A novel microscale platform for leukemia tumor treating field therapy and electrochemical screening
Currently, chemotherapy methods are among the most commonly used strategies for all cancer treatments, including leukemia. Despite the marked successes of such therapies, their inevitable side-effects and dose-limiting complications hinder reaching the maximum efficacy. Recently, Tumor Treating Fiel...
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Veröffentlicht in: | Microelectronic engineering 2022-03, Vol.257, p.111738, Article 111738 |
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description | Currently, chemotherapy methods are among the most commonly used strategies for all cancer treatments, including leukemia. Despite the marked successes of such therapies, their inevitable side-effects and dose-limiting complications hinder reaching the maximum efficacy. Recently, Tumor Treating Fields (TTFields) that exploits low intensity and intermediate frequency electric fields has shown great promise as a noninvasive cancer therapy. Combining TTFields and conventional chemotherapies allows treatment with lower drug doses, resulting in significant clinical outcomes and fewer side effects. Although such combinational therapies have been used to treat a wide range of cancer types, their potential applications on leukemia have yet to be explored. This study investigates the effects of TTFields on the leukemia cells in combination with imatinib using a novel microelectrode array platform enabling the on-chip application of TTFields. Microfabrication allows applying TTFields by conventional signal generators with a maximum 20 V peak-to-peak external voltage eliminating commonly used high voltage amplifiers. We evaluated the effectiveness of our method with several biological assays, including flow cytometry, Annexin-V staining, and MTT. Our results indicate that combining TTFields and imatinib can halve the required drug dose (1 μM to 0.5 μM) to reach the apoptotic rate (68.55%±2.4%) obtained by imatinib alone. By comparing the cells numbers, after 72 h, the K562 cells number in our combinational treatment were 7% lower than the initial values seeded, suggesting a considerable net reduction in the tumor cell. Furthermore, to explore the underlying mechanism, an electrochemical approach is employed to measure the secreting contents of the leukemia cells after treatment. We concluded that the enhancement in treatment efficacy could be attributed to the induction of intracellular reactive oxygen species by TTFields, resulting in increased cell apoptosis. Our method provides an in vitro basis to assess the application of TTFields in combination with chemotherapy for leukemia cells.
[Display omitted]
•A microelectrode array platform is presented enabling on-chip application of TTFields with maximum 20 V p-p external voltage.•We utilized the fabricated device to investigate the combinational effect of TTFields with imatinib on leukemia cells.•Combining TTF and imatinib can halve the drug dose (1 μM to 0.5 μM) to reach the apoptotic rate obtained by imatinib alone |
doi_str_mv | 10.1016/j.mee.2022.111738 |
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[Display omitted]
•A microelectrode array platform is presented enabling on-chip application of TTFields with maximum 20 V p-p external voltage.•We utilized the fabricated device to investigate the combinational effect of TTFields with imatinib on leukemia cells.•Combining TTF and imatinib can halve the drug dose (1 μM to 0.5 μM) to reach the apoptotic rate obtained by imatinib alone.•Tumor treating fields initiate apoptosis pathways by induction of intracellular reactive oxygen species (ROS).</description><identifier>ISSN: 0167-9317</identifier><identifier>EISSN: 1873-5568</identifier><identifier>DOI: 10.1016/j.mee.2022.111738</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Apoptosis ; Cancer ; Cancer therapies ; Chemotherapy ; Combinational cancer therapy ; Dosage ; Electric fields ; Flow cytometry ; In vitro methods and tests ; Intracellular reactive oxygen species (ROS) ; Label-free electrochemical analysis ; Leukemia ; Microelectrode array cell culture ; Microelectrodes ; Side effects ; Signal generators ; Tumor treating fields (TTFields) ; Tumors ; Voltage amplifiers</subject><ispartof>Microelectronic engineering, 2022-03, Vol.257, p.111738, Article 111738</ispartof><rights>2022 Elsevier B.V.