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Curcumol Reduces Aerobic Glycolysis and Overcomes Chemoresistance by Inducing Cdh1-Mediated Skp2 Ubiquitination. 姜黄酚通过诱导cdh1介导的Skp2泛素化减少有氧糖酵解和克服化学耐药。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X23500349
Yu Gan, Li Zhou, Ruike Wang, Yangnan Zhang, Xiaoying Li, Shuangze Han, Pengfei Rong, Wei Wang, Wei Li

Colorectal cancer (CRC) is the third most common cancer worldwide. The main obstacle in treating advanced CRC is tumor recurrence and metastasis due to chemoresistance. S-phase kinase associated protein 2 (Skp2), an E3 ligase, is highly associated with tumor resistance and a poor prognosis. The results of immunoblotting, immunohistochemical staining, ubiquitination analysis, and co-immunoprecipitation (co-IP) assay revealed that the plant curcuma, curcumol, is a novel Skp2 inhibitor for CRC treatment. Curcumol inhibits aerobic glycolysis in CRC by inducing Skp2 degradation. Co-immunoprecipitation results showed that curcumol enhanced the interaction between cadherin-1 (Cdh1) and Skp2 and led to the ubiquitination and degradation of Skp2. Curcumol exhibited significant antitumor effects against CRC, such as increased intrinsic apoptosis and decreased tumorigenic properties, both in vivo and in vitro. Furthermore, curcumol overcame 5-fluorouracil (5-Fu) resistance in CRC and induced apoptosis in 5-Fu-resistant CRC cells. The present data revealed a novel antitumor mechanism of glycolytic regulation by curcumol, suggesting that curcumol may be a potential chemical candidate for treating 5-Fu-resistant CRC.

结直肠癌(CRC)是全球第三大常见癌症。晚期结直肠癌治疗的主要障碍是化疗耐药引起的肿瘤复发和转移。s期激酶相关蛋白2 (Skp2)是一种E3连接酶,与肿瘤耐药和不良预后高度相关。免疫印迹、免疫组织化学染色、泛素化分析和共免疫沉淀(co-IP)实验的结果表明,姜黄素是一种治疗结直肠癌的新型Skp2抑制剂。姜黄酚通过诱导Skp2降解抑制CRC的有氧糖酵解。共免疫沉淀结果显示,姜黄酚增强了cadherin-1 (Cdh1)与Skp2的相互作用,导致Skp2泛素化和降解。姜黄酚在体内和体外均表现出显著的抗CRC作用,如增加CRC细胞的内在凋亡,降低CRC的致瘤性。此外,姜黄酚克服了CRC中5-氟尿嘧啶(5-Fu)的耐药,并诱导5-Fu耐药的CRC细胞凋亡。目前的数据揭示了姜黄酚调节糖酵解的一种新的抗肿瘤机制,提示姜黄酚可能是治疗5- fu耐药CRC的潜在候选化学物质。
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引用次数: 0
Research Progress of Immunomodulation on Anti-COVID-19 and the Effective Components from Traditional Chinese Medicine. 免疫调节抗COVID-19及中药有效成分的研究进展。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 Epub Date: 2023-07-19 DOI: 10.1142/S0192415X23500611
Ting Hu, Li Li, Qin Ma

SARS-CoV-2 has posed a threat to the health of people around the world because of its strong transmission and high virulence. Currently, there is no specific medicine for the treatment of COVID-19. However, for a wide variety of medicines used to treat COVID-19, traditional Chinese medicine (TCM) plays a major role. In this paper, the effective treatment of COVID-19 using TCM was consulted first, and several Chinese medicines that were frequently used apart from their huge role in treating it were found. Then, when exploring the active ingredients of these herbs, it was discovered that most of them contained flavonoids. Therefore, the structure and function of the potential active substances of flavonoids, including flavonols, flavonoids, and flavanes, respectively, are discussed in this paper. According to the screening data, these flavonoids can bind to the key proteins of SARS-CoV-2, 3CLpro, PLpro, and RdRp, respectively, or block the interface between the viral spike protein and ACE2 receptor, which could inhibit the proliferation of coronavirus and prevent the virus from entering human cells. Besides, the effects of flavonoids on the human body systems are expounded on in this paper, including the respiratory system, digestive system, and immune system, respectively. Normally, flavonoids boost the body's immune system. However, they can suppress the immune system when over immunized. Ultimately, this study hopes to provide a reference for the clinical drug treatment of COVID-19 patients, and more TCM can be put into the market accordingly, which is expected to promote the development of TCM on the international stage.

