Monitoring circulating platelet activity to predict cancer-associated thrombosis

A characteristic clinical complication in cancer patients is the frequent incidence of thrombotic events. Numerous studies have shown hyperactive/activated platelets to be a critical earlier trigger for cancer-associated thrombus formation. However, there currently is no viable approach to monitor s...

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Veröffentlicht in:Cell reports methods 2023-07, Vol.3 (7), p.100513-100513, Article 100513
Hauptverfasser: Li, Bozhao, Lu, Zefang, Yang, Zhenlin, Zhang, Xiuping, Wang, Meiqi, Chu, Tianjiao, Wang, Peina, Qi, Feilong, Anderson, Greg J., Jiang, Ershuai, Song, Zhenchuan, Nie, Guangjun, Li, Suping
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container_end_page 100513
container_issue 7
container_start_page 100513
container_title Cell reports methods
container_volume 3
creator Li, Bozhao
Lu, Zefang
Yang, Zhenlin
Zhang, Xiuping
Wang, Meiqi
Chu, Tianjiao
Wang, Peina
Qi, Feilong
Anderson, Greg J.
Jiang, Ershuai
Song, Zhenchuan
Nie, Guangjun
Li, Suping
description A characteristic clinical complication in cancer patients is the frequent incidence of thrombotic events. Numerous studies have shown hyperactive/activated platelets to be a critical earlier trigger for cancer-associated thrombus formation. However, there currently is no viable approach to monitor specific changes in tumor-associated platelet activity. Here, we describe a chromatograph-like microfluidic device that is highly sensitive to the activity status of peripheral circulating platelets in both tumor-bearing mice and clinical cancer patients. Our results show a strongly positive correlation between platelet activation status and tumor progression. Six-month follow-up data from advanced cancer patients reveal positive links between platelet activity level and thrombus occurrence rate, with a high predictive capacity of thrombotic events (AUC = 0.842). Our findings suggest that circulating platelet activity status determined by this microfluidic device exhibits sensitive, predictive potential for thrombotic events in cancer patients for directing well-timed antithrombosis treatment. [Display omitted] •A microfluidic device effectively detects tumor-associated platelet hyperactivity•Platelet activation status is correlated with cancer progression and thrombotic risk•The device predicts thrombotic events in advanced lung, breast, and liver cancer•This approach can guide timely antithrombotic therapy in cancer patients Cancer patients often face thrombosis due to platelet hyperactivity, impacting their prognosis. Yet, we lack a simple, sensitive method to analyze their blood coagulation status. To address this concern, our study aims to develop a microfluidic device for detecting platelet activation. It offers improved sensitivity, time-efficient measurements, user-friendly operation, and cost-effective design. This device is envisioned to enhance thrombotic disease management in cancer patients and facilitate more accurate and accessible coagulation analysis in clinical and research settings. Li et al. introduce a microfluidic device that offers a fast, cost-effective method for tracking platelet activation in cancer patients. They demonstrate a strong correlation between elevated platelet activity, tumor progression, and thrombosis risk. This device can help to enable timely and targeted antithrombotic treatment.
doi_str_mv 10.1016/j.crmeth.2023.100513
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Numerous studies have shown hyperactive/activated platelets to be a critical earlier trigger for cancer-associated thrombus formation. However, there currently is no viable approach to monitor specific changes in tumor-associated platelet activity. Here, we describe a chromatograph-like microfluidic device that is highly sensitive to the activity status of peripheral circulating platelets in both tumor-bearing mice and clinical cancer patients. Our results show a strongly positive correlation between platelet activation status and tumor progression. Six-month follow-up data from advanced cancer patients reveal positive links between platelet activity level and thrombus occurrence rate, with a high predictive capacity of thrombotic events (AUC = 0.842). Our findings suggest that circulating platelet activity status determined by this microfluidic device exhibits sensitive, predictive potential for thrombotic events in cancer patients for directing well-timed antithrombosis treatment. [Display omitted] •A microfluidic device effectively detects tumor-associated platelet hyperactivity•Platelet activation status is correlated with cancer progression and thrombotic risk•The device predicts thrombotic events in advanced lung, breast, and liver cancer•This approach can guide timely antithrombotic therapy in cancer patients Cancer patients