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1.
Clin Transl Oncol ; 25(6): 1805-1820, 2023 Jun.
Article in English | MEDLINE | ID: mdl-36899123

ABSTRACT

PURPOSE: Nowadays, the oxidative phosphorylation (OXPHOS) correlated with leukemogenesis and treatment response is extensive. Thus, exploration of novel approaches in disrupting OXPHOS in AML is urgently needed. MATERIALS AND METHODS: Bioinformatical analysis of TCGA AML dataset was performed to identify the molecular signaling of OXPHOS. The OXPHOS level was measured through a Seahorse XFe96 cell metabolic analyzer. Flow cytometry was applied to measure mitochondrial status. Real-time qPCR and western blot were used to analyze the expression of mitochondrial or inflammatory factors. MLL-AF9-induced leukemic mice were conducted to measure the anti-leukemia effect of chidamide. RESULTS: Here, we reported that AML patients with high OXPHOS level were in a poor prognosis, which was associated with high expression of HDAC1/3 (TCGA). Inhibition of HDAC1/3 by chidamide inhibited cell proliferation and induced apoptotic cell death in AML cells. Intriguingly, chidamide could disrupt mitochondrial OXPHOS as assessed by inducing mitochondrial superoxide and reducing oxygen consumption rate, as well as decreasing mitochondrial ATP production. We also observed that chidamide augmented HK1 expression, while glycolysis inhibitor 2-DG could reduce the elevation of HK1 and improve the sensitivity of AML cells exposed to chidamide. Furthermore, HDAC3 was correlated with hyperinflammatory status, while chidamide could downregulate the inflammatory signaling in AML. Notably, chidamide eradicated leukemic cells in vivo and prolonged the survival time of MLL-AF9-induced AML mice. CONCLUSION: Chidamide disrupted mitochondrial OXPHOS, promoted cell apoptosis and reduced inflammation in AML cells. These findings exhibited a novel mechanism that targeting OXPHOS would be a novel strategy for AML treatment.


Subject(s)
Leukemia, Myeloid, Acute , Animals , Mice , Leukemia, Myeloid, Acute/drug therapy , Oxidative Phosphorylation , Aminopyridines/pharmacology , Benzamides , Apoptosis , Cell Line, Tumor
2.
Braz J Med Biol Res ; 52(10): e8631, 2019.
Article in English | MEDLINE | ID: mdl-31531526

ABSTRACT

The long non-coding RNA (lncRNA) maternally expressed gene 3 (MEG3), a tumor suppressor, is critical for the carcinogenesis and progression of different cancers, including hepatocellular carcinoma (HCC). To date, the roles of lncRNA MEG3 in HCC are not well illustrated. Therefore, this study used western blot and qRT-PCR to evaluate the expression of MEG3, miR-9-5p, and Sex determining Region Y-related HMG-box 11 (SOX11) in HCC tissues and cell lines. RNA pull-down and luciferase reporter assay were used to evaluate these molecular interactions. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and flow cytometry detected the viability and apoptosis of HCC cells, respectively. The results showed that MEG3 and SOX11 were poorly expressed but miR-9-5p was highly expressed in HCC. The expression levels of these molecules suggested a negative correlation between MEG3 and miR-9-5p and a positive correlation with SOX11, confirmed by Pearson's correlation analysis and biology experiments. Furthermore, MEG3 could combine with miR-9-5p, and SOX11 was a direct target of miR-9-5p. Moreover, MEG3 over-expression promoted cell apoptosis and growth inhibition in HCC cells through sponging miR-9-5p to up-regulate SOX11. Therefore, the interactions among MEG3, miR-9-5p, and SOX11 might offer a novel insight for understanding HCC pathogeny and provide potential diagnostic markers and therapeutic targets for HCC.


Subject(s)
Carcinoma, Hepatocellular/genetics , Liver Neoplasms/genetics , MicroRNAs/genetics , RNA, Long Noncoding/genetics , SOXC Transcription Factors/genetics , Apoptosis/genetics , Carcinoma, Hepatocellular/metabolism , Carcinoma, Hepatocellular/pathology , Cell Line, Tumor , Cell Proliferation/genetics , Female , Gene Expression Regulation, Neoplastic , Humans , Liver Neoplasms/metabolism , Liver Neoplasms/pathology , Male , MicroRNAs/metabolism , Middle Aged , Neoplasm Staging , RNA, Long Noncoding/metabolism , Real-Time Polymerase Chain Reaction , SOXC Transcription Factors/metabolism , Transcriptional Activation , Transfection , Up-Regulation
3.
J Econ Entomol ; 112(3): 1120-1129, 2019 05 22.
Article in English | MEDLINE | ID: mdl-30770933

