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Ovarian cancer (OC) is one of the most common types of cancer in women with a high mortality rate, and the treatment of OC is prone to high recurrence rates and side effects. Scutellaria baicalensis (SB) is a herbal medicine with good anti-cancer activity, and several studies have shown that SB and its flavonoids have some anti-OC properties. This paper elucidated the common pathogenesis of OC, including cell proliferation and cell cycle regulation, cell invasion and metastasis, apoptosis and autophagy, drug resistance and angiogenesis. The mechanisms of SB and its flavonoids, wogonin, baicalein, baicalin, Oroxylin A, and scutellarein, in the treatment of OC, are revealed, such as wogonin inhibits proliferation, induces apoptosis, inhibits invasion and metastasis, and increases the cytotoxicity of the drug. Baicalein also inhibits vascular endothelial growth factor (VEGF) expression etc. Analyzing their advantages and disadvantages in treating OC provides a new perspective on the role of SB and its flavonoids in OC treatment. It serves as a resource for future OC research and development. [ABSTRACT FROM AUTHOR]

Biomass‐derived pyrogenic carbon is attractive for advanced oxidation processes (AOPs); however, its amorphous structure limits its activation efficiency. Graphene with highly conjugated π structure possesses superior electron transport ability and thus high usefulness. However, bygone strategies are scarcely effective for reforming pyrogenic carbon to graphene. Herein, for the first time, a state‐of‐the‐art flash Joule heating (FJH) technique is showcased for reforming pyrogenic carbon to 2–5‐layer graphene. FJH current‐induced ultrahigh temperature and stress field realize instantaneous (≈10 s) regeneration of pyrogenic carbon via synchronization actions of carbonization, graphitization, and exfoliation. Meanwhile, volatilization of doped N atoms accelerates graphitization but has less of an effect on graphene configuration. Accordingly, tuned oxygen groups at the graphene edge boost peroxydisulfate (PDS) adsorption for finer initiating activation. Subsequently, 2D graphene with excellent electron utilization rate strengthens hydroxyl radical and direct electron transfer pathways in activating PDS for sulfamethoxazole (SMX) degradation. Impressively, the SMX degradation efficiency by fabricated graphene raises ≈8.9‐fold as compared with pristine pyrogenic carbon. Additionally, fabricated graphene is more efficient in PDS activation than commercial metal catalysts. Undoubtedly, this study realizes effective transformation of pyrogenic carbon to graphene for highly efficient metal‐free carbocatalyst. [ABSTRACT FROM AUTHOR]

Statically immobilized Pd active sites leads to suboptimal hydrogenation efficacy even under harsh reaction conditions, and dynamic catalysis for individual requirements of H 2 dissociation and substrate activation is devoid. Here, we have developed an innovative All-in-one system that employs dynamic Pd catalysis assisted by porous graphene, enabling hydrogenation to be conducted under mild conditions. The conversion of vanillin at 30 °C is 99% and the yield of 2-methoxy-4-methylphenol is >95%, significantly exceeding the reported records. The uniformly distributed N-doping and thin sheets of porous graphene induce Pd single-atom (PdN 4) formation, and inhibit rapid agglomeration to nanoparticles (Pd NPs) for assisting dynamic catalysis. High–pressure process analysis and theoretical calculations reveal that excellent activity comes from the synergistic effects of PdN 4 and Pd NPs. Importantly, All-in-one system is applicable for complex bio–oil hydrogenation and for a broad spectrum of unsaturated substrates. [Display omitted] • The dynamic Pd catalysis assisted by porous graphene has superior hydrogenation activity. • The All-in-one system integrates catalyst preparation and substrate conversion. • The excellent activity comes from the synergistic effects of PdN 4 and Pd NPs. • Proposing a green strategy for bio-based chemicals production or bio-oil upgrading. [ABSTRACT FROM AUTHOR]

Fe0-based nanomaterials are extensively applied in environmental remediation, but their passivated oxide shell restricts deep application. However, efforts aimed at revitalizing Fe-oxide shells have shown limited success. Here, we report a "faster win fast" approach by preferential carbon layer deposition in milliseconds to block Fe-oxide shell growth via carbon-assisted flash Joule heating (C-FJH) reaction. C-FJH induced ultra-high temperature and electric shock promoted reductive Fe formation and subsequently melted to a phase-fusional heterostructure (Fe0/FeCl 2). Therefore, theoretical calculation confirmed that electron delocalization effect of derived heterostructure promoted electron transfer. Synchronously, rapid self-heating/quenching rate (∼102 K/ms) realized a thin aromatic-carbon layer deposition to sustain both high stability and activity of reductive Fe. The channels of thin aromatic-carbon layer favored inward diffusion of pollutants, which facilitated the subsequent reduction. Accordingly, derived heterostructure and carbon layer jointly contributed to the boosted removal of multiple pollutants (including metal oxyanions, perfluorinated compounds, and disinfection by-products). [Display omitted] • Millisecond self-heating and cooling induced superior reductive Fe/carbon synthesis. • Both oxide-shell free and heterostructure resulted in superior removal efficiency. • Carbon deposition inhibited Fe oxide-shell growth and sustained Fe/carbon stability. • Electron delocalization of as-prepared heterostructure promoted electron transfer. [ABSTRACT FROM AUTHOR]

Colorectal cancer (CRC) is a globally prevalent malignancy with a high potential for metastasis. Existing cancer treatments have limitations, including drug resistance and adverse effects. Researchers are striving to develop effective therapies to address these challenges. Impressively, contemporary research has discovered that many natural products derived from foods, plants, insects, and marine invertebrates can suppress the progression, metastasis, and invasion of CRC. In this review, we conducted a comprehensive search of the CNKI, PubMed, Embase, and Web of Science databases from inception to April 2023 to evaluate the efficacy of natural products targeting mitochondria to fight against CRC. Mitochondria are intracellular energy factories involved in cell differentiation, signal transduction, cell cycle regulation, apoptosis, and tumorigenesis. The identified natural products have been classified and summarized based on their mechanisms of action. These findings indicate that natural products can induce apoptosis in colorectal cancer cells by inhibiting the mitochondrial respiratory chain, ROS elevation, disruption of mitochondrial membrane potential, the release of pro-apoptotic factors, modulation of the Bcl-2 protein family to facilitate cytochrome c release, induction of apoptotic vesicle activity by activating the caspase protein family, and selective targeting of mitochondrial division. Furthermore, diverse apoptotic signaling pathways targeting mitochondria, such as the MAPK, p53, STAT3, JNK and AKT pathway, have been triggered by natural products. Natural products such as diosgenin, allopurinol, and clausenidin have demonstrated low toxicity, high efficacy, and multi-targeted properties. Mitochondria-targeting natural products have great potential for overcoming the challenges of CRC therapy. [Display omitted] • The mitochondrial functional state is a potential target for the treatment of carcinoma. • Many natural products can inhibit colorectal cancer by regulating mitochondrial function. • Natural products such as diosgenin, allopurinol, and clausenidin have the clinical potential to treat colorectal cancer. [ABSTRACT FROM AUTHOR]