Gu Jichun, Saiyin Hexige, Fu Deliang, Li Ji
Pancreas. 2018 Apr;47(4):382-389. doi: 10.1097/MPA.0000000000001023.
Pancreatic cancer is a uniformly lethal malignancy with an abundant dense desmoplastic stroma. Because of its dense stroma, conventional drugs were considered to not penetrate this physical barrier, and this caused a systemic drug resistance. Thus, abolishing this barrier with targeted agents is considered to improve the efficiency of chemotherapeutic treatment. The Hedgehog (Hh) signaling pathway is a critical regulator of pancreas development and plays diversified roles in pancreatic cancer stroma and neoplastic cells. Increasing Hh expression in neoplastic cells added desmoplastic stroma accumulation in orthotopic tumors, and Hh inhibitors that target the stroma have an ability to prolong the overall survival of Pdx-1-Cre/KrasG12D/p53R172H mice models via deleting the stromal components and increasing vascularity in pancreatic tumor. However, the failure of translation from bench to bedside indicate the complexity of the relationship between Hh signaling and desmoplastic stroma, and more insights into the complex relationships between Hh signaling pathway and stroma, even tumor cells, might help redesign Hh-targeted therapy. In this review, we discuss the possible mechanism of translation of Hh inhibitor in the clinic from pathology to molecular mechanism.
胰腺癌是一种致死率极高的恶性肿瘤,伴有大量致密的促纤维增生性基质。由于其基质致密,传统药物被认为无法穿透这一物理屏障,从而导致全身耐药。因此,使用靶向药物消除这一屏障被认为可以提高化疗效果。刺猬信号通路(Hh)是胰腺发育的关键调节因子,在胰腺癌基质和肿瘤细胞中发挥多种作用。肿瘤细胞中Hh表达的增加会使原位肿瘤中促纤维增生性基质积累增多,而靶向基质的Hh抑制剂能够通过去除基质成分和增加胰腺肿瘤的血管生成,延长Pdx-1-Cre/KrasG12D/p53R172H小鼠模型的总生存期。然而,从实验室到临床的转化失败表明Hh信号与促纤维增生性基质之间关系复杂,更深入了解Hh信号通路与基质甚至肿瘤细胞之间的复杂关系,可能有助于重新设计针对Hh的治疗方法。在这篇综述中,我们从病理学到分子机制探讨了Hh抑制剂在临床中转化的可能机制。