953 resultados para Carcinoma, Ductal, Breast


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Objective To investigate whether the irradiation with C-beam could enhance adenovirus-mediated transfer and expression of p53 in human hepatocellular carcinoma. Materials and methods HepG2 cells were exposed to C-beam or gamma-ray and then infected with replicationdeficient adenovirus recombinant vectors containing human wild-type p53 or green fluorescent protein, respectively. The transfer efficiency and expression level of the exogenous gene were detected by flow cytometric analysis. Cell survival fraction was detected by clonogenic assay. Results The transfer frequency in C-beam or gamma-irradiated groups increased by 50-83% and 5.7-38.0% compared with the control, respectively (P < 0.05). Compared with C-beam alone, p53 alone, and gamma-ray with p53, the percentages of p53 positive cells for 1 Gy C-beam with p53 increased by 56.0-72.0%, 63.5-82.0%, and 31.3-72.5% on first and third day after the treatments, respectively (P < 0.05). The survival fractions for the 2Gy C-bearn and AdCMV-p53 infection groups decreased to similar to 2%. Conclusion C-beam irradiation could significantly promote AdCMV-green fluorescent protein transfer and expression of p53.

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目的综述近年来banoxantrone(AQ4N)作为肿瘤治疗增敏药物在国外的研究进展,为国内开发和应用AQ4N提供参考。方法分析、归纳、总结近年来发表的相关文献。结果与结论AQ4N本身对细胞没有毒性,在乏氧条件下经还原酶的催化生成活性药物AQ4,后者通过抑制乏氧细胞中的拓扑异构酶Ⅱ活性而杀死肿瘤乏氧细胞。AQ4N选择性作用于乏氧细胞,与富氧细胞毒性剂如放疗或化疗联合应用,疗效显著。

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目的:研究肿瘤抑制子BRCA1在人乳腺癌细胞辐射抗性中的作用,并探讨其作用机制。材料和方法:利用实时细胞分析系统检测辐射对细胞存活的影响;流式细胞术检测辐射对细胞周期分布的影响;RT-PCR检测辐射导致的BRCA1、Bax和Bcl-2在 mRNA水平变化;Western blot方法检测辐射诱导的蛋白表达水平的变化; In-cell western定量检测辐射引起的蛋白表达水平的变化; AO/EB染色法检测辐射导致的细胞死亡情况。结果:第一,分别用1Gy和4Gy x射线和碳离子束辐照人乳腺癌细胞MCF-7,研究MCF-7对不同LET射线的辐射敏感性差异。结果显示,x射线组1Gy辐射导致细胞存活显著下降,4Gy辐射对细胞存活影响不明显;而碳离子束辐射对细胞生长无抑制作用。与x射线组比较,碳离子辐射诱导了更低的亚“G1”期细胞百分数和更显著的G2期阻滞现象。同时碳离子束辐射诱导BRCA1磷酸化水平和p21表达上调,Bax表达下调。以上结果表明MCF-7对辐射的耐受性与凋亡功能相关,而BRCA1 Ser-1524磷酸化作用可能参与细胞周期和凋亡的信号调控。第二,研究BRCA1在咖啡因诱导的辐射增敏效应中作用。当2mM咖啡因联合4Gy的x射线或碳离子束辐射处理MCF-7细胞后,观察到细胞存活显著下降,辐射诱导的G2期阻滞被废除,BRCA1和p21蛋白表达被抑制,而p53表达水平无明显变化。结果表明咖啡因诱导的MCF-7细胞的辐射增敏作用可能与G2期阻滞被废除相关,BRCA1可能参与该过程的信号调节。第三, 利用BRCA1功能正常的MCF-7细胞和BRCA1功能缺失的HCC1937细胞进一步研究BRCA1对细胞辐射敏感性的影响。辐射显著抑制了HCC1937细胞存活,但对MCF-7细胞存活无明显影响。与HCC1937细胞相比,辐射诱导MCF-7细胞发生显著的G2期阻滞。辐射诱导HCC1937细胞发生晚期凋亡,而MCF-7细胞则多发生早期凋亡,且MCF-7细胞凋亡数明显少于HCC1937细胞。RT-PCR检测结果显示,辐射增强了MCF-7细胞中BRCA1的mRNA 水平,抑制了Bax的mRNA 水平,对Bcl-2的影响不明显;而HCC1937细胞中Bax的mRNA表达水平则被增强。同时辐射诱导MCF-7细胞中BRCA1和p21蛋白表达增强,Bax表达下降,Bcl-2水平略有增高。而HCC1937细胞Bax表达水平增强,但p21和Bcl-2的表达水平则检测不到。这些结果表明,正常的BRCA1功能对Bcl-2的转录表达是必须的,BRCA1通过上调p21水平,下调Bax/Bcl-2影响细胞的辐射敏感性。结论: BRCA1在人乳腺癌细胞的辐射抗性发生中发挥重要作用,BRCA1通过上调p21水平诱导G2期阻滞,下调Bax/Bcl-2抑制凋亡信号,使得细胞对辐射诱导的凋亡产生抗性,最终导致细胞对辐射产生耐受性

