ABSTRACT
T-cell therapy with T cells that are re-directed to hepatitis B virus (HBV)-infected cells by virus-specific receptors is a promising therapeutic approach for treatment of chronic hepatitis B and HBV-associated cancer. Due to the high number of target cells, however, side effects such as cytokine release syndrome or hepatotoxicity may limit safety. A safeguard mechanism, which allows depletion of transferred T cells on demand, would thus be an interesting means to increase confidence in this approach. In this study, T cells were generated by retroviral transduction to express either an HBV-specific chimeric antigen receptor (S-CAR) or T-cell receptor (TCR), and in addition either inducible caspase 9 (iC9) or herpes simplex virus thymidine kinase (HSV-TK) as a safety switch. Real-time cytotoxicity assays using HBV-replicating hepatoma cells as targets revealed that activation of both safety switches stopped cytotoxicity of S-CAR- or TCR-transduced T cells within less than one hour. In vivo, induction of iC9 led to a strong and rapid reduction of transferred S-CAR T cells adoptively transferred into AAV-HBV-infected immune incompetent mice. One to six hours after injection of the iC9 dimerizer, over 90% reduction of S-CAR T cells in the blood and the spleen and of over 99% in the liver was observed, thereby limiting hepatotoxicity and stopping cytokine secretion. Simultaneously, however, the antiviral effect of S-CAR T cells was diminished because remaining S-CAR T cells were mostly non-functional and could not be restimulated with HBsAg. A second induction of iC9 was only able to deplete T cells in the liver. In conclusion, T cells co-expressing iC9 and HBV-specific receptors efficiently recognize and kill HBV-replicating cells. Induction of T-cell death via iC9 proved to be an efficient means to deplete transferred T cells in vitro and in vivo containing unwanted hepatotoxicity.
Subject(s)
Adoptive Transfer , Caspase 9/biosynthesis , Hepatitis B Antigens/immunology , Hepatitis B virus/immunology , Hepatitis B, Chronic/therapy , T-Lymphocytes/transplantation , Adoptive Transfer/adverse effects , Animals , Caspase 9/genetics , Cell Death , Cell Line , Coculture Techniques , Cytokines/metabolism , Cytotoxicity, Immunologic , DNA-Binding Proteins/genetics , DNA-Binding Proteins/metabolism , Disease Models, Animal , Enzyme Induction , Female , Hepatitis B virus/pathogenicity , Hepatitis B, Chronic/immunology , Hepatitis B, Chronic/metabolism , Hepatitis B, Chronic/virology , Humans , Interleukin Receptor Common gamma Subunit/genetics , Interleukin Receptor Common gamma Subunit/metabolism , Male , Mice, Inbred C57BL , Mice, Knockout , Receptors, Chimeric Antigen/genetics , Receptors, Chimeric Antigen/metabolism , Simplexvirus/enzymology , Simplexvirus/genetics , T-Lymphocytes/enzymology , T-Lymphocytes/immunology , T-Lymphocytes/pathology , Thymidine Kinase/genetics , Thymidine Kinase/metabolism , Transduction, GeneticABSTRACT
N-myc interactor (NMI), a member of the oncogene Myc family, has been reported to be closely related to the development of cancer. However, the character of NMI in cervical carcinoma has not been reported. Herein, we found that downregulation of NMI protein not only promoted the proliferation, migration, and invasion of HeLa cells, but also decreased their expression of Caspase-3 and Caspase-9. Silencing NMI promotes the epithelial-mesenchymal transition of human cervical carcinoma HeLa cells by upregulating N-cadherin, vimentin, and downregulating E-cadherin. Further investigation illustrated the downregulation of NMI can activate the STAT3 signaling pathway. In conclusion, we found that the downregulation of NMI plays an important role in the progression of cervical cancer, and may served as a novel therapeutic target for cervical cancer.
Subject(s)
Down-Regulation , Gene Expression Regulation, Neoplastic , N-Myc Proto-Oncogene Protein/biosynthesis , Uterine Cervical Neoplasms/metabolism , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Cell Line, Tumor , Cell Movement , Cell Proliferation , Epithelial-Mesenchymal Transition , Female , Gene Silencing , HEK293 Cells , HeLa Cells , Humans , Neoplasm Invasiveness , STAT3 Transcription Factor/metabolism , Signal TransductionABSTRACT
Ginsenoside Rd (GS-Rd), isolated from the Chinese traditional herbal medicine Panax ginseng, is used for the treatment of cardiovascular diseases, inflammation, different body pains, and trauma. Caspase-3 and Caspase-9 belong to cysteine aspartic acid specific protease (Caspase) family that plays an important role in apoptosis progression of cancers. In the present study, we investigated the anti-tumor effect of GS-Rd by MTT assay, colony formation assessment, flow cytometry, and Western blotting. Our results revealed that ginsenoside Rd significantly inhibits human gastric cancer (GC) growth and cell proliferation. Flow cytometer analysis showed that the GS-Rd could significantly induce apoptosis and arrest the G0/G1 phase in GC cells. Further, GS-Rd was found to increase the ratio of Bax/Bcl-2 and the expression of Caspase-3 and Caspase-9, respectively, and to decrease the expression of Cyclin D1. Taken together, our study suggests that GS-Rd significantly inhibits GC cell proliferation, induces cell apoptosis through increase the expression of Caspase-3, Caspase-9, and the ratio of Bax/Bcl-2. GS-Rd also induces cell cycle arrest at G0/G1 phase by down-regulation Cyclin D1. Thus, GS-Rd could serve as a lead to develop novel therapeutic agents to against human gastric cancer.