ABSTRACT

Alligatorweed, Alternanthera philoxeroide (Mart.) Griseb. (Amaranthaceae) is an invasive weed in China that is often kept under control by the alligatorweed flea beetle, Agasicles hygrophila Selman and Vogt (Coleoptera: Chrysomelidae) introduced into China from Argentina in the 1980s. Elevated CO2 levels have been shown to have a direct effect on Ag. hygrophila. In order to fully evaluate the indirect effects of three different atmospheric concentrations of CO2 (420, 550, and 750 ppm) on the population parameters of Ag. hygrophila reared on Al. philoxeroides, we collected life table data for Ag. hygrophila using the age-stage, two-sex life table method. In general, there were no significant differences in the lengths of the preadult parameters among the three treatments. The adult duration and total longevity of males, however, did increase as CO2 increased in concentration. Although the adult preoviposition and total preoviposition periods decreased, the fecundity, oviposition days, eggs per oviposition day, net reproductive rate, intrinsic rate of increase, and finite rate of increase all increased significantly at the high CO2 concentration. Consequently, we determined that the Ag. hygrophila population size will potentially increase rapidly over a short period of time at elevated CO2 concentrations. Our results suggest that 550 and 750 ppm CO2 may also cause physiological changes in Al. philoxeroides that, in turn, provide enhanced nutrition for increasing reproduction in Ag. hygrophila by accelerating maturation of their reproductive system. These results indicate that the efficacy of Ag. hygrophila as a biological control agent against Al. philoxeroides will likely be increased at 550 and 750 ppm CO2.


Subject(s)
Acanthaceae , Amaranthaceae , Coleoptera , Animals , Argentina , Carbon Dioxide , China , Female , Male
4.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;52(10): e8631, 2019. tab, graf
Article in English | LILACS | ID: biblio-1039247

ABSTRACT

The long non-coding RNA (lncRNA) maternally expressed gene 3 (MEG3), a tumor suppressor, is critical for the carcinogenesis and progression of different cancers, including hepatocellular carcinoma (HCC). To date, the roles of lncRNA MEG3 in HCC are not well illustrated. Therefore, this study used western blot and qRT-PCR to evaluate the expression of MEG3, miR-9-5p, and Sex determining Region Y-related HMG-box 11 (SOX11) in HCC tissues and cell lines. RNA pull-down and luciferase reporter assay were used to evaluate these molecular interactions. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and flow cytometry detected the viability and apoptosis of HCC cells, respectively. The results showed that MEG3 and SOX11 were poorly expressed but miR-9-5p was highly expressed in HCC. The expression levels of these molecules suggested a negative correlation between MEG3 and miR-9-5p and a positive correlation with SOX11, confirmed by Pearson's correlation analysis and biology experiments. Furthermore, MEG3 could combine with miR-9-5p, and SOX11 was a direct target of miR-9-5p. Moreover, MEG3 over-expression promoted cell apoptosis and growth inhibition in HCC cells through sponging miR-9-5p to up-regulate SOX11. Therefore, the interactions among MEG3, miR-9-5p, and SOX11 might offer a novel insight for understanding HCC pathogeny and provide potential diagnostic markers and therapeutic targets for HCC.


Subject(s)
Humans , Male , Female , Middle Aged , Carcinoma, Hepatocellular/genetics , MicroRNAs/genetics , SOXC Transcription Factors/genetics , RNA, Long Noncoding/genetics , Liver Neoplasms/genetics , Transfection , Gene Expression Regulation, Neoplastic , Transcriptional Activation , Up-Regulation , Apoptosis/genetics , Carcinoma, Hepatocellular/metabolism , Carcinoma, Hepatocellular/pathology , MicroRNAs/metabolism , Cell Line, Tumor , Cell Proliferation/genetics , SOXC Transcription Factors/metabolism , Real-Time Polymerase Chain Reaction , RNA, Long Noncoding/metabolism , Liver Neoplasms/metabolism , Liver Neoplasms/pathology , Neoplasm Staging
5.
Chem Pharm Bull (Tokyo) ; 58(4): 552-5, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20410641

ABSTRACT

Two new mexicanolides, named xylomexicanolides A and B, were isolated from the seeds of an Indian mangrove, Xylocarpus moluccensis, together with four known limonoids, khayasin, angolensic acid methyl ester, khayasin T, and 2'S-methylbutanoylproceranolide. The structures of these limonoids were established on the basis of spectroscopic data. The (13)C-NMR data of khayasin were reported for the first time. Khayasin was found to exhibit marked insecticidal activity against the fifth instar larvae of Brontispa longissima (GESTRO) at a concentration of 10 mg/l.


Subject(s)
Insecticides/chemistry , Insecticides/pharmacology , Limonins/chemistry , Limonins/pharmacology , Meliaceae/chemistry , Seeds/chemistry , Animals , Coleoptera/drug effects , Insecticides/isolation & purification , Larva/drug effects , Limonins/isolation & purification , Magnetic Resonance Spectroscopy , Models, Molecular , Molecular Structure
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