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Modified nucleosides, formed post-transcriptionally in RNA by a number of modification enzymes, are excreted in abnormal levels in the urine of patients with malignant tumors. To test their usefulness as tumor markers, and to compare them with the conventional tumor markers, a reversed-phase high-performance liquid chromatographic (RP-HPLC) method and a factor analysis method have been used to study the excretion pattern of nucleosides of breast cancer patients. A clear cut differentiation of the breast cancer group and the healthy individuals in two clusters without overlapping was obtained. Copyright (C) 2000 John Wiley & Sons, Ltd.

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以血管生成为靶点的抗肿瘤策略是抗肿瘤领域的研究热点,目前已经发现许多天然和化学合成的抗血管生成药物。鲨鱼软骨作为抗新生血管生成因子的重要来源的研究已有20多年的历史,很多研究显示鲨鱼软骨提取物有抗血管生成活性。但鲨鱼软骨活性多肽的完整分子结构一直未见报道;鲨鱼软骨活性多肽干扰血管生成通路的信号途径尚不明确。 本文应用盐酸胍抽提、丙酮分级沉淀、超滤、凝胶层析等分离技术,从青鲨(Prionace glauca)软骨中分离纯化并鉴定了一种新的具有抗新生血管生成活性的多肽。经SDS-PAGE和N-末端氨基酸序列分析显示,该多肽分子量为15500 Da,采用蛋白数据库分析表明该多肽是一种新发现的鲨鱼软骨多肽(Polypeptide from Prionace glauca,PG155)。 体外实验显示,PG155抑制内皮细胞生长因子(vascular endothelial growth factor,VEGF)介导的人脐静脉内皮细胞(human umbilical vein endothelial cell ,HUVEC)迁移和管腔形成,并呈剂量依赖关系。200 μg/ml PG155对牛主动脉内皮细胞(Bovine Aortic Endothelial Cells,BAECs)和HUVECs及以下癌细胞,包括人肝癌细胞(human hepatoma Bel-7402 cells,Bel-7402)、 口腔上皮癌细胞(human oral epidermoid carcinoma KB cells ,KB)、人结肠癌细胞(human colon cancer HCT-18 cells,HCT-18)和人乳腺癌细胞(human breast MCF7 cancer cells ,MCF7)的增殖均无抑制作用,说明PG155无细胞毒作用。20 μg/ml PG155显著抑制HUVEC的迁移和管腔形成;40-80 μg/ml PG155 对VEGF 介导的HUVEC的迁移和管腔形成几乎完全抑制。 体内实验显示,PG155显著抑制斑马鱼胚胎模型新生血管生成,并呈剂量依赖关系。形态学观察表明PG155显著抑制斑马鱼胚胎肠下静脉(subintestinal vessels, SIVs)的生长,随着浓度的升高SIVs的生长可受到完全抑制。碱性磷酸酶染色分析显示,在一定浓度范围内,PG155随着浓度的升高对斑马鱼胚胎整体血管生成抑制作用依次增强。160 μg/ml PG155会引起斑马鱼胚胎心脏功能障碍。 由海洋生物中发现新的肿瘤新生血管生成抑制剂国内外的报道较少,我们的工作表明鲨鱼软骨可作为血管生成抑制剂的重要来源,鲨鱼软骨活性多肽PG155由于具有极低的细胞毒作用,并能抑制VEGF介导的血管生成过程,有希望成为一类新型抗肿瘤药物。

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The nucleoside analogue cordycepin (3'-deoxyodenosine, 3'-dA), one of the components of cordyceps militaris, has been shown to inhibit the growth of various tumor cells. However, the probable mechanism is still obscure. In this study, the inhibition of cell growth and changes in protein expression induced by cordycepin were investigated in BEL-7402 cells. Using the MTT assay and flow cytometry, we found that cordycepin inhibits cell viability and induces apoptosis in BEL 7402 cells. Additionally. the proteins were separated using two-dimensional polyacrylamide gel electrophoresis, and eight proteins were found to be significantly, affected by cordycepin compared to untreated control; among them, two were downregulated and six were upregulated. Of the eight proteins, six were identified with peptide mass fingerprinting using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) after in-gel trypsin digestion. These proteins are involved in various aspects of cellular metabolism. It is suggested that the effect of cordycepin on the growth of tumor cells is significantly related to the metabolism-associated protein expression induced by cordycepin. Copyright 2008 Prous Science, S.A.U. or its licensors. All rights reserved.

