Image-Guided Neutron Capture Therapy Using the Gd-DO3A-BTA Complex as a New Combinatorial Treatment Approach

Gadolinium-neutron capture therapy (Gd-NCT) is based on the nuclear capture reaction that occurs when 157Gd is irradiated with low energy thermal neutrons to primarily produce gamma photons. Herein, we investigated the effect of neutron capture therapy (NCT) using a small molecular gadolinium comple...

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Veröffentlicht in:Contrast media and molecular imaging 2018-01, Vol.2018 (2018), p.1-9
Hauptverfasser: Lee, Kyo Chul, Kim, Kyeong Min, Lee, Yong Jin, Chang, Yongmin, Kim, Han-Jun, Choi, Eun-Ji, Kim, Hee-Kyung, Oh, Seyoung, Kim, Mi Hyun, Kim, Jung Young, Park, Ji-Ae, Jung, Ki-Hye, Do, Sun Hee
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container_end_page 9
container_issue 2018
container_start_page 1
container_title Contrast media and molecular imaging
container_volume 2018
creator Lee, Kyo Chul
Kim, Kyeong Min
Lee, Yong Jin
Chang, Yongmin
Kim, Han-Jun
Choi, Eun-Ji
Kim, Hee-Kyung
Oh, Seyoung
Kim, Mi Hyun
Kim, Jung Young
Park, Ji-Ae
Jung, Ki-Hye
Do, Sun Hee
description Gadolinium-neutron capture therapy (Gd-NCT) is based on the nuclear capture reaction that occurs when 157Gd is irradiated with low energy thermal neutrons to primarily produce gamma photons. Herein, we investigated the effect of neutron capture therapy (NCT) using a small molecular gadolinium complex, Gd-DO3A-benzothiazole (Gd-DO3A-BTA), which could be a good candidate for use as an NCT drug due to its ability to enter the intracellular nuclei of tumor cells. Furthermore, MRI images of Gd-DO3A-BTA showed a clear signal enhancement in the tumor, and the images also played a key role in planning NCT by providing accurate information on the in vivo uptake time and duration of Gd-DO3A-BTA. We injected Gd-DO3A-BTA into MDA-MB-231 breast tumor-bearing mice and irradiated the tumors with cyclotron neutrons at the maximum accumulation time (postinjection 6 h); then, we observed the size of the growing tumor for 60 days. Gd-DO3A-BTA showed good therapeutic effects of chemo-Gd-NCT for the in vivo tumor models. Simultaneously, the Gd-DO3A-BTA groups ([Gd-DO3A-BTA(+), NCT(+)]) showed a significant reduction in tumor size (p [Gd-DO3A-BTA(+), NCT(−)] > [Gd-DO3A-BTA(−), NCT(+)] > [Gd-DO3A-BTA(−), NCT(−)]. On day 60, the [Gd-DO3A-BTA(+), NCT(+)] and [Gd-DO3A-BTA(−), NCT(−)] groups exhibited an approximately 4.5-fold difference in tumor size. Immunohistochemistry studies demonstrated that new combinational therapy with chemo-Gd-NCT could treat breast cancer by both the inhibition of tumor cell proliferation and induction of apoptosis-related proteins, with in vivo tumor monitoring by MRI.
