基质
间质细胞
平滑
音猬因子
癌症研究
刺猬
生物
腺癌
胰腺癌
刺猬信号通路
血管生成
医学
肿瘤进展
胰腺
病理
癌症
免疫组织化学
内分泌学
细胞生物学
免疫学
信号转导
遗传学
作者
Andrew D. Rhim,Paul E. Oberstein,Dafydd Thomas,Emily T. Mirek,Carmine F. Palermo,Stephen A. Sastra,Erin N. Dekleva,Tyler Saunders,Claudia P. Becerra,Ian Tattersall,C. Benedikt Westphalen,Jan Kitajewski,Maite G. Fernández‐Barrena,Martín E. Fernández-Zapico,Christine A. Iacobuzio–Donahue,Kenneth P. Olive,Ben Z. Stanger
出处
期刊:Cancer Cell
[Cell Press]
日期:2014-05-22
卷期号:25 (6): 735-747
被引量:1866
标识
DOI:10.1016/j.ccr.2014.04.021
摘要
Sonic hedgehog (Shh), a soluble ligand overexpressed by neoplastic cells in pancreatic ductal adenocarcinoma (PDAC), drives formation of a fibroblast-rich desmoplastic stroma. To better understand its role in malignant progression, we deleted Shh in a well-defined mouse model of PDAC. As predicted, Shh-deficient tumors had reduced stromal content. Surprisingly, such tumors were more aggressive and exhibited undifferentiated histology, increased vascularity, and heightened proliferation--features that were fully recapitulated in control mice treated with a Smoothened inhibitor. Furthermore, administration of VEGFR blocking antibody selectively improved survival of Shh-deficient tumors, indicating that Hedgehog-driven stroma suppresses tumor growth in part by restraining tumor angiogenesis. Together, these data demonstrate that some components of the tumor stroma can act to restrain tumor growth.
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