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1.
Chinese Journal of Hematology ; (12): 336-341, 2022.
Artigo em Chinês | WPRIM | ID: wpr-935091

RESUMO

Objective: To retrospectively analyze the data of Chinese patients with newly diagnosed acute promyelocytic leukemia (APL) to preliminarily discuss the clinical and cytogenetic characteristics. Methods: From February 2004 to June 2020, patients with newly diagnosed APL aged ≥ 15 years who were admitted to the Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College were chosen. Clinical and laboratory features were retrospectively analyzed. Results: A total of 790 cases were included, with a male to female ratio of 1.22. The median age of the patients was 41 (15-76) years. Patients aged between 20 and 59 predominated, with 632 patients (80%) of 790 patients classified as low and intermediate risk and 158 patients (20%) of 790 patients classified as high risk. The white blood cell, platelet, and hemoglobin levels at diagnosis were 2.3 (0.1-176.1) ×10(9)/L, 29.5 (2.0-1220.8) ×10(9)/L, and 89 (15-169) g/L, respectively, and 4.8% of patients were complicated with psoriasis. The long-form type of PML-RARα was most commonly seen in APL, accounting for 58%. Both APTT extension (10.3%) and creatinine>14 mg/L (1%) are rarely seen in patients at diagnosis. Cytogenetics was performed in 715 patients with newly diagnosed APL. t (15;17) with additional chromosomal abnormalities were found in 155 patients, accounting for 21.7%; among which, +8 was most frequently seen. A complex karyotype was found in 64 (9.0%) patients. Next-generation sequencing was performed in 178 patients, and 113 mutated genes were discovered; 75 genes had an incidence rate>1%. FLT3 was the most frequently seen, which accounted for 44.9%, and 20.8% of the 178 patients present with FLT3-ITD. Conclusions: Patients aged 20-59 years are the most common group with newly diagnosed APL. No obvious difference was found in the ratio of males to females. In terms of risk stratification, patients divided into low and intermediate risk predominate. t (15;17) with additional chromosomal abnormalities accounted for 21% of 715 patients, in which +8 was most commonly seen. The long-form subtype was most frequently seen in PML-RARα-positive patients, and FLT3 was most commonly seen in the mutation spectrum of APL.


Assuntos
Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Aberrações Cromossômicas , Citogenética , Leucemia Promielocítica Aguda/genética , Mutação , Proteínas de Fusão Oncogênica/genética , Estudos Retrospectivos
2.
China Journal of Endoscopy ; (12): 106-108, 2018.
Artigo em Chinês | WPRIM | ID: wpr-702979

RESUMO

Objective?To observe the clinical effect of FURS combined with ultrasound guided all seeing needle treatment of low pole renal calculi.?Methods?From January 2016 to January 2017, 63 patients with low pole renal calculi were enrolled in this study. 16 patients with multiple stones and 47 cases with single stones were treated by FURS combined with ultrasound guided all seeing needle. We retrospectively analyzed all the patients clinical data, including the operation time, bleeding volume, stone clearance rate, the incidence of postoperative complications, then assess the safety and effectiveness of the surgical approach.?Results?The operation time was 30 ~ 60 min, the average time was 45 min, postoperative complications in 3 cases, 2 cases of pain; no blood transfusion; 2 cases of percutaneous nephrolithotomy. Postoperative hospital stay wad 2 ~ 3 d, an average of 2 d, postoperative residual stone in 3 cases, 2 weeks after the treatment of external lithotripsy, 1 case of stone clearance rate of 100.0%.?Conclusion?Retrograde FURS combined with ultrasound guided visual puncture for renal calculi is safe, effective and feasible.

3.
China Journal of Endoscopy ; (12): 105-107, 2018.
Artigo em Chinês | WPRIM | ID: wpr-702916

RESUMO

Objective To evaluate the clinical efficacy of laparoscopy and short poly FURS in treatment of UPJO combined with renal stones. Methods From May 2014 to November 2016, 20 patients with ureteropelvic junction stricture in our hospital were treated with Laparoscopy and short poly FURS lithotripsy, the clinical data of the patients before and after operation were retrospectively analyzed. Results The patients in this group were successfully operated in stage I, and the hemoglobin descent rate did not change significantly before and after operation. No need of blood transfusion, the first day after the review of urinary tract plain film observed DJ tube position, postoperative back to hospital in March pulled out of DJ tube, postoperative follow-up 6 months to 1 year, the patient recovered well, no long-term complications. Conclusion Laparoscopy and short poly FURS lithotripsy, has satisfactory effects and no significant complications which should be promoted.