Subject(s)
Antineoplastic Agents, Phytogenic/therapeutic use , Caspase 3/genetics , Caspase 9/genetics , Ginsenosides/therapeutic use , Stomach Neoplasms/drug therapy , Apoptosis/drug effects , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Cell Cycle Checkpoints/drug effects , Cell Proliferation/drug effects , Gene Expression Regulation, Neoplastic/drug effects , Humans , Proto-Oncogene Proteins c-bcl-2/metabolism , Tumor Stem Cell Assay , Up-Regulation/drug effects , bcl-2-Associated X Protein/metabolismABSTRACT
Splenic immune function was enhanced in diet-induced-obese (DIO) mice caused by Escherichia coli. The changes in spleen function on apoptosis were still unknown. Two hundred mice in groups Lean-E. coli and DIO-E. coli were intranasal instillation of E. coli. And another two hundred mice in groups Lean-PBS and DIO-PBS were given phosphate-buffered saline (PBS). Subsequently, spleen histology was analyzed. Then the rates of spleen cell (SC) apoptosis, and expression of the genes and proteins of Bcl-2, Bax, caspase-3 and caspase-9 were quantified in each group at 0 h (uninfected), 12 h, 24 h, and 72 h postinfection. The SC apoptosis rates of the DIO-E. coli groups were lower than those of the DIO-PBS groups at 12, 24 and 72 h (p < 0.05). Anti-apoptotic Bcl-2 expression gene and protein of the DIO-E. coli groups were higher than those of the DIO-PBS groups (p < 0.05). Gene expressions of pro-apoptotic Bax, caspase-3 and caspase-9 of the DIO-E. coli groups were lower than those of DIO-PBS groups at 12, 24 and 72 h (p < 0.05). The SC apoptosis rates of the Lean-E. coli groups were higher than those of the Lean- PBS groups at 12 h and 24 h (p < 0.05). Interestingly, the SC apoptosis rates in the DIO-E. coli groups were lower than those of the Lean-E. coli groups at 12 h (p < 0.05). In conclusion, our results suggested that the DIO mice presented stronger anti-apoptotic abilities than Lean mice in non-fatal acute pneumonia induced by E. coli infection, which is more conducive to protecting the spleen and improving the immune defense ability of the body.
Subject(s)
Apoptosis/immunology , Escherichia coli Infections/immunology , Escherichia coli/immunology , Obesity/immunology , Pneumonia/immunology , Spleen/immunology , Administration, Intranasal , Animals , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Escherichia coli Infections/microbiology , Escherichia coli Infections/mortality , Macrophages/immunology , Male , Megakaryocytes/immunology , Mice , Mice, Obese , Neutrophils/immunology , Pneumonia/microbiology , Pneumonia/mortality , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Spleen/cytology , bcl-2-Associated X Protein/biosynthesisABSTRACT
Aim: Sevoflurane could induce apoptosis of rat hippocampal neurons, while theaflavins (TFs) have antioxidant and anti-inflammatory properties. This study aims to explore whether TFs could alleviate sevoflurane-induced neuronal cell injury.Materials and methods: Cells were treated by concentration gradient of sevoflurane and TFs. Cell viability, level of reactive oxygen species (ROS) and apoptosis rate were determined by cell counting kit-8 (CCK-8) and flow cytometry, respectively. Quantitative PCR (qPCR) and western blot were performed to determine mRNA and protein expressions.Results: TFs promoted viability of cells under the treatment of sevoflurane, while it suppressed apoptosis and down-regulated ROS level in a concentration-dependent manner. TFs could also down-regulate expression levels of caspase-3 and caspase-9 and cytosol and intranuclear nuclear factor E2-related factor 2 (Nrf2) in rat hippocampal nerve cells, while it up-regulated those of heme oxygenase 1 (HO-1), NADPH quinine oxidoreductase 1 (NQO1), glutamate cysteine ligase (GCL) and peroxiredoxin 1 (Prx1).Conclusions: Our study suggests that TFs exert protective effects on sevoflurane-induced neurocytotoxicity and therefore could be used as a potential drug for treatment of neuronal injury.
