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RNAi knockdown of C-erbB2 expression inhibits salivary gland adenoid cystic carcinoma SACC-83 cell growthin vitro 被引量:1
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作者 Xiaohua Liu Yincheng Zhang +2 位作者 Wenhao Ren Tengteng Cao Yongjin Zhu 《The Journal of Biomedical Research》 CAS 2010年第3期215-222,共8页
Objective:To knockdown the C-erbB2 gene in salivary gland adenoid cystic carcinoma SACC-83 cells using RNA interference,and determine the effect of silencing C-erbB2 on cell proliferation.Methods:C-erbB2-siRNA was t... Objective:To knockdown the C-erbB2 gene in salivary gland adenoid cystic carcinoma SACC-83 cells using RNA interference,and determine the effect of silencing C-erbB2 on cell proliferation.Methods:C-erbB2-siRNA was transfected into SACC-83 cells.RT-PCR and immunohistochemistry were used to detect C-erbB2 expression in SACC-83 cells.Cell proliferation was measured by the MTT assay and gene knockdown was achieved by RNA interference.Apoptosis was analyzed by flow cytometry.Results:Compared with the control,C-erbB2 mRNA expression was decreased in the C-erbB2-siRNA transfection group,and immunohistochemical analysis indicated that C-erbB2 protein expression was decreased.After C-erbB2-siRNA was transfected for 48 h,absorbance at 570 nm (MTT)was 0.185±0.021 compared with 0.354±0.034,0.299±0.053,and 0.314±0.049 in the blank control,liposome control and negative control siRNA groups,respectively.The differences were statistically significant (P〈0.05)between the C-erbB2-siRNA group and the control groups.Following the C-erbB2 knockdown,the percentage of apoptotic cells was 5.63%compared with 2.04%,2.85%,and 2.98%in the three control groups,respectively.Proliferation of SACC-83 cells was inhibited,and early apoptotic cells were increased.Conclusion: RNA interference can effectively silence C-erbB2 gene expression and inhibit growth of SACC-83 cells,which indicates the potential of targeting this gene as a novel gene therapy approach for the treatment of salivary gland adenoid cystic carcinoma. 展开更多
关键词 salivary gland adenoid cystic carcinoma RNA interference C-ERBB2 gene silence
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Nerve Growth Factor and Vascular Endothelial Growth Factor: Retrospective Analysis of 63 Patients with Salivary Adenoid Cystic Carcinoma 被引量:12
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作者 Hao Li Xiao-lin Nong +3 位作者 Qi Chen Yi-ping Yang Jia-quan Li Yan-ning Li 《International Journal of Oral Science》 SCIE CAS CSCD 2010年第1期35-44,共10页
Aim To detect the expression of nerve growth factor (NGF) and vascular endothelial growth factor (VEGF) in salivary adenoid cystic carcinoma (SACC) tissues, as well as to determine the correlation between growth... Aim To detect the expression of nerve growth factor (NGF) and vascular endothelial growth factor (VEGF) in salivary adenoid cystic carcinoma (SACC) tissues, as well as to determine the correlation between growth factor expression and prognosis in SACC. Methodology Medical records of 63 patients surgically treated for SACC between January 1988 and October 2005 were reviewed. Immunohistochemistry was performed