严重急性呼吸系统综合征冠状病毒2型由于其强大的传播力和高毒力,对世界各地的人们的健康构成了威胁。目前,尚无治疗新冠肺炎的特效药。然而,对于用于治疗新冠肺炎的多种药物,中医药(TCM)发挥着重要作用。本文首先对新冠肺炎中医药的有效治疗进行了探讨,并发现了几种常用中药在治疗中的巨大作用。然后,在探索这些草药的活性成分时,发现它们大多含有黄酮类化合物。因此,本文对黄酮类化合物的潜在活性物质,包括黄酮醇、黄酮类化合物和黄烷的结构和功能进行了讨论。根据筛选数据,这些黄酮类化合物可以分别与严重急性呼吸系统综合征冠状病毒2型、3CLpro、PLpro和RdRp的关键蛋白结合,或阻断病毒刺突蛋白与ACE2受体之间的界面,从而抑制冠状病毒的增殖,阻止病毒进入人体细胞。此外,本文还阐述了黄酮类化合物对人体系统的影响,包括呼吸系统、消化系统和免疫系统。通常情况下,类黄酮能增强身体的免疫系统。然而,当过度免疫时,它们会抑制免疫系统。最终,本研究希望为新冠肺炎患者的临床药物治疗提供参考,使更多的中药能够相应地投入市场,有望推动中医药在国际舞台上的发展。
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引用次数: 0
Review on Processing Methods of Toxic Chinese Materia Medica and the Related Mechanisms of Action. 毒性中药炮制方法及其作用机制研究进展。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X23500635
Lingyun Pan, Yingshu Wang, Lixia Yue, Nan Wang, Wen Xu, Xue Liao, Haiying Wang, Yanfeng Xiu

Toxic Chinese materia medica (CMM) has both pharmacological activities and toxic effects. Based on thousands of years of experience in the application of CMMs, people have explored many practical processing methods of CMMs, also known as "Pao Zhi", to reduce/control toxicity and preserve/enhance efficacy. Toxic CMMs have been used throughout China's hospitals. Yet, the production and use of toxic CMM should be carried out in accordance with the Chinese pharmacopoeia (ChP) and the processing regulations formulated by the health administrative departments of provinces, autonomous regions, and municipalities directly under the Central Government. This paper summarizes the current understanding and awareness of toxicity and 45 toxic CMMs, the commonly used processing methods of toxic CMMs recorded in the 2020 edition of ChP, and the changes in the chemical component, toxicity, or efficacy profiles after processing. This review may provide useful information for the processing methods of toxic CMMs worldwide. We believe that with an in-depth study and understanding of toxic CMMs combined with a standardized application, the toxicity of CMMs will be predictable and controllable in the future.

有毒中药具有药理活性和毒性作用。人们在几千年的应用经验的基础上,探索出了许多实用的中药加工方法,也被称为“保治”,以减少/控制毒性,保持/增强功效。有毒的中药在中国的医院里随处可见。但是,有毒中药的生产、使用,应当按照《中国药典》和省、自治区、直辖市卫生行政部门制定的生产、使用规定执行。本文综述了目前对毒性和45种毒性中药的认识和认识,2020年版ChP中记录的毒性中药的常用加工方法,以及加工后化学成分、毒性或功效谱的变化。本文综述可为国内外有毒中药的加工方法提供参考。我们相信,随着对有毒cmm的深入研究和认识,结合标准化应用,未来cmm的毒性将是可预测和可控的。
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引用次数: 0
Ginsenoside Rd Inhibited Ferroptosis to Alleviate CCl4-Induced Acute Liver Injury in Mice via cGAS/STING Pathway. 人参皂苷Rd通过cGAS/STING途径抑制铁中毒减轻ccl4诱导的小鼠急性肝损伤
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X23500064
Yuangeng Li, Ping Yu, Wenwen Fu, Shuo Wang, Wenjun Zhao, Yue Ma, Yi Wu, Heming Cui, Xiaofeng Yu, Li Fu, Huali Xu, Dayun Sui

