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1.
J Biol Regul Homeost Agents ; 31(3): 579-587, 2017.
Article in English | MEDLINE | ID: mdl-28952290

ABSTRACT

Rough titanium surfaces enhance cell response to activation of Wnt canonical signalling, a pathway required for osteoblast differentiation. The present study investigated the effects of GSK3ß-inhibitors SB216763 and SB415286 on osteoblastic differentiation on titanium surfaces with different topography and wettability. Osteoblastic MC3T3 cells were plated on smooth (Pickled), sand-blasted/acid-etched (SLA) or hyper hydrophilic SLA (modSLA) titanium discs and transfected with a reporter vector sys-tem for Wnt canonical signalling. Cells were also seeded in the presence or in the absence of GSK3b-inhibitors SB216763 or SB415286 and their viability, morphology and the expression of Wnt target and osteoblast specific genes was assessed by Real Time PCR. Inhibitors altered cell morphology and mostly reduced cell viability at high concentration. SB415286 markedly increased the expression of ALP in MC3T3 cells on rough surfaces at the concentration of 100 nM before decreasing its expression at higher concentrations. OCN expression was unaffected. Increasing concentrations of SB216763 increased the expression of ALP in MC3T3 cells on rough surfaces but OCN expression was not changed at any con-centration. SB216763 and SB415286 inhibitors should be further investigated as potential tools to improve cell differentiation on titanium surfaces for endosseous implants.


Subject(s)
Aminophenols/pharmacology , Cell Differentiation/drug effects , Glycogen Synthase Kinase 3 beta/antagonists & inhibitors , Indoles/pharmacology , Maleimides/pharmacology , Osteoblasts/enzymology , Titanium/chemistry , Animals , Cell Line , Dose-Response Relationship, Drug , Glycogen Synthase Kinase 3 beta/metabolism , Mice , Osteoblasts/cytology , Surface Properties
2.
J Biol Regul Homeost Agents ; 28(3): 489-95, 2014.
Article in English | MEDLINE | ID: mdl-25316136

ABSTRACT

Rough titanium surfaces enhance the activation of Wnt canonical signaling, a pathway required for osteoblast differentiation. The present study investigated the effects of GSK3b-inhibitor (2'Z,3'E)- 6-Bromoindirubin-3'-oxime (BIO) on osteoblastic differentiation on titanium surfaces with different topography and wettability. C2C12 cells were plated on pickled, acid-etched/sand-blasted (SLA), modified hydrophilic SLA titanium discs (modSLA) and stimulated with increasing doses of BIO. Activation of Wnt canonical signaling was measured with a reporter system. Gene expression was measured in the same cell system by Real Time PCR. Osteoblastic MC3T3 cells were then plated on discs with or without BIO and the expression of osteoblast specific genes was assessed by Real Time PCR. One mM BIO activated Wnt canonical signaling in C2C12 cells on all surfaces, and the highest effect was on rough surfaces. BIO markedly increased the expression of Osteoprotegerin and Osteocalcin in MC3T3 cells on rough surfaces at the concentration of 100 nM, and on all surfaces at the concentration of 1 mM. BIO enhances Wnt signaling activation and the expression of osteoblastic genes on rough surfaces and could be a viable approach to improve cell response to implant surfaces.


Subject(s)
Enzyme Inhibitors/pharmacology , Glycogen Synthase Kinase 3/antagonists & inhibitors , Osteoblasts/enzymology , Titanium/chemistry , Wnt Signaling Pathway , Animals , Cell Differentiation , Cell Line , Gene Expression Regulation , Glycogen Synthase Kinase 3/metabolism , Glycogen Synthase Kinase 3 beta , Mice , Osteoblasts/cytology , Osteocalcin/biosynthesis , Osteoprotegerin/biosynthesis , Surface Properties
3.
Int J Oncol ; 6(1): 65-8, 1995 Jan.
Article in English | MEDLINE | ID: mdl-21556502

ABSTRACT

From July 1992 to December 1993, 62 patients with non-small cell lung cancer (NSCLC) were admitted to a multicentric randomized study. The patients were treated with vinorelbine (V) alone at a dose of 25 mg/m(2)/i.v. weekly or with V at a dose of 25 mg/m(2)/i.v. on day 1 and 8 plus cisplatin at a dose of 80 mg/m(2)/i.v. on day 1 every 3-4 weeks (VP). An objective response was observed in 42% of patients treated with VP versus 12.5% of those treated with vinorelbine alone (p=0.038). There was no significant difference in the median survival duration between the two groups (38 versus 30 weeks for VP and V, respectively). Toxicity was tolerable but more severe in the VP regimen. These data suggest that V is an active agent in NSCLC and that the VP regimen may yield results comparable to other cisplatin combinations for treatment of these tumors.

