Abstract
DPC4/SMAD4 mutations are associated with aggressive pancreatic cancer. In this issue of Cell, Whittle et al. demonstrate that Runx3 expression combined with Dpc4/Smad4 status can predict the metastatic propensity of pancreatic tumors, providing valuable guidance for personalized therapy for patients with pancreatic cancer.
Original language | English (US) |
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Pages (from-to) | 1245-1246 |
Number of pages | 2 |
Journal | Cell |
Volume | 161 |
Issue number | 6 |
DOIs | |
State | Published - 2015 |
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology