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Regardless of molecular subtyping, breast cancer stem cells significantly contribute to tumor heterogeneity, distant dissemination, and therapeutic resistance. The Hippo pathway is a key regulator of organogenesis and tissue development, and its deregulation is common in breast cancer and linked to cancer stem cell features across several cancer types. Dysfunctional pathway activity leads to the aberrant activation of Hippo downstream effectors, the Yes\u2010associated protein (YAP) and its paralog transcriptional co\u2010activator with PDZ\u2010binding motif (TAZ), which promote epithelial\u2010to\u2010mesenchymal transition, growth factor\u2010independent proliferation, and maintenance of the breast cancer stem cells' niche. This review summarizes the regulation of the Hippo pathway, emphasizing its significant role in coordinating stemness\u2010related mechanisms in breast cancer. An overview of how the Hippo pathway fuels stemness in triple\u2010negative breast cancer, the most aggressive BC subtype, is then provided. 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