to examine the expression of NGF and VEGF in tumor tissues. Kaplan-Meier analysis and Cox's proportional hazard regression model were applied to assess predictors of survival. Results NGF and VEGF were overexpressed in SACC tissues, compared with those in normal salivary tissues (P〈0.05), and the staining intensity of these two factors was stronger in groups of solid subtype, advanced TNM stage, perineural invasion and recurrence. Patients with high- expression of NGF and VEGF, solid subtype, advanced stage, perineural invasion, recurrence and extended resection alone had worse survival rates (P〈0.05). Conclusion NGF and VEGF are expressed increasingly in the tissues of SACC cases with invasion and metastasis. NGF expression and VEGF expression are independent prognosis factors for survival. 展开更多
关键词 nerve growth factor vascular endothelial growth factor salivary adenoid cystic carcinoma PROGNOSIS
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ANTIMETASTATIC EFFECT OF INTEGRIN IIb/IIIa INHIBITORSON SALIVARY ADENOID CYSTIC CARCINOMA 被引量:3
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作者 李风和 俞光岩 +2 位作者 李盛琳 彭师奇 傅嘉 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 2001年第3期198-201,共4页
Objectives: To investigate the relation between metastatic potential of salivary adenoid cystic carcinoma (SACC) and tumor cell-platelet adhesion, and the antimetastatic effect of integrin IIb/IIIa inhibitor on SACC. ... Objectives: To investigate the relation between metastatic potential of salivary adenoid cystic carcinoma (SACC) and tumor cell-platelet adhesion, and the antimetastatic effect of integrin IIb/IIIa inhibitor on SACC. Methods: Tumor cell-platelet adhesion of highly metastatic SACC-LM, non-highly metastatic SACC-83 and effect of aspirin, arginine-aspartate (RD), magnesium acetylsalicylate on adhesion were studiedin vitro. Antimetastafic effect of aspirin, RD, magnesium acetysalicylate on experimental metastasis of SACC was observedin vivo. Results: The tumor cell-platelet adhesion was stronger in SACC-LM than in SACC-83. Aspirin, RD and magnesium acetylsalicylate could inhibit the adhesion of SACC-LM at the concentration of 1, 5 and 25 μg/ml. RD can inhibit experimental metastasis of SACC. Conclusion: Metastasis of SACC is related to platelet-tumor cell adhesion, RD could inhibit metastasis of SACC. 展开更多
关键词 salivary adenoid cystic carcinoma Integrin IIb/IIIa PLATELET Neoplasm metastasis
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Expressions of chemokine receptor CXCR4 and its ligand CXCL12 in salivary adenoid cystic carcinoma 被引量:4
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作者 徐晓刚 吕春堂 周中华 《Journal of Medical Colleges of PLA(China)》 CAS 2004年第4期225-228,共4页
