Visualization of medical images has become an important method for the basic medical research as well as clinical diagnosis and treatment.Construction of the highly sophisticated three-dimensional(3D) models of the human body by computers has become an essential foundation for current medical research and disease treatment methods.Visualization Toolkit(VTK) is a kind of famous software in scientific visualization fields.It is convenient and efficient for programming.This paper implements three typical algorithms,Contour-connecting,Marching Cubes and Ray-casting,of medical image 3D visualization using VTK with VC++.Results show that VTK is a powerful tool with many advantages,such as simple operation,fast,and good interaction ability and can be widely used in 3D reconstruction of medical images.

40 ?m in diameter) were accounted for about 15％, and the rest were medium-and small-sized cells.

In the present study the commissural projection between the two superior colliculi in the rat was examined with horseradish peroxidase method. The result shows that when HRP was injected into the superior colliculus of one side, HRP labeled cells could be found in every part of the contralateral superior colliculus. In each case the labeled cells were relatively concentrated in the region corresponding to the site of injection. It indicates that various parts of one superior colliculus may be connected chiefly with the corresponding part of the opposite side through the commissural projection.Most of the labeled cells were found in the middle layer of the superior colliculus, especially in its upper half, less in the deep layer, and the least in the superficial layer. Neurons in the superficial layer of one side project only to the superficial layer of the contralateral side, and so are the middle-deep layers. The connections between the superficial layers of both sides were independent from those of the middledeep layers.The commissural projection of the bilateral superior colliculi passes through the commissure of the superior colliculus which could be divided into a dorsal and a ventral fiberal fasciculns. The dorsal one was smaller, predominantly related to the superficial layer and the upper half of the middle layer; the ventral one was larger, part of its fibers related to the lower half of the middle layer and the deep layer, while the rest project to other nuclei of the contralateral region of the mesencephalon (e. g. nucleus cuneiforms, etc,).Most of the labeled cells were small in size, the rest were medium-sized, and no large ones were found.

Purpose To investigate the expression of secreted frizzled-related protein 4 (SFRP4) and to evaluate its clinical significance in pancreatic ductal adenocarcinoma (PDAC).Methods RT-PCR was performed to analyze SFRP4 mRNA expression level in 30 paired PDAC lesion and matched adjacent non-tuimor tissue.Immunohistochemistry staining detection of 205 matched cases tissue microarray was conducted to explore SFRP4 protein expression pattern.The correlation between SFRP4 and clinical characteristics was also analyzed,including overall survival.Results SFRP4 expression pattern both at mRNA and protein level in PDAC lesion was higher than that in matched adjacent non-tumor tissue.At mRNA level,to found that expression of SFRP4 was elevated in 90％ (27/30) of PDAC tissues (P =0.007 2).To found that high expression of SFRP4 was detected in 56.5％ (116/205) of PDAC tissue,while only 28.8％ (59/205) in the adjacent non-tumor tissue.Moreover,no significant association was observed between SFRP4 expression and clinical characteristics.Kaplan-Meier survival analysis showed high level of SFRP4 expression was correlated with poor overall survival (x2 =3.467,P =0.024).Conclusion SFRP4 can be a novel prognostic biomarker in PDAC.

It is demonstrated that the parabigeminal nucleus of the rat is subdivided intodorsal,middle and ventral groups.The parabigeminal nucleus sends fibers to bila-teral superior colliculus,the rostral half of it predominantly projects to the rostralhalf of the contralateral superior colliculus,but the rostral end projects only to thecontralateral one;the caudal half of this nucleus predominantly projects to thecaudal half of the ipsilateral superior colliculus,but the caudal end projects only tothe ipsilateral one.The superficial layer of the superior colliculus receives projec-tions from the ipsilateral dorsal and ventral groups and from the contralateralmiddle group of the parabigeminal nucleus.The middle and deep layers receive pro-jections from the ipsilateral middle group and contralateral dorsal and ventral groups,and probably from the other groups of both sides.The superior colliculus also sends fibers to both parabigeminal nuclei,predo-minantly the ipsilateral side.The lateral tegmental area sends fibers to the middle and deep layers of the su-perior colliculus.From the results described above,it could be concluded that the parabigeminalnucleus——tectum——parabigeminal nucleus connections are not only concerned withsuperficial layer,but also with the middle and deep layers of the superior colliculus.The tegmentum——tectum——tegmentum connections are only concerned with the mid-dle and deep layers of the superior colliculus.

