髓系恶性肿瘤种系DNA分离的穿孔活检皮肤成纤维细胞的标准化培养:一种实用的床边到实验室的方法。

IF 1.1 Q3 BIOLOGY
Parampreet Kour, Nedhi Kumari, Naveen Kaushal, Tanvi Sharma, Shano Naseem, Jogeshwar Binota, Manupdesh Singh Sachdeva, Arihant Jain, Manish Rohilla, Reena Das, Pankaj Malhotra, Pulkit Rastogi
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引用次数: 0

摘要

遗传的种系变异现在被认为是血液髓系恶性肿瘤的重要贡献者,但它们的可靠检测依赖于获得未受污染的种系DNA。在实体瘤中,外周血不含肿瘤细胞,因此可作为种系检测的标准来源。相比之下,外周血通常含有肿瘤或克隆突变细胞在血液恶性肿瘤,使它不可能区分体细胞和种系变异。这一独特的挑战需要使用替代的非造血组织来源来准确评估血液学髓系恶性肿瘤患者的种系。长期以来,从穿孔活检中获得的培养皮肤成纤维细胞一直被认为是这一目的的黄金标准。然而,大多数现有的方案都是针对研究环境进行优化的,缺乏详细的、以患者为中心的日常临床使用工作流程。为了解决这一翻译空白,我们提出了一种强大的、无酶的方案,用于培养常规骨髓手术期间从床边收集的皮肤穿刺活检中提取的真皮成纤维细胞。该方法详细介绍了实用的床边收集、无菌运输、无酶消化的机械解剖、电镀策略、培养扩增和纯度验证的高产DNA分离。通过将这种标准化方法整合到常规血液病理学工作流程中,该方案确保了可靠的生殖细胞材料,将患者不适降到最低,并缩短了适合临床诊断的周转时间。•该方案将床边皮肤穿刺活检与常规骨髓取样相结合,以尽量减少患者的不适,避免额外的侵入性手术。•采用优化的无酶机械解剖方法,去除脂肪,精细切碎,划痕镀孔,减少污染,提高成纤维细胞产量。•它为原代成纤维细胞培养,电镀,扩展和收获提供了一个易于遵循的工作流程,适用于常规血液病理学实验室。•它始终产生高质量的生殖系DNA,不受造血污染,是髓系恶性肿瘤基因检测的理想选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Standardized Culture of Skin Fibroblasts From Punch Biopsies for Germline DNA Isolation in Myeloid Malignancies: A Practical Bedside-to-Laboratory Approach.

Inherited germline variants are now recognized as important contributors to hematologic myeloid malignancies, but their reliable detection depends on obtaining uncontaminated germline DNA. In solid tumors, peripheral blood remains free of tumor cells and therefore serves as a standard source for germline testing. In contrast, peripheral blood often contains neoplastic or clonally mutated cells in hematologic malignancies, making it impossible to distinguish somatic from germline variants. This unique challenge necessitates using an alternative, non-hematopoietic tissue source for accurate germline assessment in patients with hematologic myeloid malignancies. Cultured skin fibroblasts derived from punch biopsies have long been considered the gold standard for this purpose. Nevertheless, most existing protocols are optimized for research settings and lack detailed, patient-centric workflows for routine clinical use. Addressing this translational gap, we present a robust, enzyme-free protocol for culturing dermal fibroblasts from skin punch biopsies collected at the bedside during routine bone marrow procedures. The method details practical bedside collection, sterile transport, mechanical dissection without enzymatic digestion, plating strategy, culture expansion, and high-yield DNA isolation with validated purity. By integrating this standardized approach into routine hematopathology workflows, the protocol ensures reliable germline material with minimal patient discomfort and a turnaround time suitable for clinical diagnostics. Key features • This protocol integrates bedside skin punch biopsy with routine bone marrow sampling to minimize patient discomfort and avoid additional invasive procedures. • It uses an optimized enzyme-free mechanical dissection method with fat removal, fine mincing, and scratched well plating to reduce contamination and improve fibroblast yield. • It provides an easy-to-follow workflow for primary fibroblast culture, plating, expansion, and harvest, suitable for routine hematopathology laboratories. • It consistently yields high-quality germline DNA free of hematopoietic contamination, ideal for genetic testing in myeloid malignancies.

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