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1.
Cancer Research and Treatment ; : 165-171, 2014.
Article in English | WPRIM | ID: wpr-106245

ABSTRACT

PURPOSE: Evidence regarding the usefulness of 18F-fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) in predicting the prognosis of non-small cell lung cancer is increasing. However, data on small cell lung cancer (SCLC) are scarce. The aim of this study was to evaluate the prognostic value of metabolic parameters measured using 18F-FDG PET/CT in patients with SCLC. MATERIALS AND METHODS: We conducted a retrospective review of 114 patients with pathologically proven SCLC (26 cases of limited disease and 88 cases of extensive disease) who underwent pretreatment 18F-FDG PET/CT. The maximal SUV (SUVmax) was used quantitatively for determination of FDG PET activity. The SUVmax of the primary tumor (primary SUVmax), the sum of SUVmax values of malignant lesions (SUVsum), and the mean SUVmax of malignant lesions were calculated. RESULTS: The patient population was subdivided using a median SUVsum value of 24.6. High SUVsum showed a significant association with known factors for poor prognosis, including higher neuron-specific enolase (p=0.010), CYFRA 21-1 (p=0.014), and extensive disease status (p=0.007). Patients with high SUVsum had significantly shorter median overall survival (6.6 months vs. 13.0 months, p<0.001) and progression-free survival (5.2 months vs. 8.0 months, p<0.001) than patients with low SUVsum. Results of multivariate analysis showed that SUVsum, chemotherapy cycles, and the response to first-line treatment were significant prognostic factors of survival. In contrast, mean SUVmax and primary SUVmax were not significant predictors of survival. CONCLUSION: In this study, metabolic burden represented by SUVsum from pretreatment 18F-FDG PET/CT was an independent prognostic factor in patients with SCLC.


Subject(s)
Humans , Carcinoma, Non-Small-Cell Lung , Disease-Free Survival , Drug Therapy , Electrons , Fluorodeoxyglucose F18 , Multivariate Analysis , Phosphopyruvate Hydratase , Positron Emission Tomography Computed Tomography , Prognosis , Retrospective Studies , Small Cell Lung Carcinoma , Tumor Burden
2.
Tuberculosis and Respiratory Diseases ; : 323-330, 2007.
Article in Korean | WPRIM | ID: wpr-22280

ABSTRACT

Malignant pleural mesothelioma(MPM) is an uncommon neoplasm which is originated from pleural mesothelial cells. The majority of MPM is associated with prior asbestos exposure. Patients often present with chest pain and dyspnea due to pleural effusion, which might be diagnosed with tuberculous pleurisy especially in Korea. MPM is well known for its poor prognosis with a median survival time of less than 12 months after diagnosis and no established standard treatment modality. We report 3 cases of MPM confirmed by video-assisted thoracoscopic biopsy first misdiagnosed as tuberculous pleurisy.


Subject(s)
Humans , Asbestos , Biopsy , Chest Pain , Diagnosis , Dyspnea , Korea , Mesothelioma , Pleural Effusion , Prognosis , Thoracoscopy , Tuberculosis, Pleural
3.
Tuberculosis and Respiratory Diseases ; : 492-498, 2007.
Article in Korean | WPRIM | ID: wpr-8710

ABSTRACT

Background: Several lines of evidence suggest that a host's genetic factors influence the outcome of exposure to Mycobacterium tuberculosis. The aim of this study was to determine whether polymorphism in NRAMP1 (natural resistance associated macrophage protein 1) gene is associated with the susceptibility or resistance to tuberculosis infection for patients with drug-sensitive pulmonary tuberculosis (DS-TB) and multi-drug resistant pulmonary tuberculosis (MDR-TB). Methods: Eight genetic polymorphisms of the NRAMP1 gene were investigated in patients suffering with DS-TB (n=100) or MDR-TB (n=102), and in healthy normal controls (NC, n=96). The genetic polymorphisms of NRAMP1 were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Results: The frequency of D543N A/G heterogygotes was significantly higher in the DS-TB subjects than the NCs (OR=2.10, 95% CI: 1.00 to 4.41, p=0.049). The frequency of 823C/T T/C heterozygotes was significantly higher in the DS-TB subjects (OR=2.79, 95% CI: 1.11 to 7.04, p=0.029) and the MDR-TB subject (OR=3.30, 95% CI 1.33 to 8.18, p=0.010) than in the NCs. However, the frequency of these genotypes was not different between the DS-TB and MDR-TB subjects. Conclusion: A significant association was found between NRAMP1 823 C/T polymorphism and pulmonary tuberculosis. This result suggests that NRAMP1 polymorphism may be involved in the development of pulmonary tuberculosis in Koreans.