Objective: To examine expressions of chemokine receptor CXCR4 and its ligand CXCL12 in primary focus and lymphogenous metastasis of salivary adenoid cystic carcinoma (ACC) with lung metastasis. Methods: Using immunohi... Objective: To examine expressions of chemokine receptor CXCR4 and its ligand CXCL12 in primary focus and lymphogenous metastasis of salivary adenoid cystic carcinoma (ACC) with lung metastasis. Methods: Using immunohistochemical hypersensitivity catalyzed signal amplification (CSA), expressions of chemokine receptor CXCR4 and ligand CXCL12 were detected in tissue specimens from 20 cases of primary cancer focus and lymphogenous metastasis of salivary adenoid cystic carcinoma, of which 7 cases were associated with lung metastasis and 3 with lympogenous metastasis. Twenty cases of tongue carcinoma (including 10 cases with lymphogenous metastasis) and 15 cases of mucoepidermoid carcinoma (including 5 cases with lymphogenous metastasis) were used as the malignant control group;and salivary mixed tumor (n=10), tongue leukoceratosis (n=10) and cervical lymph node reactive hyperplasia (n=10) were used as the benign control group. Results: Expression of CXCR4 in the tissues and lymph metastases of oral and maxillofacial salivary ACC, mucoepidermoid carcinoma and tongue carcinoma was significantly higher than that of the benign control group (P<0.05); expression of CXCR4 in the primary focus of ACC was significantly higher than that of the malignant control group; and expression of CXCR4 in the ACC with lung metastasis was 87.1% (6/7), significantly higher than that without lung metastasis(P<0.01). There was evident positive expression of CXCL12 in endotheliocytes of microvessels within cancer and paracancer tissues and significantly high expression of CXCL12 in lymphogenous metastasis(P<0.05). Conclusion: Chemokine receptor CXCR4 and its ligand CXCL12 may be associated with local invasion and lymphogenous metastasis of oral and maxillofacial cancer, especially with lung metastasis of salivary ACC. 展开更多
关键词 salivary gland adenoid cystic carcinoma METASTASIS chemokine receptor CHEMOKINE IMMUNOHISTOCHEMISTRY
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Inhibition of Salidroside on Salivary Gland Adenoid Cystic Carcinoma
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作者 LI Mei-hua ZHOU Hong-lan +1 位作者 WANG Wei QIU Xin-ru 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2010年第6期969-973,共5页
To evaluate the role of salidroside on proliferation,apoptosis and invasiveness of salivary gland adenoid cystic carcinoma cells(SACC),immunocytochemical staining was employed to detect proliferating cell nuclear an... To evaluate the role of salidroside on proliferation,apoptosis and invasiveness of salivary gland adenoid cystic carcinoma cells(SACC),immunocytochemical staining was employed to detect proliferating cell nuclear antigen(PCNA),caspase 3 and caspase 8 expression in SACC-2 cells.Modified Boyden chamber assay combined with laser confocal microscopy(LSCM) was used to evaluate the invasion and migration abilities of SACC-2 cells at different time point.Immunohistochemistry staining revealed that the expression of PCNA was significantly decreased(P0.01) after salidroside treatment.In contrast,salidroside treatment led to increased caspase 3 and caspase 8 in SACC-2 cells.Cell migration depth and number of cells that penetrated Boyden chamber were also decreased by salidroside.Salidroside potently inhibits the proliferation and simultaneously induces the apoptosis of SACC-2 cells.Migration and invasion of SACC-2 cells are also inhibited.Our data throw light on potential clinical application of salidroside to the patients with SACC. 展开更多
