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1.
Chinese Medical Journal ; (24): 509-513, 2009.
Article in English | WPRIM | ID: wpr-311832

ABSTRACT

<p><b>BACKGROUND</b>The lung functional status could be displayed on lung perfusion images. With the images, the radiotherapy plans of lung cancer could be guided to more optimized. This study aimed to assess quantitatively the impact of incorporating functional lung imaging into 3-dimensional conformal radiotherapy (3DCRT) and intensity-modulated radiation therapy (IMRT) planning for non-small cell lung cancer (NSCLC).</p><p><b>METHODS</b>Ten patients with NSCLC who had undergone radiotherapy were included in this study. Before radiotherapy, each patient underwent CT simulation and lung perfusion imaging with single photon emission computed tomography (SPECT). The SPECT images were registered with simulation planning CT and used to contour functional lung (lung-F) and non-functional lung (lung-NF). Two 3DCRT plans and two IMRT plans were designed and compared in each patient: two anatomic plans using simulation CT alone and two functional plans using SPECT-CT in addition to the simulation CT. Dosimetric parameters of the four types of plans were compared in terms of tumor coverage and avoidance of normal tissues. Total radiation dose was set at 66 Gy (2 Gy x 33 fractions).</p><p><b>RESULTS</b>In incorporating perfusion information in 3DCRT and IMRT planning, the reductions on average in the mean doses to the functional lung in the functional plan were 168 cGy and 89 cGy, respectively, compared with those in the anatomic plans. The median reductions in the percentage of volume irradiated with > 5 Gy, > 10 Gy, > 20 Gy, > 30 Gy and > 40 Gy for functional lung in the functional plans were 6.50%, 10.21%, 14.02%, 22.30% and 23.46% in 3DCRT planning, respectively, and 3.05%, 15.52%, 14.16%, 4.87%, and 3.33% in IMRT planning, respectively. No greater degree of sparing of the functional lung was achieved in functional IMRT than in 3DCRT.</p><p><b>CONCLUSION</b>Function-guided 3DCRT and IMRT plannings both appear to be effective in preserving functional lung in NSCLC patients.</p>


Subject(s)
Humans , Carcinoma, Non-Small-Cell Lung , Diagnostic Imaging , Pathology , Radiotherapy , Radiography , Radiotherapy, Conformal , Methods , Radiotherapy, Intensity-Modulated , Methods , Tomography, Emission-Computed, Single-Photon , Methods
2.
Chinese Journal of Hepatology ; (12): 821-825, 2009.
Article in Chinese | WPRIM | ID: wpr-306636

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the role of c-Jun N-terminal kinase (JNK) signal transduction pathway in the rats of nonalcoholic fatty liver disease (NAFLD).</p><p><b>METHODS</b>Sixty four Sprague-Dawley rats were randomly divided into four groups: 8-week control group (NG8w), 12-week control group (NG12 w), 8-week high-fat diet (HG8w), and 12-week high-fat diet group (HG12w), with 16 rats in each group. Glucose infusion rate (GIR) was tested by euglycemic hyperinsulinemic clamp; aminotransferase (ALT), aspartate aminotransferase (AST), triglyceride (TG), total cholesterol (TC), free fatty acid (FFAs), fast insulin (FIns), tumor necrosis factor alpha (TNF alpha), superoxide dismutase (SOD) and malondialdehyde (MDA) were tested by biochemistry automatic analyzer or RIA; The expression of JNK1, insulin receptor substrate-1 (IRS-1), phospho-IRS-1 Ser307 (p-IRS-1 Ser307), Protein kinase B (PKB) and phospho-PKB Ser473 (p- PKB Ser473) were detected by Western blot.</p><p><b>RESULTS</b>Compared to control group, body weight, liver index, serum levels of ALT, AST, TG, TC, FIns, FFAs, TNF alpha, and TC, TG FFAs, MDA in liver homogenates were increased, while the level of SOD, and GIR were decreased. The expression of JNK1 protein and p-IRS-1 Ser307 in liver tissue was up-regulated, while expression of p-PKB Ser473 was decreased (P < 0.05). A positive correlation was found between the expression intensity of JNK1 and IR (Pearson correlation: 0.718, P < 0.01).</p><p><b>CONCLUSION</b>The high-fat could induce the expression of JNK1, which in turn modulates the phosphorylation of proteins in the insulin signaling pathway, and induces insulin resistant.</p>


Subject(s)
Animals , Male , Rats , Alanine Transaminase , Blood , Biomarkers , Blood , Dietary Fats , Disease Models, Animal , Fatty Liver , Metabolism , Pathology , Insulin Receptor Substrate Proteins , Metabolism , Insulin Resistance , JNK Mitogen-Activated Protein Kinases , Metabolism , Lipids , Blood , Liver , Metabolism , Pathology , Proto-Oncogene Proteins c-akt , Metabolism , Random Allocation , Rats, Sprague-Dawley , Signal Transduction
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