4.
National Journal of Andrology ; (12): 525-528, 2018.
Artigo em Chinês | WPRIM | ID: wpr-689697

RESUMO

<p><b>Objective</b>To explore the practicability and safety of the F4.8 visual miniature nephroscope in the diagnosis and treatment of hematospermia.</p><p><b>METHODS</b>This study included 12 cases of refractory hematospermia accompanied by perineal or lower abdominal pain and discomfort. All the patients failed to respond to two months of systemic anti-inflammatory medication and local physiotherapy. Seminal vesicle tumor and tuberculosis were excluded preoperatively by rectal seminal vesicle ultrasonography, MRI or CT. Under epidural anesthesia, microscopic examination was performed with the F4.8 miniature nephroscope through the urethra and ejaculatory duct orifice into the seminal vesicle cavity, the blood clots washed out with normal saline, the seminal vesicle stones extracted by holmium laser lithotripsy and with the reticular basket, the seminal vesicle polyps removed by holmium laser ablation and vaporization, and the seminal vesicle cavity rinsed with diluted iodophor after operation.</p><p><b>RESULTS</b>Of the 10 patients subjected to bilateral seminal vesiculoscopy, 3 with unilateral and 2 with bilateral seminal vesicle stones were treated by holmium laser lithotripsy, saline flushing and reticular-basket removal, 2 with seminal vesicle polyps by holmium laser ablation and vaporization, and the other 3 with blood clots in the seminal vesicle cavity by saline flushing for complete clearance. The 2 patients subjected to unilateral seminal vesiculoscopy both received flushing of the seminal vesicle cavity for clearance of the blood clots. The operations lasted 10-55 (25 ± 6) minutes. There were no such intra- or post-operative complications as rectal injury, peripheral organ injury, and external urethral sphincter injury. The urethral catheter was removed at 24 hours, anti-infection medication withdrawn at 72 hours, and regular sex achieved at 2 weeks postoperatively. The patients were followed up for 6-20 (7 ± 2.3) months, during which hematospermia and related symptoms disappeared in 10 cases at 3 months and recurrence was observed in the other 2 at 4 months after surgery but improved after antibiotic medication.</p><p><b>CONCLUSIONS</b>The F4.8 visual miniature nephroscope can be applied to the examination of the seminal vesicle cavity and treatment of seminal vesicle stones and polyps, with the advantages of minimal invasiveness, safety and reliability.</p>


Assuntos
Humanos , Masculino , Cálculos , Diagnóstico por Imagem , Cirurgia Geral , Ductos Ejaculatórios , Endoscópios , Endoscopia , Neoplasias dos Genitais Masculinos , Hemospermia , Diagnóstico , Terapêutica , Hólmio , Lasers de Estado Sólido , Litotripsia , Imageamento por Ressonância Magnética , Cirurgia Endoscópica por Orifício Natural , Recidiva Local de Neoplasia , Complicações Pós-Operatórias , Reprodutibilidade dos Testes , Glândulas Seminais , Diagnóstico por Imagem , Uretra
5.
International Eye Science ; (12): 1082-1086, 2017.
Artigo em Chinês | WPRIM | ID: wpr-641218

RESUMO

Vogt-Koyanagi-Harada (VKH)syndrome is an autoimmune disease attacking against pigmented cells, resulting in blindness and usually affecting multiple organs including ears, meninges, hair and skin.Correct diagnosis and immediate treatment in the early stage is vital to visual prognosis.Currently, corticosteroids is first-line drug.In addition, VKH patients refractory to corticosteroids can choose other treatment such as immunosuppressive agents and biological agents.

