Translating whole‐genome doubling into precision medicine in cancer

Whole-genome doubling (WGD) occurs in approximately 30-40% of human cancers, representing a transformative evolutionary event that fundamentally reshapes tumor biology. WGD triggers chromosomal instability (CIN) and somatic copy-number alterations (SCNAs), which accelerate tumor evolution and underlie aggressive clinical behavior. Paradoxically, the same cellular stresses that drive tumor progression also force WGD-positive cells into a heightened dependence on specific survival mechanisms, meaning that poor prognosis and therapeutic vulnerability arise from the same underlying phenomenon. Despite the widespread occurrence and clinical impact of WGD, translating its biology into actionable therapeutic strategies remains limited due to the lack of prospective evidence and integrated biomarker frameworks. This review provides a comprehensive overview of WGD biology, from mechanisms to clinical applications, examining how WGD arises and drives tumor evolution, its prevalence and prognostic impact across cancer types, and the emerging therapeutic vulnerabilities that WGD-positive tumors expose.