关键词 IMMUNOHISTOCHEMISTRY SALIDROSIDE salivary gland adenoid cystic carcinoma cell sacc-2 Boyden chamber Proliferating cell nuclear antigen
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EXPRESSION OF EPIDERMAL GROWTH FACTOR RECEPTOR IN DIFFERENT SALIVARY ADENOID CYSTIC CARCINOMA CELL LINES
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作者 马杰 宗志红 王兆元 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 2005年第3期213-216,共4页
Objective: To investigate the expression of epidermal growth factor receptor, a receptor tyrosine protein kinase, in the subcellular fractions of human salivary adenoid cystic carcinoma cell lines SACC-83 and SACC-LM... Objective: To investigate the expression of epidermal growth factor receptor, a receptor tyrosine protein kinase, in the subcellular fractions of human salivary adenoid cystic carcinoma cell lines SACC-83 and SACC-LM. Methods: Low metastatic and high metastatic cells of the adenoid cystic carcinoma, SACC-83 and SACC-LM, were cultured. Their subcellular fractions were extracted. The expression of epidermal growth factor receptor was detected with Western blot method, and the results of protein expression were quantitatively analyzed by FluorChem V2.0 software. Results: The results of Western blot analysis indicated that, EGFR expression on the membrane of SACC-83 cells was significantly higher than that of SACC-LM cells, but its expression in cytoplasm was significantly less in the former than the later (P〈0.01). In SACC-83 cell line, EGFR was over-expressed in membrane (P〈0.01), but in SACC-LM cell line, EGFR was over-expressed in cytoplasm (P〈0.01). Conclusion: The results suggest that the obtaining of metastasis ability is related to the high expression of EGFR protein in cytoplasm, so the molecular targeting therapy to EGFR may be an ideal treatment for the invasion and metastasis of salivary adenoid cystic carcinoma. 展开更多
关键词 salivary adenoid cystic carcinoma Epidermal growth factor receptor METASTASIS
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STUDIES OF TISSUE CULTURE ON THE ADENOID CYSTIC CARCINOMA OF SALIVARY GLANDS
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作者 何荣根 王峥 +1 位作者 周晓健 张秀丽 《Medical Bulletin of Shanghai Jiaotong University》 CAS 1991年第2期22-27,共6页
In this paper, the authors gave a synthetic report about sutdies of tissue culture on adenoid cystic carcinomas from human salivary glands. It includes the process of establishment of Acc-2 and Acc-3 cell lines, obser... In this paper, the authors gave a synthetic report about sutdies of tissue culture on adenoid cystic carcinomas from human salivary glands. It includes the process of establishment of Acc-2 and Acc-3 cell lines, observations to the cellular morphostructures, chromosome analysis, proliferative kinetics and some cellular physiological functions. All of these observations confirm that two cell lines have obvious malignant natures, epithelial and glandulous cellular features as well as. Both of cell lines have provided the useful experimental models in vitro for research on histogenesis and biological behaviours at adenoid cystic carcinoma and seeking new methods of clinical treatment. 展开更多