Subject(s)
Humans , Genotype , Heterozygote , Macrophages , Mycobacterium tuberculosis , Polymorphism, Genetic , Tuberculosis , Tuberculosis, Pulmonary
4.
Tuberculosis and Respiratory Diseases ; : 117-127, 2002.
Article in Korean | WPRIM | ID: wpr-228591

ABSTRACT

BACKGROUND: MUC1 mucin is a heavily glycosylated large glycoprotein and is expressed aberrantly in carcinoma. CD44 is polymorphic family of cell surface glycoproteins participating in cell-cell adhesion and modulat ion of the cell-matrix interaction. MUC1 mucin and CD44 expression have been implicated in a tumor invasion and metastasis in certain malignancies. In this study, the expression of MUC1 and the standard form of CD44(CD44s) was examined in non-small cell lung cancer (NSCLC). METHODS: Immunohistochemical staining using monoclonal antibodies including MUC1 glycoprotein and CD44s was performed on 80 NSCLC surgical specimens. The association between MUC1 and CD44s expression and the histological type and tumor stage was investigated. RESULTS: Depolarized MUC1 expression in more than 10% of cancer cells was found in 12 (27.9%) out of 43 squamous cell carcinomas (SCCs) and 12 (32.4%) out of 37 adenocarcinomas (ACs). It was not associated with the tumor histological type and the TNM-stage in SCCs. Depolarized MUC1 expression correlated with the N-stage in ACs (p=0.036). CD44s was expressed in 36 (83.7%) out of 43 SCCs and 14(37.8%) out of 37ACs. Reduced CD44s expression correlated with the N-stage (p=0.031) and the TNM-stage (p=0.0006) in SCCs. CONCLUSIONS: Depolarized MUC1 expression was related to the nodal stage in NSCLC adenocarcinoma. Reduced CD44s expression was related to nodal involvement and the TNM-stage in squamous cell carcinoma. This suggests that MUC1 and CD44s expression in NSCLC might play important roles in tumor progression and can be used as prognostic variables.


Subject(s)
Humans , Adenocarcinoma , Antibodies, Monoclonal , Carcinoma, Non-Small-Cell Lung , Carcinoma, Squamous Cell , Glycoproteins , Immunohistochemistry , Membrane Glycoproteins , Mucin-1 , Neoplasm Metastasis
5.
Korean Journal of Medicine ; : 716-719, 2002.
Article in Korean | WPRIM | ID: wpr-55464

ABSTRACT

Nasopharyngeal tuberculosis is a very rare condition and mainly secondary infection from pulmonary tuberculosis by contagious, hematogenous or lymphatic spread. However, nasopharyngeal tuberculosis may arise as a primary infection in adults without active pulmonary disease and is frequently associated with involvement of the cervical lymph node. The nasopharynx may be a portal entry for mycobacterium tuberculosis in patients who develop cervical lymphadenitis. But, involvement of the nasopharynx by tuberculosis may be underdiagnosed because it does not produce obvious symptoms or physical signs. Recently authors experienced a case of primary nasopharyngeal tuberculosis of immigrant woman from Vietnam. Here, we report a case that was confirmed by punch biopsy under telerhinoscopy and improved by combination chemotherapy.


