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1.
Horm Metab Res ; 47(3): 214-9, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25153684

ABSTRACT

Simple nodular goiter and Hashimoto's thyroiditis are 2 frequent nonmalignant thyroid diseases. Tobacco smoking has detrimental effects on the endocrine system and in particular on thyroid function and morphology. The objective of this cross-sectional study, involving 1800 Caucasian adults from a geographical area with mild iodine deficiency, was to evaluate the relationship between tobacco smoking, smoking cessation, and the prevalence of simple nodular goiter and Hashimoto's thyroiditis. Thyroid status was evaluated by ultrasonic exploration of the neck, measurement of FT3, FT4, TSH, antibodies against thyroid peroxidase and thyroglobulin, and urinary iodine excretion. The fine-needle aspiration biopsy of significant nodules was also performed. Smoking habits were evaluated by a specific questionnaire and the calculation of number of pack years. Both current and previous smokers showed an increased risk of simple nodular goiter compared to never smokers after adjustment for potential confounders and known goitrogen factors. Interestingly, the simple nodular goiter risk was similar for never smokers and for previous smokers declaring a time since cessation of smoking for more than 69 months. Smoking habit was not associated to an increased risk of Hashimoto's thyroiditis.Smoking appears to be an independent risk factor for simple nodular goiter but not for Hashimoto's thyroiditis in an area with mild iodine deficiency. A prolonged withdrawal of smoking dramatically reduces the risk of simple nodular goiter occurrence.


Subject(s)
Goiter/etiology , Hashimoto Disease/etiology , Iodine/deficiency , Smoking/adverse effects , Adult , Aged , Aged, 80 and over , Cross-Sectional Studies , Female , Goiter/blood , Goiter/epidemiology , Hashimoto Disease/blood , Hashimoto Disease/epidemiology , Humans , Iodine/blood , Italy/epidemiology , Male , Middle Aged , Prevalence , Smoking/blood , Smoking/epidemiology
2.
Cell Death Differ ; 14(5): 952-62, 2007 May.
Article in English | MEDLINE | ID: mdl-17332776

ABSTRACT

Interferon alpha (IFNalpha) induces both apoptosis and a counteracting epidermal growth factor Erk-dependent survival response in cancer cells. In this report, IFNalpha increased eukaryotic elongation factor 1A (eEF-1A) protein expression by inhibition of eEF-1A degradation via a proteasome-dependent pathway. The reduction of the expression level of eEF-1A by RNA interference enhanced the apoptosis induced by IFNalpha on the same cells. Moreover, IFNalpha induced the phosphorylation of both serine and threonine in eEF-1A. These effects were paralleled by an increased co-immunoprecipitation and colocalization of eEF-1A with C-Raf. The suppression of C-Raf kinase activity with the inhibitor BAY 43-9006 completely antagonized the increase of both eEF-1A phosphorylation and expression and of C-Raf/eEF-1A colocalization induced by IFNalpha and enhanced apoptosis and eEF-1A ubiquitination. Cell transfection with the mutated K48R ubiquitin increased EF-1A expression and desensitized tumor cells to the modulating effects of IFNalpha. The dynamic simulation of 3Dstructure of eEF-1A identified putative serine and threonine phosphorylation sites. In conclusion, the interaction between eEF-1A and C-Raf increases eEF-1A stability and induces a survival activity.


Subject(s)
Apoptosis/drug effects , Interferon-alpha/pharmacology , Lung Neoplasms/pathology , Oncogene Proteins/metabolism , Peptide Elongation Factor 1/metabolism , Proto-Oncogene Proteins c-raf/metabolism , Cell Line, Tumor , Humans , Immunoprecipitation , Lung Neoplasms/metabolism , Phosphorylation/drug effects , Phosphoserine/metabolism , Phosphothreonine/metabolism , Proteasome Endopeptidase Complex/metabolism , Protein Binding/drug effects , Protein Processing, Post-Translational/drug effects , Protein Transport/drug effects , RNA, Small Interfering/metabolism , Ubiquitin/metabolism
3.
Dig Liver Dis ; 39(2): 122-9, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17092786