Carbon tetrachloride (CCl4)-induced lipid peroxidation associated with hepatic oxidative stress and cell death is an important mechanism of acute liver injury (ALI). Ginsenoside Rd is considered an active ingredient of ginseng. Evidence suggests that ginsenoside Rd may improve ischaemic stroke, nerve damage, cancer and other diseases involving apoptosis, inflammation, oxidative stress, mitochondrial injury and autophagy. However, the effects of ginsenoside Rd on CCl4-induced ALI and its underlying mechanisms are still unclear. In this study, 0.25% CCl4 was injected intraperitoneally in mice to establish a CCl4-induced ALI model. In the Rd treatment group, Rd (10, 20[Formula: see text]mg/kg) doses were injected intraperitoneally 1[Formula: see text]h before and 23[Formula: see text]h after CCl4 administration. Ferroptosis inducer imidazole ketone erastin (IKE) was injected intraperitoneally 4[Formula: see text]h before CCl4 administration to explore the mechanism. The blood and liver were collected 24[Formula: see text]h after CCl4 administration to investigate the effect and mechanism of ginsenoside Rd on CCl4-induced ALI. Our results showed that ginsenoside Rd inhibited CCl4-induced ALI in mice. Ginsenoside Rd also downregulated CCl4-induced serum and liver iron, 4-hydroxynonenal, and 8-hydroxy-2 deoxyguanosine levels. Furthermore, it upregulated glutathione and glutathione peroxidase 4 levels. In addition, ginsenoside Rd downregulated the expression of cGAS and STING. Subsequently, the ferroptosis inducer imidazole ketone erastin significantly reversed the hepatoprotective effect and influence of ginsenoside Rd with regard to the indicators mentioned above. Our study confirmed that ginsenoside Rd ameliorated CCl4-induced ALI in mice, which was related to the reduction of ferroptosis. Simultaneously, the ginsenoside Rd-mediated inhibition of the cGAS/STING pathway contributed to its antiferroptosis effect. In conclusion, our results suggested that ginsenoside Rd inhibited ferroptosis via the cGAS/STING pathway, thereby protecting mice from CCl4-induced ALI. These results suggested ginsenoside Rd may be used as a potential intervention treatment against CCl4-induced ALI.

四氯化碳(CCl4)诱导的脂质过氧化与肝脏氧化应激和细胞死亡相关,是急性肝损伤(ALI)的重要机制。人参皂苷Rd被认为是人参的一种活性成分。有证据表明,人参皂苷Rd可能改善缺血性中风、神经损伤、癌症和其他涉及细胞凋亡、炎症、氧化应激、线粒体损伤和自噬的疾病。然而,人参皂苷Rd对ccl4诱导的ALI的作用及其机制尚不清楚。本研究通过腹腔注射0.25% CCl4,建立CCl4诱导的小鼠ALI模型。Rd组在CCl4给药前1 h,给药后23 h,分别腹腔注射Rd(10、20 mg/kg)剂量。在CCl4给药前腹腔注射铁下垂诱导剂咪唑酮erastin (imidazole酮erastin, IKE)[公式:见文],探讨其作用机制。给药24 h后取血、取肝,探讨人参皂苷Rd对CCl4诱导ALI的作用及机制。结果表明,人参皂苷Rd对ccl4诱导的小鼠ALI有抑制作用。人参皂苷Rd也下调ccl4诱导的血清和肝脏铁、4-羟基壬烯醛和8-羟基-2脱氧鸟苷水平。此外,它还上调谷胱甘肽和谷胱甘肽过氧化物酶4的水平。此外,人参皂苷Rd下调cGAS和STING的表达。随后,铁下垂诱导剂咪唑酮erastin在上述指标上显著逆转了人参皂苷Rd的肝保护作用和影响。我们的研究证实,人参皂苷Rd可以改善ccl4诱导的小鼠ALI,这与降低铁下垂有关。同时,人参皂苷rd介导的对cGAS/STING通路的抑制有助于其抗铁下垂作用。总之,我们的研究结果表明,人参皂苷Rd通过cGAS/STING途径抑制铁凋亡,从而保护小鼠免受ccl4诱导的ALI。这些结果提示人参皂苷Rd可能作为ccl4诱导的ALI的潜在干预治疗。
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引用次数: 0
Probiotic Fermentation of Herbal Medicine: Progress, Challenges, and Opportunities. 草药益生菌发酵:进展、挑战和机遇。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X23500519
Hao-Yu Yang, Lin Han, Yi-Qun Lin, Tao Li, Yu Wei, Lin-Hua Zhao, Xiao-Lin Tong

Fermentation is a processing method used in traditional Chinese medicine (TCM). However, traditional fermentation methods suffer from poor production control. In contrast, probiotic fermented herbal medicine (PFHM) offers advantages such as the use of pure strains, a controllable process, and the ability to produce a variety of active enzymes during fermentation. As a result, PFHM has become a research hotspot. This review focuses on the progress, challenges, and opportunities in the research of PFHM. The use of probiotic enzymes during fermentation alters the active ingredients of TCM, resulting in positive pharmacological effects such as increased active ingredients, reduced toxicity, new pharmacological effects, and the reuse of herbal residues. PFHM has the potential to transfer the metabolic transformation of the effective components of TCM by intestinal flora outside the body during production and preparation, which has a broad application prospect. However, due to the complexity of the chemical composition of TCM, the mechanism of PFHM requires further investigation. Finally, we discuss the prospects of industrializing PFHM, which is essential for promoting the innovation and modernization of TCM.

发酵是中药的一种加工方法。然而,传统的发酵方法存在生产控制不佳的问题。相比之下,益生菌发酵草药(PFHM)具有使用纯菌株,过程可控以及在发酵过程中产生多种活性酶的能力等优点。因此,PFHM已成为一个研究热点。本文综述了PFHM研究的进展、挑战和机遇。在发酵过程中使用益生菌酶可以改变中药的活性成分,从而产生积极的药理作用,如增加活性成分,降低毒性,产生新的药理作用,以及草药残留物的再利用。PFHM在生产和制备过程中具有通过肠道菌群在体外转移中药有效成分代谢转化的潜力,具有广阔的应用前景。然而,由于中药化学成分的复杂性,PFHM的作用机制有待进一步研究。最后,对中药产业化前景进行了展望,指出中药产业化对促进中药创新和现代化具有重要意义。
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引用次数: 1
Metabolomics Analysis of Electroacupuncture Pretreatment Induced Neuroprotection on Mice with Ischemic Stroke. 电针预处理对缺血性脑卒中小鼠神经保护的代谢组学分析。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X23500520
Su-Hao Yang, Xin-Xiao Zhang, Zhan-Qiong Zhong, Xia-Xia Luo, Yu-Fei Wang, Xing-Ping Xiao, Ze-Qin Huang, Si-Yi Yu, Jia-Yi Sun, Mei-Jun Liu, Xiao-Yi Xiong

The brain metabolic changes caused by the interruption of blood supply are the initial factors of brain injury in ischemic stroke. Electroacupuncture (EA) pretreatment has been shown to protect against ischemic stroke, but whether its neuroprotective mechanism involves metabolic regulation remains unclear. Based on our finding that EA pretreatment significantly alleviated ischemic brain injury in mice by reducing neuronal injury and death, we performed a gas chromatography-time of flight mass spectrometry (GC-TOF/MS) to investigate the metabolic changes in the ischemic brain and whether EA pretreatment influenced these changes. First, we found that some glycolytic metabolites in the normal brain tissues were reduced by EA pretreatment, which may lay the foundation of neuroprotection for EA pretreatment against ischemic stroke. Then, 6[Formula: see text]h of cerebral ischemia-induced brain metabolic changes, especially the enhanced glycolysis, were partially reversed by EA pretreatment, which was manifested by the brain levels of 11 of 35 up-regulated metabolites and 18 of 27 down-regulated metabolites caused by cerebral ischemia significantly decreasing and increasing, respectively, due to EA pretreatment. A further pathway analysis showed that these 11 and 18 markedly changed metabolites were mainly involved in starch and sucrose metabolism, purine metabolism, aspartate metabolism, and the citric acid cycle. Additionally, we found that EA pretreatment raised the levels of neuroprotective metabolites in both normal and ischemic brain tissues. In conclusion, our study revealed that EA pretreatment may attenuate the ischemic brain injury by inhibiting glycolysis and increasing the levels of some neuroprotective metabolites.

