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1.
Laryngoscope ; 121(9): 2011-8, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21792978

ABSTRACT

OBJECTIVES/HYPOTHESIS: Wood dust is a well-established risk factor for intestinal type sinonasal adenocarcinoma. The 5-year overall survival has varied from 20% to 80% according T1-T4 stages; 5-year survival according to histologic subtype has varied from 20% to 50%. To date, no study has evaluated whether environmental, occupational, and personal risk factors have any impact on both overall and cancer-specific survival. We aimed to determine whether exposure to carcinogenic risk factors besides wood exposure can influence the survival of patients with sinonasal ethmoid carcinoma. STUDY DESIGN: Retrospective cohort study of the association of survival data and occupational and personal carcinogenic risk factors. METHODS: All patients hospitalized for ethmoid adenocarcinoma at the Nantes University Hospital between 1988 and 2004 were included . Data concerning TNM classification, histology, type and quality of tumor resection at the macro- and microscopic level, and occupational and personal exposure to carcinogens were collected. Statistical analysis was conducted using univariate and multivariate linear regression. RESULTS: A total of 98 patients were included with a response rate of 98%. Data showed 86% of patients had been exposed to wood dust. The 5-year survival was 62%. We first identified four factors that independently influenced overall survival: diplopia (P = .0159), spread to the orbit (P = .0113), bilateral involvement (P = .0134), TNM stage (P < .001). When the analysis included all occupational environmental factors (wood dust, solvent, and metals exposure) as well as personal risk factors, the length of exposure to metals (P = .0307) and tobacco exposure (P = .0031) also were found to influence 5-year overall survival. We identified high prevalence of colon cancer (4%) and double cancer (18%). CONCLUSIONS: We showed exposure to both environmental (tobacco) and occupational (metal dust) factors could influence survival in the diagnosis of a cancer. Our study suggests that screening for colon cancer should be offered to wood dust workers. A prospective multicentric study should be necessary to confirm our results.


Subject(s)
Adenocarcinoma/etiology , Dust , Metals/adverse effects , Occupational Exposure/adverse effects , Paranasal Sinus Neoplasms/etiology , Tobacco Smoke Pollution/adverse effects , Adenocarcinoma/diagnosis , Adenocarcinoma/surgery , Female , Humans , Logistic Models , Male , Middle Aged , Occupations , Paranasal Sinus Neoplasms/diagnosis , Paranasal Sinus Neoplasms/surgery , Retrospective Studies , Risk Factors , Survival Rate
2.
Int J Cancer ; 123(2): 288-295, 2008 Jul 15.
Article in English | MEDLINE | ID: mdl-18412241

ABSTRACT

Our study explored the influence of diet on gliomagenesis and associated systemic effects (SE) in rats. The experimental diet contained various ingredients supposed to interfere with carcinogenesis, mainly phytochemicals (PtcD for phytochemical diet) and its effects were compared to those of the same diet without the phytochemicals (BD for basal diet). Glioma was induced by ethylnitrosourea to pregnant females fed the diets from the start of gestation until the moment of sacrifice of the offpsrings. In male rats fed the PtcD or the BD the incidence of gliomas was markedly reduced compared to rats fed a standard diet (StD). In females this effect was weaker and was limited to the PtcD. A significant proportion of rats with brain tumors and fed the StD exhibited SE evidenced by weight loss, a shorter survival, reduction in liver weight and an increased proportion of liver mitochondria, effects that were not observed in their counterpart fed PtcD. Comparison of the expression of genes involved in the balance proliferation/apoptosis and in the response to oxidative stress in male brain tumors showed that the prevention of SE was associated with an increase in bcl-2 and catalase and a decrease in ki-67, sod-1 and sod-2 transcripts. These results show that the degree of agressiveness of gliomas can be modulated by dietary interventions and suggest that some phytochemicals with antioxidant properties could participate to the mechanism.


Subject(s)
Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , Apoptosis , Brain Neoplasms/diet therapy , Brain Neoplasms/prevention & control , Glioma/diet therapy , Glioma/prevention & control , Oxidative Stress , Animals , Apoptosis/drug effects , Biomarkers, Tumor/analysis , Brain Neoplasms/chemically induced , Brain Neoplasms/metabolism , Brain Neoplasms/pathology , Cell Proliferation/drug effects , Ethylnitrosourea , Female , Fruit , Glioma/chemically induced , Glioma/metabolism , Glioma/pathology , Immunohistochemistry , Male , Mitochondria, Liver/metabolism , Polymerase Chain Reaction , Pregnancy , RNA, Neoplasm/analysis , Rats , Vegetables
3.
BMC Cancer ; 6: 234, 2006 Oct 03.
Article in English | MEDLINE | ID: mdl-17018136

