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Biomedical subjects

Q Cui

Publications and source records attributed to Q Cui.

At least 55 records · Page 3Linked to original sources

[The correlation between Burkitt's lymphoma and Epstein-Barr virus in 28 cases and their expression of p53 and bcl-2 proteins].

OBJECTIVE: To investigate the correlation between Burkitt's lymphoma and Epstein-Barr (EB) virus and its expression of p53 and bcl-2 proteins. METHODS: Polymerase chain reaction (PCR), in situ PCR and immunohistochemical techniques were applied to specimens from 28 cases of Burkitt's lymphomas on paraffin-embedded sections. RESULTS: EB virus was found in 8 (28.5%) cases by PCR, of which 3 were positive by in situ PCR. Positive rates for the expression of p53 and bcl-2 were 44.4% and 48.1% respectively. Whereas in stages I-II and III-IV, they were 3(23.0%), 9(64.2%) and 3(23.0%), 10(71.4%) respectively. Both the expression of p53 and bcl-2 were high in stages III-IV, low in stages I-II (P < 0.05). The positive cases of EB virus in combination with the expression of p53 and bcl-2 protein, p53 protein and bcl-2 protein were 4,5,4 respectively and 9 cases were positive for p53 and bcl-2 protein. In other words, the positive cases for EB virus in combination with the expression of p53 and bcl-2 were 50%, whereas 70% were positive for both p53 and bcl-2. CONCLUSIONS: The positive rates of EB virus in our series are different from some reports of African-Burkitt's and similar to many other reports of endemic Burkitt's lymphoma. The expression of p53 and bcl-2 proteins are significantly correlated with stage; high in stages III-IV and low in stages I-II. EB virus, p53 and bcl-2 proteins may affect each other.

Adolescent↗

[5 cases report of Kaposi's sarcoma].

OBJECTIVE: To aid clinical diagnosis and management of Kaposi's sarcoma. METHODS: 3 male and 2 female of classical Kaposi's sarcoma were analysed by clinical and pathological examinations. RESULTS: All the patients presented hemorrhagic or flue plagues nodules that could be fused together or ulceration. The lesions could reappear and get relived by themselves, The retroperitoneal lymphnodes was involved in one case, together with hypoxemia, oral ulceration, conjunctivitis and keratitis. The tumor behaved intensive spindle-cell sarcoma with obvious karyokinesis. CONCLUSION: The affected organ in classical kaposi's sarcoma were mainly skin, rarely internal organs. The diagnosis were verified on pathology and the treatment could rely on radiotherapy, chemotherapy and local resection.

Adult↗

Steroid-induced adipogenesis in a pluripotential cell line from bone marrow.

UNLABELLED: We studied the effect of steroids on the differentiation of a pluripotential mesenchymal cell with use of a cell line (D1) from mouse bone-marrow stroma. The cells were treated with increasing (10[-9], 10(-8), and 10(-7)-molar) concentrations of dexamethasone for increasing durations ranging from forty-eight hours to twenty-one days. The appearance of triglyceride vesicles in the cells indicated that this treatment had induced the differentiation of the cell into adipocytes. The number of cells that contained the triglyceride vesicles and the expression of a fat-cell-specific gene, 422(aP2), increased with longer durations of exposure to dexamethasone and with higher concentrations of the steroid. Treatment with dexamethasone also diminished the expression of alpha1 type-I collagen mRNA and osteocalcin mRNA. The data indicate that dexamethasone stimulates the differentiation of cells in bone-marrow stroma into adipocytes as well as the accumulation of fat in the marrow at the expense of expression of type-I collagen and osteocalcin mRNA, thereby suppressing differentiation into osteoblasts. CLINICAL RELEVANCE: Steroid-induced adipogenesis by bone progenitor cells in marrow may influence the development of osteonecrosis. It is therefore important to consider the investigation of a treatment, such as the inhibition of the metabolism and accumulation of fat in marrow, that can prevent the onset of osteonecrosis.

Adipocytes↗

[Further clinical analysis on the prognosis of chronic lymphocytic thyroiditis].