6.
Chinese Journal of Nursing ; (12): 1486-1494, 2017.
Artigo em Chinês | WPRIM | ID: wpr-665005

RESUMO

Objective To systematically review and synthesize the lived experience of family members caring for schizophrenia patients at home,in order to provide evidence for community and home nursing. Methods We searched databases including The Cochrane Library,PubMed,EMbase,ISI Web of Science,PsycINFO,CINAHL,CBM, CNKI,VIP and Wanfang from inception to April 2017,to collect qualitative studies in the experience of family members caring for schizophrenia patients at home. The quality of included studies was evaluated according to JBI Critical Appraisal Tool for qualitative studies in Australia. Results A total of 31 studies were included,and 141 complete findings were grouped according to their similarities to form 8 categories. These categories resulted in two synthesized findings:Integration Results 1:It brought family members a negative influence in care process because of excessive pressure and burden,but over time,they were slowly accepting the fact and trying to cope with dis-ease;Integration Results 2:Patients were unable to take care of themselves,and caregivers were helpless and wanted assistance from the government and the health care system. Conclusion The government and health system should pay more attention to the impact of schizophrenia on family members who take care of schizophrenia patients. In the process of care,patients should be given support,guidance and encouragement,which help family members to improve coping abilities of psychology and disease,and to promote physical and mental health of schizophrenia pa-tients and their family members.

7.
Journal of International Pharmaceutical Research ; (6): 301-306, 2016.
Artigo em Chinês | WPRIM | ID: wpr-845585

RESUMO

Objective To observe the ethanol extract from Dendrobium chrysotoxum Lindl. (DC) on the amelioration of diabetic retinopathy (DR) in mice induced by streptozotocin (STZ), and further investigate the engaged mechanism. Methods Diabetes was induced by STZ injection in C57 mice and then the diabetic mice were orally given with DC. The retinal neovascularization was evaluated by staining with cluster of differentiation 31 (CD31) and histological assessment of retinas by hematoxylin-eosin (HE) staining. The mRNA expression of signals involved in vascular endothelial growth factor (VEGF) signaling pathway was detected by realtime PCR assay. The amount of VEGF in serum and vitreous bodies was detected by enzyme-linked immunosorbent assay (ELISA). Results DC (50 and 200 mg/kg) reduced the increased retinal vessels in STZ-induced diabetic mice. Results of real-time PCR showed that DC reduced the increased mRNA expression of retinal hypoxia inducible factor-1α (HIF-1α), VEGF and its receptors including VEGFR1 and VEGFR2 in STZ- induced diabetic mice. ELISA results further demonstrated that DC reduced the increased VEGF level in serum and vitreous bodies of STZ-induced diabetic mice. Conclusions DC ameliorates DR via inhibiting retinal angiogenesis by reducing the expression of VEGF and VEGF-regulated signaling pathway.

8.
Chinese Traditional and Herbal Drugs ; (24): 1908-1913, 2016.
Artigo em Chinês | WPRIM | ID: wpr-853491

RESUMO

Objective: To observe the amelioration of ethanol extract from Dendrobium chrysotoxum (EEDC) on non-proliferative diabetic retinopathy (NPDR) induced by streptozotocin (STZ), and further to investigate its engaged mechanism. Methods: NPDR was induced by STZ injection in C57 mice and then the diabetic mice were orally given EEDC. The retinal blood-retinal barrier (BRB) breakdown was evaluated using Evans blue leakage assay. The mRNA expression of interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF) α, early growth response-1 (Egr-1), tissue factor (TF), and Serpine 1 in retinas was detected by real-time PCR. The amount of IL-1β, IL-6, TNF-α, TF, and Serpine 1 in serum was detected by enzyme-linked immunosorbent assay (ELISA). Results: EEDC at both doses reduced the increased Evans blue leakage in STZ-induced NPDR in mice. Results: of Real-Time PCR showed that EEDC reduced the increased retinal mRNA expression of IL-1β, IL-6, TNFα and Egr-1, TF, Serpine 1 in STZ-induced NPDR in mice. ELISA results also confirmed that EEDC reduced the increased serum levels of IL-1β, IL-6, TNF-α, TF, and Serpine 1 in STZ-induced NPDR in mice. Conclusion: EEDC could ameliorate the STZ-induced NPDR in mice via inhibiting retinal BRB breakdown by reducing the expression of pro-inflammatory cytokines including IL-1β, IL-6, TNF-α, and coagulation-fibrinolysis related signals such as TF and Serpine 1.

