The Hedgehog signaling pathway is overexpressed in a variety of cancers, leading to hyperactivation of target genes in Hh responding cells.1 In a number of cancers, the responding cells are stromal fibroblasts that are found near Hh ligand-expressing epithelial cells.2-5 This paracrine mechanism is one of many cell-cell interactions that take place between epithelial and mesenchymal cells. Through its role as a master regulator of other transcription factors, Hh pathway activation can have extremely potent effects on cell proliferation, behavior and survival. In pancreatic ductal adenocarcinoma (PDA), paracrine signaling from neoplastic epithelial cells to fibroblasts controls the development and maintenance of stromal desmoplasia, a very prominent feature of these tumors.4-7 We previously found that stromal desmoplasia in PDA contributes to primary chemoresistance by interfering with drug delivery.7 Inhibiting the Hh pathway with a targeted inhibitor of Smoothened (Smo) depleted the stroma from pancreatic tumors arising in a genetically engineered mouse model. This had the effect of facilitating drug delivery to the tumor parenchyma, ultimately aiding in their treatment and leading to prolonged survival. However, the precise molecular mechanisms by which Smo inhibitors target desmoplasia is unclear. To learn more about how Smo inhibitors affect stromal cells, we will examine the functional and molecular consequence of Smo inhibition in a genetically engineered mouse model of PDA. We will perform ChIP-SEQ for the downstream transcription factor Gli2 on pancreatic tumor tissues and compare the results to changes in global gene expression induced by Smo inhibition, providing insight into the differentially regulated genes whose promoters are bound by Gli transcription factors. Another effect of Smo inhibition in pancreatic tumors is the restoration of tissue vascularization, which is oddly low in pancreatic cancer. This paradoxical result is at odds with the known roles of the Hh pathway during angiogenesis. We hypothesize that angiogenesis occurs after Smo inhibition due to the relief of an anti- angiogenic signal provided by fibroblasts. We will test this by using hedgehog-independent means of depleting the stroma, and by examining several possible stroma-mediated mechanisms using tissues derived from genetically engineered mice. These experiments will leverage our expertise in mouse modeling, preclinical therapeutics and molecular biology to determine the basic mechanisms of Smo inhibition in pancreatic cancer and other systems employing paracrine Hh signaling. Currently, 25 different clinical trials have been initiated to investigate Smo inhibitors in 9 different cancers, including PDA. The experiments proposed here will aid our understanding of their results and assist in the design of future trials. More generally, we will learn about the relationship between epithelial and mesenchymal cells and the pathways that promote stromal desmoplasia in cancer.
The goal of this proposal is to learn how a new class of anticancer agent works at the molecular level. Smoothened inhibitors have recently entered clinical trials for 9 different types of cancer, including pancreatic cancer. This proposal uses preclinical trials in pancreatic cancer to better understand the effects of Smoothened inhibitors.
|Olive, Kenneth P (2017) Fanning the Flames of Cancer Chemoresistance: Inflammation and Anticancer Therapy. J Oncol Pract 13:181-183|
|Harmsen, Stefan; Huang, Ruimin; Wall, Matthew A et al. (2015) Surface-enhanced resonance Raman scattering nanostars for high-precision cancer imaging. Sci Transl Med 7:271ra7|
|Olive, Kenneth P (2015) Stroma, Stroma Everywhere (Far More Than You Think). Clin Cancer Res 21:3366-8|
|Olive, Kenneth P; Politi, Katerina (2014) Translational therapeutics in genetically engineered mouse models of cancer. Cold Spring Harb Protoc 2014:131-43|
|Delgiorno, Kathleen E; Hall, Jason C; Takeuchi, Kenneth K et al. (2014) Identification and manipulation of biliary metaplasia in pancreatic tumors. Gastroenterology 146:233-44.e5|
|Holmstrom, Sam R; Olive, Kenneth P (2014) Protein breakdown precedes pancreatic tumor development. Nat Med 20:1097-9|
|Sastra, Stephen A; Olive, Kenneth P (2014) Acquisition of mouse tumor biopsies through abdominal laparotomy. Cold Spring Harb Protoc 2014:47-56|
|Rhim, Andrew D; Oberstein, Paul E; Thomas, Dafydd H et al. (2014) Stromal elements act to restrain, rather than support, pancreatic ductal adenocarcinoma. Cancer Cell 25:735-47|
|Sastra, Stephen A; Olive, Kenneth P (2013) Quantification of murine pancreatic tumors by high-resolution ultrasound. Methods Mol Biol 980:249-66|
|Westphalen, Christoph Benedikt; Olive, Kenneth P (2012) Genetically engineered mouse models of pancreatic cancer. Cancer J 18:502-10|