血供中断引起的脑代谢变化是缺血性脑卒中脑损伤的初始因素。电针(EA)预处理已被证明对缺血性中风有保护作用,但其神经保护机制是否涉及代谢调节尚不清楚。基于我们发现EA预处理通过减少神经元损伤和死亡而显著减轻小鼠缺血性脑损伤,我们采用气相色谱-飞行时间质谱(GC-TOF/MS)研究了缺血性脑的代谢变化以及EA预处理是否影响了这些变化。首先,我们发现EA预处理后正常脑组织中部分糖酵解代谢物减少,这可能为EA预处理对缺血性脑卒中的神经保护奠定了基础。然后,EA预处理可以部分逆转脑缺血引起的脑代谢变化,特别是糖酵解的增强,表现为脑缺血引起的35种上调代谢物中有11种脑水平显著降低,27种下调代谢物中有18种脑水平显著升高。进一步的途径分析表明,这11和18的代谢产物发生了显著变化,主要参与淀粉和蔗糖代谢、嘌呤代谢、天冬氨酸代谢和柠檬酸循环。此外,我们发现EA预处理提高了正常脑组织和缺血脑组织中神经保护代谢物的水平。综上所述,我们的研究表明,EA预处理可能通过抑制糖酵解和增加一些神经保护代谢物的水平来减轻缺血性脑损伤。
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引用次数: 1
A Novel Paradigm Defines Functional Molecule Clusters for an Anti-Alzheimer's Disease Recipe from Traditional Chinese Medicine. 一种新的范式定义了一种抗阿尔茨海默病中药配方的功能分子簇。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 Epub Date: 2023-08-31 DOI: 10.1142/S0192415X23500805
Peiyi Ji, Jianrong Xu, Miaomiao Li, Chenghuan Song, Yongfang Zhang, Rui Zhang, Hongzhuan Chen, Hao Wang, Lanxue Zhao

Traditional Chinese Medicine (TCM) prescriptions are organically composed of compatible herbs according to the TCM theory. The complex ingredients of TCM could act on multiple targets through various pathways simultaneously to exert pharmacological effects, making TCM an unrivaled gem in the medical world. However, due to a lack of comprehensive and standard study methods, the research of TCM products has been quite limited. A novel paradigm that could aid in the discovery of the material basis and fully clarify the mechanism of TCM prescriptions is urgently needed. In this study, a similarity analysis based on molecular fingerprints was adopted to explore the representative molecules of the Tiaoxin recipe, a Chinese patent formula approved by the National Medical Products Administration (NMPA) for the treatment of mild-to-moderate Alzheimer's disease (AD), and 38 out of 1047 chemicals were finally screened out. Next, we tried to define a new concept of a "functional molecule cluster" for chemicals with similar pharmacological effects to elucidate how the chemical mixture from TCMs produce their therapeutic effects. Four anti-AD functional molecule clusters from the Tiaoxin recipe were identified: an anti-inflammatory cluster, an anti-ROS cluster, an anti-AChE activity cluster, and an anti-A[Formula: see text] aggregation cluster. Furthermore, the chemicals from the anti-inflammatory cluster and anti-ROS cluster were proved to display their multi-target and multi-pathway roles partially or mainly through molecules of the TLR4-MYD88-NF-[Formula: see text]B and Keap1-Nrf2-ARE pathways. The functional molecule clusters may be vital to the explanation of the efficacy of the Tiaoxin recipe, which could give us a more profound understanding of TCM prescriptions. Our paradigm may open a novel path for TCM research.

根据中医理论,中药处方是由配伍的草药有机组成的。中药的复杂成分可以通过多种途径同时作用于多个靶点,发挥药理作用,使中药成为医学界无与伦比的瑰宝。然而,由于缺乏全面、规范的研究方法,中药产品的研究一直相当有限。迫切需要一种新的范式来帮助发现中医方剂的物质基础并充分阐明其作用机制。本研究采用基于分子指纹的相似性分析方法,对经国家药品监督管理局批准用于治疗轻中度阿尔茨海默病的中成药调心方的代表性分子进行了探索,最终筛选出1047种化学物质中的38种。接下来,我们试图为具有类似药理作用的化学物质定义一个“功能分子簇”的新概念,以阐明中药的化学混合物如何产生其治疗效果。从调心方中鉴定出四个抗AD功能分子簇:抗炎簇、抗ROS簇、抗AChE活性簇和抗A[公式:见正文]聚集簇。此外,来自抗炎簇和抗ROS簇的化学物质被证明部分或主要通过TLR4-MYD88-NF-[式:见正文]B和Keap1-Nrf2-ARE途径的分子显示出其多靶点和多途径作用。功能分子簇可能对解释调心方的疗效至关重要,从而使我们对中药方剂有更深入的了解。我们的范式可能为中医学研究开辟一条新的道路。
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引用次数: 0
A New Perspective on Metabolites and Bioactive Compounds from Fungi. 真菌代谢产物和生物活性化合物研究的新视角。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 Epub Date: 2023-08-30 DOI: 10.1142/S0192415X23500799
Thananjeyan Balasubramaniyam, Seo-Ree Choi, Vinod Kumar Nathan, Abhishikta Basu, Joon-Hwa Lee