Subject(s)
Biflavonoids/pharmacology , Catechin/pharmacology , Hippocampus/drug effects , NF-E2-Related Factor 2/physiology , Neurons/metabolism , Neurotoxicity Syndromes/prevention & control , Sevoflurane/toxicity , Animals , Apoptosis/drug effects , Apoptosis/physiology , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Cell Survival/drug effects , Dose-Response Relationship, Drug , Down-Regulation/drug effects , Glutamate-Cysteine Ligase/biosynthesis , Heme Oxygenase-1/biosynthesis , Hippocampus/metabolism , NAD(P)H Dehydrogenase (Quinone)/biosynthesis , NF-E2-Related Factor 2/biosynthesis , Neurons/physiology , Neurotoxicity Syndromes/metabolism , Neurotoxicity Syndromes/physiopathology , Peroxiredoxins/biosynthesis , Primary Cell Culture , Rats , Reactive Oxygen Species/metabolism , Signal Transduction/physiology , Up-Regulation/drug effectsABSTRACT
The purpose of this study was to determine whether the mitochondrial membrane potential, pro-apoptotic gene expression, and ubiquitylation status of zona pellucida proteins (ZP1, ZP2, and ZP3) of vitrified GV-stage mature oocytes could be protected by treatment with cholesterol-loaded methyl-ß-cyclodextrin (CLC) prior to vitrification. Porcine GV oocytes were treated with CLC prior to the vitrification process, and the effects on the mitochondrial membrane potential and ZP ubiquitylation status were determined by JC-1 single staining and western blot assays. We found that porcine GV-stage oocytes were treated with CLC at different concentrations (0.5, 5, and 10â¯mg/mL) prior to vitrification improved in vitro maturation of these oocytes (Pâ¯<â¯0.05). The mitochondrial membrane potential of matured oocyte without vitrification or treated with 5â¯mg/mL CLC vitrification treatment was higher than that of the 0â¯mg/mL CLC group and other treatment groups (vitrified) (Pâ¯<â¯0.05). The expression of Caspase 3, Caspase 8, and Caspase 9 genes in the high concentration CLC treatment groups (5 and 10â¯mg/mL) was significantly lower than that in the 0 (vitrified) mg/mL CLC group (Pâ¯<â¯0.05). ZPs protein and ZP3 protein ubiquitylation were also higher in the non-vitrified controls, 5 and 10â¯mg/mL CLC-treated oocytes than in the 0 (vitrified) and 0.5â¯mg/mL vitrified groups (Pâ¯<â¯0.05). Whereas the sperm-oocyte binding capacity was improved in the CLC treatment groups (Pâ¯<â¯0.05) but the embryonic development rate was not improved. In conclusion, pretreatment with CLC can improve the survival rate and maturation rate of oocytes and protect their mitochondria and zona pellucida of porcine oocytes from cryodamage during the vitrification process.
Subject(s)
Cholesterol/pharmacology , Cryoprotective Agents/pharmacology , Oocytes/growth & development , Oogenesis/drug effects , Zona Pellucida Glycoproteins/metabolism , beta-Cyclodextrins/pharmacology , Animals , Caspase 3/biosynthesis , Caspase 8/biosynthesis , Caspase 9/biosynthesis , Cryopreservation/methods , Embryonic Development/drug effects , Female , Male , Membrane Potential, Mitochondrial/physiology , Mitochondria/physiology , Pregnancy , Spermatozoa , Swine , Ubiquitination/drug effects , Vitrification/drug effects , Zona Pellucida/metabolismABSTRACT
BACKGROUND: Central pro-inflammatory cytokine (PIC) signal is involved in neurological deficits after transient global ischemia induced by cardiac arrest (CA). The present study was to examine if blocking acid sensing ion channels (ASICs) using amiloride in the Central Nervous System can alleviate neurological deficits after the induction of CA and further examine the participation of PIC signal in the hippocampus for the effects of amiloride. METHODS: CA was induced by asphyxia and then cardiopulmonary resuscitation was performed in rats. Western blot analysis and ELISA were used to determine the protein expression of ASIC subunit ASIC1 in the hippocampus, and the levels of PICs. As noted, it is unlikely that this procedure is clinically used although amiloride and other pharmacological agents were given into the brain in this study. RESULTS: CA increased ASIC1 in the hippocampus of rats in comparison with control animals. This was associated with the increase in IL-1ß, IL-6 and TNF-α together with Caspase-3 and Caspase-9. The administration of amiloride into the lateral ventricle attenuated the upregulation of Caspase-3/Caspase-9 and this further alleviated neurological severity score and brain edema. Inhibition of central IL-6 and TNF-α also decreased ASIC1 in the hippocampus of CA rats. CONCLUSION: Transient global ischemia induced by CA amplifies ASIC1a in the hippocampus likely via PIC signal. Amiloride administered into the Central Nervous System plays a neuroprotective role in the process of global ischemia. Thus, targeting ASICs (i.e., ASIC1a) is suggested for the treatment and improvement of CA-evoked global cerebral ischemia.
