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1.
Pathol Oncol Res ; 19(3): 447-50, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23361472

ABSTRACT

Fine-needle aspiration biopsy is a method to detect malignancy for undetermined pulmonary nodules, but has the potential to spread malignant cells from the tumor to the pleural cavity or chest wall. We developed a two-step freezing method to avoid needle-tract seeding, by use of percutaneous cryoablation after biopsy but before the biopsy needle was removed. A man aged 72 years was admitted because of a large mass in right upper lobe. After biopsy, the patient underwent surgery. Pathological assessment of the resected tumor showed that tissue around the biopsy probe and cryoprobe had been killed before needle withdrawal.


Subject(s)
Biopsy, Needle/adverse effects , Cryosurgery/methods , Lung Neoplasms/pathology , Neoplasm Seeding , Aged , Humans , Lung Neoplasms/diagnosis , Lung Neoplasms/prevention & control , Male , Postoperative Complications/prevention & control
2.
World J Gastroenterol ; 17(9): 1219-26, 2011 Mar 07.
Article in English | MEDLINE | ID: mdl-21448429

ABSTRACT

AIM: To study the correlation between high metastasis-associated protein 1 (MTA1) expression and lymphangiogenesis in colorectal cancer (CRC) and its role in production of vascular endothelial growth factor-C(VEGF-C). METHODS: Impact of high MTA1 and VEGF-C expression levels on disease progression and lymphovascular density (LVD, D2-40-immunolabeled) in 81 cases of human CRC was evaluated by immunohistochemistry. VEGF-C mRNA and protein expressions in human LoVo and HCT116 cell lines were detected by real-time polymerase chain reaction and Western blotting, respectively, with a stable expression vector or siRNA. RESULTS: The elevated MTA1 and VEGF-C expression levels were correlated with lymph node metastasis and Dukes stages (P < 0.05). Additionally, high MTA1 expression level was correlated with a large tumor size (P < 0.05). A significant correlation was found between MTA1 and VEGF-C protein expressions in tumor cells (r = 0.371, P < 0.05). Similar to the VEGF-C expression level, high MTA1 expression level was correlated with high LVD in CRC (P < 0.05). Furthermore, over-expression of MTA1 significantly enhanced the VEGF-C mRNA and protein expression levels, whereas siRNAs - knocked down MTA1 decreased the VEGF-C expression level. CONCLUSION: MTA1, as a regulator of tumor-associated lymphangiogenesis, promotes lymphangiogenesis in CRC by mediating the VEGF-C expression.


Subject(s)
Colorectal Neoplasms/metabolism , Colorectal Neoplasms/pathology , Histone Deacetylases/metabolism , Lymphangiogenesis/physiology , Repressor Proteins/metabolism , Vascular Endothelial Growth Factor C/metabolism , Disease Progression , Female , Histone Deacetylases/genetics , Humans , Immunohistochemistry , Lymphatic Metastasis , Male , Middle Aged , RNA Interference , Repressor Proteins/genetics , Trans-Activators
3.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 45(4): 219-22, 2010 Apr.
Article in Chinese | MEDLINE | ID: mdl-20654197

ABSTRACT

OBJECTIVE: To examine the expression of Fas and Fas ligand (FasL) in T lymphocytes of oral lichen planus (OLP) and the effects of Fas, FasL and activation-induced cell death (AICD) on OLP. METHODS: The oral mucosa samples from patients with OLP and normal oral mucosa were assessed by in situ terminal deoxynucleotidyl transferase (TdT)-mediated deoxyuridine-5'-triphosphate (dUTP)-biotin nick end-labelling (TUNEL) assay for nucleosomal DNA fragmentation of apoptotic cells in infiltrating lymphocytes. Immunohistochemical technique was used for detection of expression level of Fas and FasL. Immunohistochemical double labeling was performed to examine the expression of Fas and FasL in CD8+ T cells and CD4+ T cells. RESULTS: The rate of apoptosis in infiltrating lymphocytes of OLP was (1.9 +/- 1.8)%, which was lower than that of normal oral mucosa (P = 0.013). The expression of Fas and FasL were increased in lymphocytes of OLP (P = 0.005 and 0.000 respectively). The positive rate of double labeled cells of CD8+ and Fas+ was not increased in OLP (P = 0.313), and of CD8+ and FasL+ in OLP was higher than that of normal oral mucosa (P = 0.002). The expression of double labeled cells of CD4+ and Fas+ in OLP was higher than that of control group (P = 0.031). The expression of CD4+ and Fas+ T cells in reticular OLP were increased (P = 0.019), and of CD4+ and FasL+ did not show remarkable change (P = 0.097). CONCLUSIONS: There was a low frequency of lymphocytic apoptosis. T cells, especially CD8+ T cells in OLP and CD4+T cells in atrophic-erosive OLP appeared to escape from AICD, which may account for the persistence of inflammation. Some CD4+ T cells in reticular OLP may go through AICD.


