ABSTRACT
A dioctofimose, causada pelo nematódeo Dioctophyme renale, acomete frequentemente cães errantes e de hábitos alimentares pouco seletivos, podendo afetar também o homem. O parasita é grande, pode medir até cem centímetros de comprimento e se aloja geralmente no rim direito. O diagnóstico é obtido pela visualização dos ovos do D. renale durante o exame do sedimento urinário ou pelo achado do parasita à necropsia. O presente trabalho descreve um caso de parasitismo por este nematoide em cão atendido no Hospital Veterinário "Governador Laudo Natel" da Faculdade de Ciências Agrárias e Veterinárias, Jaboticabal, no qual a conduta terapêutica foi a realização de nefrectomia do rim acometido, devido à destruição do parênquima renal. A nefrectomia unilateral foi eficiente para a cura do paciente e eliminação do parasita.(AU)
Dioctophimosis, caused by the nematode Dioctophyme renale, frequently attacks erratic dogs and have poorly selective eating habits and, may also affects the man. The parasite is large, can be up to one meter long and usually is lodged to the right kidney. The diagnosis is obtained by the preview of D. renale eggs during the examination of the urinary sediment or by finding the parasite at necropsy. The present study describes a case of parasitism by this nematode in a dog attended at the "Governador Laudo Natel" Veterinary Hospital of the Faculdade de Ciências Agrárias e Veterinárias, Jaboticabal, in which the therapeutic management was the nephrectomy of the affected kidney, due to the destruction of the renal parenchyma. Unilateral nephrectomy was efficient for the cure of the patient and elimination of the parasite.(AU)
Subject(s)
Animals , Dogs , Dioctophymatoidea/parasitology , Nephrectomy/veterinary , Enoplida Infections/parasitology , Enoplida Infections/veterinary , Kidney/parasitology , Helminthiasis/diagnosis , Helminthiasis/parasitologyABSTRACT
A dioctofimose, causada pelo nematódeo Dioctophyme renale, acomete frequentemente cães errantes e de hábitos alimentares pouco seletivos, podendo afetar também o homem. O parasita é grande, pode medir até cem centímetros de comprimento e se aloja geralmente no rim direito. O diagnóstico é obtido pela visualização dos ovos do D. renale durante o exame do sedimento urinário ou pelo achado do parasita à necropsia. O presente trabalho descreve um caso de parasitismo por este nematoide em cão atendido no Hospital Veterinário "Governador Laudo Natel" da Faculdade de Ciências Agrárias e Veterinárias, Jaboticabal, no qual a conduta terapêutica foi a realização de nefrectomia do rim acometido, devido à destruição do parênquima renal. A nefrectomia unilateral foi eficiente para a cura do paciente e eliminação do parasita.
Dioctophimosis, caused by the nematode Dioctophyme renale, frequently attacks erratic dogs and have poorly selective eating habits and, may also affects the man. The parasite is large, can be up to one meter long and usually is lodged to the right kidney. The diagnosis is obtained by the preview of D. renale eggs during the examination of the urinary sediment or by finding the parasite at necropsy. The present study describes a case of parasitism by this nematode in a dog attended at the "Governador Laudo Natel" Veterinary Hospital of the Faculdade de Ciências Agrárias e Veterinárias, Jaboticabal, in which the therapeutic management was the nephrectomy of the affected kidney, due to the destruction of the renal parenchyma. Unilateral nephrectomy was efficient for the cure of the patient and elimination of the parasite.