OBJECTIVE AND METHODS: There have been many reports on the incidence of hypothyroidism and thyroid carcinoma in chronic lymphocytic thyroiditis patients, however, the incidence of thyroid carcinoma had been a widely debated issue. Therefore 300 cases of chronic lymphocytic thyroiditis from 1964 to 1995 were reviewed. There were 37 males and 263 females, and 52 had a pathological diagnosis of chronic lymphocytic thyroiditis. RESULTS: Among 300 patients, 2 had coexistent thyroid papillary carcinoma. The original symptom in 64.3% patients was hypothyroidism, and the total incidence of hypothyroidism was 76%. It was also indicated in this study that the occurrence of hypothyroidism in chronic lymphocytic thyroiditis patient was associated with the elevated level of antithyroglobulin antibody, enlargement and tenderness of thyroid gland. CONCLUSION: In our study, as the low incidence of coexisted thyroid carcinoma, with the high incidence of hypothyroidism it seemed to be that the elevated antithyroglobulin antibody could be a more effective factor in the development of hypothyroidism in chronic lymphocytic thyroiditis.

Adolescent↗

The Otto Aufranc Award. Lovastatin prevents steroid induced adipogenesis and osteonecrosis.

Osteonecrosis of the femoral head was induced experimentally in chickens after the administration of a high dose of corticosteroids. Lovastatin was used to prevent the effects of the steroid on adipogenesis in cultured cells, and adipogenesis and osteonecrosis in chickens. The in vitro study, with marrow cells in culture, showed that Lovastatin inhibited steroid induced fat specific gene expression and counteracted the inhibitory effects of steroids on osteoblastic gene expression. For the in vivo study, 83 adult chickens were used: 48 received methylprednisolone 3 mg/kg weekly via intramuscular injection (Group A). Fifteen received the steroid (as in Group A) plus Lovastatin 20 mg per animal per day orally (Group B). Ten chickens received Lovastatin only (Group C). Another 10 received no medication and served as the control group (Group D). Evidence of osteonecrosis was observed in specimens from Group A, including subchondral bone death and resorption, fat cell proliferation, and new bone formation. Conversely, sections from Group B showed less adipogenesis and no bone death. It is concluded that the bipedal chicken is a useful animal model for studies of osteonecrosis and that lipid clearing agents, such as Lovastatin, may be helpful in preventing the development of steroid induced osteonecrosis.

Adipose Tissue↗

[Inducing effect of dimethy-4, 4'-dimethoxy-5, 6,5',6-dimethylenedioxybipheny-2, 2'-dicarboxylate (DDB) on differentiation of leukemia HL-60 cells].

OBJECTIVE: To study the effects of anti-hepatitis drug, DDB, on leukemia cell line HL-60. METHOD: Cytobiological methods were used. RESULT: DDB was inhibited the proliferation of HL-60 cells. About 50% of HL-60 cells treated with DDB (10(-4)mol/L) for 6 days exhibited NBT reduction, and phagocytosis activity was also enhanced by DDB (10(-4)mol/L) for 4 days. The HL-60 cells treated with DDB turned out to be mature granulocytes morphologically. CONCLUSION: The activity of acid phosphatase in DDB-treated HL-60 cells was significantly increased. DDB can induce HL-60 cells to differentiate along granulocyte lineage.

Acid Phosphatase↗

[Effect of dimethyl-4,4'-dimethoxy-5,6,5',6'-dimethylenedioxybiphenyl-2, 2'-dicarboxylate (DDB) on several phenotypes of Bel-7402 hepatocarcinoma cell line and its mechanism].

DDB is a hepatoprotectant and has been widely used for the treatment of chronic viral hepatitis in China. The drug markedly improved the abnormal liver function particularly in lowering the elevated serum transaminases in patients. It is known that there is a close correlation between primary hepatocarcinoma and chronic viral hepatitis. The aim of the present study is to evaluate the effect of DDB on hepatocarcinoma cell line. The results showed that the growth and clonogenicity of Bel-7402 human hepatocarcinoma cell line cultured with DDB were markedly inhibited. The nucleoles of the cells treated with DDB disappeared or their numbers and nucleus/cytoplasm ratio decreased under electron microscopic observation. DDB at the concentration of 10(-4) mol.L-1 significantly increased the contents of cAMP and calmodulin (CaM) in Bel-7402 hepatocarcinoma cells. DDB was also found to inhibit topoisomerase II activity of Bel-7402 hepatocarcinoma cells. These results suggest that the mechanism of inhibition of DDB on several phenotypes of Bel-7402 cell line may be related to its effect on cAMP and CaM content as well as topoisomerase II activity.