</rights><rights>Copyright Elsevier BV Mar 15, 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c325t-59cd729471dceae7ad22f45889b5aa1eee22461e3cfed788ee11cb6ce19b4e523</citedby><cites>FETCH-LOGICAL-c325t-59cd729471dceae7ad22f45889b5aa1eee22461e3cfed788ee11cb6ce19b4e523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mee.2022.111738$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Shojaee, Maryam</creatorcontrib><creatorcontrib>Soltan Khamsi, Pouya</creatorcontrib><creatorcontrib>Hosseini, Mohammad</creatorcontrib><creatorcontrib>Khodayari, Mehran</creatorcontrib><creatorcontrib>Moghtaderi, Hasan</creatorcontrib><creatorcontrib>Mousavi, Mir Razi</creatorcontrib><creatorcontrib>Farajpour, Mohsen</creatorcontrib><creatorcontrib>Mohajerzadeh, Shams</creatorcontrib><title>A novel microscale platform for leukemia tumor treating field therapy and electrochemical screening</title><title>Microelectronic engineering</title><description>Currently, chemotherapy methods are among the most commonly used strategies for all cancer treatments, including leukemia. Despite the marked successes of such therapies, their inevitable side-effects and dose-limiting complications hinder reaching the maximum efficacy. Recently, Tumor Treating Fields (TTFields) that exploits low intensity and intermediate frequency electric fields has shown great promise as a noninvasive cancer therapy. Combining TTFields and conventional chemotherapies allows treatment with lower drug doses, resulting in significant clinical outcomes and fewer side effects. Although such combinational therapies have been used to treat a wide range of cancer types, their potential applications on leukemia have yet to be explored. This study investigates the effects of TTFields on the leukemia cells in combination with imatinib using a novel microelectrode array platform enabling the on-chip application of TTFields. Microfabrication allows applying TTFields by conventional signal generators with a maximum 20 V peak-to-peak external voltage eliminating commonly used high voltage amplifiers. We evaluated the effectiveness of our method with several biological assays, including flow cytometry, Annexin-V staining, and MTT. Our results indicate that combining TTFields and imatinib can halve the required drug dose (1 μM to 0.5 μM) to reach the apoptotic rate (68.55%±2.4%) obtained by imatinib alone. By comparing the cells numbers, after 72 h, the K562 cells number in our combinational treatment were 7% lower than the initial values seeded, suggesting a considerable net reduction in the tumor cell. Furthermore, to explore the underlying mechanism, an electrochemical approach is employed to measure the secreting contents of the leukemia cells after treatment. We concluded that the enhancement in treatment efficacy could be attributed to the induction of intracellular reactive oxygen species by TTFields, resulting in increased cell apoptosis. Our method provides an in vitro basis to assess the application of TTFields in combination with chemotherapy for leukemia cells.
[Display omitted]
•A microelectrode array platform is presented enabling on-chip application of TTFields with maximum 20 V p-p external voltage.•We utilized the fabricated device to investigate the combinational effect of TTFields with imatinib on leukemia cells.•Combining TTF and imatinib can halve the drug dose (1 μM to 0.5 μM) to reach the apoptotic rate obtained by imatinib alone.•Tumor treating fields initiate apoptosis pathways by induction of intracellular reactive oxygen species (ROS).</description><subject>Apoptosis</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Combinational cancer therapy</subject><subject>Dosage</subject><subject>Electric fields</subject><subject>Flow cytometry</subject><subject>In vitro methods and tests</subject><subject>Intracellular reactive oxygen species (ROS)</subject><subject>Label-free electrochemical analysis</subject><subject>Leukemia</subject><subject>Microelectrode array cell culture</subject><subject>Microelectrodes</subject><subject>Side effects</subject><subject>Signal generators</subject><subject>Tumor treating fields (TTFields)</subject><subject>Tumors</subject><subject>Voltage amplifiers</subject><issn>0167-9317</issn><issn>1873-5568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMouK7-AG8Bz62d9CMpnpbFL1jwoueQTaZuar9M0gX_vVnq2cuEgeedyTyE3EKWQgbVfZv2iCnLGEsBgOfijKxA8Dwpy0qck1VkeFLnwC_JlfdtFvsiEyuiN3QYj9jR3mo3eq06pFOnQjO6nsZCO5y_sLeKhrmPbXCogh0-aWOxMzQc0Knph6rBUOxQBzfqQ8TjHOq1Qxwie00uGtV5vPl71-Tj6fF9-5Ls3p5ft5tdonNWhqSsteGsLjgYjQq5Mow1RSlEvS-VAkRkrKgAc92g4UIgAuh9pRHqfYEly9fkbpk7ufF7Rh9kO85uiCslq8qa1Xn0EilYqNO93mEjJ2d75X4kZPLkUrYyupQnl3JxGTMPSwbj948WnfTa4qDRWBePlma0_6R_AS3iflQ</recordid><startdate>20220315</startdate><enddate>20220315</enddate><creator>Shojaee, Maryam</creator><creator>Soltan Khamsi, Pouya</creator><creator>Hosseini, Mohammad</creator><creator>Khodayari, Mehran</creator><creator>Moghtaderi, Hasan</creator><creator>Mousavi, Mir Razi</creator><creator>Farajpour, Mohsen</creator><creator>Mohajerzadeh, Shams</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20220315</creationdate><title>A novel microscale platform for leukemia tumor treating field therapy and electrochemical screening</title><author>Shojaee, Maryam ; Soltan Khamsi, Pouya ; Hosseini, Mohammad ; Khodayari, Mehran ; Moghtaderi, Hasan ; Mousavi, Mir Razi ; Farajpour, Mohsen ; Mohajerzadeh, Shams</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-59cd729471dceae7ad22f45889b5aa1eee22461e3cfed788ee11cb6ce19b4e523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Apoptosis</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Combinational