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using an LPS-induced RAW 264.7 macrophage model demonstrated that DADS, DMDS, and propyl disulfide (PDS) effectively suppress NO and PGE2 synthesis, thereby limiting LPS-induced inflammatory responses ( in vitro and in vivo studies indicate that OSCs exert their anti-inflammatory effects primarily through the inhibition of NF- B and MAPK signaling pathways, as well as the suppression of inflammatory mediators such as IL-6, IL-10, and TNF-

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External light triggering allows the precise spatiotemporal control of drug release

Besides, Puf-A silencing also suppressed the growth of cancer cells with normal p53, indicating that Puf-A might play a decisive role in regulating tumor cell growth, even when its expression was restricted by p53

44 Another previous study indicated that L

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