The Pq Laboratory of Micro/Nano BiomeDx, Department of Biomedical Engineering, Binghamton University-SUNY, Binghamton, New York, 13902, USA.
, Biotechnology Building, Room 2625, 65 Murray Hill Road, Vestal, New York, 13850, USA.
Protein J. 2021 Feb;40(1):108-118. doi: 10.1007/s10930-020-09949-2. Epub 2021 Jan 2.
Patients with triple-negative breast cancer (TNBC) have a relatively poor prognosis and cannot benefit from endocrine and/or targeted therapy. Considerable effort has been devoted toward the elucidation of the molecular mechanisms and potential diagnostic/therapeutic targets. However, it is inefficient and often ineffective to study the biological nuances of TNBC in large-scale clinical trials. In contrast, the investigation of the association between molecular alterations induced through controlled variables and relevant physiochemical characteristics of TNBC cells in laboratory settings is simple, definite, and efficient in exploring the molecular mechanisms. In this study, microgravity was selected as the sole variable of study as it can inhibit cancer cell viability, proliferation, metastasis, and chemoresistance. Identifying the key molecules that shift cancer cells toward a less aggressive phenotype may facilitate future TNBC studies. We focused on extracellular vesicles (EV) derived from TNBC MDA-MB-231 cells in microgravity, which mediate intercellular communication by transporting signaling molecules between cells. Our results show that in comparison with cells in full gravity, EV release rate decreased in microgravity while average EV size increased. In addition, we found EVs may be superior to cells in analyzing differentially expressed proteins, especially those that are down-regulated ones and usually unidentified or neglected in analysis of intact cellular contents. Proteomic analysis of both EVs and cells further revealed a significant correlation with GTPases and proliferation of MDA-MB-231 cells in microgravity. Altogether, our findings would further inspire in-depth correlative cancer biological studies and subsequent clinical research.
患有三阴性乳腺癌(TNBC)的患者预后相对较差,不能从内分泌和/或靶向治疗中获益。人们已经投入了相当大的努力来阐明分子机制和潜在的诊断/治疗靶点。然而,在大规模临床试验中研究 TNBC 的生物学细微差别效率低下且往往效果不佳。相比之下,在实验室环境中研究通过控制变量诱导的分子改变与 TNBC 细胞相关的物理化学特征之间的关联既简单又明确,并且在探索分子机制方面非常有效。在这项研究中,选择微重力作为唯一的研究变量,因为它可以抑制癌细胞的活力、增殖、转移和化疗耐药性。确定使癌细胞向侵袭性较弱表型转变的关键分子可能有助于未来的 TNBC 研究。我们专注于源自 TNBC MDA-MB-231 细胞的在微重力条件下的细胞外囊泡(EV),它们通过在细胞之间运输信号分子来介导细胞间通讯。我们的结果表明,与在完全重力下的细胞相比,微重力下 EV 的释放速率降低,而平均 EV 尺寸增加。此外,我们发现 EV 可能优于细胞,在分析差异表达蛋白方面,尤其是那些在分析完整细胞内容物时通常未被识别或被忽视的下调蛋白。EV 和细胞的蛋白质组学分析进一步揭示了与微重力下 MDA-MB-231 细胞中的 GTPases 和增殖的显著相关性。总之,我们的发现将进一步激发深入的相关癌症生物学研究和随后的临床研究。