Arora Smriti, D'Souza Alain, Aland Gourishankar, Kale Narendra, Jadhav Bhagwat, Kad Trupti, Chaturvedi Pankaj, Singh Balram, Khandare Jayant
Actorius Innovations and Research, Pune, 411057, India.
OneCell Diagnostics, Pune, 411057, India.
Lab Chip. 2022 Apr 12;22(8):1519-1530. doi: 10.1039/d2lc00004k.
Circulating tumor cells (CTCs) are distinct cancer biomarkers established in clinical settings for early cancer detection, metastasis progression, and minimal residual disease (MRD) monitoring. Despite numerous advances, the comprehensive molecular characterization of CTCs is extremely challenging owing to their rarity and heterogeneity. Here, we present a novel cotton microfluidic substrate (CMS) as an innovative biomedical matrix that efficiently isolates CTCs while facilitating CTC expansion to enable a further downstream analysis of these rare cells. CMS enabled static and dynamic isolation of cells from the MCF-7 cancer cell line, as well as from head and neck squamous cell carcinoma (HNSCC) patients' blood and the cell capture efficiencies were further compared with a clinically regulated OncoDiscover® Liquid Biopsy Test. Further, CMS acted as a matrix on which the captured cancer cells were grown in 3D tumor models for studying anti-cancer drug efficacy and multi-drug resistance (MDR) mechanisms. The design of the CMS employed two different surface chemistries, flattened and nanostructured surfaces, each conjugated to anti-EpCAM antibodies to evaluate the CTC capture efficiency and 3D tumor growth dynamics. The nanostructured surface was highly efficient for capturing CTCs and promoted 3D tumor spheroid formation with a 5-fold increase in size from day 03 to day 10 of culture. Moreover, when treated with an anti-cancer drug, cisplatin, an almost 1/2 reduction in tumor size was achieved within 24 hours, followed by a cytostatic threshold and eventual acquisition of drug resistance within 3 days. Conclusively, the CMS matrix exhibits potential for further development of "tissue on chip" and "point-of-care" medical devices in cancer diagnostics, and chemo-therapeutic efficacy evaluations in both drug discovery and development.
循环肿瘤细胞(CTCs)是在临床环境中确立的独特癌症生物标志物,用于早期癌症检测、转移进展监测和微小残留病(MRD)监测。尽管取得了诸多进展,但由于CTCs的稀有性和异质性,对其进行全面的分子表征极具挑战性。在此,我们展示了一种新型棉花微流控基质(CMS),作为一种创新的生物医学基质,它能有效分离CTCs,同时促进CTCs扩增,以便对这些稀有细胞进行进一步的下游分析。CMS能够从MCF-7癌细胞系以及头颈部鳞状细胞癌(HNSCC)患者的血液中静态和动态分离细胞,并将细胞捕获效率与临床规范的OncoDiscover®液体活检测试进行了进一步比较。此外,CMS作为一种基质,捕获的癌细胞可在其上生长成三维肿瘤模型,用于研究抗癌药物疗效和多药耐药(MDR)机制。CMS的设计采用了两种不同的表面化学性质,即扁平表面和纳米结构表面,每种表面都与抗EpCAM抗体偶联,以评估CTCs捕获效率和三维肿瘤生长动力学。纳米结构表面在捕获CTCs方面效率极高,并促进了三维肿瘤球体的形成,从培养第3天到第10天,其大小增加了5倍。此外,用抗癌药物顺铂处理后,在24小时内肿瘤大小几乎缩小了1/2,随后出现细胞生长抑制阈值,并在3天内最终获得耐药性。总之,CMS基质在癌症诊断以及药物发现和开发中的化疗疗效评估方面,展现出了进一步开发“芯片上的组织”和“即时护理”医疗设备的潜力。