Subject(s)
Acid Sensing Ion Channels/metabolism , Amiloride/therapeutic use , Hippocampus/metabolism , Interleukin-6/metabolism , Ischemic Attack, Transient/drug therapy , Tumor Necrosis Factor-alpha/metabolism , Acid Sensing Ion Channels/genetics , Amiloride/pharmacology , Animals , Asphyxia/complications , Brain Damage, Chronic/drug therapy , Brain Damage, Chronic/etiology , Brain Damage, Chronic/prevention & control , Brain Edema/drug therapy , Brain Edema/etiology , Caspase 3/biosynthesis , Caspase 3/genetics , Caspase 9/biosynthesis , Caspase 9/genetics , Drug Evaluation, Preclinical , Hydrazines/pharmacology , Ischemic Attack, Transient/etiology , Ischemic Attack, Transient/metabolism , Male , Quinoxalines/pharmacology , Rats, Sprague-Dawley , Up-Regulation/drug effectsABSTRACT
Tetrabromobisphenol A (TBBPA) is a commonly used brominated flame retardant, which has a wide range of toxic effects on organisms. This study investigated the cytotoxic effects on human hepatocytes (L02â¯cells) after treated with 0, 5, 10, 20, and 40⯵M of TBBPA. Results showed that TBBPA significantly increased intracellular reactive oxygen species (ROS), malondialdehyde (MDA) and the ratio of oxidized/reduced glutathione (GSSG/GSH) dose-dependently. TBBPA also decreased the cell mitochondrial membrane potential (MMP), caused the release of cytochrome C (Cyt C) to cytoplasm and promoted the expression of caspase-9 and caspase-3, and finally increased the level of apoptosis. The ROS inhibitor N-acetyl-L-cysteine (NAC) relieved the oxidative stress responses, and prevented the decrease of MMP and increase of apoptosis. In addition, TBBPA promoted the expression of antioxidant genes related to Nrf2, such as quinone oxidoreductase 1 (NQO1), catalase (CAT), and heme oxygenase 1 (HO-1). Oxidative stress initiated by TBBPA, activated mitochondrial apoptosis and Nrf2 pathway, and increased the degree of apoptosis in L02â¯cells.
Subject(s)
Apoptosis/drug effects , Flame Retardants/toxicity , Mitochondria/metabolism , NF-E2-Related Factor 2/metabolism , Oxidative Stress/drug effects , Polybrominated Biphenyls/toxicity , Acetylcysteine/pharmacology , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Catalase/metabolism , Cell Line , Cytochromes c/metabolism , Glutathione/metabolism , Heme Oxygenase-1/biosynthesis , Heme Oxygenase-1/genetics , Hepatocytes/drug effects , Humans , Malondialdehyde/metabolism , Membrane Potential, Mitochondrial/drug effects , NAD(P)H Dehydrogenase (Quinone)/biosynthesis , Reactive Oxygen Species/metabolism , Signal Transduction/drug effectsABSTRACT
Epidemiological evidence showed that the particulate matter exposure is associated with atherosclerotic plaque progression, which may be related to foam cell formation, but the mechanism is still unknown. The study was aimed to investigate the toxic effects and possible mechanism of PM2.5 on the formation of macrophage foam cells induced by oxidized low density lipoprotein (ox-LDL). Results showed that PM2.5 induced cytotoxicity by decreasing the cell viability and increasing the LDH level in macrophage foam cells. PM2.5 aggravated the lipid accumulation in ox-LDL-stimulated macrophage RAW264.7 within markedly increasing level of intracellular lipid by Oil red O staining. The level of ROS increased obivously after co-exposure to PM2.5 and ox-LDL than single exposure group. In addition, serious mitochondrial damage such as the mitochondrial swelling, cristae rupturing and disappearance were observed in macrophage foam cells. The loss of the mitochondrial membrane potential (MMP) further exacerbated the mitochondrial damage in PM2.5-induced macrophage foam cells. The apoptotic rate increased more severely via up-regulated protein level of Bax, Cyt C, Caspase-9, Caspase-3, and down-regulated that of Bcl-2, indicating that PM2.5 activated the mitochondrial-mediated apoptosis pathway. In summary, our results demonstrated that PM2.5 aggravated the lipid accumulation, mitochondrial damage and apoptosis in macrophage foam cells, suggesting that PM2.5 was a risk factor of atherosclerosis progression.