9.
Clinical Medicine of China ; (12): 811-813,814, 2016.
Artigo em Chinês | WPRIM | ID: wpr-604680

RESUMO

Objective To discuss clinical characteristics and surgical treatment of patients with pulmo?nary inflammatory myofibroblastic tumor(PIMT). Methods From April 2010 to June 2015 in Beijing Tiantan Hospital Affiliated to Capital Medical University, there were 15 cases patients diagnosed as PIMT and trea?ted. The clinical datas of the patients were analyzed retrospectively. The main clinical manifestations,pathological results,clinical treatment and prognosis of the patients and follow?up outcome were analyzed. Results There were 10 males and 5 females,at the age of 39 to 6 8 years old with the median age of 52. Among the 15 cases of patients with PIMT,1 case was recurrence,14 cases were initial treatment. The treatment reason was due to the abnormal physical examination,or cough and sputum with blood,or chest pain,or chest tightness or fever. Chest CT showed that the mass was round or class round, lobulated, part of them showed the burr shape edge. Immunohistochemistry showed that Vimentin positive and smooth muscle actin positive. All patients accept?ed the open chest or thoracoscope surgery. The main operations concluded partial resection,lobectomy or lobecto?my with lymph node eradication. No perioperative death occured,no complications such as postoperative bleed?ing,bronchial pleural fistula and other complications happened. The average follow?up time was from 8 to 58 months. Follow?up rate was 100. 0%(15/15). There was no tumor recurrence. Conclusion The clinical mani?festations of the pulmonary inflammatory myofibroblastic tumor is complex. The PIMT should be confirmed by pathologic examination,the main treatment is surgical resection with good prognosis and lower recurrence.

10.
International Eye Science ; (12): 813-816, 2015.
Artigo em Chinês | WPRIM | ID: wpr-637328

RESUMO

?Acute retinal necrosis syndrome ( ARN) is a serious eye disease, which caused by Herpes virus mostly, with unknown pathogenesis. Because of the aggressive progression, treatment of ARN is difficult, and the blindness rate is extremely high. Current treatment strategies are the combination of the drug therapy and the operative treatment. Drugs commonly used are antiviral drugs, glucocorticoids, and antiplatelet drugs, and the operative treatment includes laser photocoagulation and vitrectomy.

11.
Korean Journal of Urology ; : 519-524, 2015.
Artigo em Inglês | WPRIM | ID: wpr-171067

RESUMO

PURPOSE: To assess the safety and efficacy of an ultramini nephrostomy tract, which we were using for the first time, combined with flexible ureterorenoscopy (URS) in the treatment of pediatric patients with multiple renal calculi. MATERIALS AND METHODS: Twenty pediatric patients (age, < or =6 years) underwent ultramini percutaneous nephrolithotomy (PCNL) combined with flexible URS. The group had multiple renal calculi, which were bilateral in 3 cases and were located in a total of 23 sites. The calculi were located in 2 calyces in 10 cases, scattered in more than 2 calyces in 7 cases, and limited to 1 calyx in 3 cases. The average patient age was 37.35 months (range, 14-68 months). The average stone diameter was 2.0 cm (range, 1-3.0 cm). In all patients, an ultramini nephrostomy tract was established under ultrasound guidance (dilated to F10) with simultaneous sheath placement. The flexible URS was placed into the collecting system during holmium laser lithotripsy. RESULTS: When ultramini PCNL was combined with flexible ureterorenoscopic holmium laser lithotripsy, the complete stone-free rate was 87% (20/23). The average level of hemoglobin decreased to 1.0 g/dL after the operation. No blood transfusions were needed. Levels of blood urea nitrogen, creatinine, and C-reactive protein were not significantly different before and after the operation. The average duration of hospitalization was approximately 4.85 days, and all cases were followed up for 6 to 12 months. No complications were found. CONCLUSIONS: Ultramini PCNL combined with flexible ureterorenoscopic holmium laser lithotripsy is a safe and effective treatment for children with multiple renal calculi.


Assuntos
Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Cálculos Renais/patologia , Tempo de Internação/estatística & dados numéricos , Litotripsia a Laser/métodos , Nefrostomia Percutânea/métodos , Estudos Retrospectivos , Resultado do Tratamento , Ultrassonografia de Intervenção/métodos , Ureteroscopia/métodos
12.
Chinese Medical Journal ; (24): 1854-1861, 2011.
Artigo em Inglês | WPRIM | ID: wpr-338575

