IRCCS SYNLAB SDN, Via E. Gianturco 113, 80143 Naples, Italy.
Institute for Experimental Endocrinology and Oncology (IEOS), National Research Council (CNR), Via Pansini 5, 80131 Naples, Italy.
Int J Mol Sci. 2022 Apr 3;23(7):3989. doi: 10.3390/ijms23073989.
Extracellular vesicles (EVs) shuttle proteins, RNA, DNA, and lipids crucial for cell-to-cell communication. Recent findings have highlighted that EVs, by virtue of their cargo, may also contribute to breast cancer (BC) growth and metastatic dissemination. Indeed, EVs are gaining great interest as non-invasive cancer biomarkers. However, little is known about the biological and physical properties of EVs from malignant BC lesions, and even less is understood about EVs from non-malignant lesions, such as breast fibroadenoma (FAD), which are clinically managed using conservative approaches. Thus, for this pilot study, we attempted to purify and explore the proteomic profiles of EVs from benign breast lesions, HER2+ BCs, triple-negative BCs (TNBCs), and continuous BC cell lines (i.e., BT-549, MCF-10A, and MDA-MB-231), combining experimental and semi-quantitative approaches. Of note, proteome-wide analyses showed 49 common proteins across EVs harvested from FAD, HER2+ BCs, TNBCs, and model BC lines. This is the first feasibility study evaluating the physicochemical composition and proteome of EVs from benign breast cells and primary and immortalized BC cells. Our preliminary results hold promise for possible implications in precision medicine for BC.
细胞外囊泡 (EVs) 可转运蛋白质、RNA、DNA 和脂质,这些对于细胞间通讯至关重要。最近的研究结果强调,EVs 凭借其携带的货物,也可能促进乳腺癌 (BC) 的生长和转移扩散。事实上,EVs 作为非侵入性癌症生物标志物引起了广泛关注。然而,人们对源自恶性 BC 病变的 EVs 的生物学和物理特性知之甚少,对于源自非恶性病变(如乳腺纤维腺瘤 [FAD])的 EVs 更是知之甚少,因为 FAD 采用保守方法进行临床治疗。因此,在这项初步研究中,我们尝试通过实验和半定量方法,从良性乳腺病变、HER2+ BC、三阴性 BC (TNBC) 和连续 BC 细胞系(即 BT-549、MCF-10A 和 MDA-MB-231)中纯化和探索 EV 的蛋白质组学特征。值得注意的是,蛋白质组学分析显示,源自 FAD、HER2+ BC、TNBC 和模型 BC 细胞系的 EVs 中有 49 种共同蛋白。这是第一项评估良性乳腺细胞以及原发性和永生化 BC 细胞的 EVs 的理化组成和蛋白质组学的可行性研究。我们的初步结果为 BC 的精准医学可能产生的影响提供了希望。