ABSTRACT

BACKGROUND: To understand the molecular changes underlying Helicobacter pylori-related gastric diseases is mandatory to prevent gastric cancer. Proteomic technology is providing a rapid expansion of the basic knowledge, particularly in the discovery of new biomarkers involved in the tumourigenesis. AIM: To characterise changes in protein expression level of the gastric mucosa in H. pylori-infected patients. METHODS: The population enrolled comprised 41 dyspeptic patients. Proteins extracted from gastric mucosal specimens were analysed by 2-dimensional electrophoresis, sequenced by MALDI-TOF and identified by Edman's degradation. RESULTS: Twenty-one out of 41 patients had H. pylori infection of whom 17 had anti-CagA IgG antibodies. Several proteins were identified, of which Rho guanosine diphosphatase dissociation inhibitor alpha and heat shock protein 27 increased and glutathione transferase and antrum mucosa protein-18 decreased in H. pylori-positive in respect to H. pylori-negative patients. Interestingly, antrum mucosa protein-18, currently referred as gastrokine-1, showed two isoforms differing in the first N-terminal amino acid residue. Both gastrokine-1 isoforms were observed in the H. pylori-negative group whereas a lower expression or even absence of the gastrokine-1 basic isoform was found in a subgroup (7/21) of H. pylori-positive patients with moderate-severe gastritis. CONCLUSION: Our study demonstrated the presence of gastrokine-1 isoforms of which the basic isoform was reduced in a subset of patients with H. pylori infection.


Subject(s)
Dyspepsia/metabolism , Endonucleases/biosynthesis , Gastric Mucosa/metabolism , Helicobacter Infections/metabolism , Helicobacter pylori , Adult , Blotting, Northern , Blotting, Western , Electrophoresis, Gel, Two-Dimensional , Female , Gene Expression Regulation , Guanine Nucleotide Dissociation Inhibitors/biosynthesis , HSP27 Heat-Shock Proteins , Heat-Shock Proteins/biosynthesis , Humans , Male , Middle Aged , Molecular Chaperones , Neoplasm Proteins/biosynthesis , Oligonucleotide Array Sequence Analysis , Peptide Hormones , Protein Isoforms/biosynthesis , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , rho-Specific Guanine Nucleotide Dissociation Inhibitors
4.
Expert Opin Drug Saf ; 15(10): 1329-47, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27347638

ABSTRACT

INTRODUCTION: The atypical antipsychotic (APs) drugs have become the most widely used agents to treat a variety of psychoses because of their superiority with regard to safety and tolerability profile compared to conventional/'typical' APs. AREAS COVERED: We aimed at providing a synthesis of most current evidence about the safety and tolerability profile of the most clinically used atypical APs so far marketed. Qualitative synthesis followed an electronic search made inquiring of the following databases: MEDLINE, Embase, PsycINFO and the Cochrane Library from inception until January 2016, combining free terms and MESH headings for the topics of psychiatric disorders and all atypical APs as following: ((safety OR adverse events OR side effects) AND (aripiprazole OR asenapine OR quetiapine OR olanzapine OR risperidone OR paliperidone OR ziprasidone OR lurasidone OR clozapine OR amisulpride OR iloperidone)). EXPERT OPINION: A critical issue in the treatment with atypical APs is represented by their metabolic side effect profile (e.g. weight gain, lipid and glycaemic imbalance, risk of diabetes mellitus and diabetic ketoacidosis) which may limit their use in particular clinical samples. Electrolyte imbalance, ECG abnormalities and cardiovascular adverse effects may recommend a careful baseline and periodic assessments.


Subject(s)
Antipsychotic Agents/adverse effects , Cardiovascular Diseases/chemically induced , Metabolic Diseases/chemically induced , Cardiovascular Diseases/physiopathology , Electrocardiography , Humans , Metabolic Diseases/physiopathology , Water-Electrolyte Balance/drug effects
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