同时还建立了原代培养的肿瘤细胞，提升了模型的利用效率。
We further developed the primary cell culture if the tumor cells which would lead to better use of this genetic model.
采用MTT法检测绞股蓝多糖对体外培养的肿瘤细胞增殖的抑制作用。
The inhibitory effect of polysaccharide on tumor cells proliferation was assayed by MTT method.
对体外培养的肿瘤细胞增殖抑制率可高达60.10%，与对照组比较差异有显著性（P<0.05）；
The inhibitory rate of JMME on tumor cell cultivated in vitro(60.10%)was higher than that in control group(P<0.05).
方法不同浓度的药物作用于培养的肿瘤细胞，应用MTT法和光学显微镜观察药物对细胞的生长抑制作用。
Methods MTT assay and light-microscope were used to evaluate the inhibitory effect of aloe-emodin on the cancer cells.
采用MTT比色法对体外培养的肿瘤细胞进行细胞毒作用实验，验证槲寄生蛋白注射液体外抗肿瘤效果，并且鉴定这种检测方法的有效性。
Antitumor effect of the Mistletoe protein extract was studied by analysis of cytotoxicity activity of tumor cells in vitro using MTT assay. The validity of this test method was also detected.
他精确地把那些细胞从他们的血液中抽离出来，在实验室的培养皿中让其增值数十亿倍，大到足以有可能制服一个肿瘤。
He literally pulled those cells out of their blood and grew billions more of them in laboratory dishes, enough to have a chance at overwhelming a tumor.
科学家发现用沙门氏菌培养肿瘤可引发免疫反应，从而有效的杀死癌细胞-并能阻止其生长。
Scientists have discovered that treating tumours with the Salmonella bacteria can induce an immune response that effectively kills cancer cells - and also vaccinates against further growth.
新的培养方法已经证明是对未来的肿瘤治疗方案是有益的。研究人员已能明确对于药品易感的细胞的目标受体。
The new culture has already proven useful for coming up with treatment options for the tumors. Researchers have been able to target receptors in the cells susceptible to drugs.
鱼类细胞培养已成为鱼类病毒学、肿瘤学、毒理学、遗传学和免疫学等研究的重要手段。
Cell culture of fish has provided us an important tool to study virology, tumorigenesis, cytotoxicity, genetics and immunology, etc.
结果从28例实体瘤组织和肿瘤引流淋巴结中获取的TIL前体细胞，26例培养成功，其中23例TIL数量达到治疗数量级；
Results TIL were successfully cultured in 26 out of 28 samples obtained from tumor tissues or tumor draining lymph nodes(TDLN), of which 23 samples reached the number of therapy grade.
目的：观察早期培养的PC 12细胞以了解肿瘤细胞演化过程。
Aim: to observe the proliferating process in early cultured PC12 cells so as to investigate the tumor evolving process.
已经证实在消化道以及大部分神经内分泌肿瘤活检组织和体外培养的细胞株中有sstr尤其是亚型SSTR2的表达。
It is proved that there are SSTRs, especially SSTR2 in digestive duct and neuroendocrine tumor tissue and cell strain cultured in vitro.
运用艾灸血清和小鼠胸腺细胞瘤(EL - 4)进行细胞培养，观察艾灸血清在体外对肿瘤细胞形态、细胞周期及DNA断点的影响。
By culture EL-4 tumor cells with Murine Moxibustion Serum (MS), influence of MS to cell structure, cell cycle and breaking point of DNA was studied.
在这个无血清培养基中，SSV -NIH3T3细胞可以很好地生长，并具有分泌血小板生长因子样生物学活性物质和致裸鼠肿瘤的能力。
In this SFM SSV-NIH3T3 cells grow well, they keep the ability of secreting platelet-derived growth factor-like material into culture medium and causing tumor growth in nude mice.
方法利用体外细胞培养模型，应用MTT法分析姜黄素衍生物对不同肿瘤细胞生长的影响。
METHODS Based on cell culture model in vitro, MTT test was used to study the inhibitory effect of curcumin derivatives on tumor cell lines.
目的为建立肿瘤细胞向腹膜转移的体外侵袭模型，建立改良的人腹膜间皮细胞消化培养法。
Objective To establish a modified enzymatic disaggregation method to isolate human peritoneal mesothelial cells in order to establish a invasion model of peritoneal metastasis in vitro .