Subject(s)
Animals , Dogs , Dioctophymatoidea/parasitology , Enoplida Infections/parasitology , Enoplida Infections/veterinary , Nephrectomy/veterinary , Kidney/parasitology , Helminthiasis/diagnosis , Helminthiasis/parasitologyABSTRACT
The leptin gene product is released into the blood stream, passes through the blood-brain barrier, and finds the leptin receptor (LEPR) in the central nervous system. This hormone regulates food intake, hematopoiesis, inflammation, immunity, differentiation, and cell proliferation. The LEPR Gln223Arg polymorphism has been reported to alter receptor function and expression, both of which have been related with prognostics in several tumor types. Furthermore, several studies have shown a relationship between the Gln223Arg polymorphism and tumor development, and its role in oral and oropharyngeal squamous cell carcinoma is now well understood. In this study, 315 DNA samples were used for LEPR Gln223Arg genotyping and 87 primary oral and oropharyngeal squamous cell carcinomas were used for immunohistochemical expression analysis, such that a relationship between these and tumor development and prognosis could be established. Homozygous LEPR Arg223 was found to be associated with a 2-fold reduction in oral and oropharyngeal cancer risk. In contrast, the presence of the Arg223 allele in tumors was associated with worse disease-free and disease-specific survival. Low LEPR expression was found to be an independent risk factor, increasing the risk for lymph node metastasis 4-fold. In conclusion, the Gln223Arg polymorphism and LEPR expression might be valuable markers for oral and oropharyngeal cancer, suggesting that LEPR might serve as a potential target for future therapies.
Subject(s)
Biomarkers, Tumor/genetics , Leptin/genetics , Mouth Neoplasms/genetics , Oropharyngeal Neoplasms/genetics , Polymorphism, Genetic/genetics , Receptors, Leptin/genetics , Adult , Aged , Alleles , Amino Acid Substitution , Blood-Brain Barrier , Body Mass Index , Female , Genotype , Humans , Male , Middle Aged , Prognosis , Risk FactorsABSTRACT
Five-year survival rates for oral squamous cell carcinoma (OSCC) are 30% and the mortality rate is 50%. Immunohistochemistry panels are used to evaluate proliferation, vascularization, apoptosis, HPV infection, and keratin expression, which are important markers of malignant progression. Keratins are a family of intermediate filaments predominantly expressed in epithelial cells and have an essential role in mechanical support and cytoskeleton formation, which is essential for the structural integrity and stability of the cell. In this study, we analyzed the expressions of keratins 17 and 19 (K17 and K19) by immunohistochemistry in tumoral and non-tumoral tissues from patients with OSCC. The results show that expression of these keratins is higher in tumor tissues compared to non-tumor tissues. Positive K17 expression correlates with lymph node metastasis and multivariate analysis confirmed this relationship, revealing a 6-fold increase in lymph node metastasis when K17 is expressed. We observed a correlation between K17 expression with disease-free survival and disease-specific death in patients who received surgery and radiotherapy. Multivariate analysis revealed that low expression of K17 was an independent marker for early disease relapse and disease-specific death in patients treated with surgery and radiotherapy, with an approximately 4-fold increased risk when compared to high K17 expression. Our results suggest a potential role for K17 and K19 expression profiles as tumor prognostic markers in OSCC patients.
Subject(s)
Biomarkers, Tumor/metabolism , Carcinoma, Squamous Cell/metabolism , Keratins/metabolism , Mouth Neoplasms/metabolism , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/therapy , Disease-Free Survival , Epithelial Cells/metabolism , Female , Humans , Lymphatic Metastasis/pathology , Male , Middle Aged , Mouth Neoplasms/pathology , Mouth Neoplasms/therapy , Neoplasm Recurrence, Local/metabolism , Neoplasm Recurrence, Local/pathology , PrognosisABSTRACT
The C677T and A1298C polymorphisms in methylene-tetrahydrofolate reductase (MTHFR), which regulates the release of active folate in the body, may have reduced activity. Given that folate participates in important intracellular pathways, such as nucleotide synthesis and biomolecule methylation, it seems plausible that patients with head and neck squamous cell carcinoma (HNSCC) may respond differently to radiotherapy treatments, based on genetic polymor-phisms. Therefore, this study sought to understand the role of these polymorphisms in HNSCC patient radiotherapy response. Genotypes were detected by PCR-RFLP after extraction of DNA from peripheral blood lymphocytes. Survival curves were analyzed by the Kaplan- Meier model, and significant differences were analyzed by the Wil-coxon test. Response to radiotherapy in patients with laryngeal SCC was significantly associated with the MTHFR C677T polymorphism (P = 0.030). Indeed, the presence of at least one T allele decreases the mortality rate up to 3-fold. Therefore, we propose that MTHFR C677T may represent a putative biomarker for radiotherapy prognosis in la-ryngeal SCC patients.
