食管癌干细胞(ECSCs)在裸鼠异种移植模型中的致瘤性

Ayyoob Khosravi, Fariba Kokabi, R. Behzadi, J. Asadi
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引用次数: 1

摘要

Jahanbakhsh Asadi, Golestan医科大学代谢紊乱研究中心,Gorgan,伊朗dr.asadi@goums.ac.ir摘要背景和目的:体内癌症建模是研究癌症发病机制和参与癌症进展的分子机制的重要工具。实验小鼠是在体内重建人类癌症最常用的动物。肿瘤干细胞(Cancer stem cells, CSCs)是肿瘤复发和转移导致治疗失败的主要原因。分离癌症干细胞有助于我们研究它们的功能和行为。在本研究中,我们使用球形成法分离肿瘤干细胞,然后在异种移植肿瘤模型中研究其致瘤性。方法:采用低贴壁培养皿无血清培养基(SFM)培养YM1癌细胞,富集肿瘤干细胞。将含有肿瘤干细胞样细胞的球体分离成单细胞,并注射到B6裸鼠背侧。结果:注射后数日皮下形成肿瘤。用每周记录的肿瘤长度绘制肿瘤的生长曲线。测量肿瘤的体积和重量。所产生的肿瘤大小与注射的细胞数量相适应。病理分析证实肿瘤起源于食道。结论:实验室小鼠模型为研究人类肿瘤的体内发病机制提供了一种实用的建模系统。
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Tumorigenicity of Esophageal Cancer Stem Cells (ECSCs) in nude mouse xenograft model
Jahanbakhsh Asadi, Metabolic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran dr.asadi@goums.ac.ir Abstract Background and objectives: Modeling cancer in vivo is a very important tool to investigate cancer pathogenesis and molecular mechanisms involved in cancer progression. Laboratory mice are the most common animal used for rebuilding human cancer in vivo. Cancer stem cells (CSCs) are the main reason of failure in cancer therapy because of tumor relapse and metastasis. Isolation of cancer stem cells helps us to study their function and behavior. In the current study we separate cancer stem-like cells using sphere formation assay then investigate their tumorigenicity in xenograft tumor model. Methods: YM1 cancer cells were cultured in serum-free media (SFM) in low adherent culture dishes for enrichment of cancer stem cells. The resulting spheres containing cancer stem-like cells were dissociated into single cells and were injected into the dorsal flank of B6 nude mice. Results: A few days after injection, subcutaneous tumors formed. The growth curves of the resulting tumors were plotted using their weekly recorded lengths. The tumors' volume and weight were measured. The size of resulting tumors was appropriate to the number of cells injected. Pathological analysis confirmed esophageal origin of the resulting tumors. Conclusion: Using laboratory mice models is a practical modeling system that provides us investigation of human tumors pathogenesis in vivo.
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