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基于核形态学评估微管靶向药物单药治疗或与溶瘤病毒联合治疗诱导的细胞命运

Nuclear Morphology-Based Assessment of Cell Fates Induced by a Microtubule Targeting Agent as a Single Treatment or Combined with an Oncolytic Virus.

作者信息

De Sucheta, Ehrlich Marcelo

机构信息

Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.

出版信息

Methods Mol Biol. 2025;2926:91-100. doi: 10.1007/978-1-0716-4542-0_8.

Abstract

Immunofluorescence microscopy allows for the quantitative assessment of cell fate at single-cell resolution. This is required to analyze heterogeneous cell populations, as the assessment of average values of given parameters does not faithfully describe distinct states of specific subpopulations. As a case in point, we describe a methodology for characterizing the effects of a microtubule targeting agent, 2-methoxestradiol (2ME2), on T24 human bladder cancer cells. We employ an immunofluorescence-based assessment of nuclear morphology, DNA content, and the intracellular distribution pattern of microtubules for the identification/classification of cells undergoing mitosis or mitotic slippage. When combined with imaging-based identification of cells expressing a nonstructural oncolytic virus protein, this approach enables the assessment of the potential for combined treatment with a microtubule targeting agent and an oncolytic virus (e.g., the Epizootic Hemorrhagic Disease Virus-Tel Aviv University, EHDV-TAU).

摘要

免疫荧光显微镜能够在单细胞分辨率下对细胞命运进行定量评估。这对于分析异质性细胞群体是必要的,因为给定参数的平均值评估并不能如实描述特定亚群的不同状态。作为一个例子,我们描述了一种方法,用于表征微管靶向剂2-甲氧基雌二醇(2ME2)对T24人膀胱癌细胞的影响。我们采用基于免疫荧光的方法评估核形态、DNA含量以及微管的细胞内分布模式,以识别/分类经历有丝分裂或有丝分裂滑脱的细胞。当与基于成像的表达非结构溶瘤病毒蛋白的细胞识别相结合时,这种方法能够评估微管靶向剂与溶瘤病毒(例如,流行性出血病病毒-特拉维夫大学,EHDV-TAU)联合治疗的潜力。

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