The anticancer potential of quassinoids has attracted a great deal of attention for decades,and scientific data revealing their possible applications in cancer management are continuously increasing in the literature....The anticancer potential of quassinoids has attracted a great deal of attention for decades,and scientific data revealing their possible applications in cancer management are continuously increasing in the literature.Aside from the potent cytotoxic and antitumor properties of these degraded triterpenes,several quassinoids have exhibited synergistic effects with anticancer drugs.This article provides an overview of the potential anticancer properties of quassinoids,including their cytotoxic and antitumor activities,mechanisms of action,safety evaluation,and potential benefits in combination with anticancer drugs.展开更多
The anticancer activities of synthesized benzylthio-indolyl-triazol-amine derivatives 1a^1c were investigated via theoretical scales. The experimental results show that derivative 1a has the highest anticancer activit...The anticancer activities of synthesized benzylthio-indolyl-triazol-amine derivatives 1a^1c were investigated via theoretical scales. The experimental results show that derivative 1a has the highest anticancer activity, and 1c has the lowest one. The interactions of 1a^1c with C-nanotube（5,5） were investigated. Also the quantum molecular descriptors of derivatives 1a^1c were calculated and the results show that they can interact with C-nanotube（5,5） effectively. The adsorptions of 1a^1c on C-nanotube（5,5） surface were exothermic and experimentally possible from the energetic viewpoint. The results indicated that ΔEad and ΔGad values of derivative 1a on C-nanotube（5,5） were higher than those of the corresponding derivatives 1b and 1c, so 1a has the highest ｜μ｜, ω and ｜？N｜ values and the lowest value, and the trends of theoretical anticancer activities of 1a^1c are similar to the experimental values successfully.展开更多
Oolong tea,partially fermented from Camellia sinensis leaves,exhibits significant antioxidative,anti-inflammatory,and anti-cancer activities as indicated in several in vitro and in vivo studies.However,studies on heal...Oolong tea,partially fermented from Camellia sinensis leaves,exhibits significant antioxidative,anti-inflammatory,and anti-cancer activities as indicated in several in vitro and in vivo studies.However,studies on health promoting effects of oolong tea and its characteristic compounds are limited.The potential efficacy of bioactives derived from oolong tea and their roles as promising anticancer agents,their cardio-protective benefits during hypoxic conditions,effects in treating allergic disorders,potential prebiotic activities,improvement of blood lipid status in human beings,effectivity as oral hypoglycemic agent in the treatment of type 2 diabetes,and their potentials to reduce the risk of obesity have been discussed in this review.These promising studies mainly gained from animal studies might broaden the consumption and usage of the phenolic-enriched oolong tea and its products in food and pharmaceutical industries.However,potential health beneficial effects of oolong tea in humans should be further complemented by large-sized,randomized double-blind and placebo-controlled trials to consolidate potential therapeutic applications.展开更多
OBJECTIVE： To provide in vitro evidence of Psorinum treatment against cancer cells in a controlled study. METHODS： Effects of homeopathic Psorinum 6× on cell viability were initially determined in several cance...OBJECTIVE： To provide in vitro evidence of Psorinum treatment against cancer cells in a controlled study. METHODS： Effects of homeopathic Psorinum 6× on cell viability were initially determined in several cancer cell lines, including A549, Hep G2 and MCF-7, using 3-（4,5-dimethylthiazol-2-yl）-2,5-diphenyltetrazolium bromide assay, and an ethanol 6× control. The cell line that exhibited highest inhibition was selected and used in the following experiments. A range of Psorinum 6× doses was used to explore treatment effects on cell cycle arrest, cell death（apoptosis）, generation of reactive oxygen species（ROS） and change in mitochondrial membrane potential（MMP） using fl ow cytometry and fl uorescence microscopy, respectively. Expression of several signal proteins related to apoptosis and cell survival were quantified with Western blotting and confocal microscopy. Further, circular dichroism（CD） spectroscopy was used to determine possible drug-DNA interactions, as well as the induction of conformational changes. RESULTS： Treatment of cancer cell lines with Psorinum showed greater anticancer effects in A549 cells than in others. In A549 cells Psorinum treatment inhibited cell proliferation at 24 h after treatment, and arrested cell cycle at sub-G1 stage. It also induced ROS generation, MMP depolarization, morphological changes and DNA damage, as well as externalization of phosphatidyl serine. Further, increases in p53 expression, Bax expression, cytochrome c release, along with reduction of Bcl-2 level and caspase-3 activation were observed after Psorinum 6× treatment, which eventually drove A549 cells towards the mitochondria-mediated caspase-3-dependent pathway. CD spectroscopy revealed direct interaction of Psorinum with DNA, using calf thymus-DNA as target.CONCLUSION： Psorinum 6× triggered apoptosis in A549 cells via both up- and down-regulations of relevant signal proteins, including p53, caspase-3, Bax and Bcl-2.展开更多
基金supported by the National Natural Science Foundation of China(82274085)the Natural Science Foundation of Jiangsu Province(BK20220478)the Natural Science Foundation of Jiangsu Higher Education institutions of China(22KJB360010).