RESUMO

<p><b>BACKGROUND</b>Signal transducer and activator of transcription 3 (STAT3) is usually constitutively activated in a variety of malignancies. It directly contributes to tumorigenesis, invasion, and metastasis. The surgical treatment of breast cancer has made no breakthroughs in terms of treatment effect, in spite of its long history. Current biotherapies bring a note of optimism to breast cancer treatment. To explore the possibility of a siRNA targeted STAT3 blocking treatment for over-activated tumor cells, we evaluated the efficacy of a STAT3 siRNA on human breast cancer cells in vitro and in vivo.</p><p><b>METHODS</b>Three MCF-7 human breast cancer cell lines were tested: control MCF-7 cells, non-specific siRNA transfected MCF-7 cells and STAT3 siRNA transfected MCF-7 cells. Expression of STAT3 in MCF-7 cells was inhibited by RNA interference (RNAi). The STAT3 mRNA and protein levels were detected by semi-quantity RT-PCR and Western blotting. Cell proliferation and apoptosis were determined by MTT method and flow cytometry. The three groups of MCF-7 cells mentioned above were transplanted subcutanuously into nude mice and their tumorgenic ability observed. The STAT3 mRNA and protein levels of the samples from tumors in different groups were determined by semi-quantity RT-PCR and Western blotting and compared.</p><p><b>RESULTS</b>In STAT3 siRNA transfected MCF-7 cells, the expressions (STAT3/β-actin) of STAT3 mRNA (0.327 ± 0.020) and protein (0.153 ± 0.006) were significantly lower than that in control MCF-7 cells (mRNA 1.093 ± 0.018, protein 1.374 ± 0.022) and non-specific siRNA transfected MCF-7 cells (mRNA 1.035 ± 0.050, protein 1.320 ± 0.033) (P < 0.05). MTT showed that cell proliferation was significantly reduced and the cell growth inhibition ratio in the STAT3-siRNA group was (44.00 ± 5.10)%, significantly higher than that in non-specific siRNA transfected MCF-7 cells ((16.10 ± 1.05)%, P < 0.05). Flow cytometry results showed that more apoptosis was observed in the STAT3-siRNA group. The rate of apoptosis was (14.79 ± 0.22)%, much higher than in control MCF-7 cells (7.06 ± 0.71) and non-specific siRNA transfected MCF-7 cells (8.45 ± 0.43) (P < 0.05). The tumor growth in the STAT3 siRNA transfected MCF-7 cells was significantly slower than in the two control groups. On the 22th day after transplantation the tumor weight ((21.40 ± 10.57) mg) and volume ((41.15 ± 12.17) mm(3)) in the STAT3 siRNA transfected group were significantly lower than in control group (weight (88.60 ± 12.16) mg, volume (118.45 ± 24.68) mm(3)) and non-specific siRNA transfected group (weight (57.20 ± 21.86) mg, volume (101.36 ± 21.90) mm(3)) (P < 0.05). Both the STAT3 mRNA and protein levels in the tumors from the STAT3 siRNA transfected group were significantly lower than in the tumors from the two control groups.</p><p><b>CONCLUSIONS</b>STAT3 siRNA can effectively silence the STAT3 gene in vitro and in vivo, increase cell apoptosis rate and significantly decrease cell proliferation, which inhibits the growth of breast cancer cell in vitro. Tumor growth of xenograft mice is significantly inhibited. The results obtained in vivo are in consistency with those in vitro. STAT3 may be a novel therapeutic target for breast cancer and RNA interference has potential clinical application.</p>


Assuntos
Animais , Feminino , Humanos , Camundongos , Apoptose , Linhagem Celular Tumoral , Neoplasias Mamárias Experimentais , Patologia , Terapêutica , Camundongos Nus , RNA Interferente Pequeno , Genética , Fator de Transcrição STAT3 , Genética , Ensaios Antitumorais Modelo de Xenoenxerto
13.
National Journal of Andrology ; (12): 1011-1013, 2011.
Artigo em Chinês | WPRIM | ID: wpr-239041

RESUMO

<p><b>OBJECTIVE</b>To investigate the effect of transurethral resection of the prostate (TURP) in the treatment of urinary retention following seed implantation for prostate cancer.</p><p><b>METHODS</b>We treated 2 cases of urinary retention following seed implantation for prostate cancer by TURP, and analyzed their clinical data.</p><p><b>RESULTS</b>The operations were successful in both of the cases, with mean operation time of 60 min. Postoperative nocturnal urination of the patients averaged 2 times per night as compared with 5 - 6 times per night preoperatively, and their scores on IPSS and quality of life were significantly improved after surgery.</p><p><b>CONCLUSION</b>TURP affords satisfactory results in the treatment of urinary retention following seed implantation for prostate cancer patients.</p>


