双siRNA精准靶向弥漫性胸膜间皮瘤的合成致死脆弱性

Diffuse pleural mesothelioma (DPM) remains a lethal malignancy with limited benefit from existing therapies, underscoring the urgent need for molecularly precise treatments that act directly at the disease interface. Previously, we identified WEE1 and PKMYT1 as consistently overexpressed in DPM and demonstrated that their combined inhibition induces synthetic lethality. Here, we evaluate a dual-siRNA therapeutic strategy targeting this kinase pair and position it within a platform engineered for localized RNA delivery. Across three DPM subtypes (epithelioid, sarcomatoid, and biphasic), siRNA constructs achieved robust knockdown of WEE1 and PKMYT1, with >70% reduction in mRNA levels at 48-96 h post-transfection. Single-gene silencing induced only modest reductions in cell viability, with >70-80% survival across most lines relative to controls. In contrast, combined WEE1/PKMYT1 knockdown consistently elicited a marked decrease in viability, ranging from 60% to 85% depending on the cell line (p < 0.001). Cell-cycle analysis revealed that dual knockdown, unlike individual siRNAs, induced significant G2/M arrest accompanied by a depletion of S-phase cells, indicating disruption of DNA damage checkpoints. Flow cytometry demonstrated a 3- to 5-fold increase in apoptotic cell fractions compared with single knockdowns and controls (p < 0.0001), confirming synergistic induction of programmed cell death. These data show that although individual siRNAs exert limited effects, their combination produces robust anti-proliferative, pro-apoptotic, and cell-cycle disruptive phenotypes consistent with synthetic lethality. Collectively, these data validate dual-siRNA synthetic lethality as a promising therapeutic approach for DPM and underscore the potential of a nanoparticle-hydrogel delivery system that we have developed for precise, localized RNA therapy. This work paves the way for RNA nanomedicine in mesothelioma and other anatomically restricted, treatment-refractory cancers.