Saa3 is a key mediator of the protumorigenic properties of cancer-associated fibroblasts in pancreatic tumors

Magdolna Djurec(Spanish National Cancer Research Centre), Osvaldo Graña‐Castro(Spanish National Cancer Research Centre), Albert Lee(Columbia University Irving Medical Center), Kevin Troulé(Spanish National Cancer Research Centre), Elisa Espinet(German Cancer Research Center), Lavinia Cabras(Spanish National Cancer Research Centre), Carolina Navas(Spanish National Cancer Research Centre), Maria Blasco(Spanish National Cancer Research Centre), Laura Martín-Díaz(Spanish National Cancer Research Centre), Miranda Burdiel(Spanish National Cancer Research Centre), Jing Li(Spanish National Cancer Research Centre), Zhaoqi Liu(Columbia University Irving Medical Center), Mireia Vallespinós(Instituto Ramón y Cajal de Investigación Sanitaria), Francisco Sanchez Bueno(Instituto Murciano de Investigación Biosanitaria), Martin R. Sprick(Heidelberg Institute for Stem Cell Technology and Experimental Medicine), Andreas Trumpp(German Cancer Research Center), Bruno Sáinz(Instituto Ramón y Cajal de Investigación Sanitaria), Fátima Al‐Shahrour(Spanish National Cancer Research Centre), Raúl Rabadán(Columbia University Irving Medical Center), Carmen Guerra(Spanish National Cancer Research Centre), Mariano Barbacid(Spanish National Cancer Research Centre)
Proceedings of the National Academy of Sciences
January 19, 2018
Cited by 176Open Access
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Abstract

Significance Pancreatic ductal adenocarcinoma is one of the most malignant human tumors for which there are no efficacious therapeutic strategies. This tumor type is characterized by an abundant desmoplastic stroma that promotes tumor progression. Yet recent studies have shown that physical or genetic elimination of the stroma leads to more aggressive tumor development. Here, we decided to reprogram the stromal tissue by identifying and subsequently targeting genes responsible for their protumorigenic properties. Comparative transcriptome analysis revealed several genes overexpressed in cancer-associated fibroblasts compared with those present in normal pancreata. We provide genetic evidence that one of these genes, Saa3 , plays a key role on the protumorigenic properties of the stroma, opening the door to the design of future therapeutic strategies.


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