关键词 adenoid cystic carcinoma tissue culture cell line salivary GLAND
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Adenoid Cystic Carcinoma of Parotid Salivary Gland—A Case Study
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作者 Shuaib Kayode Aremu 《Case Reports in Clinical Medicine》 2018年第11期576-581,共6页
Adenoid Cystic Carcinoma (ACC) is an infrequent slow growing epithelial tumour constituting for around less than 1% of all the oral and maxillo-facial malignancies and almost 10% of all the salivary gland tumors. Paro... Adenoid Cystic Carcinoma (ACC) is an infrequent slow growing epithelial tumour constituting for around less than 1% of all the oral and maxillo-facial malignancies and almost 10% of all the salivary gland tumors. Parotid gland is the second most common site to be involved in the head and neck region along with submandibular gland, Palate being the most common site involved in the oral cavity. Key feature of these tumors include its asymptomatic presentation, indolent nature, typically showing infiltrative growth and peri-neural invasion. Herein, we report a case of adenoid cystic carcinoma of right parotid gland of a 33-year-old male who presented with complaint of painless slow enlargement of left parotid gland and facial muscle weakness. On Examination firm mass in the region of the left parotid gland as well as left facial paralysis was seen. Biopsy results and further management is discussed here within. 展开更多
关键词 adenoid cystic carcinoma PAROTID GLAND MALIGNANT salivary GLAND Tumor
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抑制miR-130a表达对SACC-83顺铂化疗敏感性及XIAP MDR1蛋白表达的影响
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作者 石佳佩 王秋林 +3 位作者 易笑冉 刘俊杰 严梦 李鹏程 《贵州医科大学学报》 CAS 2024年第9期1326-1334,共9页
目的研究抑制miR-130a表达对人涎腺腺样囊性癌细胞株(SACC-83)顺铂(DDP)化疗敏感性及X染色体连锁凋亡抑制蛋白(XIAP)、多药耐药基因(MDR1)表达的影响。方法构建人涎腺腺样囊性癌DDP耐药细胞株(SACC-83/DDP),采用实时荧光定量(qRT-PCR)检... 目的研究抑制miR-130a表达对人涎腺腺样囊性癌细胞株(SACC-83)顺铂(DDP)化疗敏感性及X染色体连锁凋亡抑制蛋白(XIAP)、多药耐药基因(MDR1)表达的影响。方法构建人涎腺腺样囊性癌DDP耐药细胞株(SACC-83/DDP),采用实时荧光定量(qRT-PCR)检测SACC-83、SACC-83/DDP细胞中miR-130a表达水平;将SACC-83/DDP细胞随机分为对照组、mir-130a inhibitor组(转染mir-130a inhibitor)、DDP+mir-130a inhibitor阴性对照组(30μmol/L DDP+转染mir-130a inhibitor阴性对照)及DDP+mir-130a inhibitor组(30μmol/L DDP+转染mir-130a inhibitor),采用CCK-8法测定各组细胞生存率以及对DDP的耐药性,流式细胞术检测细胞凋亡率,TUNEL染色检测细胞凋亡指数;qRT-PCR检测细胞miR-130a、XIAP、MDR1、PTEN mRNA水平,免疫印记法检测细胞XIAP、MDR1、PTEN蛋白表达。结果与SACC-83细胞相比,miR-130a在SACC-83/DDP细胞中高表达(P<0.05);与对照组和mir-130a inhibitor组相比,DDP+mir-130a inhibitor组细胞生存率降低,凋亡率和凋亡指数升高(P<0.05);与mir-130a inhibitor组相比,DDP+mir-130a inhibitor组细胞生存率降低,凋亡率和凋亡指数升高(P<0.05);与对照组相比,mir-130a inhibitor组、DDP+mir-130a inhibitor组细胞miR-130a水平、XIAP mRNA及蛋白、MDR1 mRNA及蛋白表达降低(P<0.05),凋亡率、凋亡指数和PTEN蛋白表达升高(P<0.05);与DPP+mir-130a inhibitor组相比,DDP+mir-130a inhibitor阴性对照组细胞miR-130a水平、XIAP mRNA及蛋白、MDR1 mRNA及蛋白表达升高(P<0.05),凋亡率、凋亡指数和PTEN蛋白表达下降(P<0.05);SACC-83/DDP细胞对DDP的耐药性明显高于SACC-83细胞,抑制miR-130a表达逆转了SACC-83/DDP细胞的DDP耐药性。结论抑制miR-130a表达,可能下调XIAP表达,增强人涎腺腺样囊性癌细胞株对顺铂化疗的敏感性。 展开更多
关键词 miR-130a X染色体连锁凋亡抑制蛋白 人涎腺腺样囊性癌细胞株 顺铂 化疗敏感性
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POLQ表达降低对SACC-83细胞DNA损伤敏感性的影响
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作者 白晗 刘涵 +3 位作者 朱蕾 刘超 李楠 肖晶 《上海口腔医学》 CAS 北大核心 2023年第2期120-125,共6页
