2.Genetic polymorphism of T6235C mutation in 3' non-coding region of CYP1A1 and GSTM1 genes and lung cancer susceptibility in the Mongolian population
Fuhou CHANG ; Minjie WANG ; Jun QI ; Qin YIN ; Lei FAN ; Ruilan HAN ; Guang WANG
Journal of Pharmaceutical Analysis 2009;21(4):225-229
Objective To estimate the relative risk for lung cancer associated with genetic polymorphism of T6235C mutation in 3' non-coding region (Msp Ⅰ) of cytochrome P450 1A1 (CYP1A1) and glntathione S-transferase M1 (GSTM1) in the Mongolian population in Inner Mongolian Region of China. Methods Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and multiplex PCR methods were used to analyze blood samples obtained from 263 case subjects and 263 control subjects to determine their genotypes for CYP1A1 and GSTM1.Control subjects were matched with case subjects by ethnic background, age and gender. Results The frequencies of the variant CYP1A1 genotypes (CYP1A1C) and GSTM1-null in lung cancer groups were higher than those in control groups (38.4% vs. 28. 5% and 57.8% vs. 48.0%). The individuals who corried with CYP1A1C genotype had a significantly higher risk of lung cancer (OR=1.56, 95% CI=1.08 to 2.25, P=0.016) than those who carried with non-variation CYP1A1 genotype. The ones who carried with GSTM1-null genotype also had a significantly higher risk of lung cancer (OR=1.49, 95% CI=1.06 to 2.10, P=0.023) than these who carried with GSTM1-present genotype.When combination of polymorphisms of CYP1A1 and GSTM1 genotypes was analyzed, the risk of lung cancer for combination of CYP1A1C and GSTM1-null genotypes was increased significantly (OR=2.084, 95e CI=1.27 to 3.42, P=0.003). Susceptibility to lung cancer was related to smoking (OR=2.10, 95% CI=1.48 to 2.98, P=0.000). Considering smoking status, the risk of lung cancer for combination of smoking and CYP1A1C genotype was remarkably increased (OR=2.76, 950/0 CI=1.74 to 4. 37, P=0.000). It was the same case with combination of smoking and GSTM1-null genotype (OR=4. 38, 95% CI=2.35 to 8.15, P=0.000). Conclusion The polymorphisms of CYP1A1C genotype and GSTM1-null are the risk factors of lung cancer in the Mongolian population in Inner Mongolia Region of China. Smoking is also related to susceptibility to lung cancer. There may be a synergetic interaction between CYP1A1C and GSTM1-null in the elevated susceptibility of lung cancer. Smoking may have a synergetic interaction with CYP1A1C and GSTM1-null in the elevated susceptibility of lung cancer.
3.Thoracic spinal trauma associated with closed thoracoabdominal injury.
Lei LU ; Li-wen WU ; Guang-yu FAN
Chinese Journal of Traumatology 2003;6(3):171-173
OBJECTIVETo explore the management of thoracic spinal trauma (TST) associated with closed thoracoabdominal injuries (CTAI).
METHODSA retrospective study was made on 259 patients with TST admitted to our department as an emergency treatment from January 1996 to June 2001. We summarized the clinical features of TST associated with CTAI.
RESULTSAmong 259 patients with thoracic spinal trauma, 112 were associated with CTAI. Traffic accident was the most common cause. The force causing upper TST was more violent than that causing the lower. Pulmonary complications were the leading cause of death in this group. Surgery could not improve neurological function for completely paraplegic patients.
CONCLUSIONSThe reason that upper TST has the tendency to be associated with CTAI is its special anatomical feature. Routine ultrasonic examination can avoid misdiagnosis of latent closed abdominal injuries associated with spinal injury. The presence of potential injuries, especially CTAI, should be considered when deciding whether or not to perform surgery early.
