机构:Univ Penn, Med Ctr, Abramson Canc Ctr, Abramson Family Canc Res Inst,Dept Canc Biol, Philadelphia, PA 19104 USA
DeNicola, G
Tuveson, DA
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机构:
Univ Penn, Med Ctr, Abramson Canc Ctr, Abramson Family Canc Res Inst,Dept Canc Biol, Philadelphia, PA 19104 USAUniv Penn, Med Ctr, Abramson Canc Ctr, Abramson Family Canc Res Inst,Dept Canc Biol, Philadelphia, PA 19104 USA
Tuveson, DA
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机构:
[1] Univ Penn, Med Ctr, Abramson Canc Ctr, Abramson Family Canc Res Inst,Dept Canc Biol, Philadelphia, PA 19104 USA
[2] Univ Penn, Med Ctr, Abramson Canc Ctr, Abramson Family Canc Res Inst,Dept Med, Philadelphia, PA 19104 USA
Pancreatic ductal adenocarcinoma (PDA) is arguably the most lethal malignancy in the United States. Despite the identification of many molecular alterations in PDA, this information has not translated into effective therapeutic strategies to date. A recent report in Cancer Cell (Fernandez-Zapico et al, Cancer Cell 2005, 7:39-49) reveals an unexpected role for the hematopoietic-specific RhoGEF VAV1 in pancreatic tumorigenesis, where ectopic expression of VAV1 as a result of promoter demethylation was identified in the I majority of established cell lines and PDA tissue samples. Importantly, VAV1 expression was functionally required for optimal proliferation, transformation and survival of pancreatic cancer cell lines. This study provides the first evidence of VAV1 promoter demethylation as an event in cancer progression, suggesting that aberrant signaling pathways driven by VAV1 are potential therapeutic targets in PDA.