共查询到20条相似文献,搜索用时 140 毫秒
1.
2.
3.
目的: 研究4种肿瘤-睾丸抗原(CT)基因在膀胱移行细胞癌中的表达及其临床意义.方法: 采用反转录聚合酶链反应(RT-PCR)技术检测49例膀胱移行细胞痈患者癌组织(新鲜标本,Ta-T1期28例,T2-T4期21例;G1 20例,G2 16例,G3 13例)及其中15例患者癌旁组织的cTAGE-1、cTAGE-2、MAGE-A1及NY-ESO-1等4种CT基因mRNA的表达.结果: 49例膀胱移行细胞癌组织中MAGE-A1表达最高,其次为cTAGE-1,cTAGE-2及NY-ESO-1,分别为59%(29/49),55%(27/49),51%(25/49)及47%(23/49).15例癌旁组织表达均阴性.膀胱移行细胞癌组织中肿瘤不同分期、不同分级之间4种CT基因表达的差异均无统计学意义(Pearson x2检验法,P>0.05).结论: CT基因在膀胱移行细胞癌组织中有较高表达,而在癌旁组织无表达,可以进一步研究作为膀胱移行细胞癌特异性免疫治疗靶基因的可行性. 相似文献
4.
膀胱移行细胞癌p16、增殖细胞核抗原的表达及临床意义 总被引:1,自引:0,他引:1
应用免疫组化染色技术检测p16及PCNA基因在膀胱移行细胞癌中的表达,旨在探讨两者与膀胱移行细胞癌分级及预后的关系。 1 材料与方法 1.1 材料 收集我院1978~1992年间,手术切除膀胱移行细胞癌55例。其中男性44例,女性11例,年龄28~77岁,中位年龄58.87岁。随访时间术后1~15年,随访率100%。组织学分级Ⅰ级16例,Ⅱ级20例,Ⅲ级19例。膀胱正常粘膜6例作为对照,标本均经10%福尔马林固定,石蜡包埋,4μm连续切片。 相似文献
5.
6.
克隆性增殖T细胞的检测和研究进展 总被引:2,自引:0,他引:2
杨学宁 《国外医学(肿瘤学分册)》2000,27(6):359-362
肿瘤部位出现大量淋巴细胞浸润的病人常有较好的预后,推测这是宿主对肿瘤相关抗原的一种直接反应。目前理想的检测是否存在针对肿瘤细胞的克隆性增殖T细胞的方法是CDR3长度分析法。克隆性增殖了细胞的研究有助于进一步阐明肿瘤免疫机制,并有可能用于过继细胞免疫治疗。 相似文献
7.
陈卫 《中国肿瘤生物治疗杂志》1995,2(4):241-242
肿瘤的抗原性是肿瘤免疫学的核心问题。长期以来,免疫学家们对肿瘤细胞是否表达与正常组织所不同的抗原及其能否被机体免疫系统所识别,诱发特异的抗肿瘤免疫应答反应进行了大量的研究,但一直未能揭示肿瘤抗原的本质问题。关键原因乃是受限于人们对肿瘤的发病学以及免疫细胞识别抗原的分子机制的认识。 相似文献
8.
9.
目的:通过鳞癌抗原(squamous cell carcinoma antigen,SCCAg)在喉鳞状细胞癌中的表达来评价其在喉癌诊断和预后中的意义。方法:采用微粒子酶免疫法(microparticle enzyme immunoassay,MEIA)检测46例喉鳞状细胞癌患者血清SCCAg的水平,以41例喉部良性疾病患者作为对照。结果:喉鳞状细胞癌患者与对照组的SCCAg值有明显差异(P<0.05),喉鳞状细胞癌组SCCAg阳性率为36.96%,良性病变组仅1例阳性,阳性率为2.44%。SCCAg阳性率与喉鳞状细胞癌TNM分期、淋巴结转移相关。复发患者SCCAg治疗1周后表达水平明显下降(P<0.05),但半年后又明显升高(P<0.05)。结论:SCCAg与喉鳞状细胞癌关系密切,有可能成为喉鳞状细胞癌的进展和预后的指标。 相似文献
10.
膀胱癌抗原在膀胱移行细胞癌诊断中的价值 总被引:3,自引:0,他引:3
目的评价膀胱癌抗原(UBC)对膀胱移行细胞癌(BTCC)的诊断价值.方法采用ELISA法对89例BTCC及108例泌尿系非移行细胞癌(TCC)患者的尿UBC进行检测,并同时行尿脱落细胞学检查.结果 BTCC患者尿UBC均值为30.5 μg/L,与泌尿系非TCC患者8.2μg/L的均值比较,差别有显著性意义(P<0.01).尿UBC(以8.4μg/L为最适临界值)和尿细胞学诊断BTCC的敏感性分别为75.3%和16.9%,特异性分别为77.8%和100%,两者差别均有显著性意义(P<0.01).结论尿UBC检测对BTCC的诊断是一种较为敏感、特异且无创的方法,敏感性明显优于尿细胞学,但临床上不能完全替代尿细胞学检查. 相似文献
11.
The aim of this study was to explore the diagnostic value of levels of the serum-soluble receptor-binding cancer antigen expressed on SiSo cells (sRCAS1) expressed in lung cancer patients. Enzyme-linked immunosorbent assay was performed to detect serum sRCAS1 levels in 138 patients with lung cancers of various types and in 40 healthy controls. Our results showed that the patients with lung cancer had higher serum sRCAS1 levels than the controls. As disease stages progressed in lung cancer, serum sRCAS1 levels increased; patients with lymph node and distant metastases had higher levels than those without metastases, regardless of histology, age, and gender. At a cutoff value of 19.2 U/ml, sRCAS1 was 91.3 % sensitive and 72.5 % specific for lung cancer. In conclusion, these results suggest that sRCAS1 levels could have a clinical value for the diagnosis and management of lung cancer and could be used as a new tumor marker of lung cancer. 相似文献
12.