Subject(s)
Apoptosis/drug effects , Foam Cells/pathology , Lipoproteins, LDL/metabolism , Membrane Potential, Mitochondrial/physiology , Particulate Matter/toxicity , Plaque, Atherosclerotic/pathology , Animals , Atherosclerosis/pathology , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Cell Line , Cytochromes c/biosynthesis , Lipid Metabolism/drug effects , Mice , RAW 264.7 Cells , Reactive Oxygen Species/metabolism , Signal Transduction/drug effects , Up-Regulation , bcl-2-Associated X Protein/biosynthesisABSTRACT
BACKGROUND Ursolic acid is an important bioactive triterpenoid that has been reported to be of tremendous pharmacological importance. However, the anticancer potential of ursolic acid has not been examined against metastatic melanoma cells. Therefore, in this study we examined the anticancer potential of ursolic acid and its mode of action. MATERIAL AND METHODS WST-1 and colony formation assays were used for cell viability assessment. Cell cycle analysis was performed by flow cytometry. Apoptosis was detected by AO/EB staining using fluorescence microscopy. Cell migration and invasion were assessed by Boyden chamber assay. Protein expression was checked by Western blotting. RESULTS The results revealed that ursolic acid exerts significant (p<0.01) growth-inhibitory effects on SK-MEL-24 cells. The IC50 of ursolic acid against SK-MEL-24 cells was 25 µM. Our investigation of the underlying mechanism revealed that ursolic acid prompts apoptotic cell death of the SK-MEL-24 cells, which was linked with increased expression of Bax and Caspase 3 and 9, and decreased expression of Bcl-2. Ursolic acid also halted the SK-MEL-24 cells at G0/G1 phase of the cell cycle and also downregulated the expression of Cyclin B1 and Cdc25. Ursolic acid significantly (p<0.01) inhibited the migration and invasion of SK-MEL-2 cells, indicative of its anti-metastatic potential. Finally, ursolic acid inhibited the MAPK/ERK pathway by suppressing the expression of p-P38 and p-ERK. CONCLUSIONS Ursolic acid appears to be a potent molecule for the treatment of melanoma.
Subject(s)
MAP Kinase Signaling System/drug effects , Melanoma/drug therapy , Triterpenes/pharmacology , Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Cell Cycle Checkpoints/drug effects , Cell Line, Tumor , Cell Movement/drug effects , Cell Proliferation/drug effects , Cell Survival/drug effects , Humans , Melanoma/enzymology , Melanoma/pathology , Mitogen-Activated Protein Kinases/metabolism , Neoplasm Invasiveness , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Ursolic AcidABSTRACT
Benzophenone-3 (BP-3) is the most commonly used chemical UV filter. This compound can easily be absorbed through the skin and the gastrointestinal tract and can disturb sex hormone receptor function. BP-3 is lipophilic and should cross the blood-brain barrier and it may reduce the survival of neurons, although so far, its effects on nerve cells have been studied in only in vitro cultures. The aim of the present study was to determine the effects of BP-3 on apoptosis and the expression of oestrogen, androgen and arylhydrocarbon receptors (AhR) in the rat frontal cortex and hippocampus. This compound was administered dermally to female rats during pregnancy and next to their male offspring through 6 and 7 weeks of age. BP-3 in the frontal cortex induced the mitochondrial apoptosis pathway by increasing the active forms of caspase-3 and caspase-9, inducing the pro-apoptotic proteins Bax and Bak and increasing the number of cells with apoptotic DNA fragmentation. In the hippocampus, an increase in the caspase-9 level and a downward trend in the level of anti-apoptotic proteins were observed. In both brain regions, the contents of ERß in the nuclear fraction and GPR30 in the membrane fraction were significantly reduced. BP-3 significantly increased AhR in the cytosol of the frontal cortex but had no effect on the content of this receptor in the hippocampus. This is the first study showing that exposure to BP-3 induces the mitochondrial apoptosis pathway in the rat frontal cortex and this effect may result from a weakening of the neuroprotective effects of oestrogen and/or an intensification of AhR-mediated apoptosis.
