一种分离恶性胸腔积液cd45阳性和cd45阴性细胞的新方法

Jimin Choi, Jeong Uk Lim, Wooil Kim, Dong Woo Lee, S. Kwon, Sang-Hyun Lee
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摘要

背景:患者来源的恶性胸腔积液(MPE)样本可用于确定患者特异性药物组合,因为MPE样本容易获得且成本低廉的肿瘤细胞来源。然而,从MPE中分离靶癌细胞的效率一直很低,因为MPE样本包含免疫细胞、非癌细胞和癌细胞的复杂混合物。因此,需要开发新的方法来有效地从MPE样品中分离出可用于三维(3D)细胞培养的靶癌细胞。患者来源的体外3D肿瘤模型有望促进更精确的药物治疗。方法:经既往诊断为肺腺癌的患者同意,MPE样本从韩国天主教大学首尔圣玛丽医院获得。我们使用两种不同的percol -梯度离心方法从MPE样品中分离靶细胞。结果:与传统的44%和67% percol梯度离心法相比,40%和75% percol梯度离心法能更清晰地分离cd45阳性(CD45pos)和cd45阴性(CD45neg)细胞。结论:我们的研究结果强烈表明,40%和75% percol -梯度离心方法比先前描述的percol -梯度离心方法更适用于CD45pos或CD45neg细胞的分离。此外,我们的新方法可用于分离mpe衍生的靶癌细胞,这些癌细胞可用于构建体外患者特异性3D肿瘤模型。
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A novel method for the isolation of CD45-positive and CD45-negative cells from malignant pleural effusion
Background: Patient-derived malignant pleural effusion (MPE) samples can be used to identify a patient-specific drug combination since MPE samples are readily available and cost-effective tumor cell sources. However, the isolation of target cancer cells from MPE has been inefficient because MPE samples contain a complex mixture of immune cells, non-cancerous cells, and cancer cells. Hence, new methods need to be developed to effectively isolate target cancer cells from MPE samples that can be used for 3-dimensional (3D) cell culture. Patient-derived in vitro 3D tumor models are expected to facilitate more precise drug treatment.Methods: MPE samples were obtained from Seoul St. Mary’s Hospital, The Catholic University of Korea with consent from patients previously diagnosed with lung adenocarcinoma. We isolated target cells from MPE samples using 2 different Percoll-gradient centrifugation methods.Results: The use of 40% and 75% Percoll-gradient centrifugation led to a clearer separation of CD45-positive (CD45pos) and CD45-negative (CD45neg) cells than the traditional 44% and 67% Percoll-gradient centrifugation method.Conclusion: Our findings strongly suggest that the 40% and 75% Percoll-gradient centrifugation method is more useful for the isolation of CD45pos or CD45neg cells than the previously described Percoll-gradient centrifugation method. Furthermore, our novel method was useful for the isolation of MPE-derived target cancer cells that can be used to construct in vitro patient-specific 3D tumor models.
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