ABSTRACT

BACKGROUND: Accumulating data suggest that liver is a major target organ of systemic effects observed in the presence of a cancer. In this study, we investigated the consequences of the presence of chemically induced brain tumors in rats on biophysical parameters accounting for the dynamics of water in liver mitochondria. METHODS: Tumors of the central nervous system were induced by intraveinous administration of ethylnitrosourea (ENU) to pregnant females on the 19th day of gestation. The mitochondrial crude fraction was isolated from the liver of each animal and the dynamic parameters of total water and its macromolecule-associated fraction (structured water, H2Ost) were calculated from Nuclear Magnetic Resonance (NMR) measurements. RESULTS: The presence of a malignant brain tumor induced a loss of water structural order that implicated changes in the physical properties of the hydration shells of liver mitochondria macromolecules. This feature was linked to an increase in the membrane cholesterol content, a way to limit water penetration into the bilayer and then to reduce membrane permeability. As expected, these alterations in mitochondrial plasticity affected ionic exchanges and led to abnormal features of mitochondrial biogenesis and caspase activation. CONCLUSION: This study enlightens the sensitivity of the structured water phase in the liver mitochondria machinery to external conditions such as tumor development at a distant site. The profound metabolic and functional changes led to abnormal features of ion transport, mitochondrial biogenesis and caspase activation.


Subject(s)
Brain Neoplasms/chemistry , Mitochondria, Liver/chemistry , Water/chemistry , Animals , Brain Neoplasms/enzymology , Caspases/metabolism , Cholesterol/analysis , Fatty Acids, Unsaturated/analysis , Female , Ions/analysis , Liver/enzymology , Nuclear Magnetic Resonance, Biomolecular , Rats
4.
J Leukoc Biol ; 78(3): 794-803, 2005 Sep.
Article in English | MEDLINE | ID: mdl-15961579

ABSTRACT

Dendritic cell (DC) maturation is the process by which immature DC in the periphery differentiate into fully competent antigen-presenting cells that initiate the T cell response. However, DC respond to many distinct maturation stimuli, and different types of mature DC induce qualitatively different T cell responses. As DC maturation involves the coordinated regulation of hundreds of genes, comprehensive assessment of DC maturation status would ideally involve monitoring the expression of all of these transcripts. However, whole-genome microarrays are not well-suited for routine phenotyping of DC, as the vast majority of genes represented on such chips are not relevant to DC biology, and their cost limits their use for most laboratories. We therefore developed a DC-dedicated microarray, or "DC Chip", incorporating probes for 121 genes up-regulated during DC maturation, 93 genes down-regulated during maturation, 14 DC-specific genes, and 90 other genes with known or probable immune functions. These microarrays were used to study the kinetics of DC maturation and the differences in maturation profiles among five healthy donors after stimulation with tumor necrosis factor-alpha + polyI:C. Results obtained with the DC Chip were consistent with flow cytometry, enzyme-linked immunosorbent assay, and real-time polymerase chain reaction, as well as previously published data. Furthermore, the coordinated regulation of a cluster of genes (indoleamine dioxygenase, kynureninase, kynurenine monoxygenase, tryptophanyl tRNA synthetase, and 3-hydroxyanthranilate 3,4-dioxygenase) involved in tryptophan metabolism was observed. These data demonstrate the use of the DC Chip for monitoring the molecular processes involved in the orientation of the immune response by DC.


Subject(s)
Cell Differentiation/immunology , Dendritic Cells/immunology , Gene Expression Profiling/methods , Oligonucleotide Array Sequence Analysis/methods , Antigens, CD/analysis , Antigens, CD/genetics , Dendritic Cells/chemistry , Dendritic Cells/drug effects , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Humans , Interleukin-12/analysis , Interleukin-12/genetics , Kinetics , Phenotype , Poly I-C/pharmacology , RNA, Messenger/analysis , RNA, Messenger/genetics , Reference Values , Reproducibility of Results , Research Design , Reverse Transcriptase Polymerase Chain Reaction , Tryptophan/metabolism , Tumor Necrosis Factor-alpha/pharmacology
5.
FEBS Lett ; 579(11): 2364-8, 2005 Apr 25.
Article in English | MEDLINE | ID: mdl-15848173

ABSTRACT

We have shown previously that calcium could trigger nuclear fragmentation, which was associated with a caspase 3 (C3)-like activity [Juin, P., Pelletier, M., Oliver, L., Tremblais, K., Gregoire, M., Meflah, K. and Vallette, F.M. (1998) Induction of a caspase-3-like activity by calcium in normal cytosolic extracts triggers nuclear apoptosis in a cell-free system. J. Biol. Chem. 273, 17559]. Here, we report that this activation is associated with a non-canonical truncation of C3, which induces a weak DEVDase activity. The cleavage of C3 via calcium-dependent proteolysis is independent of caspase 9; lysate exposure to calcium prevents further cleavage and activation by the cytochrome c and dATP pathway. Altogether, our data suggest that calcium could favour a necrotic mechanism by inducing the generation of a form of C3 insensitive to mitochondrial activation.