Adult ; Female ; Hemopneumothorax ; diagnosis ; Humans ; Male ; Paracentesis ; Retrospective Studies ; Spinal Cord Injuries ; diagnosis ; Thoracic Injuries ; diagnosis
4.Comparative study of myocardial perfusion imaging and 64 multi-slice spiral CT for the diagnosis of coronary artery disease
Jun, ZHAO ; Long-bao, XU ; Ren-ming, WAN ; Guang-lei, FAN ; Jian-wen, LIU ; Shu-xing, HUANG
Chinese Journal of Nuclear Medicine 2010;30(6):367-371
Objective To compare the diagnostic value of myocardial perfusion imaging (MPI) and 64 multi-slice spiral CT (64-MSCT) for coronary artery disease (CAD). Methods Fifty-two patients with suspected or known CAD were included in the study. Each patient underwent both stress and rest MPI,MSCT as well as conventional coronary angiography (CAG) within 1 month. The stress and rest MPI were scored by a 5-grade criteria (0 ~ 4) based on 17 coronary artery segments. The difference between summed stress and rest scores > 1 was defined as myocardial ischemia. Stenosis in one main vessel or one main branch of the main vessel ≥50% was defined as myocardial ischemia by MSCT. CAG was used as the reference for comparison. Statistical analysis was performed using SPSS 13. 0 software. Kappa value was used to test the accordance of MPI and MSCT results. X2 test was used to evaluate the difference between MPI and MSCT results. Results The patient-based sensitivity, specificity, positive and negative predictive values and accuracy of MPI and MSCT for the diagnosis of CAD were 86.7% (26/30), 77.3% ( 17/22),83.9% (26/31), 81.0% ( 17/21), 82.7% (43/52) and 83.3% ( 25/30), 86.4% ( 19/22), 89.3%( 25/28), 79.2% ( 19/24), 84.6% (44/52), respectively. The vessel-based sensitivity, specificity, positive and negative predictive values and accuracy of MPI and MSCT were 74.5% (38/51), 81.0% (85/105 ), 65.5% (38/58), 86.7% ( 85/98), 78.8% ( 123/156 ) and 90.2% (46/51 ), 88.6% ( 93/105 ),79.3 % (46/58), 94.9% (93/98), 89.1% ( 139/156), respectively. There was no statistically significant difference between MPI and MSCT for either patient or lesion-based diagnosis (X2 =0.44, 0.21, both P >0.05 ). 96.0% (24/25) patients with both abnormal MPI and MSCT positive were valified by CAG while 83.3% (15/18) patients with both MPI and MSCT negative were excluded by CAG. Conclusions Both MPI and MSCT are reliable diagnostic modalities for CAD. They also provide complementary diagnostic value to each other.
5.Not Available.
Qi fan YANG ; Zhi ling TIAN ; Lei WAN ; Dong hua ZOU ; Yan bin WANG ; Guang zheng ZHANG ; Ning guo LIU
Journal of Forensic Medicine 2022;38(4):551-554
6.Congenital dyserythropoietic anemia type II: a case report and literature review.
Yuan LI ; Xin ZHAO ; Kang ZHOU ; Yang LI ; Jian-ping LI ; Lei YE ; Guang-xin PENG ; Hui-hui FAN ; Li-ping JING ; Li ZHANG ; Feng-kui ZHANG
Chinese Journal of Hematology 2012;33(4):270-273
OBJECTIVETo investigate the clinical and laboratory features of congenital dyserythropoietic anemia type II (CDA-II) in order to improve the recognition of the disease.
METHODSA case of CDA-II was reported and the related literatures were reviewed.
RESULTSThe 32-years old female presented with moderate anemia, jaundice and hepatosplenomegaly from her childhood and was misdiagnosed as hereditary spherocytosis for a long time. There were no increased reticulocytes in the peripheral blood and her bone marrow showed erythroid hyperplasia with 43% of binucleated erythroblasts. Electron microscopy examination revealed stretches of double membrane lining the inner surface of the erythroblast cell membrane.
CONCLUSIONSCDA-II is a rare congenital anemia characterized by ineffective erythropoiesis with unique laboratory features, and is relatively easy to be misdiagnosed. It is necessary to improve the awareness of CDA-II, and to set-up its responsible gene analysis, i.e., CDAN2 gene and SEC23B gene detection.
Adult ; Anemia, Dyserythropoietic, Congenital ; diagnosis ; genetics ; Female ; Humans ; Vesicular Transport Proteins ; genetics
7.Imageology change of the intervertebral foramen degenerative intervertebral disc in different degrees and its clinical.