Subject(s)
Apoptosis/drug effects , Benzophenones/toxicity , Frontal Lobe/metabolism , Gonadal Steroid Hormones/metabolism , Hippocampus/metabolism , Sunscreening Agents/toxicity , Animals , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Female , Frontal Lobe/drug effects , Hippocampus/drug effects , Male , Pregnancy , Prenatal Exposure Delayed Effects , Rats , Rats, Sprague-Dawley , Receptors, Androgen/biosynthesis , Receptors, Androgen/drug effects , Receptors, Aryl Hydrocarbon/drug effects , Receptors, Estrogen/biosynthesis , Receptors, Estrogen/drug effects , bcl-2 Homologous Antagonist-Killer Protein/biosynthesis , bcl-2-Associated X Protein/biosynthesisABSTRACT
Hypoxia is a type of cellular stress that may result in apoptosis and autophagy. The molecular mechanisms underlying the association between autophagy and apoptosis remain unclear, particularly in hypoxic conditions. Transmission electron microscope, AOPI staining, flow cytometry and western blot were used to examine the crosstalk between autophagy and apoptosis in hypoxic conditions. Rat alveolar type II epithelial RLE6TN cells were cultured in a longterm hypoxic environment established by cobalt (II) chloride. It was demonstrated that autophagy and apoptosis occurred in RLE6TN cells under hypoxic conditions. Treatment of RLE6TN cells with the autophagy inhibitor 3methyladenine increased the generation of reactive oxygen species, mitochondrial damage and hypoxiainduced apoptosis. The expression of caspases, particularly caspase9, increased and may have participated in these processes. The data indicated that the inhibition of autophagy enhanced apoptosis through the mitochondriamediated intrinsic pathway. These findings provide important insight into the molecular mechanism of autophagy and apoptosis crosstalk. This may provide new insights into pulmonary disease surveillance, diagnosis and treatment.
Subject(s)
Alveolar Epithelial Cells/enzymology , Apoptosis/drug effects , Autophagy/drug effects , Caspase 9/biosynthesis , Cobalt/pharmacology , Gene Expression Regulation, Enzymologic/drug effects , Alveolar Epithelial Cells/pathology , Animals , Cell Line , RatsABSTRACT
As one type of adult stem cells (ASCs), human dental pulp stem cells (HDPSCs) have several properties, including high proliferation rate, selfrenewal capability, and multilineage differentiation. However, the apoptotic mechanism underlying the development of dental pulp cells remains unclear. In the present study, a significant increase of apoptosis was observed in HDPSCs from the deciduous teeth compared with that from adult permanent teeth. In addition, the occurrence of cytochrome c expression and mitochondrialmediated apoptosis pathway activity in HDPSCs were confirmed by quantitative polymerase chain reaction, and western blotting. Although caspase8 and caspase9 showed higher expression in deciduous teeth than in adult permanent teeth, only the knockdown of caspase9 via RNA interference in HDPSC cells exhibited a significant reduction in apoptosis, and caspase3 expression and activity. All these results revealed that caspase9 and activated caspase3 predominantly regulates cell apoptosis in HDPSCs from deciduous teeth.
Subject(s)
Adult Stem Cells/enzymology , Apoptosis , Caspase 9/biosynthesis , Dental Pulp/enzymology , Gene Expression Regulation, Enzymologic , Tooth, Deciduous/enzymology , Adolescent , Adult , Adult Stem Cells/cytology , Caspase 3/biosynthesis , Child , Dental Pulp/cytology , Female , Humans , Male , Tooth, Deciduous/cytologyABSTRACT
This study aimed to develop novel 1,3,5-triazine derivatives as potent anti-cervical cancer agents. The compounds were synthesized in short steps with an excellent yield and characterized via various spectroscopic and analytical methods. A structure-activity relationship study suggested that electron-withdrawing substituents showed greater anticancer activity than electron-donating groups. Compound 7p (p-fluoro) showed the highest activity against cervical cancer cells. In a nude mouse xenograft model inoculated with HeLa cells, 7p showed dose-dependent inhibition of cervical tumour growth. Histopathological examination of excised tumour-bearing tissues showed that 7p improved the microstructure in a dose-dependent manner. Compound 7p also increased the proportions of HeLa cells in G0/G1 and S-phase and significantly decreased that of G2/M-phase. The effects of 7p on C-caspase-3, C-caspase-9, Bcl-2 and Bax expression in HeLa cells were also determined.
Subject(s)
Antineoplastic Agents , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Gene Expression Regulation, Neoplastic/drug effects , Neoplasms , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Triazines , bcl-2-Associated X Protein/biosynthesis , Animals , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Cell Cycle/drug effects , HeLa Cells , Humans , Jurkat Cells , Mice , Mice, Nude , Neoplasms/drug therapy , Neoplasms/metabolism , Neoplasms/pathology , Triazines/chemical synthesis , Triazines/chemistry , Triazines/pharmacology , Xenograft Model Antitumor AssaysABSTRACT
Objective To investigate the expressions and correlations of gastrin and apoptosis-associated proteins involved in mitochondrial apoptotic pathway in gastric cancer tissues, and explore their clinicopathological characteristics. Methods The tissue chip technology and immunohistochemistry (IHC) were used to detect the expressions of gastrin and apoptosis-associated proteins (Bcl2, caspase-9 and caspase-3) in human gastric cancer tissues and their paracancerous tissues. The correlations of these markers and their clinicopathological characteristics were analyzed using Spearman rank correlation analysis and Chi-square test. Results The expressions of gastrin and Bcl2 in gastric cancer tissues were significantly higher than those in the corresponding paracancerous tissues, whereas the expressions of caspase-9 and caspase-3 in gastric cancer tissues was significantly lower than those in the corresponding tissues. There was a significant positive correlation between the expressions of gastrin and Bcl2 in gastric cancer tissues (r=0.237). The expression of gastrin was associated with tumor position, and the expression of Bcl2 was associated with tumor size, TNM stage and lymph node metastasis. Conclusion Gastrin and Bcl2 are highly expressed in gastric cancer tissues, and they are correlated with the clinicopathologic features.
