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Raloxifene inhibits pancreatic adenocarcinoma growth by interfering with ERβ and IL-6/gp130/STAT3 signaling.

Ioannis Pozios | Nina N Seel | Nina A Hering | Lisa Hartmann | Verena Liu | Peter Camaj | Mario H Müller | Lucas D Lee | Christiane J Bruns | Martin E Kreis | Hendrik Seeliger
Cellular oncology (Dordrecht) | 2021

Currently, the exact role of estrogen receptor (ER) signaling in pancreatic cancer is unknown. Recently, we showed that expression of phosphorylated ERβ correlates with a poor prognosis in patients with pancreatic ductal adenocarcinoma (PDAC). Here, we hypothesized that raloxifene, a FDA-approved selective ER modulator (SERM), may suppress PDAC tumor growth by interfering with ERβ signaling. To test this hypothesis, we studied the impact of raloxifene on interleukin-6/glycoprotein-130/signal transducer and activator of transcription-3 (IL-6/gp130/STAT3) signaling.

Pubmed ID: 32940862

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Dako (tool)

RRID:SCR_013530

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