Subject(s)
Carcinoma, Squamous Cell/genetics , Carcinoma, Squamous Cell/radiotherapy , Head and Neck Neoplasms/genetics , Head and Neck Neoplasms/radiotherapy , Methylenetetrahydrofolate Reductase (NADPH2)/genetics , Polymorphism, Single Nucleotide , Adult , Aged , Alleles , Carcinoma, Squamous Cell/diagnosis , Carcinoma, Squamous Cell/mortality , Female , Genotype , Head and Neck Neoplasms/diagnosis , Head and Neck Neoplasms/mortality , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Neoplasm Staging , Prognosis , Squamous Cell Carcinoma of Head and Neck , Treatment OutcomeABSTRACT
The aims of this study were to analyze the polymorphisms XRCC1 Arg194Trp, XRCC1 Arg399Gln, XRCC3 Thr241Met, XPC Lys939Gln, ERCC1 Asn118Asn, and RAD51 -98G>C and to verify their influence on radiotherapy response and prognosis of patients with head and neck squamous cell carcinoma (HNSCC). Peripheral blood DNA was extracted from 311 patients and analyzed by PCR-RFLP. Our results showed that in irradiated oral and oropharyngeal patients, the 939Gln allele increased 6-fold local disease relapse risk (OR = 6.04; CI = 1.47-24.88) and over 2-fold the earliness of relapse (HR = 2.63; CI = 1.04-6.70). As for the XRCC3 polymorphism, multivariate analysis showed that the 241Met allele increases over 33-fold local relapse risk (OR = 33.64; CI = 3.23-350.85), over 12-fold earliness of relapse (HR = 12.55; CI = 2.47-63.73) and over 3-fold earliness of death (HR = 3.04; CI = 1.08-8.61). For polymorphism RAD51 -98, multivariate analysis showed that allele C increases over 3-fold the risk of relapse (OR = 3.13; CI = 1.12-8.78) and over 2-fold the earliness of relapse (HR = 2.84; CI = 1.25-6.47). For polymorphism XRCC1 Arg399Gln, multivariate analysis showed that the 399Gln allele increased the risk of local disease relapse for irradiated oral and oropharyngeal patients (OR = 3.35; CI = 1.10-10.13) by over 3-fold. Based on these results, we suggest that these polymorphisms may be useful markers of prognosis in HNSCC.
Subject(s)
Head and Neck Neoplasms/genetics , Head and Neck Neoplasms/pathology , Polymorphism, Single Nucleotide/genetics , DNA-Binding Proteins/genetics , Female , Genetic Predisposition to Disease/genetics , Humans , Male , Middle Aged , Neoplasm Recurrence, Local/genetics , Neoplasm Recurrence, Local/pathology , Prognosis , X-ray Repair Cross Complementing Protein 1ABSTRACT
Death-associated protein 1 (DAP1) is a member of the DAP family. Its expression is associated with cell growth and normal death of the neoplastic cells, regulated by the mammalian target of the rapamycin protein. Activated DAP1 negatively regulates autophagy, which has been associated with the development and progression of several diseases, such as cancer, and with prognosis and survival of diverse tumor types. Therefore, in this study we analyzed DAP1 expression in 54 oral squamous cell carcinoma tumor samples and in 20 non-tumoral margins by immunohistochemistry. The results showed that DAP1 is more frequently expressed in tumor tissues compared with marginal non-tumoral cells. Additionally, high DAP1 expression is associated with a 4-fold increase in the risk of lymph node metastases. Our results suggest that the DAP1 protein can be used as a potential marker of lymph node metastases predisposition, helping define the best therapy for each patient to minimize risk of developing metastases.