Subject(s)
Calcium/pharmacology , Caspases/chemistry , Caspases/metabolism , Apoptosis , Calcium/metabolism , Caspase 3 , Caspases/genetics , Cell Extracts/chemistry , Cell Line, Tumor , Cytochromes c/metabolism , Deoxyadenine Nucleotides/pharmacology , Enzyme Activation/drug effects , Humans , Mutation/genetics , Peptide Hydrolases/metabolism , Protein Subunits/chemistry , Protein Subunits/genetics , Protein Subunits/metabolism
6.
Cancer Immunol Immunother ; 54(1): 78-86, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15693142

ABSTRACT

We have shown recently that some indigestible carbohydrate (short-chain fructo-oligosaccharides [sc-FOS]) reduced colon tumor incidence in Apc+/Min mice, and that this effect depended on a functional local immune system. In addition, IL-15 mRNA was concomitantly modulated in the mucosa. Since intraepithelial lymphocytes (IELs) are in close contact with intestinal epithelial cells, these cells are the candidates most likely to be involved in early cancer immunosurveillance. The present study documents the effects of sc-FOS on large intestine IELs (LI-IELs) from Apc+/+ or Apc+/Min mice by analyzing markers related to their phenotype, their activation status, and the cell surface IL-15/IL-5R alpha. In the colons of Apc+/Min mice, fewer LI-IELs expressed surface IL-15/IL-15R alpha. In addition, a lower number of CD4+ LI-IELs expressed CD25, although more LI-IELs expressed CD69, as compared to normal mice. The sc-FOS enriched diet caused a decrease in the proportion of CD25+ LI-IELs and an increase in the percentage of LI-IELs bearing surface IL-15/IL-15R alpha, independently of the Apc gene status. The IL-15/IL-15R alpha increase was, however, higher in Min mice, and returned to a level very similar to that of Apc+/+ mice when the latter mice were fed a low-fiber diet. The sc-FOS-enriched diet specifically induced an increase in CD69+ cells in Apc+/+ mice, and a decrease in the proportion of CD4+ CD25+ LI-IELs in Apc+/Min mice. Some of these modulations could contribute to the development of a better immune anticancer response in the early steps of cancer development.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Dietary Carbohydrates/pharmacology , Interleukin-15/immunology , Intestine, Large/drug effects , Lymphocytes/immunology , Receptors, Interleukin-2/immunology , Animals , CD4-Positive T-Lymphocytes/drug effects , Dietary Carbohydrates/immunology , Female , Flow Cytometry , Gene Expression Regulation/drug effects , Genes, APC , Interleukin-15/genetics , Intestine, Large/cytology , Intestine, Large/immunology , Lymphocytes/drug effects , Mice , Mice, Inbred C57BL , Mice, Mutant Strains , Mutation , Phenotype , RNA, Messenger/drug effects , RNA, Messenger/genetics , Receptors, Interleukin-15 , Receptors, Interleukin-2/drug effects , Receptors, Interleukin-2/genetics
7.
J Biol Chem ; 280(11): 10587-98, 2005 Mar 18.
Article in English | MEDLINE | ID: mdl-15590655

ABSTRACT

The translocation of Bax from the cytosol into the mitochondrial outer membrane is a central event during apoptosis. We report that beyond the addressing step, which involves its first alpha-helix (halpha1), the helices alpha5 and alpha6 (halpha5alpha6) are responsible for the insertion of Bax into mitochondrial outer membrane bilayer. The translocation of Bax to mitochondria is associated with specific changes in the conformation of the protein that are under the control of two prolines: Pro-13, which controls the unfolding of halpha1, and Pro-168, a proline located immediately before the hydrophobic carboxyl-terminal end (i.e. helix alpha9, halpha9), which controls the disclosure of halpha5alpha6. An additional step, the disruption of an electrostatic bond formed between Asp-33 (halpha1) and Lys-64 (BH3), allows the mitochondria addressing of Bax. We conclude that, although the intramolecular interactions of halpha1 with the BH3 region control the addressing of Bax to mitochondria, the Pro-168 is involved in the control of its membrane insertion through halpha5alpha6.