Subject(s)
Apoptosis , Fas Ligand Protein/metabolism , Lichen Planus, Oral/metabolism , Lichen Planus, Oral/pathology , fas Receptor/metabolism , Adult , CD4-Positive T-Lymphocytes/metabolism , CD8-Positive T-Lymphocytes/metabolism , Female , Humans , In Situ Nick-End Labeling , Male , Middle Aged , Mouth Mucosa/metabolism , Mouth Mucosa/pathology
4.
Arch Med Res ; 40(4): 268-75, 2009 May.
Article in English | MEDLINE | ID: mdl-19608016

ABSTRACT

BACKGROUND AND AIMS: Recent observations suggest an implication of cyclooxygenase-2 (COX-2) in tumor lymphangiogenesis through an upregulation of vascular endothelial growth factor-C (VEGF-C) expression. However, it is unclear whether COX-2 is also associated with VEGF-C expression, tumor lymphangiogenesis and lymph node metastasis in human prostate cancer. METHODS: COX-2 and VEGF-C expression were examined in tumor tissues from 58 prostate cancer patients using immunohistochemical staining. We also analyzed the association of COX-2 and VEGF-C expression with tumor lymphangiogenesis quantified as lymphatic vessel density (LVD), lymph node metastasis, and patients' biochemical progression-free survival (b-PFS). RESULTS: High expression of either COX-2 or VEGF-C was correlated with tumor lymphangiogenesis and lymph node metastasis, as well as poor b-PFS. Moreover, a strong correlation was found between expression of COX-2 and VEGF-C (r = 0.631, p <0.001). CONCLUSIONS: COX-2 is positively associated with VEGF-C expression, tumor lymphangiogenesis and lymphatic metastasis in prostate cancer. These findings suggest that COX-2 may play a pivotal role in lymphangiogenesis and lymph node metastasis of prostate cancer via the regulation of VEGF-C expression.


Subject(s)
Biomarkers, Tumor/biosynthesis , Cyclooxygenase 2/biosynthesis , Prostatic Neoplasms/mortality , Prostatic Neoplasms/pathology , Vascular Endothelial Growth Factor C/biosynthesis , Aged , Biomarkers, Tumor/analysis , Cyclooxygenase 2/analysis , Humans , Lymphangiogenesis , Lymphatic Metastasis , Male , Middle Aged , Survival Analysis , Vascular Endothelial Growth Factor C/analysis
5.
Nan Fang Yi Ke Da Xue Xue Bao ; 29(5): 946-8, 2009 May.
Article in Chinese | MEDLINE | ID: mdl-19460716

ABSTRACT

OBJECTIVE: To investigate the expressions of proliferating cell nuclear antigen (PCNA), B cell lymphoma-2 (Bcl-2) and Bcl-associated X (Bax) in the lymphocytes of patients with oral lichen planus (OLP). METHODS: Immunohistochemistry was used for detecting the expressions of PCNA, Bcl-2 and Bax proteins in oral lichen planus tissue and normal oral mucosa (NOM). RESULTS: The expressions of PCNA and Bcl-2 proteins increased significantly in the lymphocytes of patients with OLP compared with those in NOM. The expressions of PCNA and Bcl-2 proteins showed no significant differences between patients with OLP of general type and erosive type. CONCLUSION: Increased expression of PCNA and the imbalance of Bcl-2/Bax expressions in the lymphocytes of patients with OLP can be important causes for continuous lymphocyte infiltration in OLP.


Subject(s)
Lichen Planus, Oral/metabolism , Lymphocytes/metabolism , Proliferating Cell Nuclear Antigen/metabolism , Proto-Oncogene Proteins c-bcl-2/metabolism , bcl-X Protein/metabolism , Adult , Female , Humans , Male , Middle Aged , Mouth Mucosa/metabolism
6.
Org Lett ; 10(20): 4569-72, 2008 Oct 16.
Article in English | MEDLINE | ID: mdl-18816120

ABSTRACT

Galaxamide (1), a rare cyclic pentapeptide, was isolated from the marine algae Galaxaura filamentosa. A preliminary bioassay of Galaxamide showed remarkable in vitro antiproliferative activities against GRC-1 and HepG2 cell lines. The first total synthesis of the cyclic peptide was achieved for further biological evaluation.


Subject(s)
Peptides, Cyclic/chemistry , Peptides, Cyclic/isolation & purification , Rhodophyta/chemistry , Animals , Cell Line , Cell Survival/drug effects , Humans , Magnetic Resonance Spectroscopy , Molecular Structure , Peptides, Cyclic/chemical synthesis , Peptides, Cyclic/toxicity
7.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 43(2): 99-100, 2008 Feb.
Article in Chinese | MEDLINE | ID: mdl-18683732

ABSTRACT

OBJECTIVE: To investigate the expression of TGF-beta receptors in CD8+ T cells of oral lichen planus (OLP). METHODS: Immunohistochemical double labeling technique was used to examine the expression of TGF-betaR I and TGF-betaR II in CD8+ T cells of 28 OLP patients and in 10 controls. The results were compared between the two groups. RESULTS: The double labeled cells were negative in controls. The positive rates of double labeled cells of CD8+/TGF-betaR I and CD8+/TGF-betaR II in OLP were (8.82 +/- 9.98)% and (1.11 +/- 2.94)% respectively. CONCLUSIONS: The expression level of TGF-betaR II in CD8+ T cells of OLP did not increase compared with the controls, but the expression of TGF-betaR I increased. The results indicate the abnormal TGF-beta signal transduction in CD8+ T cells of OLP, which may contribute to the persistence of the chronic inflammation in OLP.


Subject(s)
CD8-Positive T-Lymphocytes/metabolism , Lichen Planus, Oral/metabolism , Protein Serine-Threonine Kinases/metabolism , Receptors, Transforming Growth Factor beta/metabolism , Adult , Case-Control Studies , Female , Humans , Lichen Planus, Oral/pathology , Male , Mouth Mucosa/metabolism , Mouth Mucosa/pathology , Receptor, Transforming Growth Factor-beta Type I , Receptor, Transforming Growth Factor-beta Type II , Signal Transduction
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