treatment target for MPM. Mol Cancer Ther; 15(5); 1095-105. ©2016 AACR.
在恶性胸膜间皮瘤(MPM)中,已发现刺猬信号通路(Hh)存在自分泌驱动的上调,其中配体沙漠刺猬因子(DHH)由肿瘤细胞产生。然而,我们的研究表明,Hh信号通路在MPM肿瘤标本的肿瘤和基质以及原位免疫活性大鼠MPM模型中均被激活。这通过胶质瘤相关癌基因1(GLI1)和patched1(PTCH1)在肿瘤和基质部分的阳性免疫组化染色得以证实。DHH主要在肿瘤部分表达。为进一步研究Hh信号通路在MPM基质中的作用,我们在MPM大鼠模型中使用Hh拮抗剂维莫德吉(100 mg/kg口服)拮抗Hh信号。维莫德吉每日治疗有效下调Hh靶基因Gli1、刺猬因子相互作用蛋白(Hhip)和Ptch1,并导致肿瘤体积显著减小和肿瘤生长延迟。免疫组化分析显示,维莫德吉治疗主要下调基质区室中的GLI1和HHIP,同时降低先前描述的成纤维细胞Hh反应性基因如纤连蛋白(Fn1)和Vegfa的表达。从在3%氧气中培养的大鼠模型分离的原代细胞继续表达Dhh,但在体外对维莫德吉无反应。然而,这些细胞的培养上清液刺激小鼠胚胎成纤维细胞中Gli1、Ptch1和Fn1的表达,而维莫德吉可抑制这种表达。我们的研究为Hh信号在MPM基质维持肿瘤生长中的作用提供了新证据,强调Hh信号作为MPM的治疗靶点。《分子癌症治疗》;15(5);1095 - 105。©2016美国癌症研究协会。