Subject(s)
Mitochondria/metabolism , Proto-Oncogene Proteins c-bcl-2/chemistry , Amino Acid Sequence , Animals , Apoptosis , Aspartic Acid/chemistry , Base Sequence , Cell-Free System , Cytosol/metabolism , Electrophoresis, Polyacrylamide Gel , Immunoprecipitation , Lipid Bilayers , Liver/metabolism , Lysine/chemistry , Microscopy, Confocal , Models, Molecular , Molecular Sequence Data , Mutagenesis, Site-Directed , Mutation , Plasmids/metabolism , Proline/chemistry , Protein Conformation , Protein Folding , Protein Structure, Secondary , Protein Structure, Tertiary , Protein Transport , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Static Electricity , Subcellular Fractions/metabolism , Transfection , Transgenes , Two-Hybrid System Techniques , bcl-2-Associated X Protein
8.
Mol Cell ; 16(5): 807-18, 2004 Dec 03.
Article in English | MEDLINE | ID: mdl-15574335

ABSTRACT

The mechanism by which some BH3-only proteins of the Bcl-2 family directly activate the "multidomain" proapoptotic member Bax is poorly characterized. We report that the first alpha helix (Halpha1) of Bax specifically interacts with the BH3 domains of Bid and PUMA but not with that of Bad. Inhibition of this interaction, by a peptide comprising Halpha1 or by a mutation in this helix, prevents ligand-induced activation of Bax by Bid, PUMA, or their BH3 peptides. Halpha1-mutated Bax, which can mediate death induced by Bad or its BH3 peptide, does not mediate that induced by Bid, PUMA, or their BH3 peptides. The response of Halpha1-mutated Bax to Bid can be restored by a compensating mutation in Bid BH3. Thus, a specific interaction between Bax Halpha1 and their BH3 domains allows Bid and PUMA to function as "death agonists" of Bax, whereas Bad recruits Bax activity through a distinct pathway.


Subject(s)
Carrier Proteins/chemistry , Proto-Oncogene Proteins c-bcl-2/chemistry , Proto-Oncogene Proteins/chemistry , Tumor Suppressor Protein p53/chemistry , Apoptosis , Apoptosis Regulatory Proteins , BH3 Interacting Domain Death Agonist Protein , Cell Line , Cell-Free System , Dose-Response Relationship, Drug , Humans , Immunoprecipitation , Ligands , Microscopy, Fluorescence , Mitochondria/metabolism , Mutation , Peptides/chemistry , Plasmids/metabolism , Protein Binding , Protein Conformation , Protein Structure, Secondary , Protein Structure, Tertiary , Protein Transport , Proto-Oncogene Proteins c-bcl-2/metabolism , Recombinant Proteins/chemistry , Surface Plasmon Resonance , Time Factors , Two-Hybrid System Techniques , bcl-2-Associated X Protein
9.
FEBS Lett ; 578(1-2): 41-6, 2004 Dec 03.
Article in English | MEDLINE | ID: mdl-15581613

ABSTRACT

The change in the conformation of Bax at the onset of apoptosis is a determinant for the execution of this cell death programme. However, very few models can account for this modification and the factors involved in this process remain elusive. We have analysed the modifications in the conformation induced by a variation in pH using a cell-free assay. We show that a moderate basic or acidic pH can induce apoptotic-like changes in the conformation of Bax, such as the exposure of the N-terminal or the BH3 domain. These changes in the conformation are associated with the binding of Bax to mitochondria and an enhanced Bax homo- and oligomerisation. Our results suggest that variations in the pH, in a range consistent with that often observed during apoptosis, are sufficient to trigger Bax translocation to mitochondria and the subsequent release of apoptogenic factors from this organelle.


Subject(s)
Hydrogen-Ion Concentration , Mitochondria/metabolism , Protein Conformation , Proto-Oncogene Proteins c-bcl-2/chemistry , Proto-Oncogene Proteins c-bcl-2/metabolism , Animals , Apoptosis/physiology , Cell-Free System , Dimerization , Epitopes , Rats , Trypsin/metabolism , bcl-2-Associated X Protein , bcl-X Protein
10.
BMC Cancer ; 4: 54, 2004 Aug 24.
Article in English | MEDLINE | ID: mdl-15331018

ABSTRACT

BACKGROUND: The relative role of anti apoptotic (i.e. Bcl-2) or pro-apoptotic (e.g. Bax) proteins in tumor progression is still not completely understood. METHODS: The rat glioma cell line A15A5 was stably transfected with human Bcl-2 and Bax transgenes and the viability of theses cell lines was analyzed in vitro and in vivo. RESULTS: In vitro, the transfected cell lines (huBax A15A5 and huBcl-2 A15A5) exhibited different sensitivities toward apoptotic stimuli. huBax A15A5 cells were more sensitive and huBcl-2 A15A5 cells more resistant to apoptosis than mock-transfected A15A5 cells (pCMV A15A5). However, in vivo, in syngenic rat BDIX, these cell lines behaved differently, as no tumor growth was observed with huBax A15A5 cells while huBcl-2 A15A5 cells formed large tumors. The immune system appeared to be involved in the rejection of huBax A15A5 cells since i) huBax A15A5 cells were tumorogenic in nude mice, ii) an accumulation of CD8+ T-lymphocytes was observed at the site of injection of huBax A15A5 cells and iii) BDIX rats, which had received huBax A15A5 cells developed an immune protection against pCMV A15A5 and huBcl-2 A15A5 cells. CONCLUSIONS: We show that the expression of Bax and Bcl-2 controls the sensitivity of the cancer cells toward the immune system. This sensitization is most likely to be due to an increase in immune induced cell death and/or the amplification of an anti tumour immune response