Subject(s)
Apoptosis Regulatory Proteins/genetics , Carcinoma, Squamous Cell/genetics , Genetic Predisposition to Disease , Lymph Nodes/pathology , Mouth Neoplasms/genetics , Adult , Aged , Apoptosis Regulatory Proteins/metabolism , Autophagy/genetics , Carcinoma, Squamous Cell/metabolism , Carcinoma, Squamous Cell/mortality , Carcinoma, Squamous Cell/pathology , Female , Gene Expression , Humans , Immunohistochemistry , Lymph Nodes/metabolism , Lymphatic Metastasis , Male , Middle Aged , Mouth/metabolism , Mouth/pathology , Mouth Neoplasms/metabolism , Mouth Neoplasms/mortality , Mouth Neoplasms/pathology , Neoplasm Staging , Prognosis , Risk , Survival AnalysisABSTRACT
Currently, the most important prognostic factor in oral squamous cell carcinoma (OSCC) is the presence of regional lymph node metastases, which correlates with a 50% reduction in life expectancy. We have previously observed that expression of hypoxia genes in the tumor inflammatory infiltrate is statistically related to prognosis in OSCC. FAS and FASL expression levels in OSCC have previously been related to patient survival. The present study analyzed the relationship between FASL expression in the inflammatory infiltrate lymphoid cells and clinical variables, tumor histology, and prognosis of OSCC. Strong FASL expression was significantly associated with lymph node metastases (P = 0.035) and disease-specific death (P = 0.014), but multivariate analysis did not confirm FASL expression as an independent death risk factor (OR = 2.78, 95%CI = 0.81-9.55). Disease-free and disease-specific survival were significantly correlated with FASL expression (P = 0.016 and P = 0.005, respectively). Multivariate analysis revealed that strong FASL expression is an independent marker for earlier disease relapse and disease-specific death, with approximately 2.5-fold increased risk compared with weak expression (HR = 2.24, 95%CI = 1.08-4.65 and HR = 2.49, 95%CI = 1.04-5.99, respectively). Our results suggest a potential role for this expression profile as a tumor prognostic marker in OSCC patients.
Subject(s)
Carcinoma, Squamous Cell/metabolism , Fas Ligand Protein/metabolism , Mouth Neoplasms/metabolism , Adult , Aged , Aged, 80 and over , Biomarkers, Tumor/metabolism , Carcinoma, Squamous Cell/mortality , Carcinoma, Squamous Cell/secondary , Female , Humans , Kaplan-Meier Estimate , Lymphatic Metastasis , Lymphocytes, Tumor-Infiltrating/metabolism , Male , Middle Aged , Mouth Neoplasms/mortality , Mouth Neoplasms/pathology , Multivariate Analysis , Prognosis , Proportional Hazards ModelsABSTRACT
Since anemia is indicated as an important compromising factor for the quality of life of dogs with chronic kidney disease (CKD), bone marrow cytological analysis may provide more information on the hematological profile these dogs and, therefore, allow clinicians to not only choose the most adequate treatment but also monitor the response to therapy. The aim of this study was to investigate the feasibility with sternal bone marrow puncture in chronic kidney disease (CKD) using only local anesthesia and check if the cytological analysis is helpful to determine the hematological status. We found that erythroid hypoplasia occurred only in terminal CKD patients, and that the bone marrows of dogs with CKD stages 2 and 3 were quantitatively similar to those of elderly dogs. All dogs tolerated the bone marrow puncture using only local anesthesia with lidocaine and bone marrow cytological evaluation may be a useful tool for hematopoietic evaluation of anemic dogs with CKD.(AU)
Sendo a anemia apontada como um importante fator comprometedor da qualidade de vida dos cães portadores de doença renal crônica (DRC), a análise citológica da medula óssea poderia fornecer mais informações acerca do perfil hematológico desses animais e, portanto, possibilitar ao clínico não somente optar por um tratamento mais adequado, mas também monitorar a resposta à terapia. Diante disso, objetivou-se com este estudo avaliar a praticabilidade e a aceitação do procedimento de coleta de medula óssea do osso esterno de cães com doença renal crônica (DRC) utilizando somente anestesia local, bem como verificar se os resultados fornecidos na análise citológica fazem-se úteis à composição do quadro hematológico desses pacientes. Observou-se que a manifestação de hipoplasia da série eritroide só ocorreu nos pacientes em estádio terminal da DRC, e que as medulas ósseas dos DRC em estádio 2 e 3 assemelharam-se quantitativamente à medula de animais idosos. Os cães de todos dos grupos toleraram bem a punção do osso esterno somente com uso de lidocaína, podendo ser esta, portanto, uma ferramenta útil na complementação da abordagem hematopoiética de cães anêmicos com DRC.(AU)
Subject(s)
Animals , Dogs , Renal Insufficiency, Chronic/veterinary , Anemia/veterinary , Erythropoiesis , Cytological Techniques , Bone Marrow , Hematologic Tests , Hematologic Diseases/veterinaryABSTRACT
Since anemia is indicated as an important compromising factor for the quality of life of dogs with chronic kidney disease (CKD), bone marrow cytological analysis may provide more information on the hematological profile these dogs and, therefore, allow clinicians to not only choose the most adequate treatment but also monitor the response to therapy. The aim of this study was to investigate the feasibility with sternal bone marrow puncture in chronic kidney disease (CKD) using only local anesthesia and check if the cytological analysis is helpful to determine the hematological status. We found that erythroid hypoplasia occurred only in terminal CKD patients, and that the bone marrows of dogs with CKD stages 2 and 3 were quantitatively similar to those of elderly dogs. All dogs tolerated the bone marrow puncture using only local anesthesia with lidocaine and bone marrow cytological evaluation may be a useful tool for hematopoietic evaluation of anemic dogs with CKD...