上述过程目前只在培养的癌细胞上试验过，但理论上讲，它借助外部光源也适用于人体部位较深的肿瘤的治疗。
In theory, the process, which so far has been studied only in cancer cells grown in culture, could work on tumors located too deep within the body to be reached by an external light source.
为了更为有效地利用该模型小鼠，我们通过原代培养建立了该模型的肿瘤细胞系。
We also established the cell line of this transgenic mice model through primary cell culture to make use this model more efficiently.
本实验目的：本实验进一步研究RH-01对体外培养的人源骨肉瘤HOS细胞和动物移植性肿瘤的抑制作用及特点，并初步探讨其作用机制。
The aim of the exprements is to investigate RH-01's inhibition to HOS cell in vitro and to transplantable tumor in mice, and to discuss basically its mechanism of action.
本文运用不连续密度离心的方法从鼠b 16黑色素瘤体中分离到肿瘤浸润性淋巴细胞(TIL)，并对TIL的体外培养的条件及细胞性质进行了研究。
The separation of tumor-infiltrating lymphocytes (TIL) from tumor mass of B16 melanoma was achieved by discontinuous density gradients centrifugation and the in vitro culture of TIL were investigated.
目的探讨由动员人外周造血祖细胞体外培养扩增获得的树突状细胞(DC)的生物学特性，为临床应用肿瘤树突状细胞疫苗建立制备方法。
Objective to obtain dendritic cells (DCs) from peripheral blood stem cells and hematopoietic precursor cells in vitro, and assess the feasibility of clinical application of tumor vaccine.
目的研究肿瘤细胞不同浓度及不同培养时间与超微弱发光强度之间的关系。
ObjectiveTo study the relation of different concentrations and culture time of esophageal cancer cells with their ultra-weak photon emission intensity.
方法用MTT检恻LHRH-PE40对体外培养的人肿瘤细胞的细胞毒作用，找出敏感肿瘤细胞系。
Methods The cytotoxic activity of LHRH-PE40 to the human tumor cell lines cultured in vitro was detected by MTT method, and sensitive tumor cell lines were selected out.
具有丰富的肿瘤细胞培养经验，能够解决各种细胞培养中出现的问题；
The candidate should be proficient in cell culture and trouble shooting.
然后通过免疫磁性细胞分选技术分离出播散的肿瘤细胞并进行培养，对培养成活的肿瘤细胞在鉴定来源的同时进行生物学活性检测，从细胞学角度判断入血肿瘤细胞形成转移灶的能力。
Secondly, we separated the tumor cells in blood samples by IMS and cultured it carefully, activities of the tumor cells has been tested to confirm their ability to form a successful metastasis.
本文以原代培养的人脐静脉内皮细胞（HUVEC）为材料，研究了肿瘤坏死因子（TNF）对HUVEC的损伤作用及循环内皮细胞（CEC）的形成机制。
The effects of tumor necrosis factor (TNF) on cultured human umbilical vein endothelial cells (HUVEC) and the mechanism of circulating endothelial cell (CEC) formation had been studied.
方法：采用体外培养S180肿瘤细胞为模型，观察肿瘤细胞的增殖、细胞膜上脂肪酸和唾液酸含量的变化，以及细胞膜流动性的改变。
Methods: S180 cell incubated in vitro was used as model. The change of proliferation of S180 cell, fatty acid and sialic acid in membrane and membrane fluidity of S180 cell were investigated.
方法：采用体外细胞培养以及小鼠动物模型，观察spa对培养肿瘤细胞的抑制，及其对小鼠动物模型肿瘤增殖、免疫及白介素1和2产生的影响。
Methods: Using in vitro cell culture and animal model to observe the effects of SPA given by oral administration on tumor proliferation, immune function and the ability of IL1, IL2 secretion.
因此，树突状细胞(DC细胞)递呈肿瘤抗原给共培养的CIK细胞，希望可以增强CIK细胞识别肿瘤的能力以及提高其肿瘤杀伤活性。
Hence, dendritic cells (DC) were cultured and engineered to present tumor antigens to CIK cells hoping that this might enhance the recognition of tumor cells and its subsequent killing.
结论小鼠脾脏细胞体外诱导培养可生成大量功能成熟的DC，为进一步抗肿瘤疫苗的研究奠定了基础。
Conclusion the functional DC could be induced by amplification cultivation mice spleen derived mononuclear cells in vitro. It would be the foundation of further step to produce antitumor vaccine.
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