Subject(s)
Apoptosis , Glioma/immunology , Glioma/metabolism , Proto-Oncogene Proteins c-bcl-2/metabolism , Animals , Antigens, Surface/analysis , CD8-Positive T-Lymphocytes/immunology , Clone Cells , Disease Progression , Lectins, C-Type/analysis , Lymphocyte Count , Mice , Mice, Nude , NK Cell Lectin-Like Receptor Subfamily B , Rats , Transfection , Tumor Cells, Cultured , bcl-2-Associated X Protein
11.
J Biol Chem ; 279(45): 46542-50, 2004 Nov 05.
Article in English | MEDLINE | ID: mdl-15328340

ABSTRACT

We have investigated the mechanism responsible for mitochondria permeabilization occurring during cell apoptosis. We have developed an in vivo model of apoptotic rat liver. Mitochondria appeared as an homogenous population in control liver. On the contrary, mitochondria varied in size, morphology, and the matrical density in apoptotic liver. Mitochondria were purified from control and apoptotic livers. In control conditions, a single mitochondrial population was identified; whereas three populations of mitochondria were purified from apoptotic liver. Our data show that these apoptotic populations correspond to early, intermediate, and late apoptotic mitochondria, which are characterized by an increasing extent of permeabilization of their outer membrane and a gradual enrichment in oligomerized Bax protein. Remarkably, a new ionic channel was observed in apoptotic but not in control mitochondria. The biophysical and pharmacological properties of this channel are in good agreement with those reported for a previously described mitochondrial apoptosis-induced channel (MAC) (Pavlov, E. V., Priault, M., Pietkiewicz, D., Cheng, E. H., Antonsson, B., Manon, S., Korsmeyer, S. J., Mannella, C. A., and Kinnally, K. W. (2001) J. Cell Biol. 155, 725-731). However, MAC activity was only observed in the late apoptotic mitochondrial population. Thus, our study establishes that MAC activity is related to the overall apoptotic process but corresponds to a late event.


Subject(s)
Apoptosis , Ion Channels/chemistry , Ion Channels/physiology , Liver/pathology , Mitochondria/pathology , Mitochondrial Proteins/chemistry , Mitochondrial Proteins/physiology , Animals , Anions , Biophysical Phenomena , Biophysics , Caspase 3 , Caspases/metabolism , Cell Membrane/metabolism , Electrophoresis, Polyacrylamide Gel , Electrophysiology , Immunoblotting , Intracellular Membranes/metabolism , Ions , Liver/metabolism , Liver/ultrastructure , Microscopy, Electron , Mitochondria/metabolism , Permeability , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Time Factors , bcl-2-Associated X Protein
12.
Int J Cancer ; 111(4): 575-83, 2004 Sep 10.
Article in English | MEDLINE | ID: mdl-15239136

ABSTRACT

Apoptosis is a physiologic process in normal development, tissue remodeling and cell turnover. This cell death is noninflammatory and nonimmunogenic, but when associated with a danger signal, it can activate the immune system. However, the capacity of apoptotic cells to activate the immune system is not clearly established, although dead tumor cells have been largely exploited as a source of TAA in cellular therapy against cancer. From these cellular preparations, contradictory results have been reported on the effect of apoptotic cells as an effective source of TAA and their immunologic properties. These conflicting data strongly suggest that the optimal preparation of apoptotic cells derived from tumor cells remains to be determined. In this work, we studied and compared the efficacy of antitumor immune responses derived from repeated injections using different preparations of apoptotic cells. We investigated the importance of HSP70 and TGF-beta expression in apoptotic cells used in the treatment of an established and nonimmunogenic rat carcinoma. UVB-mediated apoptosis did not affect TGF-beta expression in tumor cells, whereas HS treatment sharply downregulated it. Thus, downregulation of TGF-beta permits normal DC activation and maturation and the induction of tumor immunity. We conclude that HS followed by UVB irradiation is a superior source of tumor antigen for the treatment of established tumors. Future work will determine whether HS independently upregulates HSP70, thereby suppressing expression of active TGF-beta, or whether the 2 are linked via a still undefined mechanism.