Antineoplastic Agents↗

[Detection of c-Ki-ras oncogene codon 12 point mutations in lung carcinoma, gastric carcinoma and hepatic carcinoma].

DNA extracted from paraffin-embedded tissues of 30 lung carcinomas, 40 gastric carcinomas and 22 hepatocellular carcinomas was tested for the presence of c-Ki-ras codon 12 point mutation by PCR-RFLP technique. The results showed that 20% (6/30) lung carcinomas and 2.5% (1/40) gastric carcinomas had Ki-ras codon 12 point mutation, but non of the 22 hepatocellular carcinomas displayed this point mutation. Among 6 cases of lung carcinomas of mutation, 4 were squamous carcinomas and 2 were adenocarcinomas.

Adenocarcinoma↗

Pulmonary leiomyosarcoma--report of three cases.

Three cases of pulmonary leiomyosarcoma were presented. The characteristic clinical features were described with review of literature. In comparison with bronchogenic carcinoma, the leiomyosarcoma has some characteristics: 1) On chest X-ray, it usually appears as a sharply demarcated, even density round mass, growing rapidly within the lung, it rarely accompanies with hilar or mediastinal lymph node metastasis. 2) The preoperative cytological or pathological diagnosis is difficult either by sputum smear or by bronchoscopic biopsy or by fine needle percutaneous aspiration biopsy. 3) Pathological differential diagnosis of leiomyosarcoma of lung from anaplastic lung cancer is difficult. In conclusion, the primary pulmonary leiomyosarcoma is a rare malignant tumor, detecting the present illness seriously, paying attention to the chest X-ray films characterize, early surgical resection is the only way to get diagnosis and effective treatment method.

Adult↗

[The role of amylase in abdominal fluid in evaluating severity of acute pancreatitis and its prognosis].

Acute pancreatitis (AP) was induced on 22 cats, by injecting the mixture of bile and trypsin at different doses into the main pancreatic duct (MPD). In Group A, 7 cats revealed pancreatic interstitial edema after the injection of the mixture at 0.8 mg/kg. In Group B, 8 cats received the injection of the MPD at 1.0 mg/kg which resulted in significant extensive necrosis of the pancreas. The same pathological change was found in Group C (7 cats), combined with lesions of the lung and the liver. The survival time was different, more than 7 days in Group A, 50.4 hours in Group B and 10.4 hours in Group C (P < 0.001). Amylase concentration also showed marked difference in different groups, 4,890 U/L in Group A; 13 952 U/L in Group B and 23,810 U/L (P < 0.001) in Group C. These results are directly proportional to the severity of AP, but inversely proportional to the survival time. It suggests that amylase concentration in abdominal fluid can be used as an important marker to evaluate the severity of AP and its prognosis.

Acute Disease↗

[Construction of a retroviral vector expressing antisense N-myc gene].

In their previous studies the authors demonstrated that nerve growth factor-induced differentiation of neuroblastoma cell lines was closely related with nerve growth factor receptors and amplification of N-myc oncogenes. The authors have also successfully restored the nerve growth factor receptor expression in the cell lines which lacked expression of nerve growth factor receptors. In order to clearify the role of N-myc oncogenes during nerve growth factor-induced differentiation of neuroblastoma cell lines, a new retroviral vector was constructed to express antisense N-myc genes. This new vector contained a puromycin resistant gene, which allowed the authors to express another gene in the cell lines which had already been neomycin resistant.

Antisense Elements (Genetics)↗

[Gene expression of growth factors, growth factor receptor and oncogenes in human lung cancer cell lines].