目的:探讨DNA损伤环境中抑制POLQ对唾液腺腺样囊性癌(salivary adenoid cystic carcinoma,SACC)细胞SACC-83增殖及克隆形成能力、细胞周期及DNA损伤修复通路的影响。方法:应用shRNA(short hairpin RNA)瞬时转染方法构建POLQ敲减的SACC-8... 目的:探讨DNA损伤环境中抑制POLQ对唾液腺腺样囊性癌(salivary adenoid cystic carcinoma,SACC)细胞SACC-83增殖及克隆形成能力、细胞周期及DNA损伤修复通路的影响。方法:应用shRNA(short hairpin RNA)瞬时转染方法构建POLQ敲减的SACC-83细胞模型,利用qRT-PCR及Western免疫印迹实验检测POLQ干扰效率。应用不同浓度DNA损伤剂依托泊苷(etoposide,ETP/VP-16-213)诱导SACC-83细胞发生DNA损伤,利用Western免疫印迹实验检测γH2AX的表达水平,评价DNA双链断裂水平。在不同浓度依托泊苷诱导形成的DNA损伤环境中,通过CCK-8细胞增殖实验检测抑制POLQ对SACC-83细胞增殖能力的影响。采用平板克隆实验观察抑制POLQ对SACC-83细胞克隆形成能力的影响,应用流式细胞仪分析抑制POLQ对SACC-83细胞周期的影响,应用Western免疫印迹实验检测抑制POLQ对SACC-83细胞γH2AX、RAD51及PARP1表达水平的影响。采用SPSS 20.0软件包对数据进行统计学分析。结果:应用shRNA瞬时转染方法抑制SACC-83细胞POLQ mRNA及蛋白的表达。依托泊苷以剂量依赖的方式促进SACC-83细胞γH2AX表达。POLQ表达降低可抑制SACC-83细胞增殖能力(P<0.001),且抑制作用随ETP浓度增加而减小。在依托泊苷诱导形成的DNA损伤环境中,POLQ表达降低可抑制SACC-83细胞克隆形成能力(P<0.001),诱导细胞发生S期阻滞(P<0.01)。POLQ通过促进γH2AX(P<0.05)及同源重组(homologous recombination,HR)通路相关蛋白RAD51(P<0.05)、抑制非同源末端连接(alternative non-homologous end joining,altNHEJ)通路相关蛋白PARP1(P<0.01),调节DNA损伤修复。结论:POLQ表达降低,会促进SACC-83细胞对DNA损伤的敏感性。 展开更多
关键词 唾液腺腺样囊性癌 POLQ DNA修复 依托泊苷
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姜黄素对涎腺腺样囊性癌细胞系SACC-83增殖和凋亡的影响 被引量:4
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作者 杨威 陈彪 +5 位作者 张英怀 贾志宇 屈鹏飞 郭利华 张平 唐全勇 《现代口腔医学杂志》 CAS CSCD 2009年第2期142-144,共3页
目的体外研究姜黄素对涎腺腺样囊性癌细胞系SACC-83增殖和凋亡的影响。方法用终浓度为2.5、5、10、15、20mg/L的姜黄素处理SACC-83。应用MTT比色试验,倒置显微镜,Giemsa染色,Annexin-V-FITC和PI双标记活细胞后流式细胞仪和透射电镜检测... 目的体外研究姜黄素对涎腺腺样囊性癌细胞系SACC-83增殖和凋亡的影响。方法用终浓度为2.5、5、10、15、20mg/L的姜黄素处理SACC-83。应用MTT比色试验,倒置显微镜,Giemsa染色,Annexin-V-FITC和PI双标记活细胞后流式细胞仪和透射电镜检测和观察SACC-83的生长抑制率和细胞凋亡情况。结果姜黄素对SACC-83的生长抑制率与药物浓度和作用时间具有明显的正相关性(P<0.01)。用药组细胞明显凋亡,凋亡率随处理时间延长和药物浓度增加而上升,各组间有显著差异(P<0.01)。结论姜黄素具有抑制涎腺腺样囊性癌细胞系SACC-83增殖和诱导其凋亡的作用,且具有浓度和时间依赖性。 展开更多
关键词 姜黄素 腺样囊性癌 涎腺 增殖 凋亡
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TROP2蛋白在涎腺腺样囊性癌中的表达及与患者预后的关系
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作者 董博 姚曼曼 +2 位作者 尚宏悦 杨凯成 刘铁军 《口腔疾病防治》 2024年第10期765-771,共7页
目的 探讨滋养层细胞表面抗原2(trophoblast cell-surface antigens 2,TROP2)在涎腺腺样囊性癌(salivary adenoid cystic carcinoma,SACC)中的表达,并分析其与临床病理特征之间的关系,明确TROP2的表达与SACC患者预后的相关性。方法 本... 目的 探讨滋养层细胞表面抗原2(trophoblast cell-surface antigens 2,TROP2)在涎腺腺样囊性癌(salivary adenoid cystic carcinoma,SACC)中的表达,并分析其与临床病理特征之间的关系,明确TROP2的表达与SACC患者预后的相关性。方法 本研究获得单位伦理委员会的批准,采用免疫组织化学方法检测TROP2在85例SACC组织及各自癌旁组织中的表达情况,分析其表达情况与临床病理特征的关系;利用Kaplan-Meier法对40例SACC患者进行TROP2蛋白表达与患者术后五年无病生存期(disease-free survival,DFS)的关系分析;同时,采用Logistic回归模型分析影响SACC患者预后的因素。结果 TROP2在SACC组织中的低表达或不表达率显著高于癌旁组织(P<0.001);TROP2低表达或不表达与SACC患者肿瘤的生长以及临床分期呈显著正相关性(P<0.05);Kaplan-Meier生存分析显示:TROP2蛋白低表达或不表达的SACC患者的DFS显著低于高表达患者(P<0.05),预后不良。Logistic回归模型预后分析显示:TROP2蛋白低表达或不表达(OR=5.37;95%CI:1.03~28.08;P=0.046)与Ⅲ-Ⅳ临床分期(OR=6.89;95%CI:1.37~34.77;P=0.019)均为影响SACC患者预后的危险因素。结论 TROP2蛋白在SACC组织中低表达或不表达,患者预后不良,与肿瘤的生长、临床分期呈正相关,且TROP2低表达或不表达可作为SACC患者预后不良的独立危险因素,TROP2为SACC患者预后不良的标志物。 展开更多
关键词 涎腺腺样囊性癌 预后 免疫组织化学 TROP2 生物标志物 临床分期 临床病理特征 无病生存期 生存分析
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Genistein对唾液腺腺样囊性癌细胞株SACC-83的体外抗增殖作用 被引量:6
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作者 马杰 钟鸣 王兆元 《上海口腔医学》 CAS CSCD 2005年第1期55-58,共4页
