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黄芪多糖抑制黑色素瘤干细胞自我更新的实验研究 被引量:5
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作者 杨敏 王元花 程晓东 《中华中医药学刊》 CAS 北大核心 2021年第3期96-101,I0017,I0018,共8页
目的观察黄芪多糖对黑色素瘤干细胞自我更新的作用,并探究了其可能的分子机制。方法采用无血清培养的方法从人源A375及鼠源B16F10黑色素瘤细胞中诱导黑色素瘤干细胞,建立黑色素瘤干细胞体外培养体系,通过二次球落形成实验探讨黄芪多糖... 目的观察黄芪多糖对黑色素瘤干细胞自我更新的作用,并探究了其可能的分子机制。方法采用无血清培养的方法从人源A375及鼠源B16F10黑色素瘤细胞中诱导黑色素瘤干细胞,建立黑色素瘤干细胞体外培养体系,通过二次球落形成实验探讨黄芪多糖对黑色素瘤干细胞自我更新的作用,荧光定量PCR及蛋白质免疫印迹法检测黄芪多糖对黑色素瘤干细胞表面标志物ALDH1A3及核转录因子SOX2、OCT4、Nanog在mRNA及蛋白水平的表达情况。结果在无血清培养法培养的黑色素瘤干细胞球落中,黑色素瘤干细胞表面标志物ALDH1A3及核转录因子SOX2、OCT4、Nanog在mRNA及蛋白水平表达增高,表明本研究成功的建立了黑色素瘤干细胞的体外培养体系。用黄芪多糖作用于黑色素瘤干细胞后,二次球落形成实验发现黄芪多糖可以抑制黑色素瘤干细胞的球落形成数量及体积。荧光定量PCR及蛋白质免疫印迹法显示:与对照组相比,黄芪多糖可降低黑色素瘤干细胞表面标志物ALDH1A3及核转录因子SOX2、OCT4、Nanog在mRNA及蛋白水平的表达。结论黄芪多糖可抑制黑色素瘤干细胞的自我更新,其作用机制可能与下调ALDH1A3、SOX2、OCT4、Nanog的表达有关。 展开更多
关键词 黄芪多糖 黑色素瘤干细胞 自我更新
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Nestin in gastrointestinal and other cancers: Effects on cells and tumor angiogenesis 被引量:11
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作者 Toshiyuki Ishiwata Yoko Matsuda Zenya Naito 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第4期409-418,共10页
Nestin is a class Ⅵ intermediate filament protein that was originally described as a neuronal stem cell marker during central nervous system (CNS) development, and is currently widely used in that capacity. Nestin is... Nestin is a class Ⅵ intermediate filament protein that was originally described as a neuronal stem cell marker during central nervous system (CNS) development, and is currently widely used in that capacity. Nestin is also expressed in non-neuronal immature or progenitor cells in normal tissues. Under pathological conditions, nestin is expressed in repair processes in the CNS, muscle, liver, and infarcted myocardium. Furthermore, increased nestin expression has been reported in various tumor cells, including CNS tumors, gastrointestinal stromal tumors, pancreatic cancer, prostate cancer, breast cancer, malignant melanoma, dermatofibrosarcoma protuberances, and thyroid tumors. Nestin is reported to correlate with aggressive growth, metastasis, and poor prognosis in some tumors; however, the roles of nestin in cancer cells have not been well characterized. Furthermore, nestin is more specifically expressed in proliferating small-sized tumor vessels in glioblastoma and gastric, colorectal, and prostate cancers than are other tumor vessel markers. These findings indicate that nestin may be a marker for newly synthesized tumor vessels and a therapeutic target for tumor angiogenesis. It has received a lot of attention recently as a cancer stem cell marker in various cancer cells including brain tumors, malignant rhabdoid tumors, and uterine, cervical, prostate, bladder, head and neck, ovarian, testicular, and pancreatic cancers. The purpose of this review is to clarify the roles of nestin in cancer cells and in tumor angiogenesis, and to examine the association between nestin and cancer stem cells. Nestin has the potential to serve as a molecular target for cancers with nestin-positive cancer cells and nestin-positive tumor vasculature. 展开更多
关键词 Cancer growth Intermediate filament protein Cancer invasion Tumor migration NESTIN Stem cell marker Tumor angiogenesis
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Science Letters:Brain metastases of melanoma-mechanisms of attack on their defence system by engineered stem cells in the microenvironment
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作者 DIMITROV Borislav D. ATANASSOVA Penka A. RACHKOVA Mariana I. 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2007年第9期609-611,共3页
This report gives a better emphasis on the role of targeted effectors (e.g. a combination of 5-FC with CD-NSPCs as compared to the application of NSPCs alone) and how such delivery of pro-drug activating enzymes and o... This report gives a better emphasis on the role of targeted effectors (e.g. a combination of 5-FC with CD-NSPCs as compared to the application of NSPCs alone) and how such delivery of pro-drug activating enzymes and other tumor-killing substances may overcome melanocytic defence system, interact with and promote the host defence and immune response modulations not only in melanoma but, potentially, in other highly-metastatic cancers. 展开更多
关键词 MELANOMA Brain metastases Neural stem/progenitor cells (NSPCs) Cytosine deaminase
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