Assuntos
Idoso , Humanos , Masculino , Período Pós-Operatório , Neoplasias da Próstata , Cirurgia Geral , Ressecção Transuretral da Próstata , Métodos , Retenção Urinária , Cirurgia Geral
14.
Chinese Journal of Experimental Ophthalmology ; (12): 673-675, 2011.
Artigo em Chinês | WPRIM | ID: wpr-635682

RESUMO

Basic research program is essential to the investigation of the pathogenesis of ocular diseases and the development of novel strategies for the prevention and treatment for these diseases. With increasing support of research grants at various levels, basic research in ophthalmology has gained great achievement in China in recent years. A number of studies have recently been published in well known peer-review international journals and won the State Scientific and Technological Progress Awards. However, we have to keep it in mind that basic research in ophthalmology should be improved qualitatively meanwhile, the imbalance in basic study among different areas needs to be resolved in the near future.

15.
National Journal of Andrology ; (12): 527-530, 2010.
Artigo em Chinês | WPRIM | ID: wpr-252789

RESUMO

<p><b>OBJECTIVE</b>To explore the diagnosis and treatment of primary epididymal tumor.</p><p><b>METHODS</b>We retrospectively analyzed the clinical data of 35 cases of pathologically confirmed primary epididymal tumor. Of the total number of patients, 10 underwent tumor excision, 23 received epididymectomy, 1 was treated by simple orchidoepididymectomy, and by radical orchidoepididymectomy with second-stage retroperitoneal lymph node dissection.</p><p><b>RESULTS</b>Postoperative pathology confirmed 33 cases of benign tumor (including 21 adenomatoid tumor, 7 leiomyoma, 4 fibroma, and 1 papillary cystadenoma), and 2 cases of malignancy (1 malignant fibrous histiocytoma and 1 adenocarcinoma). The follow-up lasted 10 months to 6 years, which revealed no recurrence, metastasis and death.</p><p><b>CONCLUSION</b>Primary epididymal tumor is difficult to be definitely diagnosed preoperatively. Surgical exploration is the first choice for those highly suspected of the disease. Tumor excision or epididymectomy can be considered for benign cases, while radical orchidoepididymectomy with retroperitoneal lymph node dissection is recommended in case of malignancy.</p>


Assuntos
Adulto , Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Epididimo , Cirurgia Geral , Neoplasias dos Genitais Masculinos , Diagnóstico , Cirurgia Geral , Excisão de Linfonodo , Estudos Retrospectivos , Resultado do Tratamento
16.
Chinese Journal of Oncology ; (12): 819-824, 2010.
Artigo em Chinês | WPRIM | ID: wpr-293473

RESUMO

<p><b>OBJECTIVE</b>To observe the effect of signal transducers and activators of transcription 3 (STAT3) gene silence on the growth of breast cancer cell line MCF7 in vitro and in vivo and discuss the feasibility and effectiveness of STAT3 used as gene therapeutic target for breast cancer.</p><p><b>METHODS</b>Human breast cancer cell line MCF7 cells were divided into 3 groups: mock control group, control group transfected with scrambled sequence siRNA, and experimental group transfectod with STAT3 siRNA. The STAT3 mRNA and protein levels were detected by semi-quantity RT-PCR and Western blotting, respectively. The cell proliferation and apoptosis were examined by MTT method and flow cytometry. MCF7 cells treated with STAT3-siRNA were transplanted subcutaneously in nude mice and their tumorgenic ability was observed. The STAT3 mRNA and protein levels of the samples from nude mice of different groups were detected by semi-quantity RT-PCR and Western blotting and compared.</p><p><b>RESULTS</b>After treatment with STAT3-siRNA, STAT3 mRNA (0.327 ± 0.020 vs. 1.035 ± 0.050, 1.093 ± 0.018) and ptotein (0.153 ± 0.006 vs. 1.320 ± 0.033, 1.374 ± 0.022) levels in the MCF7 cells transfected with STAT3-siRNA were significantly lower than that in the two control groups (P < 0.05). MTT assay showed that after transfection of the STAT3-siRNA into MCF7 cells, cell proliferation was significantly reduced and the cell growth inhibition ratio in the STAT3-siRNA group was (44.00 ± 5.10)%, significantly higher than that in the control group (16.1 ± 1.05)% (P < 0.05). Flow cytometry results suggested that more apoptosis was observed in the STAT3-siRNA group. The apoptosis rate was (14.79 ± 0.22)%, much higher than that in the control group [(7.06 ± 0.71)%, (8.45 ± 0.43)%, P < 0.05]. The tumor growth in the experimental group was significantly slower than that in the two control groups. 0n the 22th day after transplantation, the tumor weight [(21.4 ± 10.6) mg vs. (88.6 ± 12.2) mg, (57.2 ± 21.9) mg] and volume [(41.15 ± 12.17) mm³ vs. (118.45 ± 24.68) mm³, (101.36 ± 21.90) mm³] in the experimental group were significantly lower than that in the two control groups (P < 0.05). The STAT3 mRNA and protein levels of the samples from nude mice in the experimental group were significantly lower than that in the two control groups.</p><p><b>CONCLUSION</b>siRNA targeting STAT3 can inhibit the proliferation of MCF7 cells in vitro and in vivo. STAT3 may become a novel therapeutic target for breast cancer.</p>