Sheng MIAO ; Lei FAN ; Ning WANG ; Lian-Qi YAN ; Zheng GUO ; Guang-Zhao SHA ; Yong-Dong WANG
China Journal of Orthopaedics and Traumatology 2009;22(10):730-732
OBJECTIVETo study the imageology change of the intervertebral foramen degenerative intervertebral disc in different degrees and explore its clinical significance.
METHODSThe imageology data (MRI and CT) of 37 patients with degenerative disc disease of L4,5 (male 23, female 14, age from 28 to 62 years with an average of 41.6 years)were investigated. The patients were divided into three groups depending on the mean signal intensity rate of degenerative disc and cerebrospinal fluid:light degenerative group (group A) of 11 cases, intermediate degenerative group (group B) of 13 cases, and severe degenerative group (group C) of 13 cases. The extreme altitude, maximum width and areas of the intervertebral foramen were measured from the CT 1.25 mm scan reconstitution. The changes of the intervertebral foramen were analyzed.
RESULTS(1) 1. The extreme altitude and areas of the intervertebral foramen gradually diminished among the light degenerative group, intermediate degenerative group and severe degenerative group, there was no significant deviation between intermediate degenerative group and the light degenerative group (P > 0.05), there was statistical significance between severe degenerative group and intermediate degenerative group (P < 0.05), there was statistical significance between severe degenerative group and light degenerative group (P < 0.01). (2) There was no statistical significance of the maximum width of intervertebral foramen among three groups (P > 0.05).
CONCLUSIONThe extreme altitude and areas of the intervertebral foramen gradually diminished when the disc are differently degenerative. But there was not significant correlation to width of the intervertebral foramen; the dimin height and area of intervertebral foramen should result in root compression.
Adult ; Female ; Humans ; Intervertebral Disc ; chemistry ; diagnostic imaging ; Intervertebral Disc Degeneration ; diagnostic imaging ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Tomography, X-Ray Computed
8.Imageology change of degenerative cartilage endplate to different degree and its clinical significance.
Sheng MIAO ; Guang-Zhao SHA ; Yong-Dong WANG ; Lian-Qi YAN ; Liang-Yu SONG ; Zheng GUO ; Lei FAN ; Lin SHAO
China Journal of Orthopaedics and Traumatology 2008;21(6):414-417
OBJECTIVETo study the imageology changes of degenerative cartilage endplate to different degree, and to explore its clinical significances.
METHODSThe imageology data (MRI or CT) of 58 patients with degenerative disc disease of L4, 5 (including 34 patients with lumbar disc herniation). The patients were divided into three groups depending on the mean signal intensity rate of degenerative disc and cerebrospinal fluid: light degenerative group of 17 cases, intermediate degenerative group of 17 cases, and severe degenerative group of 24 cases. The signals of intervertebral disks on T2WI of sagittal magnetic resonance imaging were inputted into the computer and the concave angles of endplate were measured. Anteroposterior diameter and transverse diameter of the endplate were measured from the CT scan of L4, 5, and then the relative curvature of endplate was got. The change patterns of the concave angle and the relative curvature of vertebral endplates were analyzed when the lumbar disc was differently degenerative.
RESULTS(1) The concave angle of endplate (L4 inferior endplate, L5 superior endplate) gradually increased among the light degenerative group, intermediate degenerative group and severe degenerative group (P < 0.01). (2) The relative curature of endplate (L4 inferior endplate, L5 superior endplate) gradually increased. There was significant difference between the light degenerative group and intermediate degenerative group (P < 0.0l), and there was significant difference between the light degenerative group and severe degenerative group (P < 0.0l). There were no significant difference between intermediate degenerative group and severe degenerative group (P < 0.05). (3) The concave angle of endplate had positive correlation with relative circularity (r = 0.786, 0.490).
CONCLUSIONThe concave angle and relative curvature of endplate generate corresponding changes when the lumbar disc are differently degenerative. The changes of concave angle and relative curvature of endplate are important factors of lumbar disc hernia and lower back pain, which may evaluate the probability of intervertebral disk hernia.
Adult ; Cartilage ; pathology ; Female ; Humans ; Intervertebral Disc Displacement ; pathology ; Lumbar Vertebrae ; pathology ; Magnetic Resonance Imaging ; Male ; Middle Aged
9.Inhibitory effect of knocking down microRNA-221 and microRNA-222 on glioma cell growth in vitro and in vivo.