Sendo a anemia apontada como um importante fator comprometedor da qualidade de vida dos cães portadores de doença renal crônica (DRC), a análise citológica da medula óssea poderia fornecer mais informações acerca do perfil hematológico desses animais e, portanto, possibilitar ao clínico não somente optar por um tratamento mais adequado, mas também monitorar a resposta à terapia. Diante disso, objetivou-se com este estudo avaliar a praticabilidade e a aceitação do procedimento de coleta de medula óssea do osso esterno de cães com doença renal crônica (DRC) utilizando somente anestesia local, bem como verificar se os resultados fornecidos na análise citológica fazem-se úteis à composição do quadro hematológico desses pacientes. Observou-se que a manifestação de hipoplasia da série eritroide só ocorreu nos pacientes em estádio terminal da DRC, e que as medulas ósseas dos DRC em estádio 2 e 3 assemelharam-se quantitativamente à medula de animais idosos. Os cães de todos dos grupos toleraram bem a punção do osso esterno somente com uso de lidocaína, podendo ser esta, portanto, uma ferramenta útil na complementação da abordagem hematopoiética de cães anêmicos com DRC...
Subject(s)
Animals , Dogs , Anemia/veterinary , Erythropoiesis , Renal Insufficiency, Chronic/veterinary , Bone Marrow , Cytological Techniques , Hematologic Diseases/veterinary , Hematologic TestsABSTRACT
Ectopic ureters are rarely observed in cats. Therefore, for a better chance of success in the corrective surgical procedure and survival of the patient, diagnosis should be confirmed early. This report illustrates the occurrence of bilateral ectopic ureters in a seven month old Maine Coon cat and describes the medical and surgical management adopted for correction of the abnormality.
A ectopia dos ureteres é raramente observada em gatos. Assim, para aumentar as chances de sucesso do procedimento cirúrgico corretivo e promover a sobrevivência, o diagnóstico deve ser firmado precocemente. O relato em tela ilustra a ocorrência de ureter ectópico bilateral em uma gata Maine Coon, de sete meses, e descrevem-se as manobras médico-cirúrgicas adotadas na correção dessa anormalidade.