Gene expression of growth factors including epidermal growth factor (EGF), transforming growth factor alpha (TGF alpha), epidermal growth factor receptor (EGFR), oncogenes such as c-myc, N-ras, c-erbB2 and tumor suppressor gene P53 were studied in 4 human lung cancer cell lines using Northern blot technique. Among these cell lines were 2 adenocarcinoma cell lines, one large cell carcinoma cell line and one small cell carcinoma cell line. Expression of EGF and TGF alpha mRNAs were found in all 4 cell lines and EFGR mRNA was seen in 3 out of 4 cell lines. Among these cell lines, 2 cell lines with weaker expression of EGF and TGF alpha, expressed c-myc mRNA. Another 2 cell lines had no c-myc but expressed large amounts of EGF and TGF alpha mRNA. No expression of N-ras, c-erbB2 and p53 were found in these cell lines. The results indicate the presence of autocrine loop of growth factors in these cancer cells. The autostimulation of growth factors may be the main cause for the uncontrolled growth of cancer cells. After treating the cancer cells with EGF, anti-EGF and anti-EGFR antibodies, EGF was found to exert a mild stimulating effect on the growth of one cell line, but no effect on the other cell lines. Anti-EGF and anti-EGFR antibodies inhibited the cell growth on all cell lines. These results provided further evidence for the presence of autocrine loop of growth factors in these lung cancer cell lines.

Adenocarcinoma↗

At least two mechanisms are involved in the death of retinal ganglion cells following target ablation in neonatal rats.

Removal of the superior colliculus (SC) in neonatal Wistar rats results in a rapid loss of retinal ganglion cells (RGCs). There is an early twofold increase in RGC death 4-8 hr postlesion (PL) followed by a later 10-11-fold increase in pyknosis about 24 hr PL. We have now used neurotrophic factors (BDNF, NT-4/5, NT-3, NGF, LIF), glutamate receptor antagonists (MK-801, DNQX, CNQX), an antioxidant (N-ace-tyl-L-cysteine), and an NOS inhibitor (L-NAME) to determine whether the early and late phases of lesion-induced RGC death involved similar or different mechanisms. Normal and pyknotic nuclei of tectally projecting RGCs were visualized by injecting the left s.c. of 2 d old rats with diamidino yellow (DY). Two days later the injection site was removed. In most rats, right eyes were injected with factors immediately after the s.c. ablation. Rats were perfused either 6 or 24 hr PL. In the latter group a second intravitreal injection of the appropriate factor was sometimes made 12 hr PL. NT- 4/5 and BDNF significantly decreased RGC pyknosis 6 and 24 hr PL, whereas NT-3 was only protective 6 hr PL. LIF slightly reduced RGC death 24 hr PL, but NGF had no influence on RGC survival at either time point. NT-4/5 also reduced the rate of naturally occurring RGC death. MK-801, DNQX, CNQX, N-acetylcysteine, and L-NAME all prevented the early lesion-induced increase in RGC death but had no significant effect on RGC death measured 24 hr PL; none of these factors significantly reduced the rate of naturally occuring RGC death. Cycloheximide, shown previously to reduce RGC pyknosis 24 hr PL, did not prevent RGC death 6 hr PL. The data indicate that there are at least two mechanisms involved in RGC death after neonatal target ablation. The early increase is related to excitotoxic effects mediated by glutamate receptors and involves NOS and the production of free radicals. We found no evidence that RGC death measured 24 hr PL is dependent on these processes, but the later death does require protein synthesis and, most likely, the activation of an endogenous suicide program. NT-4/5 and BDNF protected RGCs from both types of lesion-induced death.

Animals↗

NT-4/5 reduces naturally occurring retinal ganglion cell death in neonatal rats.

The retrograde nucleophilic tracer diamidino yellow (DY) was injected into the left superior colliculi of 2-day-old rats. Two days later, right eyes were injected with either neurotrophin NT-4/5, cycloheximide (CHX), MK-801 and DNQX (glutamate receptor antagonists), or saline. Almost all rats were perfused 6-7 h later and the numbers of normal and pyknotic DY-labelled retinal ganglion cells (RGCs) were determined from retinal whole mounts. In controls (no eye injection) the proportion of pyknotic RGCs was 1.04%. This level of naturally occurring death was significantly reduced after injection of NT-4/5 (0.34%); normal RGC density was also higher in this group. RGC pyknosis was increased after saline (1.21%), MK-801/DNQX (1.22%) or CHX (1.48%) injections but only in the latter case was the increase significantly greater than control.