Subject(s)
Apoptosis/genetics , Apoptosis/immunology , Cancer Vaccines , HSP70 Heat-Shock Proteins/biosynthesis , Immunotherapy , Transforming Growth Factor beta/biosynthesis , Animals , Carcinoma/immunology , Carcinoma/pathology , Carcinoma/veterinary , Colonic Neoplasms/immunology , Colonic Neoplasms/pathology , Colonic Neoplasms/veterinary , Dendritic Cells/immunology , Down-Regulation , HSP70 Heat-Shock Proteins/immunology , Humans , Rats , Transforming Growth Factor beta/immunology , Ultraviolet Rays , Up-Regulation
13.
Biochem Biophys Res Commun ; 316(1): 93-9, 2004 Mar 26.
Article in English | MEDLINE | ID: mdl-15003516

ABSTRACT

We report that the induction and completion of the apoptotic program is delayed in a doxorubicin-resistant cell line (HL60/ADR). This hindrance to cell death occurred downstream of the multidrug-resistant protein (mrp), a transmembrane transporter. In vitro studies showed that these cells were incapable of correctly activating procaspase 3 (pC3), the main executioner of apoptosis. Sequencing of HL60/ADR pC3 revealed point mutations in a sequence located in the N-terminal region of the large subunit of caspase 3 (C3, amino acids 31-37; i.e., immediately after the propeptide). We called this particular form of C3, the C3 N-terminal modified (C3-NTM), and show that it is partially active when transfected into MCF-7 cells shown to have little or no endogenous pC3. As a deletion of the amino acids 31-37 in wild-type C3 leads to the same phenotype, we conclude that this sequence is involved in C3 activation during apoptosis.


Subject(s)
Caspases/chemistry , Caspases/metabolism , Amino Acid Sequence , Apoptosis , Caspase 3 , Caspases/genetics , Cell Line , Drug Resistance , Enzyme Activation , HL-60 Cells , Humans , Molecular Sequence Data , Point Mutation , Protein Subunits/chemistry , Protein Subunits/metabolism , Sequence Alignment
14.
J Biol Chem ; 279(12): 11503-12, 2004 Mar 19.
Article in English | MEDLINE | ID: mdl-14681224

ABSTRACT

p21(Bax) is a pro-apoptotic member of the Bcl-2 family and is converted by calpain into a truncated form called p18(Bax). This proteolysis enhanced the apoptogenic properties of Bax by a mechanism not yet elucidated. We have shown recently that the first alpha helix (Halpha1) of p21(Bax) contained a mitochondrial addressing sequence, which appeared to be necessary for p21(Bax)-induced apoptosis (Cartron, P. F., Priault, M., Oliver, L., Meflah, K., Manon, S., and Vallette, F. M. (2003) J. Biol. Chem. 278, 11633-11641). This feature is in contradiction with the high apoptogenic profile of p18(Bax), because the Halpha1 is lost during the calpain cleavage of p21(Bax). We investigated the role of p18(Bax) in apoptosis and found that its activity required the presence of p21(Bax). In addition, p18(Bax) exhibited a higher affinity for Bcl-Xl than p21(Bax) did, a property that seems to be essential for the fulfillment of its pro-apoptotic role. In conclusion, calpain proteolysis converts the multi-domain p21(Bax) into a Bcl-2 homology 3-like protein capable of overcoming the inhibition of apoptosis due to Bcl-Xl.


Subject(s)
Proto-Oncogene Proteins c-bcl-2/physiology , Proto-Oncogene Proteins/physiology , Apoptosis , Base Sequence , Brain Neoplasms/metabolism , Brain Neoplasms/pathology , Cell Line, Tumor , DNA Primers , Glioma/metabolism , Glioma/pathology , Humans , Mitochondria/metabolism , Proto-Oncogene Proteins/chemistry , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-bcl-2/chemistry , Proto-Oncogene Proteins c-bcl-2/metabolism , bcl-2-Associated X Protein
15.
Expert Rev Anticancer Ther ; 3(4): 563-70, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12934667

ABSTRACT

The cell death program, apoptosis, is currently viewed as the ultimate obstacle in cancer therapy. Inhibition of apoptosis is thought to be involved in both tumorigenesis and resistance to chemo- and radiotherapy. Considerable efforts are underway to design new tools capable of overcoming this inhibition. In this review, the current understanding of mechanisms of apoptosis in normal and tumor cells as well as possible or existing strategies designed to induce specific and efficient cell death in cancers are summarized.


Subject(s)
Apoptosis/physiology , Membrane Proteins/physiology , Neoplasms/physiopathology , Proto-Oncogene Proteins c-bcl-2 , Proto-Oncogene Proteins/physiology , Humans , Neoplasms/pathology , Neoplasms/therapy , bcl-2 Homologous Antagonist-Killer Protein , bcl-2-Associated X Protein
16.
Cell Immunol ; 223(1): 70-6, 2003 May.
Article in English | MEDLINE | ID: mdl-12914760

ABSTRACT

Adenomatous polyposis coli (APC) functions are involved in the heterotypic interactions occurring between intestinal epithelial cells (IECs) and intra-epithelial lymphocytes (IELs). These interactions may be of interest in cancer prevention, since recent data provide evidence for lymphocyte mediated immunosurveillance of epithelial cancers. The present study attempts to determine if APC inactivation induces changes in the cross-talk between IEC and large intestine IEL (LI-IEL) through intercellular adhesion molecule (ICAM-1)/leukocyte function-associated (LFA-1) interactions. Mouse Apc+/+ and Apc+/Min colonocytes were co-cultivated with LI-IEL. When co-cultured with LI-IEL Apc+/Min IEC but not Apc+/+ IEC expressed high levels of ICAM-1. The presence of ICAM-1 was linked to TNFalpha production in both co-cultures and TNFR expression only in co-cultivated Apc+/Min IEC. Finally, butyrate enhanced the expression of ICAM-1 in Apc+/Min IEC co-cultured with LI-IEL, and the secretion of TNFalpha by both types of co-cultures. These events could participate in determining the Apc+/Min IEC immunogenicity under different in vivo conditions.


