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The phrase "dual signaling pathways in tumor development" describes a phenomenon in cancer biology where key cell signaling pathways (such as TGF-β, Hippo/YAP, Wnt/β-catenin, and others) can exert context-dependent effects—acting as tumor suppressors in early cancer stages but promoting tumor progression, invasion, or metastasis at later stages through complex pathway crosstalk and regulatory mechanisms. This is not a molecular entity, receptor, protein, or gene, and thus cannot serve as a specific therapeutic target, biomarker, or drug target in itself[1][2][3].
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