Amidines↗

The effect of cycloheximide and ganglioside GM1 on the viability of retinotectally projecting ganglion cells following ablation of the superior colliculus in neonatal rats.

The time-course and extent of death of retinal ganglion cells (RGCs) following ablation of the superior colliculus (SC) in neonatal Wistar rats has recently been described [Harvey, A. R. and Robertson, D. (1992) J. Comp. Neurol., 325, 83-94]. Normal and pyknotic nuclei of retinotectally projecting ganglion cells were visualized using the fluorescent retrograde tracer diamidino yellow (DY), which had been injected into the SC at P2 (day of birth = P0), 2 days prior to tectal removal. The present report sets out to determine whether cycloheximide, an inhibitor of protein synthesis, or ganglioside GM1 reduced this lesion-induced RGC death. All surgery was carried out under ether anaesthesia; DY was injected into the left SC at P2 and the injected area was removed at P4. Cycloheximide (20-500 ng) was injected into the vitreous chamber of the right eye immediately after the lesion and again 11-12 h later. In some rats, cycloheximide administration was delayed until 12 h after the SC ablation. Control rats received SC lesions alone or lesions plus sham eye injections of saline. Different doses of GM1 were applied i.p. or intraocularly. Rats were perfused 24 h after the SC lesion, at the time of peak RGC death. Retinae of lesion only or sham eye injected rats contained approximately 11% pyknotic RGCs and the density of normal RGCs was approximately 3400/mm2. The rate of pyknosis in cycloheximide treated retinae was reduced to approximately 3%. Normal RGC density in these retinae was approximately 5500/mm2, similar to that found in retinae of unlesioned animals.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[Point mutation at codon 12 of c-Ki-ras oncogene in human pancreatic neoplasms and normal human pancreas tissue].

Point mutation at codon 12 of c-Ki-ras oncogene was tested from 2 normal human pancreas, 7 pancreatic endocrine neoplasms and 15 pancreatic adenocarcinomas, including 5 resected pancreatic adenocarcinomas, 3 cell lines of pancreatic adenocarcinoma and 7 nude mice transplanted tumors by dot blot and single-strand conformation polymorphism (SSCP) after PCR amplification, c-Ki-ras codon 12 point mutation was found only in pancreatic adenocarcinomas (11/15 by dot blot and 13/15 by SSCP). No mutation was detected in normal human pancreatic tissue and endocrine tumors. By our experience, SSCP is more convenient and faster than dot blot in detecting gene mutation. Point mutation at codon 12 of c-Ki-ras oncogene may play an important role in the development of human pancreatic carcinoma.

Adenocarcinoma↗

Ultrastructural study of moniliformin induced lesions of myocardium in rats and mice.

Effects of moniliformin on the ultrastructure of the myocardium of mice and rats were studied. Mice were given moniliformin orally at a dose of 29.46 mg.kg-1 the LD50. One h after dosing, lesions of the mitochondria of the myocardial cells were found which became more severe in 2 and 3 h. Ultrastructural lesions were also observed in the myofibrils and sarcolemma. Rats were given moniliformin orally at the dosage of 6 mg.kg-1 once daily for 56 d. Lesions of mitochondria and myofibrils were relatively mild. In the myocardiac specimens taken from the 21d post-toxin administration, lesions of the sarcolemma became more obvious. These moniliformin-induced lesions were similar to the ultrastructural changes in the myocardium of patients with Keshan disease. Our findings indicate that there may be a close and important relationship between moniliformin intoxication and Keshan disease.

Animals↗

Noninvasive estimation of cardiac output.

A noninvasive method of measuring cardiac output is described. The method uses adaptive aorta models in conjunction with femoral and carotid pulse contour waveform measurements to calculate aortic flow. Results are presented from measurements on dogs using internal pressure recordings made with fluid-filled catheters and compared with electromagnetic flow measurements taken in the ascending aorta. Preliminary results using external pulse measurements on patients are also presented and compared with thermal dilution measurements.

Animals↗