文摘The anticancer potential of quassinoids has attracted a great deal of attention for decades,and scientific data revealing their possible applications in cancer management are continuously increasing in the literature.Aside from the potent cytotoxic and antitumor properties of these degraded triterpenes,several quassinoids have exhibited synergistic effects with anticancer drugs.This article provides an overview of the potential anticancer properties of quassinoids,including their cytotoxic and antitumor activities,mechanisms of action,safety evaluation,and potential benefits in combination with anticancer drugs.
文摘The anticancer activities of synthesized benzylthio-indolyl-triazol-amine derivatives 1a^1c were investigated via theoretical scales. The experimental results show that derivative 1a has the highest anticancer activity, and 1c has the lowest one. The interactions of 1a^1c with C-nanotube（5,5） were investigated. Also the quantum molecular descriptors of derivatives 1a^1c were calculated and the results show that they can interact with C-nanotube（5,5） effectively. The adsorptions of 1a^1c on C-nanotube（5,5） surface were exothermic and experimentally possible from the energetic viewpoint. The results indicated that ΔEad and ΔGad values of derivative 1a on C-nanotube（5,5） were higher than those of the corresponding derivatives 1b and 1c, so 1a has the highest ｜μ｜, ω and ｜？N｜ values and the lowest value, and the trends of theoretical anticancer activities of 1a^1c are similar to the experimental values successfully.
基金funded by Hubei Science and Technology Plan Key Project(G2019ABA100)Open fund of Hubei Key Laboratory of Economic Forest Germplasm Improvement and Resources Comprehensive Utilization(201932103)fund from Assessment and Comprehensive Utilization of Characteristic Biological resources in Dabie Mountains(4022019006)。
文摘Oolong tea,partially fermented from Camellia sinensis leaves,exhibits significant antioxidative,anti-inflammatory,and anti-cancer activities as indicated in several in vitro and in vivo studies.However,studies on health promoting effects of oolong tea and its characteristic compounds are limited.The potential efficacy of bioactives derived from oolong tea and their roles as promising anticancer agents,their cardio-protective benefits during hypoxic conditions,effects in treating allergic disorders,potential prebiotic activities,improvement of blood lipid status in human beings,effectivity as oral hypoglycemic agent in the treatment of type 2 diabetes,and their potentials to reduce the risk of obesity have been discussed in this review.These promising studies mainly gained from animal studies might broaden the consumption and usage of the phenolic-enriched oolong tea and its products in food and pharmaceutical industries.However,potential health beneficial effects of oolong tea in humans should be further complemented by large-sized,randomized double-blind and placebo-controlled trials to consolidate potential therapeutic applications.
文摘OBJECTIVE： To provide in vitro evidence of Psorinum treatment against cancer cells in a controlled study. METHODS： Effects of homeopathic Psorinum 6× on cell viability were initially determined in several cancer cell lines, including A549, Hep G2 and MCF-7, using 3-（4,5-dimethylthiazol-2-yl）-2,5-diphenyltetrazolium bromide assay, and an ethanol 6× control. The cell line that exhibited highest inhibition was selected and used in the following experiments. A range of Psorinum 6× doses was used to explore treatment effects on cell cycle arrest, cell death（apoptosis）, generation of reactive oxygen species（ROS） and change in mitochondrial membrane potential（MMP） using fl ow cytometry and fl uorescence microscopy, respectively. Expression of several signal proteins related to apoptosis and cell survival were quantified with Western blotting and confocal microscopy. Further, circular dichroism（CD） spectroscopy was used to determine possible drug-DNA interactions, as well as the induction of conformational changes. RESULTS： Treatment of cancer cell lines with Psorinum showed greater anticancer effects in A549 cells than in others. In A549 cells Psorinum treatment inhibited cell proliferation at 24 h after treatment, and arrested cell cycle at sub-G1 stage. It also induced ROS generation, MMP depolarization, morphological changes and DNA damage, as well as externalization of phosphatidyl serine. Further, increases in p53 expression, Bax expression, cytochrome c release, along with reduction of Bcl-2 level and caspase-3 activation were observed after Psorinum 6× treatment, which eventually drove A549 cells towards the mitochondria-mediated caspase-3-dependent pathway. CD spectroscopy revealed direct interaction of Psorinum with DNA, using calf thymus-DNA as target.CONCLUSION： Psorinum 6× triggered apoptosis in A549 cells via both up- and down-regulations of relevant signal proteins, including p53, caspase-3, Bax and Bcl-2.