often face thrombosis due to platelet hyperactivity, impacting their prognosis. Yet, we lack a simple, sensitive method to analyze their blood coagulation status. To address this concern, our study aims to develop a microfluidic device for detecting platelet activation. It offers improved sensitivity, time-efficient measurements, user-friendly operation, and cost-effective design. This device is envisioned to enhance thrombotic disease management in cancer patients and facilitate more accurate and accessible coagulation analysis in clinical and research settings. Li et al. introduce a microfluidic device that offers a fast, cost-effective method for tracking platelet activation in cancer patients. They demonstrate a strong correlation between elevated platelet activity, tumor progression, and thrombosis risk. 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Numerous studies have shown hyperactive/activated platelets to be a critical earlier trigger for cancer-associated thrombus formation. However, there currently is no viable approach to monitor specific changes in tumor-associated platelet activity. Here, we describe a chromatograph-like microfluidic device that is highly sensitive to the activity status of peripheral circulating platelets in both tumor-bearing mice and clinical cancer patients. Our results show a strongly positive correlation between platelet activation status and tumor progression. Six-month follow-up data from advanced cancer patients reveal positive links between platelet activity level and thrombus occurrence rate, with a high predictive capacity of thrombotic events (AUC = 0.842). Our findings suggest that circulating platelet activity status determined by this microfluidic device exhibits sensitive, predictive potential for thrombotic events in cancer patients for directing well-timed antithrombosis treatment. [Display omitted] •A microfluidic device effectively detects tumor-associated platelet hyperactivity•Platelet activation status is correlated with cancer progression and thrombotic risk•The device predicts thrombotic events in advanced lung, breast, and liver cancer•This approach can guide timely antithrombotic therapy in cancer patients Cancer patients often face thrombosis due to platelet hyperactivity, impacting their prognosis. Yet, we lack a simple, sensitive method to analyze their blood coagulation status. To address this concern, our study aims to develop a microfluidic device for detecting platelet activation. It offers improved sensitivity, time-efficient measurements, user-friendly operation, and cost-effective design. This device is envisioned to enhance thrombotic disease management in cancer patients and facilitate more accurate and accessible coagulation analysis in clinical and research settings. Li et al. introduce a microfluidic device that offers a fast, cost-effective method for tracking platelet activation in cancer patients. They demonstrate a strong correlation between elevated platelet activity, tumor progression, and thrombosis risk. This device can help to enable timely and targeted antithrombotic treatment.</description><subject>Animals</subject><subject>Blood Platelets - pathology</subject><subject>cancer-associated thrombosis</subject><subject>circulating platelets</subject><subject>fibrin network</subject><subject>Mice</subject><subject>microfluidic device</subject><subject>Neoplasms - complications</subject><subject>Platelet Activation - physiology</subject><subject>Thrombosis - etiology</subject><issn>2667-2375</issn><issn>2667-2375</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1LJDEQhoMoKq7_QKSPXnrMx3QyuSgiugou62H3HJLqaidDd2dMMgP-ezO0K3rZS6qoPFWVvC8hZ4zOGGXycjWDOGBezjjlopRow8QeOeZSqpoL1ex_yY_IaUorSikvkNDskByVqhBSqGPy_CuMPofox5cKfIRNb_MuX5eIPebKQvZbn9-qHKp1xNZDrsCOgLG2KQXwhWurvIxhcCH59IMcdLZPePoRT8jf-7s_tw_10--fj7c3TzXM5TzXLXAtGJUNMKW4FFxo1yFVqHVHXafRYfmUblTXONegc1YtlFt0ugUBbTlOyPU0d71xA7aAY462N-voBxvfTLDefL8Z_dK8hK1htGggxKJMuPiYEMPrBlM2g0-AfW9HDJtk-GLeyEZSpgs6n1CIIaWI3eceRs3OELMykyFmZ4iZDClt51_f-Nn0T_4CXE0AFqW2HqNJ4LGI2_qIkE0b_P83vANDQ6EY</recordid><startdate>20230724</startdate><enddate>20230724</enddate><creator>Li, Bozhao</creator><creator>Lu, Zefang</creator><creator>Yang, Zhenlin</creator><creator>Zhang, Xiuping</creator><creator>Wang, Meiqi</creator><creator>Chu, Tianjiao</creator><creator>Wang, Peina</creator><creator>Qi, Feilong</creator><creator>Anderson, Greg J.