Laboratory of Molecular Oncology, ICMR-National Institute of Pathology, Safdarjung Hospital Campus, New Delhi, 110029, India.
Jamia Hamdard-Institute of Molecular Medicine, Jamia Hamdard, New Delhi, 110062, India.
Sci Rep. 2021 Dec 7;11(1):23554. doi: 10.1038/s41598-021-02923-7.
Gallbladder carcinoma (GBC) is a major cancer of the gastrointestinal tract with poor prognosis. Reliable and affordable biomarker-based assays with high sensitivity and specificity for the detection of this cancer are a clinical need. With the aim of studying the potential of the plasma-derived extracellular vesicles (EVs), we carried out quantitative proteomic analysis of the EV proteins, using three types of controls and various stages of the disease, which led to the identification of 86 proteins with altered abundance. These include 29 proteins unique to early stage, 44 unique to the advanced stage and 13 proteins being common to both the stages. Many proteins are functionally relevant to the tumor condition or have been also known to be differentially expressed in GBC tissues. Several of them are also present in the plasma in free state. Clinical verification of three tumor-associated proteins with elevated levels in comparison to all the three control types-5'-nucleotidase isoform 2 (NT5E), aminopeptidase N (ANPEP) and neprilysin (MME) was carried out using individual plasma samples from early or advanced stage GBC. Sensitivity and specificity assessment based on receiver operating characteristic (ROC) analysis indicated a significant association of NT5E and ANPEP with advanced stage GBC and MME with early stage GBC. These and other proteins identified in the study may be potentially useful for developing new diagnostics for GBC.
胆囊癌 (GBC) 是一种预后较差的胃肠道主要癌症。可靠且经济实惠的基于生物标志物的检测方法,具有高灵敏度和特异性,可用于检测这种癌症,这是临床的需求。为了研究血浆来源的细胞外囊泡 (EVs) 的潜力,我们使用三种类型的对照和不同疾病阶段,对 EV 蛋白进行了定量蛋白质组学分析,这导致鉴定出 86 种丰度改变的蛋白质。其中包括 29 种仅存在于早期阶段的蛋白质、44 种仅存在于晚期阶段的蛋白质和 13 种存在于两个阶段的蛋白质。许多蛋白质与肿瘤状况具有功能相关性,或者在 GBC 组织中也被证明存在差异表达。其中一些也以游离状态存在于血浆中。与所有三种对照类型相比,三种肿瘤相关蛋白(5'-核苷酸酶同工酶 2 (NT5E)、氨肽酶 N (ANPEP) 和脑啡肽酶 (MME))在个体血浆样本中的水平升高,对其进行了临床验证。基于接受者操作特征 (ROC) 分析的灵敏度和特异性评估表明,NT5E 和 ANPEP 与晚期 GBC 显著相关,而 MME 与早期 GBC 显著相关。该研究中鉴定出的这些和其他蛋白质可能对开发新的 GBC 诊断方法具有潜在的用途。