目的:研究酪氨酸蛋白激酶抑制剂Genistein(4',5,7-三羟基异黄酮)对人唾液腺腺样囊性癌细胞株SACC-83的体外抗增殖作用及其对细胞增殖周期的影响。方法:用Genistein处理体外培养的SACC-83细胞,采用MTT检测法计算细胞存活率,显微照相... 目的:研究酪氨酸蛋白激酶抑制剂Genistein(4',5,7-三羟基异黄酮)对人唾液腺腺样囊性癌细胞株SACC-83的体外抗增殖作用及其对细胞增殖周期的影响。方法:用Genistein处理体外培养的SACC-83细胞,采用MTT检测法计算细胞存活率,显微照相记录细胞生长状态及形态学的改变,流式细胞仪测定细胞周期,AnnexinⅤ/PI法定量检测细胞凋亡,采用SPSS11.5统计软件对结果进行统计方差分析。结果:Genistein对SACC-83细胞有一定的抗增殖作用,且当其作用到一定时间、达到一定的浓度后,该作用与浓度及时间呈依赖关系;细胞形态发生改变,体积缩小,悬浮细胞逐渐增多;SACC-83细胞经220μmol/LGenistein作用3d,其生长受到明显抑制,阻断细胞生长于G2/M期,并明显诱导细胞凋亡(P<0.01)。结论:Genistein可以显著抑制人唾液腺腺样囊性癌细胞株SACC-83的生长,阻断细胞周期于G2/M期,并诱导细胞凋亡;提示酪氨酸蛋白激酶在唾液腺腺样囊性癌的发生、发展中起着重要作用。 展开更多
关键词 酪氨酸蛋白激酶 GENISTEIN 唾液腺腺样囊性癌 细胞周期 细胞凋亡
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单次不同X线剂量照射对SACC-83细胞的放射生物学效应 被引量:3
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作者 郑瑛 周昌龙 +2 位作者 李旭奎 张引成 饶国州 《现代肿瘤医学》 CAS 2005年第1期26-29,共4页
目的 了解体外培养的SACC-83细胞对不同剂量X线照射的反应。方法 采用SACC-83细胞系,于体外分别给予 2Gy、5Gy、lOGy、15Gy、20Gy、25Gy和 30Gy的X线照射,进行集落细胞数、集落形成率、凋亡DNA电泳梯状图谱、流式细胞仪凋亡率的检测... 目的 了解体外培养的SACC-83细胞对不同剂量X线照射的反应。方法 采用SACC-83细胞系,于体外分别给予 2Gy、5Gy、lOGy、15Gy、20Gy、25Gy和 30Gy的X线照射,进行集落细胞数、集落形成率、凋亡DNA电泳梯状图谱、流式细胞仪凋亡率的检测和细胞形态学观察。结果 对照组细胞倍增迅速,2Gy、5Gy、l0Gy细胞增殖缓慢, 15Gy以上的其余各组细胞未见增殖;集落形成率检测显示, 15Gy以上剂量照射各组均为 0. 2~15Gy照射能检测到凋亡带, 15Gy以上为明显的坏死带。15Gy已达体外SACC-83细胞的致死剂量。在形态学上 20~30Gy为坏死,在 10Gy^15Gy为凋亡与坏死的过渡区,在l0Gy剂量时表现为单纯的细胞凋亡, 2~5Gy表现为凋亡细胞与活细胞同时并存。经 2, 5Gy剂量照射细胞主要表现为S期细胞的比例减少,G2 /M期细胞的比例增多,经 10、15、2OGy剂量照射细胞主要表现为S期细胞和G2 /M期细胞的比例均减少。结论 通过SACC-83建立的射线细胞模型,提示在单次连续低剂量的放射线作用下表现为凋亡和活细胞共存,随着放射剂量的增加为凋亡,进而为凋亡和坏死并存,大剂量时,为细胞的坏死,这说明放射线对腺样囊性癌的作用为致细胞凋亡和直接细胞毒作用。照射剂量不同可能引起不同时相的细胞发生凋亡。 展开更多
关键词 放射剂量 凋亡 腺样囊性癌 sacc-83
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Genistein对腺样囊性癌细胞SACC-83中细胞周期蛋白表达的影响 被引量:3
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作者 马杰 王洁 +1 位作者 钟鸣 王兆元 《上海口腔医学》 CAS CSCD 2006年第1期69-72,共4页
目的:研究酪氨酸蛋白激酶抑制剂Genistein诱导人唾液腺腺样囊性癌细胞株SACC-83细胞周期阻滞的分子机制。方法:用Genistein处理体外培养的SACC-83细胞,采用Western印迹技术检测CyclinB1、Cdk1和CyclinD1、Cdk4蛋白的表达,并利用电泳凝... 目的:研究酪氨酸蛋白激酶抑制剂Genistein诱导人唾液腺腺样囊性癌细胞株SACC-83细胞周期阻滞的分子机制。方法:用Genistein处理体外培养的SACC-83细胞,采用Western印迹技术检测CyclinB1、Cdk1和CyclinD1、Cdk4蛋白的表达,并利用电泳凝胶成像分析软件,对其结果进行量化分析,采用SPSS11.5统计软件对结果进行方差分析。结果:随着Genistein作用时间的延长和浓度的增加,CyclinB1、Cdk1和CyclinD1、Cdk4蛋白的表达明显减少。SACC-83细胞经220μmol/LGenistein作用3d,其CyclinB1、Cdk1和CyclinD1、Cdk4蛋白的表达量分别是对照组的58%、64%和46%、43%,差异非常显著(P<0.01)。结论:Genistein诱导SACC-83细胞周期阻滞于G2/M期,与其下调CyclinB1、Cdk1和CyclinD1、Cdk4蛋白的表达有关。 展开更多
关键词 酪氨酸蛋白激酶 GENISTEIN 唾液腺 腺样囊性癌 细胞周期
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姜黄素与β-榄香稀联用对涎腺腺样囊性癌细胞株SACC-LM生长抑制和凋亡的协同作用 被引量:4
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作者 白亮 李耀辉 王如 《大连医科大学学报》 CAS 2010年第1期26-30,共5页
[目的]研究姜黄素与β-榄香稀联合对体外培养涎腺腺样囊性癌细胞株SACC-LM生长抑制和凋亡的情况。[方法]应用MTT测定法、流式细胞术和透射电镜观察等方法观察姜黄素协同β-榄香稀(浓度比1∶1)诱导SACC-LM细胞凋亡率及凋亡方式。[结果]1)... [目的]研究姜黄素与β-榄香稀联合对体外培养涎腺腺样囊性癌细胞株SACC-LM生长抑制和凋亡的情况。[方法]应用MTT测定法、流式细胞术和透射电镜观察等方法观察姜黄素协同β-榄香稀(浓度比1∶1)诱导SACC-LM细胞凋亡率及凋亡方式。[结果]1)用MTT测定法,姜黄素协同β-榄香稀(浓度比1∶1)作用SACC-LM细胞24 h后,其抑制率有明显协同效应。2)联合用药对SACC-LM肿瘤细胞Caspase-3的表达阳性率为(46.2±3.2)%明显高于单独用药组。3)用流式细胞术,10μg/mL姜黄素与10μg/mLβ-榄香稀联合作用SACC-LM细胞24 h后诱导SACC-LM细胞发生凋亡,并将细胞周期阻滞于S期。4)用透射电镜观察,协同用药(浓度比1∶1)作用SACC-LM细胞24 h后,出现明显细胞凋亡特征。[结论]姜黄素和β-榄香稀(浓度比1∶1)联合应用可增强对SACC-LM细胞株的敏感作用,并诱导其产生凋亡,使其细胞周期阻滞于S期。 展开更多
关键词 涎腺腺样囊性癌细胞株sacc—LM 细胞周期 姜黄素 β-榄香稀