Fungi play an important role in the solution to important global problems. Making use of processes and goods that are based on fungi can help promote sustainability by making the most efficient use of natural resources. Fungi stand apart from other organisms due to their extraordinary capacity to generate organic compounds. They are necessary for the psychological and physiological well-being of people worldwide. They are excellent producers of vitamins, pigments, hydrolytic enzymes, biofuels, organic acids, polysaccharides, and secondary metabolites such as antibiotics, anticancer treatments, hypocholesterolemic pharmaceuticals, and immunosuppressants. Other secondary metabolites include biofuels. In addition, polysaccharides are produced by them. We provide a condensed explanation of the significance of secondary metabolites in a variety of industries, such as the pharmaceutical industry, the food industry, the textile industry, and the transportation industry. In addition to providing a better understanding of biosynthetic regulation and the possibilities of genetic engineering, improved laboratory processes for the selection of nontoxigenic fungal strains have permitted the manufacture of larger quantities of safe commercial items. The significance of fungi in industrial settings is the topic that will be investigated in this review.

真菌在解决重要的全球问题方面发挥着重要作用。利用以真菌为基础的工艺和产品可以通过最有效地利用自然资源来促进可持续性。真菌因其产生有机化合物的非凡能力而与其他生物不同。它们对于全世界人民的心理和生理健康是必要的。它们是维生素、色素、水解酶、生物燃料、有机酸、多糖和次级代谢产物的优秀生产商,如抗生素、抗癌治疗、降胆固醇药物和免疫抑制剂。其他次级代谢产物包括生物燃料。此外,它们还产生多糖。我们简要解释了次级代谢产物在各种行业中的重要性,如制药行业、食品行业、纺织行业和运输行业。除了更好地了解生物合成调控和基因工程的可能性外,改进了非毒素真菌菌株的实验室选择过程,允许生产大量安全的商业产品。真菌在工业环境中的重要性是本综述将要研究的主题。
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引用次数: 0
Solasonine Inhibits Cancer Stemness and Metastasis by Modulating Glucose Metabolism via Wnt/β-Catenin/Snail Pathway in Osteosarcoma. 茄碱通过Wnt/β-Catenin/Snail通路调节骨肉瘤的糖代谢抑制肿瘤的发生和转移。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X23500593
Bangjun Wang, Yi Zhou, Peng Zhang, Jun Li, Xinyan Lu

Solasonine (SS) is a natural glycoalkaloid compound that has been reported to possess a significant anticancer function. However, its anticancer effects and related mechanisms in osteosarcoma (OS) have not been studied. This study sought to investigate the impact of SS on the growth of OS cells. OS cells were treated with different concentrations of SS for 24[Formula: see text]h, and the results showed that SS attenuated the survival of OS cells in a dose-dependent manner. Additionally, SS suppressed cancer stem-like properties and epithelial-mesenchymal transition (EMT) by inhibiting aerobic glycolysis in OS cells in an ALDOA-dependent manner. Additionally, SS reduced the levels of Wnt3a, [Formula: see text]-catenin, and Snail in OS cells in vitro. Furthermore, Wnt3a activation reversed the SS-induced inhibition of glycolysis in OS cells. Collectively, this study discovered a novel effect of SS in inhibiting aerobic glycolysis, in addition to cancer stem-like features and EMT, implying that SS could be a therapeutic candidate for OS treatment.