</creator><creator>Jiang, Ershuai</creator><creator>Song, Zhenchuan</creator><creator>Nie, Guangjun</creator><creator>Li, Suping</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0294-8861</orcidid></search><sort><creationdate>20230724</creationdate><title>Monitoring circulating platelet activity to predict cancer-associated thrombosis</title><author>Li, Bozhao ; Lu, Zefang ; Yang, Zhenlin ; Zhang, Xiuping ; Wang, Meiqi ; Chu, Tianjiao ; Wang, Peina ; Qi, Feilong ; Anderson, Greg J. ; Jiang, Ershuai ; Song, Zhenchuan ; Nie, Guangjun ; Li, Suping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-dc2931065c177263239bfe07e99f0bf9ebe005957f5bb5ebba787b8f9dc3cddc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Blood Platelets - pathology</topic><topic>cancer-associated thrombosis</topic><topic>circulating platelets</topic><topic>fibrin network</topic><topic>Mice</topic><topic>microfluidic device</topic><topic>Neoplasms - complications</topic><topic>Platelet Activation - physiology</topic><topic>Thrombosis - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Bozhao</creatorcontrib><creatorcontrib>Lu, Zefang</creatorcontrib><creatorcontrib>Yang, Zhenlin</creatorcontrib><creatorcontrib>Zhang, Xiuping</creatorcontrib><creatorcontrib>Wang, Meiqi</creatorcontrib><creatorcontrib>Chu, Tianjiao</creatorcontrib><creatorcontrib>Wang, Peina</creatorcontrib><creatorcontrib>Qi, Feilong</creatorcontrib><creatorcontrib>Anderson, Greg J.</creatorcontrib><creatorcontrib>Jiang, Ershuai</creatorcontrib><creatorcontrib>Song, Zhenchuan</creatorcontrib><creatorcontrib>Nie, Guangjun</creatorcontrib><creatorcontrib>Li, Suping</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell reports methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Bozhao</au><au>Lu, Zefang</au><au>Yang, Zhenlin</au><au>Zhang, Xiuping</au><au>Wang, Meiqi</au><au>Chu, Tianjiao</au><au>Wang, Peina</au><au>Qi, Feilong</au><au>Anderson, Greg J.</au><au>Jiang, Ershuai</au><au>Song, Zhenchuan</au><au>Nie, Guangjun</au><au>Li, Suping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monitoring circulating platelet activity to predict cancer-associated thrombosis</atitle><jtitle>Cell reports methods</jtitle><addtitle>Cell Rep Methods</addtitle><date>2023-07-24</date><risdate>2023</risdate><volume>3</volume><issue>7</issue><spage>100513</spage><epage>100513</epage><pages>100513-100513</pages><artnum>100513</artnum><issn>2667-2375</issn><eissn>2667-2375</eissn><abstract>A characteristic clinical complication in cancer patients is the frequent incidence of thrombotic events. Numerous studies have shown hyperactive/activated platelets to be a critical earlier trigger for cancer-associated thrombus formation. However, there currently is no viable approach to monitor specific changes in tumor-associated platelet activity. Here, we describe a chromatograph-like microfluidic device that is highly sensitive to the activity status of peripheral circulating platelets in both tumor-bearing mice and clinical cancer patients. Our results show a strongly positive correlation between platelet activation status and tumor progression. Six-month follow-up data from advanced cancer patients reveal positive links between platelet activity level and thrombus occurrence rate, with a high predictive capacity of thrombotic events (AUC = 0.842). Our findings suggest that circulating platelet activity status determined by this microfluidic device exhibits sensitive, predictive potential for thrombotic events in cancer patients for directing well-timed antithrombosis treatment. [Display omitted] •A microfluidic device effectively detects tumor-associated platelet hyperactivity•Platelet activation status is correlated with cancer progression and thrombotic risk•The device predicts thrombotic events in advanced lung, breast, and liver cancer•This approach can guide timely antithrombotic therapy in cancer patients Cancer patients often face thrombosis due to platelet hyperactivity, impacting their prognosis. Yet, we lack a simple, sensitive method to analyze their blood coagulation status. To address this concern, our study aims to develop a microfluidic device for detecting platelet activation. It offers improved sensitivity, time-efficient measurements, user-friendly operation, and cost-effective design. This device is envisioned to enhance thrombotic disease management in cancer patients and facilitate more accurate and accessible coagulation analysis in clinical and research settings. Li et al. introduce a microfluidic device that offers a fast, cost-effective method for tracking platelet activation in cancer patients. They demonstrate a strong correlation between elevated platelet activity, tumor progression, and thrombosis risk. This device can help to enable timely and targeted antithrombotic treatment.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>37533637</pmid><doi>10.1016/j.crmeth.2023.100513</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0294-8861</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Blood Platelets - pathology
cancer-associated thrombosis
circulating platelets
fibrin network
Mice
microfluidic device
Neoplasms - complications
Platelet Activation - physiology
Thrombosis - etiology
title Monitoring circulating platelet activity to predict cancer-associated thrombosis
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