Assuntos
Animais , Feminino , Humanos , Camundongos , Apoptose , Neoplasias da Mama , Genética , Metabolismo , Patologia , Linhagem Celular Tumoral , Proliferação de Células , Inativação Gênica , Camundongos Endogâmicos BALB C , Camundongos Nus , Transplante de Neoplasias , RNA Mensageiro , Metabolismo , RNA Interferente Pequeno , Genética , Fator de Transcrição STAT3 , Genética , Fisiologia , Transfecção , Carga Tumoral
17.
National Journal of Andrology ; (12): 627-630, 2010.
Artigo em Chinês | WPRIM | ID: wpr-295027

RESUMO

<p><b>OBJECTIVE</b>To explore the clinical value and safety of TRUS-guided transperineal biopsy with the 9 + X method in the diagnosis of prostate carcinoma.</p><p><b>METHODS</b>A total of 420 men underwent TRUS-guided transperineal biopsy with the 9 + X method for suspected prostate carcinoma. Their clinical data were retrospectively analyzed.</p><p><b>RESULTS</b>Prostate carcinoma was detected in 160 (38.1%) of the 420 cases, accounting for 7.4%, 17.8% and 65.4% in those with PSA < 4.0 microg/L, 4 -10 microg/L and > 10 microg/L respectively, 25.0% in those with abnormal findings on digital rectal examination (DRE), and 22.2% in those with abnormal echoes on TRUS or abdominal ultrasound examination. Complications after prostatic biopsy included gross hematuria in 79 cases (18.8%), acute urinary retention in 13 (3.1%) and fever in 9 (2.1%), but no other serious complications were observed.</p><p><b>CONCLUSION</b>TRUS-guided transperineal biopsy with the 9 + X method, with high accuracy and fewer complications, is an ideal approach to the diagnosis of prostate carcinoma.</p>


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Humanos , Masculino , Pessoa de Meia-Idade , Biópsia por Agulha , Métodos , Períneo , Próstata , Patologia , Reto , Diagnóstico por Imagem , Estudos Retrospectivos , Ultrassonografia
18.
International Eye Science ; (12): 883-886, 2007.
Artigo em Chinês | WPRIM | ID: wpr-641459

RESUMO

· AIM: To investigate the expression and the possible implication of CD40/CD40L costimulatory molecules in erythema nodosum of patients with Beh(c)et's disease.· METHODS: Sampling was done from erythema nodosum of 5 patients with Beh(c)et's disease and normal skin of 2 healthy individuals. Immunohistochemical staining was performed to examine the expression of CD4, CD8, CD19, CD68, HLA-DR,CD40 and CD40L molecules in the obtained tissues.· RESULTS: Approximately 90% of epidermic cells in erythema nodosum expressed CD40 molecule. In the dermis and subcutaneous tissue, a significantly increased number of CD4+Tcells, CD8+Tcells, CD19+cells, CD68+cells, HLA-DR+cells,CD40L+cells, and CD40+cells were observed in the erythema nodosum as compared with that in normal skin. Double staining showed that CD40L molecules were expressed on 45% of CD4+T cells. CD40 molecules were expressed on 100% CD68+ cells and 59.2% of HLA-DR+cells respectively.· CONCLUSION: A number of CD40/CD40L costimulatory molecules are upreguiated in the erythema nodosum of patients with Behcet's disease.