To construct a lentiviral shRNA vector targeting human protein phosphatase 1D magnesium-dependent (PPM1D) gene and detect its effectiveness of gene silencing in human gliomas, specific siRNA targets with short hairpin frame were designed and synthesized. DNA oligo was cloned into the pFU-GW-iRNA lentiviral expression vector, and then PCR and sequencing analyses were conducted to verify the constructs. After the verified plasmids were transfected into 293T cells, the lentivirus was produced and the titer of virus was determined. Real-time quantitative PCR and Western blot were performed to detect the PPM1D expression level in the infected glioma cells. PCR and Western blot analyses revealed the optimal interfering target, and the virus with a titer of 6×10(8) TU/mL was successfully packaged. The PPM1D expression in human glioma cells was knocked down at both mRNA and protein levels by virus infection. The expression of PPM1D mRNA and protein was decreased by 76.3% and 87.0% respectively as compared with control group. The multiple functions of human glioma cells after PPM1D RNA interference were detected by flow cytometry and cell counting kit-8 (CCK-8). Efficient down-regulation of PPM1D resulted in significantly increased cell apoptosis and reduced cell proliferation and invasion potential in U87-MG cells. We have successfully constructed the lentiviral shRNA expression vector capable of stable PPM1D gene silencing at both mRNA and protein levels in glioma cells. And our data gave evidence that the reduced cell growth observed after PPM1D silencing in glioma cells was at least partly due to increased apoptotic cell death.

Objective To investigate the relationship between human papilloma virus(HPV)infection and the development of laryngeal squamous cell carcinoma(LSCC).Methods To elucidate the role of HPV in the development of LSCC,we employed polymerase chain reaction(PCR)based on four pairs of primers an4 in situ hybridization(ISH)to screen the HPV infection in 84 ISCC tissues.Results Using HPV L1 general primer amplification,HPV DNA was detected in 23(27.4%)of the 84 LSCC samples.However,when specific primers for HPV-16 or-18 were used to amplify E6 and E7 in all samples,29 cases(34.5%)were positive for HPV-16,while 6 cases(7.1%)were positive for HPV 18.Coinfeetion of HPV-16 and-18 were found in 4cases (4.8%).Overall,HPV type 16 and 18 infections were present in 36.9% of the LSCC samples.In addition,the positive rate of HPV 16 E6 mRNA was 30.9%(26/84)in LSCC by ISH with digoxin-labeled sense probes of HPV 16 E6.Conclusion High-risk HPV-16may be an etiologic factor in the development of laryngeal squamous cell carcinoma, while the complicated molecular mechanism of HPV16 inducedtumorgenesis needs a further study.

Dihydroartemisinin (DHA),the major active metabolite of artemisinin,participates in tumor progression through the following ways:forming free radicals to induce cancer cells death dependent on iron,inducing apoptosis,inhibiting angiogenesis,tumor cells invasion and metastasis,modulating muhidrug resistance,controlling intracellular Ca2+ concentration,regulating cell cycles,cell autophagy and the immune system and so on.Generally,it is considered to be a potential anti-tumor drug.

Objective To observe enhancing effect of nerve regeneration on peripheral nerve defect models bridged by silicone tube idled with valproic acid (VPA). Methods In present research we demon-strate the effect of VPA on peripheral nerve regeneration and recovery of motor function following sciatic nerve transaction in rats. An 8-mm sciatic nerve deficit was created in a rat mode land bridged by a 1-cm silicone tube.Then, 10 lad of 8% VPA were perfused into the silicone chamber in the VPA group. The same volume of normal saline was delivered in the control group. Results Each animal was observed sciatic nerve function index (SFI) at 2-week intervals and studied electrophysiology at 4-week intervals for 12 weeks. Histological and morphometrical analyses were performed at the end of the experiment, 12 weeks after operation. Using the digital image-analysis system, thickness of the myelin sheath was measured, and total numbers of regenerated axons were counted. There was a significant difference in SFI, electrophysiological index (motor-nerve conduct velocity, MCV), and morphometrical results (regenerated axon number and thickness of myelin sheath) in nerve regeneration between the VPA group and controls (P ＜ 0.05). Conclusion The results demonstrated that VPA is able to enhance sciatic nerve regeneration in rats, suggesting the potential clinical application of VPA for the treatment of peripheral nerve injury in humans.

Objective: To explore the safety and efficacy of intravenous thrombolysis therapy with tissue plasminogen activator ( tPA) in aged acute ischemic stroke patients. Methods:The patients treated with intravenous tPA were analyzed and divided into≥80-year group (n=16) and <80-year group (n=79), and 30 hospitalized patients with the age above 80 years without thrombolytic therapy were selected as the control group. The prognosis of the three groups was compared. Results:①The incidence of ICH in the two thrombolysis therapy groups was 13. 9% and 18. 7% in 24h, and that of SICH was 5. 1% and 6. 3% with no significant difference (P>0. 05). ② No significant difference was found in favorable prognosis between the two therapy groups 90 days after thrombolysis (P=0. 771), while very bad prognosis rate was higher in the≥80-year group than in the <80-year group (P<0. 05). ③The≥80 years group had an increased favorable outcome compared with the control group (P<0. 05), while the very bad prognosis rate in the two groups showed no significant difference (P>0. 05). Conclusion:It is safe and effective for old patients to receive IV-tPA throm-bolysis therapy.