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肾癌细胞系的集落、悬滴和甲基纤维素三维缺氧生长优化

Colony, hanging drop, and methylcellulose three dimensional hypoxic growth optimization of renal cell carcinoma cell lines.

作者信息

Matak Damian, Brodaczewska Klaudia K, Lipiec Monika, Szymanski Łukasz, Szczylik Cezary, Czarnecka Anna M

机构信息

Laboratory of Molecular Oncology, Department of Oncology, Military Institute of Medicine, Szaserow 128, 04-141, Warsaw, Poland.

School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.

出版信息

Cytotechnology. 2017 Aug;69(4):565-578. doi: 10.1007/s10616-016-0063-2. Epub 2017 Mar 20.

Abstract

Renal cell carcinoma (RCC) is the most lethal of the common urologic malignancies, comprising 3% of all human neoplasms, and the incidence of kidney cancer is rising annually. We need new approaches to target tumor cells that are resistant to current therapies and that give rise to recurrence and treatment failure. In this study, we focused on low oxygen tension and three-dimensional (3D) cell culture incorporation to develop a new RCC growth model. We used the hanging drop and colony formation methods, which are common in 3D culture, as well as a unique methylcellulose (MC) method. For the experiments, we used human primary RCC cell lines, metastatic RCC cell lines, human kidney cancer stem cells, and human healthy epithelial cells. In the hanging drop assay, we verified the potential of various cell lines to create solid aggregates in hypoxic and normoxic conditions. With the semi-soft agar method, we also determined the ability of various cell lines to create colonies under different oxygen conditions. Different cell behavior observed in the MC method versus the hanging drop and colony formation assays suggests that these three assays may be useful to test various cell properties. However, MC seems to be a particularly valuable alternative for 3D cell culture, as its higher efficiency of aggregate formation and serum independency are of interest in different areas of cancer biology.

摘要

肾细胞癌(RCC)是常见泌尿外科恶性肿瘤中致死率最高的,占所有人类肿瘤的3%,且肾癌的发病率每年都在上升。我们需要新的方法来靶向那些对当前疗法耐药、会导致复发和治疗失败的肿瘤细胞。在本研究中,我们聚焦于低氧张力和三维(3D)细胞培养整合,以开发一种新的肾细胞癌生长模型。我们使用了3D培养中常见的悬滴法和集落形成法,以及一种独特的甲基纤维素(MC)法。在实验中,我们使用了人原发性肾细胞癌细胞系、转移性肾细胞癌细胞系、人肾癌干细胞和人健康上皮细胞。在悬滴试验中,我们验证了各种细胞系在低氧和常氧条件下形成固体聚集体的潜力。通过半软琼脂法,我们还确定了各种细胞系在不同氧气条件下形成集落的能力。在MC法与悬滴法和集落形成试验中观察到的不同细胞行为表明,这三种试验可能有助于测试各种细胞特性。然而,MC似乎是3D细胞培养特别有价值的替代方法,因为其更高的聚集体形成效率和血清非依赖性在癌症生物学的不同领域都受到关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6f3/5507837/592176bc9408/10616_2016_63_Fig1_HTML.jpg

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