19.
Chinese Medical Journal ; (24): 740-748, 2006.
Artigo em Inglês | WPRIM | ID: wpr-267054

RESUMO

<p><b>BACKGROUND</b>T-cell receptor (TCR) plays an important role in the development of autoimmune diseases. Recently, it was reported that immunization of animals with TCR peptide derived from the pathogenic cells could prevent autoimmune diseases. The aim of this study was to investigate whether vaccination with a synthetic peptide from the hypervariable region of TCR V(beta) 8.3, an experimental autoimmune uveoretinitis (EAU)-associated gene, was able to prevent the disease.</p><p><b>METHODS</b>EAU was induced in Lewis rats by immunization with IRBP R16 peptide emulsified in complete Freund's adjuvant (CFA). The clinical and histological appearances were scored. Delayed type hypersensitivity (DTH) and lymphocyte proliferation were detected. Cytokine levels of aqueous humour, supernatants of cells from spleen and draining lymph nodes were measured by enzyme linked immunosorbent assay (ELISA). Gene expression of TCR V(beta) 8.3 on CD(4)(+) T cells was examined by real time quantitative polymerase chain reaction (PCR).</p><p><b>RESULTS</b>After vaccination, the intraocular inflammation was significantly mitigated, antigen specific DTH and lymphocyte proliferation responses were suppressed, interleukin (IL)-2 in aqueous humour, interferon (IFN)-gamma and IL-2 produced by the spleen and draining lymph node cells were significantly decreased, whereas the production of IL-4 and IL-10 were increased. The response of draining lymph node cells to TCR V(beta) 8.3 peptide was enhanced after vaccination. Inoculation with CFA alone did not affect the severity of EAU and the above parameters. The suppression of EAU was much stronger in the group of four fold inoculations than the group of two fold inoculations. The expression of TCR V(beta) 8.3 gene was significantly reduced in the group of fourfold inoculations.</p><p><b>CONCLUSION</b>Vaccination with the synthetic TCR V(beta) 8.3 peptide could remarkably inhibit the development of EAU.</p>


Assuntos
Animais , Feminino , Ratos , Doenças Autoimunes , Citocinas , Genes Codificadores da Cadeia beta de Receptores de Linfócitos T , Ratos Endogâmicos Lew , Receptores de Antígenos de Linfócitos T alfa-beta , Alergia e Imunologia , Retinite , Proteínas de Ligação ao Retinol , Alergia e Imunologia , Células Th1 , Alergia e Imunologia , Células Th2 , Alergia e Imunologia , Uveíte , Vacinação
20.
Chinese Medical Journal ; (24): 2000-2004, 2005.
Artigo em Inglês | WPRIM | ID: wpr-282832

RESUMO

<p><b>BACKGROUND</b>Anterior chamber associated immune deviation (ACAID) is characterized by a Th2 cell response. GATA-3 has been shown to be necessary for the activation of Th2 cells. This study was designed to examine the expression of GATA-3 in the development of ACAID.</p><p><b>METHODS</b>ACAID was induced by injection of 50 microg interphotoreceptor retinoid binding protein (IRBP) into the anterior chamber (AC) of Wistar rats. Delayed-type hypersensitivity (DTH) was evaluated on day 3, 7, 14, 21, 28 after IRBP inoculation. GATA-3 expression was detected using immunohistochemical staining. The expression of GATA-3 mRNA at different time points after AC injection of IRBP was assayed by reverse transcriptase polymerase chain reaction (RT-PCR).</p><p><b>RESULTS</b>A significant DTH reaction was observed in Wistar rats on day 3 and 5 after IRBP inoculation. The DTH reaction was decreased 7 days after IRBP inoculation. GATA-3 expression was weak at both mRNA and protein levels in the normal spleen, but was significantly increased on day 5, 7, 14, and 21 after AC injection of IRBP.</p><p><b>CONCLUSION</b>The expression of GATA-3 is increased during ACAID, suggesting that GATA-3 may be involved in the development of ACAID.</p>


Assuntos
Animais , Feminino , Ratos , Câmara Anterior , Alergia e Imunologia , Proteínas do Olho , Alergia e Imunologia , Fator de Transcrição GATA3 , Genética , Fisiologia , Hipersensibilidade Tardia , Alergia e Imunologia , RNA Mensageiro , Ratos Wistar , Proteínas de Ligação ao Retinol , Alergia e Imunologia , Baço , Metabolismo , Células Th2 , Alergia e Imunologia
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