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NCAM基因对人涎腺腺样囊性癌细胞系SACC-83生长抑制作用的研究 被引量:4
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作者 李淑薇 李兴强 +1 位作者 张引成 张静莹 《现代口腔医学杂志》 CAS CSCD 北大核心 2008年第1期25-28,共4页
目的探讨NCAM基因对人涎腺腺样囊性癌细胞株SACC-83体外生长的抑制作用。方法应用电穿孔转染方法将NCAMcDNA转入人涎腺腺样囊性癌细胞系SACC-83中,经G418筛选2~3周,用兔抗人NCAM抗体进行免疫组化染色鉴定,然后绘制细胞生长曲线,进行软... 目的探讨NCAM基因对人涎腺腺样囊性癌细胞株SACC-83体外生长的抑制作用。方法应用电穿孔转染方法将NCAMcDNA转入人涎腺腺样囊性癌细胞系SACC-83中,经G418筛选2~3周,用兔抗人NCAM抗体进行免疫组化染色鉴定,然后绘制细胞生长曲线,进行软琼脂培养。结果应用电穿孔方法可成功将NCAM基因转染入人涎腺腺样囊性癌细胞株SACC-83中,免疫组化染色鉴定显示转染NCAM的SACC-83细胞有NCAM蛋白的表达。与对照组相比,经NCAM基因转染后的SACC-83细胞增殖明显受到抑制。转染了NCAM基因的SACC-83细胞克隆形成率明显降低。结论NCAM基因对人涎腺腺样囊性癌细胞系SACC-83的生长有一定的抑制作用。 展开更多
关键词 涎腺腺样囊性癌 NCAM基因 基因治疗
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Genistein对腺样囊性癌细胞SACC-83中细胞凋亡相关蛋白表达的影响 被引量:2
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作者 马杰 王洁 +1 位作者 钟鸣 王兆元 《上海口腔医学》 CAS CSCD 2008年第2期196-199,共4页
目的:研究酪氨酸蛋白激酶抑制剂Genistein诱导人唾液腺腺样囊性癌细胞株SACC-83细胞凋亡的分子机制。方法:用Genistein处理体外培养的SACC-83细胞,采用Western印迹技术检测bax、bcl-2和survivin蛋白的表达,并利用电泳凝胶成像分析软件,... 目的:研究酪氨酸蛋白激酶抑制剂Genistein诱导人唾液腺腺样囊性癌细胞株SACC-83细胞凋亡的分子机制。方法:用Genistein处理体外培养的SACC-83细胞,采用Western印迹技术检测bax、bcl-2和survivin蛋白的表达,并利用电泳凝胶成像分析软件,对其结果进行量化分析,采用SPSS11.5软件包对结果进行方差分析。结果:随着Genistein作用时间的延长和浓度的增加,bax蛋白的表达明显增加,bcl-2和survivin蛋白的表达明显减少。SACC-83细胞经220μmol/LGenistein作用3d,其bax蛋白的表达量是对照组的3.43倍(P<0.01),而bcl-2和survivin蛋白的表达量分别是对照组的85%(P<0.05)和35%(P<0.01)。结论:Genistein诱导SACC-83细胞凋亡,与其上调bax蛋白的表达,以及下调bcl-2和survivin蛋白的表达有关。 展开更多
关键词 酪氨酸蛋白激酶 GENISTEIN 唾液腺 腺样囊性癌 细胞凋亡
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阻断FAK表达对涎腺腺样囊性癌细胞SACC-LM的侵袭行为的影响 被引量:4
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作者 张斌 孙长伏 +2 位作者 李岩峰 于涛 黄汉 《中华老年口腔医学杂志》 2009年第2期68-70,102,共4页
目的:研究探讨阻断黏着斑激酶(focal adhesion kinase,FAK)表达对涎腺腺样囊性癌肺转移亚系细胞(salivary adenoid cystic carcinoma-Lung metastasis,SACC-LM)侵袭行为的影响及相关机制。方法:应用酪氨酸蛋白激酶抑制剂Genistein处理... 目的:研究探讨阻断黏着斑激酶(focal adhesion kinase,FAK)表达对涎腺腺样囊性癌肺转移亚系细胞(salivary adenoid cystic carcinoma-Lung metastasis,SACC-LM)侵袭行为的影响及相关机制。方法:应用酪氨酸蛋白激酶抑制剂Genistein处理体外培养的SACC-LM细胞,应用transwell小室观察Genistein对SACC-LM细胞侵袭的影响,并应用RT-PCR法检测FAK和细胞外信号调节激酶(extracellular signal-regulated kinase,ERK)mRNA的表达。所得实验数据采用SPSS10.0统计软件t检验进行分组分析。结果:Genistein使SACC-LM细胞侵袭能力减弱;检测到随着Genistein抑制剂浓度的增高和作用时间的延长,FAK和ERKmRNA的表达水平均降低。结论:阻断FAK表达导致SACC-LM细胞侵袭能力减弱,原因可能是FAK和ERK表达水平的改变。 展开更多
关键词 黏着斑激酶 阻断 涎腺腺样囊性癌 侵袭
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紫杉醇及β-榄香烯对人涎腺腺样囊性癌细胞株SACC-LM细胞毒作用的研究 被引量:2
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作者 白亮 张福胤 王如 《口腔医学研究》 CAS CSCD 2004年第5期486-488,共3页
目的 :研究紫杉醇及 β -榄香烯联合应用对体外培养人涎腺腺样囊性癌细胞株SACC -LM的细胞毒作用。方法 :应用药物敏感性MTT测定法、流式细胞术和透射电子显微镜观察等方法 ,探讨紫杉醇与 β -榄香烯 (浓度比 1∶1)联合应用诱导SACC -L... 目的 :研究紫杉醇及 β -榄香烯联合应用对体外培养人涎腺腺样囊性癌细胞株SACC -LM的细胞毒作用。方法 :应用药物敏感性MTT测定法、流式细胞术和透射电子显微镜观察等方法 ,探讨紫杉醇与 β -榄香烯 (浓度比 1∶1)联合应用诱导SACC -LM细胞凋亡及其与G1期阻滞关系。结果 :1)应用MTT比色法 ,紫杉醇与 β -榄香烯联合 (浓度比 1∶1)作用SACC -LM细胞 2 4h后 ,其抑制率呈现出明显协同效应。 2 )流式细胞仪分析 ,2 5 μg/mL紫杉醇与 2 5 μg/mLβ-榄香烯协同用药作用SACC -LM细胞 2 4h后诱导SACC -LM细胞发生凋亡 ,并将细胞周期阻滞在G1期。3)电镜观察 ,协同用药对SACC -LM细胞作用 2 4h后 ,具有典型的凋亡细胞特征。结论 :紫杉醇与 β-榄香烯 (浓度比 1∶1)对SACC -LM细胞的抑制有协同作用 ,并诱导其产生凋亡 ,G1期阻滞能诱导SACC-LM细胞凋亡。 展开更多
关键词 涎腺腺样囊性癌 细胞周期 紫杉醇 Β-榄香烯
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