Subject(s)
Animals , Cats , Postoperative Complications/veterinary , Early Diagnosis , Ureter/anatomy & histology , Urography/methods , Cats/classificationABSTRACT
Ectopic ureters are rarely observed in cats. Therefore, for a better chance of success in the corrective surgical procedure and survival of the patient, diagnosis should be confirmed early. This report illustrates the occurrence of bilateral ectopic ureters in a seven month old Maine Coon cat and describes the medical and surgical management adopted for correction of the abnormality.(AU)
A ectopia dos ureteres é raramente observada em gatos. Assim, para aumentar as chances de sucesso do procedimento cirúrgico corretivo e promover a sobrevivência, o diagnóstico deve ser firmado precocemente. O relato em tela ilustra a ocorrência de ureter ectópico bilateral em uma gata Maine Coon, de sete meses, e descrevem-se as manobras médico-cirúrgicas adotadas na correção dessa anormalidade.(AU)
Subject(s)
Animals , Cats , Ureter/anatomy & histology , Early Diagnosis , Urography/methods , Postoperative Complications/veterinary , Cats/classificationABSTRACT
The association of education, tobacco smoking, alcohol consumption, and interleukin-2 (IL-2 +114 and -384) and -6 (IL-6 -174) DNA polymorphisms with head and neck squamous cell carcinoma (HNSCC) was investigated in a cohort study of 445 subjects. IL-2 and IL-6 genotypes were determined by real-time PCR. Cox regression was used to estimate hazard ratios (HR) and 95 percent confidence intervals (95 percentCI) of disease-specific survival according to anatomical sites of the head and neck. Mean age was 56 years and most patients were males (87.6 percent). Subjects with 5 or more years of schooling had better survival in larynx cancer. Smoking had no effect on HNSCC survival, but alcohol consumption had a statistically significant effect on larynx cancer. IL-2 gene +114 G/T (HR = 0.52; 95 percentCI = 0.15-1.81) and T/T (HR = 0.22; 95 percentCI = 0.02-3.19) genotypes were associated with better survival in hypopharynx cancer. IL-2 +114 G/T was a predictor of poor survival in oral cavity/oropharynx cancer and larynx cancer (HR = 1.32; 95 percentCI = 0.61-2.85). IL-2 -384 G/T was associated with better survival in oral cavity/oropharynx cancer (HR = 0.80; 95 percentCI = 0.45-1.42) and hypopharynx cancer (HR = 0.68; 95 percentCI = 0.21-2.20), but an inverse relationship was observed for larynx cancer. IL-6 -174 G/C was associated with better survival in hypopharynx cancer (HR = 0.68; 95 percentCI = 0.26-1.78) and larynx cancer (HR = 0.93; 95 percentCI = 0.42-2.07), and C/C reduced mortality in larynx cancer. In general, our results are similar to previous reports on the value of education, smoking, alcohol consumption, and IL-2 and IL-6 genetic polymorphisms for the prognosis of HNSCC, but the risks due to these variables are small and estimates imprecise.
Subject(s)
Aged , Female , Humans , Male , Middle Aged , Carcinoma, Squamous Cell/mortality , Head and Neck Neoplasms/mortality , /genetics , /genetics , Polymorphism, Genetic/genetics , Alcohol Drinking/adverse effects , Cohort Studies , Carcinoma, Squamous Cell/etiology , Disease-Free Survival , Educational Status , Genotype , Head and Neck Neoplasms/etiology , Prognosis , Risk Factors , Smoking/adverse effectsABSTRACT
The association of education, tobacco smoking, alcohol consumption, and interleukin-2 (IL-2 +114 and -384) and -6 (IL-6 -174) DNA polymorphisms with head and neck squamous cell carcinoma (HNSCC) was investigated in a cohort study of 445 subjects. IL-2 and IL-6 genotypes were determined by real-time PCR. Cox regression was used to estimate hazard ratios (HR) and 95% confidence intervals (95%CI) of disease-specific survival according to anatomical sites of the head and neck. Mean age was 56 years and most patients were males (87.6%). Subjects with 5 or more years of schooling had better survival in larynx cancer. Smoking had no effect on HNSCC survival, but alcohol consumption had a statistically significant effect on larynx cancer. IL-2 gene +114 G/T (HR = 0.52; 95%CI = 0.15-1.81) and T/T (HR = 0.22; 95%CI = 0.02-3.19) genotypes were associated with better survival in hypopharynx cancer. IL-2 +114 G/T was a predictor of poor survival in oral cavity/oropharynx cancer and larynx cancer (HR = 1.32; 95%CI = 0.61-2.85). IL-2 -384 G/T was associated with better survival in oral cavity/oropharynx cancer (HR = 0.80; 95%CI = 0.45-1.42) and hypopharynx cancer (HR = 0.68; 95%CI = 0.21-2.20), but an inverse relationship was observed for larynx cancer. IL-6 -174 G/C was associated with better survival in hypopharynx cancer (HR = 0.68; 95%CI = 0.26-1.78) and larynx cancer (HR = 0.93; 95%CI = 0.42-2.07), and C/C reduced mortality in larynx cancer. In general, our results are similar to previous reports on the value of education, smoking, alcohol consumption, and IL-2 and IL-6 genetic polymorphisms for the prognosis of HNSCC, but the risks due to these variables are small and estimates imprecise.
