He Gan, Wang Weixuan, Zhou Yongxia, Zhao Guowei, Liao Juan
Gastrointestinal Surgery, Yongchuan Hospital of Chongqing Medical University, Chongqing, China.
Institute of Life Sciences, Chongqing Medical University, Chongqing, China.
Front Oncol. 2024 May 8;14:1397680. doi: 10.3389/fonc.2024.1397680. eCollection 2024.
For liquid biopsy of cancer, the extraction of circulating cell-free DNA (cfDNA) from plasma is required. We evaluated the efficacy of use of magnetic submicron particles coated with abundant small zwitterions (MSP-ZEWBs) for extracting short fragments of cfDNA.
We developed and optimized an MSP-ZEWB-based cfDNA extraction method using ampholytic ion-exchange materials and compared its results with those using a control kit. We measured the cfDNA concentration by quantitative polymerase-chain-reaction and using the Qubit method and analyzed cfDNA fragmentation patterns using a bioanalyzer.
The fragment size of cfDNA isolated from glycine hydrochloric acid at a pH of 2.2 exhibited a better alignment with the DNA marker. The highest DNA intensity was observed at the final concentration of 0.8% polyethylene glycol 8000. The intensity of cfDNA decreased significantly when isolated from plasma with DNA marker using MSP-ZEWBs with an adsorption buffer containing guanidine hydrochloride or isothiocyanoguanidine. All fragments were successfully extracted using MSP-ZEWBs from both plasma and phosphate-buffered saline. Notably, the intensity of short cfDNA fragments isolated using MSP-ZEWBs remained consistent for recovery of long DNA fragments. indicating a potential selective of small fragments.
The extraction of plasma cfDNA with MSP-ZEWBs requires no protein denaturation, shows resistance to cells remaining in plasma, and demonstrates higher overall efficiency and better reproducibility than other extraction methods. Use of MSP-ZEWBs may greatly enhance liquid biopsy of cancers through the analysis of plasma cfDNA in clinical practice.
对于癌症的液体活检,需要从血浆中提取循环游离DNA(cfDNA)。我们评估了使用涂覆有大量小两性离子的磁性亚微米颗粒(MSP-ZEWB)提取cfDNA短片段的效果。
我们开发并优化了一种基于MSP-ZEWB的cfDNA提取方法,该方法使用两性离子交换材料,并将其结果与使用对照试剂盒的结果进行比较。我们通过定量聚合酶链反应和Qubit方法测量cfDNA浓度,并使用生物分析仪分析cfDNA片段化模式。
在pH为2.2的甘氨酸盐酸中分离出的cfDNA片段大小与DNA标记物的匹配度更好。在最终浓度为0.8%的聚乙二醇8000时观察到最高的DNA强度。当使用含有盐酸胍或异硫氰酸胍的吸附缓冲液的MSP-ZEWB从含有DNA标记物的血浆中分离时,cfDNA的强度显著降低。使用MSP-ZEWB从血浆和磷酸盐缓冲盐水中均成功提取了所有片段。值得注意的是,使用MSP-ZEWB分离的短cfDNA片段的强度在回收长DNA片段时保持一致,表明对小片段具有潜在的选择性。
使用MSP-ZEWB提取血浆cfDNA无需蛋白质变性,对血浆中残留的细胞具有抗性,并且与其他提取方法相比具有更高的整体效率和更好的重现性。在临床实践中,通过分析血浆cfDNA,使用MSP-ZEWB可能会大大增强癌症的液体活检。