doi_str_mv 10.1155/2018/3727109
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Herein, we investigated the effect of neutron capture therapy (NCT) using a small molecular gadolinium complex, Gd-DO3A-benzothiazole (Gd-DO3A-BTA), which could be a good candidate for use as an NCT drug due to its ability to enter the intracellular nuclei of tumor cells. Furthermore, MRI images of Gd-DO3A-BTA showed a clear signal enhancement in the tumor, and the images also played a key role in planning NCT by providing accurate information on the in vivo uptake time and duration of Gd-DO3A-BTA. We injected Gd-DO3A-BTA into MDA-MB-231 breast tumor-bearing mice and irradiated the tumors with cyclotron neutrons at the maximum accumulation time (postinjection 6 h); then, we observed the size of the growing tumor for 60 days. Gd-DO3A-BTA showed good therapeutic effects of chemo-Gd-NCT for the in vivo tumor models. Simultaneously, the Gd-DO3A-BTA groups ([Gd-DO3A-BTA(+), NCT(+)]) showed a significant reduction in tumor size (p&lt;0.05), and the inhibitory effect on tumor growth was exhibited in the following order: [Gd-DO3A-BTA(+), NCT(+)] &gt; [Gd-DO3A-BTA(+), NCT(−)] &gt; [Gd-DO3A-BTA(−), NCT(+)] &gt; [Gd-DO3A-BTA(−), NCT(−)]. On day 60, the [Gd-DO3A-BTA(+), NCT(+)] and [Gd-DO3A-BTA(−), NCT(−)] groups exhibited an approximately 4.5-fold difference in tumor size. Immunohistochemistry studies demonstrated that new combinational therapy with chemo-Gd-NCT could treat breast cancer by both the inhibition of tumor cell proliferation and induction of apoptosis-related proteins, with in vivo tumor monitoring by MRI.</description><identifier>ISSN: 1555-4309</identifier><identifier>EISSN: 1555-4317</identifier><identifier>DOI: 10.1155/2018/3727109</identifier><identifier>PMID: 30515066</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animal models ; Apoptosis ; Benzothiazole ; Breast cancer ; Cancer therapies ; Cell proliferation ; Chemistry ; Combinatorial analysis ; Contrast agents ; Cyclotrons ; Gadolinium ; Gadolinium isotopes ; Image enhancement ; Immunohistochemistry ; Lipids ; Magnetic resonance imaging ; Medical imaging ; Nanoparticles ; Neutrons ; NMR ; Nuclear capture ; Nuclear magnetic resonance ; Nuclei (cytology) ; Nuclei (nuclear physics) ; Pharmaceutical sciences ; Photons ; Proteins ; Therapy ; Thermal neutrons ; Tumor cells ; Tumors</subject><ispartof>Contrast media and molecular imaging, 2018-01, Vol.2018 (2018), p.1-9</ispartof><rights>Copyright © 2018 Ki-Hye Jung et al.</rights><rights>Copyright © 2018 Ki-Hye Jung et al. 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Simultaneously, the Gd-DO3A-BTA groups ([Gd-DO3A-BTA(+), NCT(+)]) showed a significant reduction in tumor size (p&lt;0.05), and the inhibitory effect on tumor growth was exhibited in the following order: [Gd-DO3A-BTA(+), NCT(+)] &gt; [Gd-DO3A-BTA(+), NCT(−)] &gt; [Gd-DO3A-BTA(−), NCT(+)] &gt; [Gd-DO3A-BTA(−), NCT(−)]. On day 60, the [Gd-DO3A-BTA(+), NCT(+)] and [Gd-DO3A-BTA(−), NCT(−)] groups exhibited an approximately 4.5-fold difference in tumor size. 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Kim, Kyeong Min ; Lee, Yong Jin ; Chang, Yongmin ; Kim, Han-Jun ; Choi, Eun-Ji ; Kim, Hee-Kyung ; Oh, Seyoung ; Kim, Mi Hyun ; Kim, Jung Young ; Park, Ji-Ae ; Jung, Ki-Hye ; Do, Sun Hee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c537t-f23c04d08713cde190dfa7012b28aef1b9b273481613688226cef5dae89b04413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animal models</topic><topic>Apoptosis</topic><topic>Benzothiazole</topic><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Cell proliferation</topic><topic>Chemistry</topic><topic>Combinatorial analysis</topic><topic>Contrast agents</topic><topic>Cyclotrons</topic><topic>Gadolinium</topic><topic>Gadolinium isotopes</topic><topic>Image enhancement</topic><topic>Immunohistochemistry</topic><topic>Lipids</topic><topic>Magnetic resonance imaging</topic><topic>Medical imaging</topic><topic>Nanoparticles</topic><topic>Neutrons</topic><topic>NMR</topic><topic>Nuclear capture</topic><topic>Nuclear magnetic resonance</topic><topic>Nuclei (cytology)</topic><topic>Nuclei (nuclear