Hu Mingchao, Li Cheng, Wang Zhili, Ding Pi, Pei Renjun, Wang Qiang, Xu Hua, Xing Chungen
Department of Gastrointestinal Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
School of Nano-Tech and Nano-Bionics, University of Science and Technology of China, Hefei, China.
Front Bioeng Biotechnol. 2022 Feb 7;10:806238. doi: 10.3389/fbioe.2022.806238. eCollection 2022.
Circulating tumor cells (CTCs) have been well-established as promising biomarkers that can be leveraged to gauge the prognosis of patients with cancers and to guide patient treatment efforts. Although the scarcity of CTCs within peripheral circulation and the associated phenotypic changes that they exhibit owing to the epithelial-mesenchymal transition (EMT) process make the reliable isolation of these cells very challenging. Recently, several studies have discussed platforms capable of mediating the efficient and sensitive isolation of CTCs, but these approaches are nonetheless subject to certain limitations that preclude their clinical application. For example, these platforms are poorly-suited to minimizing damage in the context of cellular capture and release or the culture of captured cells for subsequent molecular analyses, which would better enable clinicians to select appropriate precision treatments on an individualized basis. In this study, we report the layer-by-layer assembly approach to synthesize a novel composite nanomaterial consisting of modified zirconium-based metal-organic-frameworks (MOFs) on the surface of magnetic beads with dual antibody surface modifications capable of capturing CTCs without being hampered by the state of cellular EMT process. Our analyses indicated that these dual antibody-modified nanomaterials exhibited greater capture efficiency than that observed for single antibody. Importantly, captured cells can be gradually released following capture and undergo subsequent proliferation following water molecule-induced MOF structural collapse. This release mechanism, which does not require operator intervention, may be effective as a means of minimizing damage and preserving cellular viability such that cells can be more reliably utilized for downstream molecular analyses and associated treatment planning. To further confirm the potential clinical applicability of the developed nanomaterial, it was successfully utilized for capturing CTCs from peripheral blood samples collected from cases diagnosed with gastrointestinal tumors.
循环肿瘤细胞(CTCs)已被确认为很有前景的生物标志物,可用于评估癌症患者的预后并指导患者的治疗工作。尽管外周血中CTCs数量稀少,且由于上皮-间质转化(EMT)过程而表现出相关的表型变化,使得可靠分离这些细胞极具挑战性。最近,多项研究讨论了能够介导高效、灵敏分离CTCs的平台,但这些方法仍存在某些局限性,阻碍了它们的临床应用。例如,这些平台不太适合在细胞捕获和释放过程中或捕获细胞用于后续分子分析的培养过程中尽量减少损伤,而这将更有助于临床医生根据个体情况选择合适的精准治疗方法。在本研究中,我们报告了一种逐层组装方法,以合成一种新型复合纳米材料,该材料由磁性微珠表面修饰的改性锆基金属有机框架(MOFs)组成,具有双抗体表面修饰,能够捕获CTCs,且不受细胞EMT过程状态的阻碍。我们的分析表明,这些双抗体修饰的纳米材料比单抗体表现出更高的捕获效率。重要的是,捕获的细胞在捕获后可逐渐释放,并在水分子诱导的MOF结构坍塌后进行后续增殖。这种释放机制无需操作人员干预,可能有效地减少损伤并保持细胞活力,从而使细胞能更可靠地用于下游分子分析和相关治疗规划。为进一步证实所开发纳米材料的潜在临床适用性,它被成功用于从胃肠道肿瘤确诊病例采集的外周血样本中捕获CTCs。