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癌症存在和治疗对血小板蛋白质组的影响。

Effects of Cancer Presence and Therapy on the Platelet Proteome.

机构信息

Amsterdam UMC, Cancer Center Amsterdam, Vrije Universiteit Amsterdam, Medical Oncology, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands.

Cardiovascular Research Institute Maastricht, Department of Physiology, Maastricht University Medical Center, 6229 ER Maastricht, The Netherlands.

出版信息

Int J Mol Sci. 2021 Jul 30;22(15):8236. doi: 10.3390/ijms22158236.

DOI:10.3390/ijms22158236
PMID:34361002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8347210/
Abstract

Platelets are involved in tumor angiogenesis and cancer progression. Previous studies indicated that cancer could affect platelet content. In the current study, we investigated whether cancer-associated proteins can be discerned in the platelets of cancer patients, and whether antitumor treatment may affect the platelet proteome. Platelets were isolated from nine patients with different cancer types and ten healthy volunteers. From three patients, platelets were isolated before and after the start of antitumor treatment. Mass spectrometry-based proteomics of gel-fractionated platelet proteins were used to compare patients versus controls and before and after treatment initiation. A total of 4059 proteins were detected, of which 50 were significantly more abundant in patients, and 36 more in healthy volunteers. Eight of these proteins overlapped with our previous cancer platelet proteomics study. From these data, we selected potential biomarkers of cancer including six upregulated proteins (RNF213, CTSG, PGLYRP1, RPL8, S100A8, S100A9) and two downregulated proteins (GPX1, TNS1). Antitumor treatment resulted in increased levels of 432 proteins and decreased levels of 189 proteins. In conclusion, the platelet proteome may be affected in cancer patients and platelets are a potential source of cancer biomarkers. In addition, we found in a small group of patients that anticancer treatment significantly changes the platelet proteome.

摘要

血小板参与肿瘤血管生成和癌症进展。先前的研究表明,癌症可能会影响血小板含量。在本研究中,我们研究了癌症患者的血小板中是否可以识别出与癌症相关的蛋白质,以及抗肿瘤治疗是否会影响血小板蛋白质组。从 9 名患有不同癌症类型的患者和 10 名健康志愿者中分离血小板。从 3 名患者中,在开始抗肿瘤治疗之前和之后分离血小板。使用基于质谱的凝胶分离血小板蛋白质组学来比较患者与对照以及治疗开始前后的差异。共检测到 4059 种蛋白质,其中 50 种在患者中明显更丰富,36 种在健康志愿者中更丰富。其中 8 种蛋白质与我们之前的癌症血小板蛋白质组学研究重叠。从这些数据中,我们选择了包括 6 种上调蛋白(RNF213、CTSG、PGLYRP1、RPL8、S100A8、S100A9)和 2 种下调蛋白(GPX1、TNS1)在内的癌症潜在生物标志物。抗肿瘤治疗导致 432 种蛋白质水平升高和 189 种蛋白质水平降低。总之,癌症患者的血小板蛋白质组可能受到影响,血小板是癌症生物标志物的潜在来源。此外,我们在一小部分患者中发现,抗癌治疗显著改变了血小板蛋白质组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/5c364e656939/ijms-22-08236-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/6a0658025c2f/ijms-22-08236-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/ccd42b7e6a6c/ijms-22-08236-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/781c567c01e4/ijms-22-08236-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/a07300fe9d75/ijms-22-08236-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/aa338d2a4391/ijms-22-08236-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/5c364e656939/ijms-22-08236-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/6a0658025c2f/ijms-22-08236-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/ccd42b7e6a6c/ijms-22-08236-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/781c567c01e4/ijms-22-08236-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/a07300fe9d75/ijms-22-08236-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/aa338d2a4391/ijms-22-08236-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1072/8347210/5c364e656939/ijms-22-08236-g006.jpg

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