Subject(s)
Gastrins/biosynthesis , Mitochondria/metabolism , Proto-Oncogene Proteins c-bcl-2/biosynthesis , Signal Transduction , Stomach Neoplasms/metabolism , Adult , Aged , Biomarkers, Tumor/biosynthesis , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Female , Humans , Immunohistochemistry , Male , Middle Aged , Stomach Neoplasms/pathologyABSTRACT
BACKGROUND/AIMS: Aloe-emodin (1,8-dihydroxy-3-hydroxymethyl-anthraquinone), an anthraquinone active compounds, is isolated from some traditional medicinal plants such as Rheum palmatum L. and Cassia occidentalis, which induce hepatotoxicity in rats. The aim of this study was to determine potential cytotoxic effects of aloe-emodin on HepaRG cells and to define the underlying mechanism. METHODS: MTT was used to evaluate cell viability. Apoptotic cell death was analyzed via Annexin V-FITC/PI double staining. Intracellular reactive oxygen species (ROS) and mitochondrial membrane potential (MMP) were determined by flow cytometry, while the expression of apoptosis-related proteins was determined by Western blot analysis. RESULTS: Treatment with aloe-emodin significantly reduced cell viability and induced apoptosis in HepaRG cells in a dose- and time-dependent manner. It provoked ROS generation and depolarization of MMP in HepaRG cells when compared with controls. Aloe-emodin dose-dependently increased release of mitochondrial cytochrome c, and levels of Fas, p53, p21, Bax/Bcl-2 ratio, as well as activation of caspase-3, caspase-8, caspase-9, and subsequent cleavage of poly(ADP-ribose)polymerase (PARP). It also induced S-phase cell cycle arrest by increasing the expression of p21 and cyclin E proteins while significantly decreasing the expression of cyclin A and CDK2. CONCLUSION: These results suggest that aloe-emodin inhibits cell proliferation and induces apoptosis in HepaRG cells, most probably through a mechanism involving both Fas death pathway and the mitochondrial pathway by generation of ROS. These findings underscore the need for risk assessment of human exposure to aloe-emodin.
Subject(s)
Anthraquinones/administration & dosage , Apoptosis/drug effects , Cell Proliferation/drug effects , Mitochondria/metabolism , Animals , Apoptosis Regulatory Proteins/biosynthesis , Caspase 3/biosynthesis , Caspase 8/biosynthesis , Caspase 9/biosynthesis , Cell Cycle Checkpoints/drug effects , Cell Survival/drug effects , Gene Expression Regulation/drug effects , Humans , Metabolic Networks and Pathways/drug effects , Mitochondria/drug effects , Mitochondria/pathology , Rats , Reactive Oxygen Species/metabolismABSTRACT
Photodynamic therapy is widely used in the clinical treatment of tumors, especially skin cancers. It has been reported that the photosensitizer curcumin, in combination with ultraviolet radiation B, induces HaCaT cell apoptosis, and this effect may be due to the activation of caspase pathways. In this study, we examined the photodynamic effects of demethoxycurcumin, a more stable analogue of curcumin, to determine whether it could induce apoptosis in skin cancer cells. We investigated the effects of a combination of ultraviolet radiation B and demethoxycurcumin on apoptotic cell death in A431 and HaCaT cells and determined the molecular mechanism of action. Our results showed increased apoptosis with a combination of ultraviolet radiation B with demethoxycurcumin, as compared to ultraviolet radiation B or demethoxycurcumin alone. The combination of ultraviolet radiation B irradiation with demethoxycurcumin synergistically induced apoptotic cell death in A431 and HaCaT cells through activation of p53 and caspase pathways, as well as through upregulation of Bax and p-p65 expression and downregulation of Bcl-2, Mcl-1, and nuclear factor-κB expression. In addition, we found that reactive oxygen species significantly increased with treatment, and mitochondrial membrane potential depolarization was remarkably enhanced. In conclusion, our data indicate that demethoxycurcumin may be a promising photosensitizer for use in photodynamic therapy to induce apoptosis in skin cancer cells.