Subject(s)
Adult , Female , Humans , Biopsy , Coinfection , Drug Therapy, Combination , Emigrants and Immigrants , Lung Diseases , Lymph Nodes , Lymphadenitis , Mycobacterium tuberculosis , Nasopharynx , Tuberculosis , Tuberculosis, Pulmonary , Vietnam
6.
Tuberculosis and Respiratory Diseases ; : 94-105, 2001.
Article in Korean | WPRIM | ID: wpr-29919

ABSTRACT

BACKGROUND: Examining the biological susceptibility of Mycobacterium tuberculosis to pyrazinamide (PZA) in vitro is very difficult as PZA is inactive under normal culture conditions. The susceptibility test, an enzyme assay for Pzase activity, and a genetic test for pncA gene mutations, were performed in order to predict PZA resistance. METHODS: 28 cultured clinical isolates of Mycobacterium tuberculosis were tested. The biological susceptibility was performed by the absolute concentration method using Lowenstein-Jensen media. The PZase activity was tested by means of Wayne's method. A 710-bp region includes the entire open reading frame of pncA was amplified and sequenced. RESULTS: All six strains with positive PZase activity exhibited no pncA mutations with one strain showing a false resistance in the biological susceptibility test. Among the 22 strains with no PZase activity, 21 exhibited showed pncA mutations. In the biological suscaptibility test, 20 strains were resistant, and one was susceptible, and the other failed to test. The mutation types varied with ten missense, one silent and one nonsense mutation 1 slipped-strand mispairing, and 6 frameshift mutations. Three strains had an adenine to guanine mutation at position - 11 upstream of the start codon. CONCLUSION: The mutation at the pncA promotor region is frequent at -11 upstream position. Automatic sequencing of pncA is a useful tool for rapid and accurate detection of PZA resistant M.tuberculosis, and for demonstrating the epidemiological relatedness of the PZA-resistant M.tubersulosis strains.


Subject(s)
Adenine , Codon, Initiator , Codon, Nonsense , Enzyme Assays , Frameshift Mutation , Guanine , Mycobacterium tuberculosis , Mycobacterium , Open Reading Frames , Promoter Regions, Genetic , Pyrazinamide
7.
Tuberculosis and Respiratory Diseases ; : 205-212, 2001.
Article in Korean | WPRIM | ID: wpr-15132

ABSTRACT

BACKGROUND: The information on nasal transport and the metabolism of peptides have been obtained from pharmacokinetic investigations in experimental animals. However, there are no transport and metabolic studies of human nasal epithelial cells. In this study, the permeability characteristics and the metabolic properties of in vitro human nasal cell monolayers were investigated. Material and METHODS: Normal human inferior nasal conchal tissue samples were obtained from patients undergoing endoscopic nasal cavitary surgery. The specimens were cultured in a transwell using an air-liquid interface (ALI) culture, and the transepithelial electrical resistance (TEER) value of the blank filter and confluent cell monolayers were measured. To determine the % leakage of mannitol, 4µmol 14C-labelled mannitol was added and the % leakage was measured every 10 minute for 1 hour. RESULT: Human nasal epithelial cells in the primary culture grew to a confluent monolayer within 7 days and expressed microvilli. The tight junction between the cells was confirmed by transmission electron microscopy. The TEER value of the blank filter, fifth day and seventh day reached 108.5 ohm.cm2, 141 ohm.cm2 and 177.5 ohm.cm2, respectively. Transcellular % leakage of the 14C-mannitol at 10, 20, 30, 40, 50 and 60 minutes was 35.67±5.43, 34.42±5.60, 32.75±5.71, 31.76±4.22, 30.96±3.49 and 29.60±3.68 %, respectively. CONCLUSION: The human nasal epithelial monolayer using ALI using techniques is suitable for a transcellular permeability study. The data suggests that human nasal epithelial cells in as ALI culture technique shows some promise for a nasal transport and metabolism study.


Subject(s)
Animals , Humans , Culture Techniques , Electric Impedance , Epithelial Cells , Mannitol , Metabolism , Microscopy, Electron, Transmission , Microvilli , Peptides , Permeability , Tight Junctions
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