茄碱(Solasonine, SS)是一种天然的糖生物碱化合物,据报道具有显著的抗癌作用。然而,其在骨肉瘤(OS)中的抗癌作用及其相关机制尚未得到研究。本研究旨在探讨SS对骨肉瘤细胞生长的影响。用不同浓度的SS处理OS细胞24 h,结果显示SS呈剂量依赖性地降低OS细胞的存活率。此外,SS以依赖aldoa的方式抑制OS细胞的有氧糖酵解,从而抑制肿瘤干细胞样特性和上皮-间质转化(EMT)。此外,SS还能降低体外OS细胞中Wnt3a、catenin和Snail的水平。此外,Wnt3a激活逆转了ss诱导的OS细胞糖酵解抑制。总的来说,本研究发现了SS在抑制有氧糖酵解方面的新作用,以及癌症干细胞样特征和EMT,这意味着SS可能是OS治疗的候选治疗方法。
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引用次数: 1
Traditional Chinese Patent Medicine in the Treatment of Alzheimer's Disease: A Systematic Review and Network Meta-Analysis. 中成药治疗阿尔茨海默病:系统评价和网络荟萃分析。
IF 5.7 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-01-01 DOI: 10.1142/S0192415X2350026X
Changning Liu, Lijuan Zhang, Ying Li, Mingxiang Li, Huan Han, Kangfeng Wang

The objective of this study was to evaluate the efficacy and safety of Chinese patent medicine compared with western medicine in the treatment of Alzheimer's disease using the Network Meta-analysis. This study retrieved relevant studies from 7 databases, and the retrieval time was from the establishment of each database to June 2022. After the screening, data extraction, and quality assessment, 47 studies were finally analyzed, involving 11 Chinese patent medicines. The results demonstrated that Chinese patent medicine intervention was superior to oral western medicine treatment in improving the patient's condition as assessed by the Mini-mental State Examination (MMSE), Activities of Daily Living (ADL), effective rate, and Alzheimer's Disease Assessment Scale-Cognitive section (ADAS-Cog). Particularly, the effect of Chinese patent medicine combined with western medicine intervention was prominent. Meanwhile, Chinese patent medicine intervention in AD did not significantly increase the risk of adverse reactions. The results of the Network Meta-analysis demonstrated that Chinese patent medicine combined with western medicine had statistically significant differences in the MMSE score, ADL score, effective rate, and ADAS-Cog score, compared with both western medicine alone and Chinese patent medicine alone. In terms of adverse reactions, the difference between Chinese patent medicine intervention and simple oral western medicine was statistically significant. The results of further ranking probability analysis demonstrated that Chinese patent medicine combined with western medicine intervention ranked first in terms of MMSE, ADL, effective rate, and ADAS-Cog. Additionally, oral Chinese patent medicine intervention alone ranked first in reducing adverse reactions. In the funnel plots of the MMSE, ADL, and effective rate, most studies were symmetrically distributed on both sides of the midline, where small sample effects and publication bias might exist to some extent. However, this conclusion still needs to be combined with clinical syndrome differentiation and treatment, and more large-sample, multi-center, high-quality studies are needed for further verification.

本研究采用网络meta分析方法,比较中成药与西药治疗阿尔茨海默病的疗效和安全性。本研究从7个数据库中检索相关研究,检索时间为每个数据库建立至2022年6月。经过筛选、数据提取和质量评价,最终分析了47项研究,涉及11种中成药。结果表明,中成药干预在改善患者病情方面优于口服西药治疗,包括最小精神状态检查(MMSE)、日常生活活动能力(ADL)、有效率和阿尔茨海默病评估量表-认知部分(ADAS-Cog)。特别是中成药结合西药干预效果突出。同时,中成药干预对AD的不良反应风险没有显著增加。网络meta分析结果显示,中成药联合西药治疗患者MMSE评分、ADL评分、有效率、ADAS-Cog评分与单用西药和单用中成药比较,差异均有统计学意义。在不良反应方面,中成药干预与单纯口服西药干预差异有统计学意义。进一步排序概率分析结果显示,中成药联合西药干预在MMSE、ADL、有效率、ADAS-Cog方面均居首位。单独口服中成药干预在减少不良反应方面排名第一。在MMSE、ADL和有效率的漏斗图中,大多数研究对称分布在中线两侧,可能存在一定程度的小样本效应和发表偏倚。但这一结论仍需与临床辨证论治相结合,需要更多大样本、多中心、高质量的研究进一步验证。
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American Journal of Chinese Medicine
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