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Rhein, an anthraquinone derivative of rhubarb, inhibits the proliferation of various human cancer cells. In this paper, we focused on studying the effects of rhein on human hepatocelluar carcinoma BEL-7402 cells and further understanding the underlying molecular mechanism in an effort to make the potential development of rhein in the treatment of cancers. Using MTT assay and flow cytometry, we demonstrate a critical role of rhein in the suppression of BEL-7402 cell proliferation in a concentration- and time-dependent manner. The increase of apoptosis rate was observed after incubation of BEL-7402 cells with rhein at 50-200 mu M for 48 hours, and the cells exhibit typical apoptotic features including cellular morphological change and chromatin condensation. Moreover, rhein-induced cell cycle S-phase arrest. Additionally, after rhein treatment, expression levels of c-Myc gene were decreased, while those of caspase-3 gene were increased in a dose-dependent manner by using real-time PCR assay. The results demonstrate for the first time that cell cycle S-phase arrest is one of the mechanisms of rhein in inhibition of BEL-7402 cells. Rhein plays its role by inducing cell cycle arrest via downregulation of oncogene c-Myc and apoptosis through the caspase-dependent pathway. It is expected that rhein will be effective and useful as a new agent in hepatocelluar carcinoma treatment in the future.

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Emodin, a natural anthraquinone compound isolated from the rhizome of rhubarb, is reported to suppress the growth of tumor in many clinical situations. In this study, we focused on the effect of emodin in human breast cancer BCap-37 cells and further understand the underlying molecular mechanism in treating breast cancer. Using MTT assay and flow cytometry, we demonstrated the critical role of emodin in the suppression of the proliferation of BCap-37 cells based on a concentration- and time-dependent manner. The increase of apoptotic rate was also observed after incubation of BCap-37 cells on emodin at 20 mu M and 50 mu M for 48 h. The cells exhibited typical apoptotic features including cellular morphological change, chromatin condensation and membrane blebbing. The results of the study further showed that Bcl-2 level decreased, while Bax and cytosolic cytochrome c levels in sample cells increased after the emodin treatment by using Western blot. The decline in the Bcl-2/Bax ratio and the increase of cytosolic cytochrome c concentration were consistent with the increase of the apoptotic ratio. The results strongly suggest that the disruption of the mitochondrial signaling pathway was involved in emodin-induced apoptosis in BCap-37 cells.

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Objective: Thirteen urinary nucleosides, primarily degradation products of tRNA, were evaluated as potential tumor markers for breast cancer patients.

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Breast region measurements are important for research, but they may also become significant in the legal field as a quantitative tool for preoperative and postoperative evaluation. Direct anthropometric measurements can be taken in clinical practice. the aim of this study was to compare direct breast anthropometric measurements taken with a tape measure and a compass.Forty women, aged 18-60 years, were evaluated. They had 14 anatomical landmarks marked on the breast region and arms. the union of these points formed eight linear segments and one angle for each side of the body. the volunteers were evaluated by direct anthropometry in a standardized way, using a tape measure and a compass.Differences were found between the tape measure and the compass measurements for all segments analyzed (p > 0.05).Measurements obtained by tape measure and compass are not identical. Therefore, once the measurement tool is chosen, it should be used for the pre- and postoperative measurements in a standardized way.This journal requires that authors assign a level of evidence to each article. for a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266.

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Background and purpose: Accelerated partial breast irradiation (APBI) is the strategy that allows adjuvant treatment delivery in a shorter period of time in smaller volumes. This study was undertaken to assess the effectiveness and outcomes of APBI in breast cancer compared with whole-breast irradiation (WBI). Material and methods: Systematic review and meta-analysis of randomized controlled trials of WBI versus APBI. Two authors independently selected and assessed the studies regarding eligibility criteria. Results: Eight studies were selected. A total of 8653 patients were randomly assigned for WBI versus APBI. Six studies reported local recurrence outcomes. Two studies were matched in 5 years and only one study for different time of follow-up. Meta-analysis of two trials assessing 1407 participants showed significant difference in the WBI versus APBI group regarding the 5-year local recurrence rate (HR = 4.54, 95% CI: 1.78-11.61, p = 0.002). Significant difference in favor of WBI for different follow-up times was also found. No differences in nodal recurrence, systemic recurrence, overall survival and mortality rates were observed. Conclusions: APBI is associated with higher local recurrence compared to WBI without compromising other clinical outcomes. (C) 2014 Elsevier Ireland Ltd. All rights reserved.

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Oliver, A., Freixenet, J., Marti, R., Pont, J., Perez, E., Denton, E. R. E., Zwiggelaar, R. (2008). A novel breast tissue density classification framework. IEEE Transactions on Information Technology in BioMedicine, 12 (1), 55-65

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Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

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Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

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Trabalho de Projeto apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Análises Laboratoriais Especializadas, área de especialização em Análise Biomédica