The
technology of aggregation-induced emission (AIE) presents a
promising avenue for fluorescence imaging-guided photodynamic cancer
therapy. However, existing near-infrared AIE photosensitizers (PSs)
frequently encounter limitations, including tedious synthesis, poor
tumor retention, and a limited understanding of the underlying molecular
biology mechanism. Herein, an effective molecular design paradigm
of anion−π+ interaction combined with the
inherently crowded conformation that could enhance fluorescence efficacy
and reactive oxygen species generation was proposed through a concise
synthetic method. Mechanistically, upon photosensitization, the Hippo
signaling pathway contributes to the death of melanoma cells and promotes
the nuclear location of its downstream factor, yes-associated protein,
which regulates the transcription and expression of apoptosis-related
genes. The finding in this study would trigger the development of
high-performance and versatile AIE PSs for precision cancer therapy
based on a definite regulatory mechanism.