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基质细胞起到抑制而非支持胰腺导管腺癌的作用。

Stromal elements act to restrain, rather than support, pancreatic ductal adenocarcinoma.

机构信息

Division of Gastroenterology, Department of Internal Medicine and Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Gastroenterology Division, Department of Medicine and Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Division of Hematology and Oncology, Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY 10032, USA.

出版信息

Cancer Cell. 2014 Jun 16;25(6):735-47. doi: 10.1016/j.ccr.2014.04.021. Epub 2014 May 22.

Abstract

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.

摘要

声波刺猬(Shh)是胰腺导管腺癌(PDAC)中肿瘤细胞过度表达的可溶性配体,它驱动富含成纤维细胞的纤维母细胞性间质的形成。为了更好地了解其在恶性进展中的作用,我们在 PDAC 的明确定义的小鼠模型中删除了 Shh。正如所预测的那样,Shh 缺陷型肿瘤的基质含量减少。令人惊讶的是,这些肿瘤更具侵袭性,表现出未分化的组织学特征,血管生成增加,增殖活性增强——这些特征在接受 Smoothened 抑制剂治疗的对照小鼠中得到了完全再现。此外,VEGFR 阻断抗体的给药选择性地改善了 Shh 缺陷型肿瘤的存活,表明 Hedgehog 驱动的基质通过抑制肿瘤血管生成在一定程度上抑制肿瘤生长。总之,这些数据表明,肿瘤基质的某些成分可以抑制肿瘤生长。

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