cancer therapy</topic><topic>Dosage</topic><topic>Electric fields</topic><topic>Flow cytometry</topic><topic>In vitro methods and tests</topic><topic>Intracellular reactive oxygen species (ROS)</topic><topic>Label-free electrochemical analysis</topic><topic>Leukemia</topic><topic>Microelectrode array cell culture</topic><topic>Microelectrodes</topic><topic>Side effects</topic><topic>Signal generators</topic><topic>Tumor treating fields (TTFields)</topic><topic>Tumors</topic><topic>Voltage amplifiers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shojaee, Maryam</creatorcontrib><creatorcontrib>Soltan Khamsi, Pouya</creatorcontrib><creatorcontrib>Hosseini, Mohammad</creatorcontrib><creatorcontrib>Khodayari, Mehran</creatorcontrib><creatorcontrib>Moghtaderi, Hasan</creatorcontrib><creatorcontrib>Mousavi, Mir Razi</creatorcontrib><creatorcontrib>Farajpour, Mohsen</creatorcontrib><creatorcontrib>Mohajerzadeh, Shams</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Microelectronic engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shojaee, Maryam</au><au>Soltan Khamsi, Pouya</au><au>Hosseini, Mohammad</au><au>Khodayari, Mehran</au><au>Moghtaderi, Hasan</au><au>Mousavi, Mir Razi</au><au>Farajpour, Mohsen</au><au>Mohajerzadeh, Shams</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel microscale platform for leukemia tumor treating field therapy and electrochemical screening</atitle><jtitle>Microelectronic engineering</jtitle><date>2022-03-15</date><risdate>2022</risdate><volume>257</volume><spage>111738</spage><pages>111738-</pages><artnum>111738</artnum><issn>0167-9317</issn><eissn>1873-5568</eissn><abstract>Currently, chemotherapy methods are among the most commonly used strategies for all cancer treatments, including leukemia. Despite the marked successes of such therapies, their inevitable side-effects and dose-limiting complications hinder reaching the maximum efficacy. Recently, Tumor Treating Fields (TTFields) that exploits low intensity and intermediate frequency electric fields has shown great promise as a noninvasive cancer therapy. Combining TTFields and conventional chemotherapies allows treatment with lower drug doses, resulting in significant clinical outcomes and fewer side effects. Although such combinational therapies have been used to treat a wide range of cancer types, their potential applications on leukemia have yet to be explored. This study investigates the effects of TTFields on the leukemia cells in combination with imatinib using a novel microelectrode array platform enabling the on-chip application of TTFields. Microfabrication allows applying TTFields by conventional signal generators with a maximum 20 V peak-to-peak external voltage eliminating commonly used high voltage amplifiers. We evaluated the effectiveness of our method with several biological assays, including flow cytometry, Annexin-V staining, and MTT. Our results indicate that combining TTFields and imatinib can halve the required drug dose (1 μM to 0.5 μM) to reach the apoptotic rate (68.55%±2.4%) obtained by imatinib alone. By comparing the cells numbers, after 72 h, the K562 cells number in our combinational treatment were 7% lower than the initial values seeded, suggesting a considerable net reduction in the tumor cell. Furthermore, to explore the underlying mechanism, an electrochemical approach is employed to measure the secreting contents of the leukemia cells after treatment. We concluded that the enhancement in treatment efficacy could be attributed to the induction of intracellular reactive oxygen species by TTFields, resulting in increased cell apoptosis. Our method provides an in vitro basis to assess the application of TTFields in combination with chemotherapy for leukemia cells.
[Display omitted]
•A microelectrode array platform is presented enabling on-chip application of TTFields with maximum 20 V p-p external voltage.•We utilized the fabricated device to investigate the combinational effect of TTFields with imatinib on leukemia cells.•Combining TTF and imatinib can halve the drug dose (1 μM to 0.5 μM) to reach the apoptotic rate obtained by imatinib alone.•Tumor treating fields initiate apoptosis pathways by induction of intracellular reactive oxygen species (ROS).</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.mee.2022.111738</doi></addata></record> |
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subjects | Apoptosis Cancer Cancer therapies Chemotherapy Combinational cancer therapy Dosage Electric fields Flow cytometry In vitro methods and tests Intracellular reactive oxygen species (ROS) Label-free electrochemical analysis Leukemia Microelectrode array cell culture Microelectrodes Side effects Signal generators Tumor treating fields (TTFields) Tumors Voltage amplifiers |
title | A novel microscale platform for leukemia tumor treating field therapy and electrochemical screening |
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