Chun-zhi ZHANG ; Chun-sheng KANG ; Pei-yu PU ; Guang-xiu WANG ; Zhi-fan JIA ; An-ling ZHANG ; Lei HAN ; Peng XU
Chinese Journal of Oncology 2009;31(10):721-726
OBJECTIVETo study the inhibitory effect of knocking down microRNA(miR)-221 and miR-222 on human glioma cell growth and its possible mechanism.
METHODSmiRNA-221/222 antisense oligonucleotides (antisense miR221/222) were transfected into human glioma U251 cells by lipofectamine. Northern blot analysis was conducted to detect the mRNA expression of miR-221/222 in the control and transfected cell groups. The proliferation activity of cells was determined by MTT assay. Cell invasion ability was examined by transwell assay, and cell cycle kinetics and apoptosis were detected with flow cytometry. The expression of relevant proteins was analyzed by Western blotting. The therapeutic efficacy of antisense miR221/222 on the growth of xenograft tumors in nude mice were also observed.
RESULTSIn the antisense miR-221/222-transfected cells, the expression of miR-221/222 was significantly reduced; the cell invasion ability was suppressed, cell cycle was blocked at G(0)/G(1) phase, and apoptotic cells were increased. The growth of xenograft tumors treated with antisense miR-221/222 was also inhibited. In antisense miR-221/222 treated tumor cells, the expression of bcl-2 was down-regulated while connexin43, p27, PUMA, caspase-3, PTEN, TIMP3 and Bax up-regulated, and p53 expression not changed.
CONCLUSIONThere is a significant inhibitory effect of antisense miR-221/222 on the growth of human glioma U251 cells. miR-221/222 may be considered as a candidate target for gene therapy of human gliomas.
Animals ; Apoptosis ; Base Sequence ; Caspase 3 ; metabolism ; Cell Cycle ; Cell Line, Tumor ; Cell Proliferation ; Down-Regulation ; Gene Expression Regulation, Neoplastic ; Gene Knockdown Techniques ; Genetic Therapy ; Glioma ; metabolism ; pathology ; Humans ; Ki-67 Antigen ; metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; MicroRNAs ; biosynthesis ; genetics ; Molecular Sequence Data ; Neoplasm Transplantation ; Oligonucleotides, Antisense ; pharmacology ; PTEN Phosphohydrolase ; metabolism ; Proto-Oncogene Proteins c-bcl-2 ; metabolism ; RNA, Messenger ; metabolism ; Tissue Inhibitor of Metalloproteinase-3 ; metabolism ; Transfection
10.The effect of silencing Dicer by small interference RNA on the biological characteristics of human glioma cells.
An-ling ZHANG ; Chun-sheng KANG ; Lei HAN ; Guang-xiu WANG ; Zhi-fan JIA ; Pei-yu PU
Chinese Journal of Medical Genetics 2009;26(5):521-524
OBJECTIVETo study the effect of silencing Dicer by small interference RNA (siRNA) to suppress the global microRNA (miRNAs) expression on the biological characteristics of TJ905 glioblastoma cells.
METHODSThe silencing effect of RNA interference on Dicer expression was evaluated by reverse transcription-polymerase chain reaction (RT-PCR), Western blot analysis and immunofluorescence staining. The cell proliferation rate and cell cycle kinetics were detected by MTT assay and flow cytometry respectively, and the cell invasive ability was evaluated by transwell assay.
RESULTSThe siRNA targeting Dicer suppressed the expression of Dicer in TJ905 cells. Meanwhile, the proliferation activity and invasive ability were significantly enhanced in cells transfected with Dicer siRNA compared to those cells transfected with scrambled siRNA and the control cells.
CONCLUSIONSuppression of Dicer expression renders the glioma cells harboring more aggressive phenotype. This preliminary finding suggests that global lower expression of miRNAs may play an oncogenic role.
Cell Cycle ; Cell Line, Tumor ; Cell Proliferation ; DEAD-box RNA Helicases ; genetics ; metabolism ; Gene Expression Regulation, Neoplastic ; Gene Silencing ; Glioblastoma ; genetics ; metabolism ; physiopathology ; Humans ; RNA, Small Interfering ; genetics ; metabolism ; Ribonuclease III ; genetics ; metabolism