Subject(s)
Curcumin/analogs & derivatives , Photochemotherapy , Skin Neoplasms/drug therapy , Skin Neoplasms/radiotherapy , Caspase 3/biosynthesis , Caspase 9/biosynthesis , Cell Line, Tumor , Cell Survival/drug effects , Cell Survival/radiation effects , Curcumin/administration & dosage , Diarylheptanoids , Gene Expression Regulation, Neoplastic , Humans , Mitochondria/drug effects , Mitochondria/radiation effects , Neoplasm Proteins/biosynthesis , Photosensitizing Agents/administration & dosage , Reactive Oxygen Species , Signal Transduction/drug effects , Signal Transduction/radiation effects , Skin Neoplasms/genetics , Skin Neoplasms/pathology , Ultraviolet RaysABSTRACT
Ferrichrome is known to be a siderophore, but it was recently identified as a tumor-suppressive molecule derived from Lactobacillus casei ATCC334 ( L. casei). In the present study, we investigated the effects of ferrichrome in gastric cancer cells. Cell lines and xenograft models treated with ferrichrome demonstrated growth suppression. The expression levels of cleaved poly (adenosine diphosphate-ribose) polymerase, and cleaved caspase-9 were increased by ferrichrome treatment. Although the tumor-suppressive effects of ferrichrome were almost completely diminished by the iron chelation, the reduction in the intracellular iron by ferrichrome did not correlate with its tumor-suppressive effects. An exhaustive docking simulation indicated that iron-free ferrichrome can make stable conformations with various mammalian molecules, including transporters and receptors. In conclusion, probiotic-derived ferrichrome induced apoptosis in gastric cancer cells. The iron binding site of ferrichrome is the structure responsible for its tumor suppressive function.
Subject(s)
Apoptosis/drug effects , Ferrichrome/administration & dosage , Ferrichrome/chemistry , Stomach Neoplasms/drug therapy , Animals , Binding Sites , Caspase 9/biosynthesis , Cell Line, Tumor , Ferrichrome/isolation & purification , Humans , Iron/metabolism , Lacticaseibacillus casei/chemistry , Mice , Molecular Docking Simulation , Stomach Neoplasms/pathology , Xenograft Model Antitumor AssaysABSTRACT
A number of drugs as well as lead molecules are isolated from natural sources. Phytol is one of such lead molecule belongs to terpenes group distributed widely in medicinal plants. In the present work, we investigated the cytotoxic behavior of phytol on human lung carcinoma cells (A549). Phytol was found to cause characteristic apoptotic morphological changes and generation of ROS in A549 cells. The mechanism of phytol involved the activation of TRAIL, FAS and TNF-α receptors along with caspase 9 and 3. In silico molecular docking studies revealed that phytol has a good binding affinity with glucose-6-phosphate dehydrogenase (G6PD), which is known to promote tumor proliferation. The ability of phytol to become potential drug candidate has been revealed from the pharmacokinetic study performed in the present study.
Subject(s)
Caspase 3/biosynthesis , Caspase 9/biosynthesis , Glucosephosphate Dehydrogenase/metabolism , Lung Neoplasms/metabolism , Phytol/pharmacology , Reactive Oxygen Species/metabolism , A549 Cells , Apoptosis/drug effects , Apoptosis/physiology , Cell Line, Tumor , Enzyme Induction/drug effects , Enzyme Induction/physiology , Humans , Phytol/chemistry , Phytol/therapeutic use , Protein Structure, Secondary , Receptors, TNF-Related Apoptosis-Inducing Ligand/metabolism , Receptors, Tumor Necrosis Factor/metabolism , fas Receptor/metabolismABSTRACT
OBJECTIVE: Previous studies found bone resorption and chondrocytes loss in mouse models of mid-palatal suture when given continuous compressive force, although chondrocytes response remained unknown. Herein, we design this study to determine how continuous compression force induces chondrocytes apoptosis. METHODS: Thirty C57BL/6 male mice (aged 6 weeks) were randomly assigned into controls (not ligated to a spring), blank controls (ligated with no compression) and the compression group (ligated with 20-g compression). After 4 d, palatal tissues were sampled and stained by TB and safranin-O. Tunel staining measured the percentage of apoptotic chondrocytes, and immunohistochemistry was performed to label apoptosis-associated proteins (e.g., Bcl-2, Bcl-xl, Bax, Bak, Bid, Bad, caspase-3, caspase-8 and caspase-9). Intergroup comparison was made by the rank sum test, and P < 0.05 was defined as statistical significance. RESULTS: After 7d of induction, TB and safranin-O staining revealed that the cartilage area in the compression group was significantly decreased, while the control group remained largely unaltered. Tunel staining showed that apoptotic cell numbers in the mid-palatal suture were significantly higher than the control group. Immunohistochemistry showed that mice in the compression group had significantly increased expression of caspase-3, caspase-9, Bad, Bak, Bax and Bid; However, caspase-8 remained unaltered. No expression of Bcl-2 and Bcl-xl was detected. CONCLUSIONS: Continuous compression force induces chondrocytes apoptosis in the mid-palatal suture. This process might be associated with the mitochondrial pathway.