physics)</topic><topic>Pharmaceutical sciences</topic><topic>Photons</topic><topic>Proteins</topic><topic>Therapy</topic><topic>Thermal neutrons</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Kyo Chul</creatorcontrib><creatorcontrib>Kim, Kyeong Min</creatorcontrib><creatorcontrib>Lee, Yong Jin</creatorcontrib><creatorcontrib>Chang, Yongmin</creatorcontrib><creatorcontrib>Kim, Han-Jun</creatorcontrib><creatorcontrib>Choi, Eun-Ji</creatorcontrib><creatorcontrib>Kim, Hee-Kyung</creatorcontrib><creatorcontrib>Oh, Seyoung</creatorcontrib><creatorcontrib>Kim, Mi Hyun</creatorcontrib><creatorcontrib>Kim, Jung Young</creatorcontrib><creatorcontrib>Park, Ji-Ae</creatorcontrib><creatorcontrib>Jung, Ki-Hye</creatorcontrib><creatorcontrib>Do, Sun Hee</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; 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Herein, we investigated the effect of neutron capture therapy (NCT) using a small molecular gadolinium complex, Gd-DO3A-benzothiazole (Gd-DO3A-BTA), which could be a good candidate for use as an NCT drug due to its ability to enter the intracellular nuclei of tumor cells. Furthermore, MRI images of Gd-DO3A-BTA showed a clear signal enhancement in the tumor, and the images also played a key role in planning NCT by providing accurate information on the in vivo uptake time and duration of Gd-DO3A-BTA. We injected Gd-DO3A-BTA into MDA-MB-231 breast tumor-bearing mice and irradiated the tumors with cyclotron neutrons at the maximum accumulation time (postinjection 6 h); then, we observed the size of the growing tumor for 60 days. Gd-DO3A-BTA showed good therapeutic effects of chemo-Gd-NCT for the in vivo tumor models. Simultaneously, the Gd-DO3A-BTA groups ([Gd-DO3A-BTA(+), NCT(+)]) showed a significant reduction in tumor size (p&lt;0.05), and the inhibitory effect on tumor growth was exhibited in the following order: [Gd-DO3A-BTA(+), NCT(+)] &gt; [Gd-DO3A-BTA(+), NCT(−)] &gt; [Gd-DO3A-BTA(−), NCT(+)] &gt; [Gd-DO3A-BTA(−), NCT(−)]. On day 60, the [Gd-DO3A-BTA(+), NCT(+)] and [Gd-DO3A-BTA(−), NCT(−)] groups exhibited an approximately 4.5-fold difference in tumor size. Immunohistochemistry studies demonstrated that new combinational therapy with chemo-Gd-NCT could treat breast cancer by both the inhibition of tumor cell proliferation and induction of apoptosis-related proteins, with in vivo tumor monitoring by MRI.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30515066</pmid><doi>10.1155/2018/3727109</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0755-3893</orcidid><orcidid>https://orcid.org/0000-0001-6109-802X</orcidid><orcidid>https://orcid.org/0000-0002-7140-354X</orcidid><orcidid>https://orcid.org/0000-0001-8959-5730</orcidid><orcidid>https://orcid.org/0000-0002-0585-8714</orcidid><orcidid>https://orcid.org/0000-0001-6284-0644</orcidid><orcidid>https://orcid.org/0000-0003-2372-5269</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animal models
Apoptosis
Benzothiazole
Breast cancer
Cancer therapies
Cell proliferation
Chemistry
Combinatorial analysis
Contrast agents
Cyclotrons
Gadolinium
Gadolinium isotopes
Image enhancement
Immunohistochemistry
Lipids
Magnetic resonance imaging
Medical imaging
Nanoparticles
Neutrons
NMR
Nuclear capture
Nuclear magnetic resonance
Nuclei (cytology)
Nuclei (nuclear physics)
Pharmaceutical sciences
Photons
Proteins
Therapy
Thermal neutrons
Tumor cells
Tumors
title Image-Guided Neutron Capture Therapy Using the Gd-DO3A-BTA Complex as a New Combinatorial Treatment Approach
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T10%3A27%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Image-Guided%20Neutron%20Capture%20Therapy%20Using%20the%20Gd-DO3A-BTA%20Complex%20as%20a%20New%20Combinatorial%20Treatment%20Approach&rft.jtitle=Contrast%20media%20and%20molecular%20imaging&rft.au=Lee,%20Kyo%20Chul&rft.date=2018-01-01&rft.volume=2018&rft.issue=2018&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=1555-4309&rft.eissn=1555-4317&rft_id=info:doi/10.1155/2018/3727109&rft_dat=%3Cproquest_pubme%3E2190116421%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2190116421&rft_id=info:pmid/30515066&rfr_iscdi=true