Subject(s)
Carcinoma, Squamous Cell/mortality , Head and Neck Neoplasms/mortality , Interleukin-2/genetics , Interleukin-6/genetics , Polymorphism, Genetic/genetics , Aged , Alcohol Drinking/adverse effects , Carcinoma, Squamous Cell/etiology , Cohort Studies , Disease-Free Survival , Educational Status , Female , Genotype , Head and Neck Neoplasms/etiology , Humans , Male , Middle Aged , Prognosis , Risk Factors , Smoking/adverse effects , Squamous Cell Carcinoma of Head and NeckABSTRACT
BACKGROUND: The development and progression of cancer depend on its genetic characteristics as well as on the interactions with its microenvironment. Understanding these interactions may contribute to diagnostic and prognostic evaluations and to the development of new cancer therapies. Aiming to investigate potential mechanisms by which the tumor microenvironment might contribute to a cancer phenotype, we evaluated soluble paracrine factors produced by stromal and neoplastic cells which may influence proliferation and gene and protein expression. METHODS: The study was carried out on the epithelial cancer cell line (Hep-2) and fibroblasts isolated from a primary oral cancer. We combined a conditioned-medium technique with subtraction hybridization approach, quantitative PCR and proteomics, in order to evaluate gene and protein expression influenced by soluble paracrine factors produced by stromal and neoplastic cells. RESULTS: We observed that conditioned medium from fibroblast cultures (FCM) inhibited proliferation and induced apoptosis in Hep-2 cells. In neoplastic cells, 41 genes and 5 proteins exhibited changes in expression levels in response to FCM and, in fibroblasts, 17 genes and 2 proteins showed down-regulation in response to conditioned medium from Hep-2 cells (HCM). Nine genes were selected and the expression results of 6 down-regulated genes (ARID4A, CALR, GNB2L1, RNF10, SQSTM1, USP9X) were validated by real time PCR. CONCLUSIONS: A significant and common denominator in the results was the potential induction of signaling changes associated with immune or inflammatory response in the absence of a specific protein.
Subject(s)
Gene Expression Regulation, Neoplastic , Mouth Neoplasms/metabolism , Proteome/metabolism , Annexin A5/metabolism , Apoptosis , Cell Proliferation , Down-Regulation , Electrophoresis, Gel, Two-Dimensional , Fibroblasts/metabolism , Genomics , Hep G2 Cells , Humans , Keratins/metabolism , Mouth Neoplasms/genetics , Nucleic Acid Hybridization , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Stromal Cells/metabolism , Vimentin/metabolismABSTRACT
AIMS: Annexin A1 (ANXA1) is a soluble cytoplasmic protein, moving to membranes when calcium levels are elevated. ANXA1 has also been shown to move to the nucleus or outside the cells, depending on tyrosine-kinase signalling, thus interfering in cytoskeletal organization and cell differentiation, mostly in inflammatory and neoplastic processes. The aim was to investigate subcellular patterns of immunohistochemical expression of ANXA1 in neoplastic and non-neoplastic samples from patients with laryngeal squamous cell carcinomas (LSCC), to elucidate the role of ANXA1 in laryngeal carcinogenesis. METHODS AND RESULTS: Serial analysis of gene expression experiments detected reduced expression of ANXA1 gene in LSCC compared with the corresponding non-neoplastic margins. Quantitative polymerase chain reaction confirmed ANXA1 low expression in 15 LSCC and eight matched normal samples. Thus, we investigated subcellular patterns of immunohistochemical expression of ANXA1 in 241 paraffin-embedded samples from 95 patients with LSCC. The results showed ANXA1 down-regulation in dysplastic, tumourous and metastatic lesions and provided evidence for the progressive migration of ANXA1 from the nucleus towards the membrane during laryngeal tumorigenesis. CONCLUSIONS: ANXA1 dysregulation was observed early in laryngeal carcinogenesis, in intra-epithelial neoplasms; it was not found related to prognostic parameters, such as nodal metastases.