Subject(s)
Cell Communication/immunology , Genes, APC/physiology , Intercellular Adhesion Molecule-1/biosynthesis , Intestine, Large/cytology , Lymphocytes/cytology , Receptors, Tumor Necrosis Factor/biosynthesis , Animals , Butyrates/pharmacology , Coculture Techniques , Epithelial Cells/cytology , Epithelial Cells/drug effects , Epithelial Cells/immunology , Epithelial Cells/metabolism , Female , Flow Cytometry , Intercellular Adhesion Molecule-1/genetics , Intercellular Adhesion Molecule-1/immunology , Interferon-gamma/immunology , Intestine, Large/drug effects , Intestine, Large/immunology , Intestine, Large/metabolism , Lymphocyte Function-Associated Antigen-1/biosynthesis , Lymphocyte Function-Associated Antigen-1/genetics , Lymphocyte Function-Associated Antigen-1/immunology , Lymphocytes/immunology , Lymphocytes/metabolism , Male , Mice , Mice, Inbred C57BL , Receptors, Tumor Necrosis Factor/genetics , Receptors, Tumor Necrosis Factor/immunology , Tumor Necrosis Factor-alpha/biosynthesis
17.
Nutr Cancer ; 45(1): 84-92, 2003.
Article in English | MEDLINE | ID: mdl-12791508

ABSTRACT

Loss of function of the Apc gene product is an early and frequent event in colorectal carcinogenesis. Altered migration of intestinal epithelial cells has been described in vivo in the Min mouse Apc+/Min model. Using cell lines established from this model we show in vitro that Apc+/Min cells are less motile than Apc+/+ cells and exhibit a disordered actin cytoskeletal network. This would increase the probabilities of the initiated cell to acquire additional genetic alterations leading to neoplasia. Butyrate, a product of indigestible carbohydrate fermentation by the colonic flora, is able to restore both motility and actin cytoskeletal organization. This feature may contribute to explain the protective effect exerted by butyrogenic diets on colon carcinogenesis in animal models.


Subject(s)
Actins/metabolism , Adenomatous Polyposis Coli Protein/physiology , Butyrates/pharmacology , Colorectal Neoplasms/prevention & control , Cytoskeleton/physiology , Genes, APC , Actins/drug effects , Actins/genetics , Adenomatous Polyposis Coli Protein/genetics , Animals , Cell Division/drug effects , Cell Movement/drug effects , Cell Movement/genetics , Colorectal Neoplasms/genetics , Colorectal Neoplasms/metabolism , Cytoskeleton/metabolism , Disease Models, Animal , Epithelial Cells , Flow Cytometry , Genes, Tumor Suppressor , Mice , Mice, Inbred C57BL , Mice, Transgenic , Microscopy, Fluorescence , Mutation , Polymerase Chain Reaction , Sensitivity and Specificity , Tumor Cells, Cultured
18.
Mol Cell Biol ; 23(13): 4701-12, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12808108

ABSTRACT

Animal models suggest that Bax and Bak play an essential role in the implementation of apoptosis and as a result can hinder tumorigenesis. We analyzed the expression of these proteins in 50 human glioblastoma multiforme (GBM) tumors. We found that all the tumors expressed Bak, while three did not express Bax. In vitro, Bax-deficient GBM (BdGBM) exhibited an important resistance to various apoptogenic stimuli (e.g., UV, staurosporine, and doxorubicin) compared to the Bax-expressing GBM (BeGBM). Using an antisense strategy, we generated Bak(-) BeGBM and Bak(-) BdGBM, which enabled us to show that the remaining sensitivity of the BdGBM to apoptosis was due to the overexpression of Bak. Bax/Bak single or double deficiency had no influence on either the clonogenicity or the growth of tumors in Swiss nude mice. Of note, Bak(-) BeGBM cells were resistant to apoptosis induced by caspase 8 (C8) but not to that induced by granzyme B (GrB). Cells lacking both Bax and Bak (i.e., Bak(-) BdGBM) were completely resistant to all stimuli including the microinjection of C8 and GrB. We show that GrB-cleaved Bid and C8-cleaved Bid differ in size and utilize preferentially Bax and Bak, respectively, to promote cytochrome c release from mitochondria. Our results suggest that Bax deficiency is compensated by an increase of the expression of Bak in GBM and show, for the first time in human cancer, that the double Bax and Bak deficiency severely impairs the apoptotic program.


