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Angiogenesis Factors Associated with New Breast Cancer Cell Line AMJ13 Cultured in Vitro

机译:与体外培养的新乳腺癌细胞系AMJ13相关的血管生成因子

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Background: AMJ13 is a new breast cancer cell line that has been established from a 70-year-old Iraqi woman with a histological diagnosis of infiltrating ductal carcinoma. It is the first for an Iraqi population. In breast cancer, angiogenesis provides the tumor tissue, which is rapidly proliferated with oxygen and nutrients, removes wastes and increases the opportunity of cancer cells to invade other organs. Methods: The AMJ13 breast cancer cell line was represented at three different passages and incubated for interval times. Microarray panel of 43 different angiogenesis markers was used to scan the supernatant for the factors. ELISA was used to quantify some of the important angiogenesis factors released in the culture medium and to confirm absence of those who was not detected by the antibody array. RT-PCR was used to confirm the gene expression (mRNA) of studied factors. Results: Microarray analysis showed that TIMP1 and two secreted at highest levels compared to the rest of the factors with low presence of endostatin. Other non-detectable factors by microarray examined by ELISA assay that showed highest expression level of VEGF-A were obtained at earliest passage, while the highest levels of FGF-b were obtained at late passage. The VEGF-D secretion was shown low concentrations at all studied passages. There is no detectable level of EGF protein in different passages and times interval tested. There are no significant differences in secretion of sICAM between different passages and incubation periods. Conclusion is that AMJ13 cell line depends on VEGF-A as main angiogenesis factor to induce micro-vessels supported by low levels of VEGF-D for lymphatic vessels formation. AMJ13 cell line depends on FGF as growth factors as in late passages it was shifted to depend mainly on FGF completely. All of this process may be regulated by TGF-β. TIMP-1 has proangiogentic effect and has feedback talk with TIMP-2. Understanding the angiogenesis process for breast cancer can give us better targets for therapy and more effective treatments.
机译:背景:AMJ13是一种新的乳腺癌细胞系,由一名70岁的伊拉克妇女建立,具有组织学诊断为浸润性导管癌。这是伊拉克人的第一个。在乳腺癌中,血管生成提供了肿瘤组织,该组织迅速被氧气和营养物质增殖,清除了废物并增加了癌细胞侵袭其他器官的机会。方法:将AMJ13乳腺癌细胞系以三个不同的代数表示,并孵育一段时间。使用43种不同血管生成标记物的微阵列面板扫描上清液中的因子。 ELISA用于量化培养基中释放的一些重要血管生成因子,并确认抗体阵列未检测到的那些因子的缺失。 RT-PCR用于确认所研究因子的基因表达(mRNA)。结果:微阵列分析表明,与其余内皮抑素含量低的因子相比,TIMP1和TIMP1的分泌水平最高。通过ELISA测定法检测的通过微阵列的其他不可检测的因子显示在早期传代中获得最高的VEGF-A表达水平,而在晚期传代中获得最高的FGF-b表达。在所有研究的传代中均显示出低浓度的VEGF-D分泌。在测试的不同传代和时间间隔中没有检测到EGF蛋白水平。在不同传代和潜伏期之间,sICAM的分泌没有显着差异。结论是AMJ13细胞系依赖VEGF-A作为主要的血管生成因子来诱导低水平的VEGF-D支持的微血管形成淋巴管。 AMJ13细胞系依赖FGF作为生长因子,因为在晚期传代过程中,它已转变为完全完全依赖FGF。所有这些过程都可以由TGF-β调节。 TIMP-1具有促血管生成作用,并与TIMP-2有反馈对话。了解乳腺癌的血管生成过程可以为我们提供更好的治疗目标和更有效的治疗方法。

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