13.
Tumor Biology - Diagnosis of malignant pleural effusion (MPE) remains a major clinical challenge. The aim of this study was to evaluate the diagnostic value of combined detection of... 相似文献
14.
Sonoda K Miyamoto S Yamazaki A Kobayashi H Nakashima M Mekada E Wake N 《Cancer》2007,110(9):1979-1990
BACKGROUND: The expression of receptor-binding cancer antigen expressed on SiSo cells (RCAS1) is related significantly to the overall survival of patients with various cancers. RCAS1 reportedly induces apoptotic cell death in peripheral lymphocytes, which may contribute to the escape of tumor cells from immune surveillance. RCAS1 expression also has been related to tumor invasiveness and size in uterine cervical cancer. To clarify whether RCAS1 exacerbates tumor progression, the authors investigated the association between RCAS1 expression and tumor growth potential. METHODS: The authors constructed small interfering ribonucleic acid (RNA) (siRNA) to target RCAS1. After transfection of siRNA and the RCAS1-encoding gene, growth of tumor cells was assessed in vitro and in vivo. The correlation between RCAS1 expression and angiogenesis was investigated in the transfected cells and in inoculated tumors from nude mice. In addition, the same association was investigated immunohistochemically with tissue samples from patients with uterine cervical cancer. RESULTS: Knockdown of RCAS1 expression by siRNA significantly suppressed the in vivo growth of SiSo and HOUA tumor cells (P < .005); however, in vitro cell growth was not affected significantly. Enhanced RCAS1 expression significantly promoted in vivo growth, but not in vitro growth, of tumors derived from COS-7 cells (P = .0039). Introduction of the RCAS1-encoding gene increased expression of vascular endothelial growth factor (VEGF). In uterine cervical cancer, RCAS1 expression was associated significantly with VEGF expression (P = .0407) and with microvessel density (P = .0108). CONCLUSIONS: RCAS1 may be a pivotal regulator of tumor growth through angiogenesis. Continued exploration of the biologic function of RCAS1 may allow the development of novel therapeutic strategies for uterine cancer. 相似文献
15.
来源于骨髓的血管内皮祖细胞具有高度的扩增潜能。各种恶性肿瘤患者外周血中血管内皮祖细胞均有不同程度的增多,血管内皮祖细胞可能成为抗血管生成治疗的监测标记和可能的治疗靶点。 相似文献
16.
17.
目的:研究CD40激发凋亡肿瘤细胞致敏的树突状细胞(dendritic cells,DCs)对细胞因子诱导杀伤(cytokine-inducedkiller,CIK)细胞的细胞表型、增殖活性及细胞毒活性的影响。方法:常规方法从健康人外周血单个核细胞中诱导DCs和CIK细胞,采用凋亡肿瘤细胞负载DCs,并用或不用激发型CD40单克隆抗体(CD40mAb)激活DCs成熟;成熟DCs与同源的CIK细胞共育5d,分别获得DC40Ag-CIK细胞及DCAg-CIK细胞;观察细胞增殖活性;流式细胞仪检测细胞表型;酶联免疫吸附实验(enzyme-linked immunosorbent assays,ELISA)法检测细胞培养上清液中IFN-γ的含量;[3H]-TdR掺入法测定细胞杀伤活性。结果:凋亡肿瘤细胞负载激发可使DCs上调表达CD1a、CD80、CD86、CD83、HLR-DR,联合CD40mAb激发可进一步促进DCs成熟;培养至第14天时,DC40Ag-CIK细胞、DCAg-CIK细胞、CIK细胞分别扩增(18.2±1.7)倍、(15.0±1.2)倍、(9.3±1.8)倍;DC40Ag-CIK细胞中的CD3 CD56 比例较DCAg-CIK细胞和CIK细胞明显上调(P<0.05);DC40Ag-CIK细胞、DCAg-CIK细胞对A549杀伤活性强于CIK细胞(P<0.05),并且DC40Ag-CIK细胞强于DCAg-CIK细胞(P<0.05);CIK细胞、DCAg-CIK细胞、DC40Ag-CIK细胞培养上清液中IFN-γ的含量递增,分别为(1494.7±246.3)pg/mL、(2706.3±197.0)pg/mL、(3676.3±335.0)pg/mL。结论:与单独凋亡肿瘤细胞负载的DCs相比,CD40激发的凋亡肿瘤细胞负载的DCs可进一步提高CIK细胞的增殖活性及细胞毒活性。 相似文献
18.
19.
20.
胰腺癌是一种致死率高、治疗困难的恶性肿瘤。近期虽然吉西他滨等化疗药物用于其治疗取得一定的疗效,但生存率改善不明显。过去的十年,诸多学者开展大量涉及胰腺肿瘤对吉西他滨代谢及耐药机制的研究。最近有资料影响胰腺癌治疗疗效的相关分子和基因的检测,对于应用吉西他滨治疗胰腺癌预测疗效有很大的应用价值,特别是在个体化治疗领域。本文主要叙述影响治疗吉西他滨治疗胰腺癌疗效的相关分子和基因的研究进展。 相似文献