Subject(s)
Annexin A1/metabolism , Carcinoma, Squamous Cell/metabolism , Laryngeal Neoplasms/metabolism , Adult , Aged , Aged, 80 and over , Annexin A1/analysis , Annexin A1/genetics , Blotting, Western , Carcinoma, Squamous Cell/pathology , Female , Gene Expression , Humans , Immunohistochemistry , Laryngeal Neoplasms/pathology , Male , Middle AgedABSTRACT
In this work, we further develop the multidimensional multiscale parser (MMP) algorithm, a recently proposed universal lossy compression method which has been successfully applied to images as well as other types of data, as video and ECG signals. The MMP is based on approximate multiscale pattern matching, encoding blocks of an input signal using expanded and contracted versions of patterns stored in a dictionary. The dictionary is updated using expanded and contracted versions of concatenations of previously encoded blocks. This implies that MMP builds its own dictionary while the input data is being encoded, using segments of the input itself, which lends it a universal flavor. It presents a flexible structure, which allows for easily adding data-specific extensions to the base algorithm. Often, the signals to be encoded belong to a narrow class, as the one of smooth images. In these cases, one expects that some improvement can be achieved by introducing some knowledge about the source to be encoded. In this paper, we use the assumption about the smoothness of the source in order to create good context models for the probability of blocks in the dictionary. Such probability models are estimated by considering smoothness constraints around causal block boundaries. In addition, we refine the obtained probability models by also exploiting the existing knowledge about the original scale of the included blocks during the dictionary updating process. Simulation results have shown that these developments allow significant improvements over the original MMP for smooth images, while keeping its state-of-the-art performance for more complex, less smooth ones, thus improving MMP's universal character.
Subject(s)
Algorithms , Data Compression/methods , Image Enhancement/methods , Image Interpretation, Computer-Assisted/methods , Pattern Recognition, Automated/methods , Signal Processing, Computer-Assisted , Computer Simulation , Models, Statistical , Numerical Analysis, Computer-Assisted , Reproducibility of Results , Sensitivity and SpecificityABSTRACT
Alterações morfológicas de 11 casos de cães com insuficiência renal foram caracterizadas e classificadas de acordo com os padrões estabelecidos pela Organização Mundial de Saúde para seres humanos. Glomerulonefrite esclerosante difusa foi diagnosticada em 82,0 por cento dos animais e nefrite intersticial crônica nos 18,0 por cento restantes. Os tipos e freqüência das lesões identificadas foram similares às encontradas na literatura para a insuficiência renal crônica.
Morphologic alterations of 11 cases of dogs with renal failure were characterized and classified according to the patterns established by the World Health Organization for human beings. Diffuse sclerosing glomerulonephritis was diagnosed in 82.0 percent of the animals and chronic interstitial nephritis in the remaining 18.0 percent. The types and frequencies of lesions were similar to the those noticed in the literature for chronic renal failure.
Subject(s)
Animals , Male , Female , Dogs , Glomerulonephritis/classification , Glomerulonephritis/diagnosis , Renal Insufficiency, Chronic/classification , Renal Insufficiency, Chronic/diagnosis , Renal Insufficiency, Chronic/veterinary , Nephritis, Interstitial/classification , Nephritis, Interstitial/diagnosisABSTRACT
Alterações morfológicas de 11 casos de cães com insuficiência renal foram caracterizadas e classificadas de acordo com os padrões estabelecidos pela Organização Mundial de Saúde para seres humanos. Glomerulonefrite esclerosante difusa foi diagnosticada em 82,0% dos animais e nefrite intersticial crônica nos 18,0% restantes. Os tipos e freqüência das lesões identificadas foram similares às encontradas na literatura para a insuficiência renal crônica.(AU)
Morphologic alterations of 11 cases of dogs with renal failure were characterized and classified according to the patterns established by the World Health Organization for human beings. Diffuse sclerosing glomerulonephritis was diagnosed in 82.0% of the animals and chronic interstitial nephritis in the remaining 18.0%. The types and frequencies of lesions were similar to the those noticed in the literature for chronic renal failure.(AU)