4.
Pancreas ; 6(4): 489-90, 1991 Jul.
Article in English | MEDLINE | ID: mdl-1876605

ABSTRACT

Acute pancreatitis may result from viral infections, including mumps, coxsackie B, Epstein-Barr, and varicella. However, viral pancreatitis has not been reported after immunization with viral vaccines. We report the occurrence of acute pancreatitis in an adult who had received measles, mumps, and rubella II vaccine (MMR II).


Subject(s)
Measles Vaccine/adverse effects , Mumps Vaccine/adverse effects , Pancreatitis/etiology , Rubella Vaccine/adverse effects , Adult , Drug Combinations , Female , Humans , Measles/prevention & control , Measles-Mumps-Rubella Vaccine , Mumps/prevention & control , Rubella/prevention & control
5.
Acta Diabetol ; 40 Suppl 1: S187-90, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14618469

ABSTRACT

Little is known about body composition in Parkinson's disease (PD). We studied 35 patients (20 male, 15 female subjects; mean age 69.7+/-5.8 years) with advanced PD by anthropometry, dual-energy X-ray absorptiometry (DEXA), and serum 25-OH vitamin D measurement. Over 70% of patients had a disease duration of more than 4 years; all were on L-dopa treatment. Low levels of serum 25-OH vitamin D were present in 41% of the patients. The mean body mass index (BMI) was 25.3+/-4.3 kg/m(2) (range 17.1-37.3). Mid-arm muscle circumference was below the 10th percentile in 23%. For whole-body mean (+/-SD) bone mineral density, the T score was below -1 SD in 35% of patients, and the Z score was below -1 SD in 24%. Percent fat mass measured with DEXA was 30.6+/-11.4% (range 10.1-45.5) in the overall sample; it was 21.1+/-8.8% (range 10.1-30.4) in male subjects and 38.1+/-9.2% (range 25.8-45.5) in female subjects. We conclude that advanced-stage PD may show excess adiposity coexisting with depletion of lean body mass (sarcopenic obesity), in addition to decreased whole-body bone mineral density associated with low serum 25-OH vitamin D. A low level of physical activity and inadequate exposure to sunlight are likely to be among the putative causes.


Subject(s)
Body Composition/physiology , Parkinson Disease/physiopathology , Absorptiometry, Photon/methods , Aged , Antiparkinson Agents/therapeutic use , Body Mass Index , Bone Density , Female , Humans , Hydroxycholecalciferols/blood , Levodopa/therapeutic use , Male , Muscle, Skeletal/anatomy & histology , Parkinson Disease/blood , Parkinson Disease/drug therapy , Skinfold Thickness
7.
J Clin Microbiol ; 42(1): 487-9, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14715813

ABSTRACT

Mucormycosis is a rare complication in cancer patients. This report presents the case of a acute myeloblastic leukemia patient who developed an ascending paralysis due to disseminated mucormycosis. The presentation was unusual because the early symptoms were fever and pain, and the disease was misdiagnosed because of a concomitant infection by Enterococcus faecium.


Subject(s)
Enterococcus faecium , Gram-Positive Bacterial Infections/diagnosis , Leukemia, Myeloid, Acute/complications , Mucormycosis/diagnosis , Aged , Diagnostic Errors , Female , Humans , Mucormycosis/etiology
8.
Haematologica ; 86(4): 440-1, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11325656

ABSTRACT

A topotecan/cytarabine combination has been reported to be effective in patients with myelodysplastic syndromes. We report our experience with this regimen in 12 patients with relapsed or secondary acute myeloid leukemia. Extra-hematologic toxicity was low, but the response to the treatment was very poor. In our opinion, this association is not a treatment option for these patients, but the addition of other agents could improve this results.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cytarabine/administration & dosage , Leukemia, Myeloid/drug therapy , Topotecan/administration & dosage , Acute Disease , Adult , Aged , Female , Humans , Leukemia, Myeloid/mortality , Male , Maximum Tolerated Dose , Middle Aged , Neoplasms, Second Primary/drug therapy , Neoplasms, Second Primary/mortality , Recurrence , Therapeutic Equivalency , Topotecan/toxicity , Treatment Outcome
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