Netrin G1 Promotes Pancreatic Tumorigenesis through Cancer-Associated Fibroblast–Driven Nutritional Support and Immunosuppression

Ralph Francescone(Fox Chase Cancer Center), Débora B. Vendramini‐Costa(Fox Chase Cancer Center), Janusz Franco‐Barraza(Fox Chase Cancer Center), Jessica Wagner(Fox Chase Cancer Center), Alexander Muir(May Institute), Allison N. Lau(Massachusetts Institute of Technology), Linara Gabitova(Fox Chase Cancer Center), Tatiana Pazina(Fox Chase Cancer Center), Sapna Gupta(Fox Chase Cancer Center), Tiffany Luong(Fox Chase Cancer Center), Dustin Rollins(Fox Chase Cancer Center), Ruchi Malik(Fox Chase Cancer Center), Roshan J. Thapa(Fox Chase Cancer Center), Diana Restifo(Fox Chase Cancer Center), Yan Zhou(Fox Chase Cancer Center), Kathy Q. Cai(Fox Chase Cancer Center), Harvey H. Hensley(Fox Chase Cancer Center), Yinfei Tan(Fox Chase Cancer Center), Warren D. Kruger(Fox Chase Cancer Center), Karthik Devarajan(Fox Chase Cancer Center), Siddharth Balachandran(Fox Chase Cancer Center), Andres J. Klein–Szanto(Fox Chase Cancer Center), Huamin Wang(The University of Texas MD Anderson Cancer Center), Wafik S. El‐Deiry(Fox Chase Cancer Center), Matthew G. Vander Heiden(Dana-Farber Cancer Institute), Suraj Peri(Fox Chase Cancer Center), Kerry S. Campbell(Fox Chase Cancer Center), Igor Astsaturov(Fox Chase Cancer Center), Edna Cukierman(Fox Chase Cancer Center)
Cancer Discovery
October 30, 2020
Cited by 205Open Access
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Abstract

Abstract Pancreatic ductal adenocarcinoma (PDAC) has a poor 5-year survival rate and lacks effective therapeutics. Therefore, it is of paramount importance to identify new targets. Using multiplex data from patient tissue, three-dimensional coculturing in vitro assays, and orthotopic murine models, we identified Netrin G1 (NetG1) as a promoter of PDAC tumorigenesis. We found that NetG1+ cancer-associated fibroblasts (CAF) support PDAC survival, through a NetG1-mediated effect on glutamate/glutamine metabolism. Also, NetG1+ CAFs are intrinsically immunosuppressive and inhibit natural killer cell–mediated killing of tumor cells. These protumor functions are controlled by a signaling circuit downstream of NetG1, which is comprised of AKT/4E-BP1, p38/FRA1, vesicular glutamate transporter 1, and glutamine synthetase. Finally, blocking NetG1 with a neutralizing antibody stunts in vivo tumorigenesis, suggesting NetG1 as potential target in PDAC. Significance: This study demonstrates the feasibility of targeting a fibroblastic protein, NetG1, which can limit PDAC tumorigenesis in vivo by reverting the protumorigenic properties of CAFs. Moreover, inhibition of metabolic proteins in CAFs altered their immunosuppressive capacity, linking metabolism with immunomodulatory function. See related commentary by Sherman, p. 230. This article is highlighted in the In This Issue feature, p. 211


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