Subject(s)
Apoptosis , Carrier Proteins/metabolism , Membrane Proteins/physiology , Proto-Oncogene Proteins c-bcl-2 , Proto-Oncogene Proteins/physiology , Animals , Astrocytoma/immunology , Astrocytoma/metabolism , BH3 Interacting Domain Death Agonist Protein , Cell Division , Cell-Free System , Dose-Response Relationship, Drug , Humans , Immunoblotting , Mice , Mice, Nude , Microscopy, Confocal , Microscopy, Fluorescence , Models, Biological , Proto-Oncogene Proteins/metabolism , RNA/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Time Factors , Transfection , Tumor Cells, Cultured , bcl-2 Homologous Antagonist-Killer Protein , bcl-2-Associated X Protein
19.
Cancer Immunol Immunother ; 52(7): 445-54, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12700941

ABSTRACT

Dendritic cells (DC) are activated by pathogens, cytokines and activated T cells. We investigated the impact of a transient initial DC stimulation on the kinetics of maturation using a combination of double-stranded RNA and TNFalpha and subsequent restimulation by T cell-derived stimuli. Transient stimulation of DC was sufficient to start an irreversible program of phenotypic maturation which proceeded in the absence of the initial stimulus. Transiently stimulated DC secreted lower amounts of IL-12 during the 48-h period of the first stimulation than cells activated for 48 h. Although both DC preparations expressed the same level of maturation-associated markers at 48 h, DC stimulated for shorter periods preserved higher sensitivity to boosting upon subsequent stimulation by T cell-derived signals. We showed that DC initially stimulated for shorter periods were more potent stimulators of T lymphocytes and they induced a more polarized Th1 response. These results indicate that short exposure of DC to maturation stimuli enables an efficient defensive immune response induction by differentially regulating phenotypic maturation and cytokine production of DC.


Subject(s)
Dendritic Cells/immunology , T-Lymphocytes/immunology , Antigen Presentation , Antigens, CD/metabolism , Cell Communication/immunology , Cell Differentiation/immunology , Cells, Cultured , Coculture Techniques , Dendritic Cells/drug effects , Drug Combinations , Humans , Immunophenotyping , Interleukins/metabolism , Poly I-C/pharmacology , Tumor Necrosis Factor-alpha/pharmacology
20.
J Biol Chem ; 278(21): 19426-35, 2003 May 23.
Article in English | MEDLINE | ID: mdl-12642586

ABSTRACT

The pro-apoptotic "BH3 domain-only" proteins of the Bcl-2 family (e.g. Bid and Bad) transduce multiple death signals to the mitochondrion. They interact with the anti-apoptotic Bcl-2 family members and induce apoptosis by a mechanism that requires the presence of at least one of the multidomain pro-apoptotic proteins Bax or Bak. Although the BH3 domain of Bid can promote the pro-apoptotic assembly and function of Bax/Bak by itself, other BH3 domains do not function as such. The latter point raises the question of whether, and how, these BH3 domains induce apoptosis. We show here that a peptide comprising the minimal BH3 domain from Bax induces apoptosis but is unable to stimulate the apoptotic activity of microinjected recombinant Bax. This relies on the inability of the peptide to directly induce Bax translocation to mitochondria or a change in its conformation. This peptide nevertheless interferes with Bax/Bcl-xL interactions in vitro and stimulates the apoptotic activity of Bax when combined with Bcl-xL. Similarly, a peptide derived from the BH3 domain of Bad stimulates Bax activity only in the presence of Bcl-xL. Thus, BH3 domains do not necessarily activate multidomain pro-apoptotic proteins directly but promote apoptosis by releasing active multidomain pro-apoptotic proteins from their anti-apoptotic counterparts.


Subject(s)
Apoptosis/drug effects , Peptide Fragments/pharmacology , Proto-Oncogene Proteins/pharmacology , Amino Acid Sequence , Animals , Cell Line , Dimerization , Fibroblasts/cytology , Fibroblasts/drug effects , Gene Expression , Kinetics , Membrane Proteins/antagonists & inhibitors , Membrane Proteins/chemistry , Membrane Proteins/pharmacology , Microinjections , Mitochondria, Liver/metabolism , Molecular Sequence Data , Peptide Fragments/administration & dosage , Peptide Fragments/chemistry , Protein Conformation , Proto-Oncogene Proteins/administration & dosage , Proto-Oncogene Proteins/antagonists & inhibitors , Proto-Oncogene Proteins/chemistry , Proto-Oncogene Proteins c-bcl-2/antagonists & inhibitors , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Recombinant Proteins/pharmacology , Transfection , bcl-2 Homologous Antagonist-Killer Protein , bcl-2-Associated X Protein , bcl-X Protein
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