Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO, USA.
Department of Biomedical Engineering, Washington University, St. Louis, MO, USA.
Leuk Lymphoma. 2021 Oct;62(10):2457-2465. doi: 10.1080/10428194.2021.1919657. Epub 2021 May 17.
Chronic myeloid leukemia (CML), acute myeloid leukemia (AML), and chronic lymphocytic leukemia (CLL) are hematological malignancies that remain incurable despite novel treatments. In order to improve current treatments and clinical efficacy, there remains a need for more complex models that mimic the intricate human leukemic microenvironment. This study aimed to use 3D tissue engineered plasma cultures (3DTEPC) derived from CML, AML and CLL patients to promote proliferation of leukemic cells for use as a drug screening tool for treatment. 3DTEPC supported the growth of primary CML, AML and CLL cells and also induced significantly more drug resistance in CML, AML and CLL cell lines compared to 2D. The 3DTEPC created a more physiologically relevant environment for leukemia cell proliferation, provided a reliable model for growing leukemia patient samples, and serves as a relevant tool for drug screening and personalized medicine.
慢性髓性白血病 (CML)、急性髓系白血病 (AML) 和慢性淋巴细胞白血病 (CLL) 是血液系统恶性肿瘤,尽管有新的治疗方法,但仍无法治愈。为了改善目前的治疗方法和临床疗效,仍然需要更复杂的模型来模拟复杂的人类白血病微环境。本研究旨在使用源自 CML、AML 和 CLL 患者的 3D 组织工程血浆培养物 (3DTEPC) 促进白血病细胞的增殖,用作治疗药物筛选工具。3DTEPC 支持原发性 CML、AML 和 CLL 细胞的生长,并且与 2D 相比,还显著诱导 CML、AML 和 CLL 细胞系产生更多的耐药性。3DTEPC 为白血病细胞增殖创造了更接近生理的环境,为白血病患者样本的生长提供了可靠的模型,并可作为药物筛选和个性化医疗的相关工具。