Combination therapy of lymphatic drug delivery and total body irradiation in a metastatic lymph node and lung mouse model
Chemotherapy using a lymphatic drug delivery system (LDDS) targeting lymph nodes (LNs) in the early stage of metastasis has a superior antitumor effect to systemic chemotherapy. An LDDS produces a higher drug retention rate and tissue selectivity in LNs. To expand the therapeutic coverage of LDDS fr...
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description | Chemotherapy using a lymphatic drug delivery system (LDDS) targeting lymph nodes (LNs) in the early stage of metastasis has a superior antitumor effect to systemic chemotherapy. An LDDS produces a higher drug retention rate and tissue selectivity in LNs. To expand the therapeutic coverage of LDDS from local treatment of metastatic LNs to prevention of distant metastases, the combination of treatment with therapies that enhance systemic tumor immune effects is an important therapeutic strategy. Recently, total body irradiation (TBI) has been shown to activate immune responses and alter the tumor microenvironment. Here we show that combination therapy with TBI and LDDS improves the antitumor effect of metastatic LNs and lung metastasis. Tumor cells were inoculated into the subiliac LN (SiLN) to induce metastasis into the proper axillary LN (PALN) and lung in a mouse model. TBI was carried out on day 4 after inoculation using a gamma irradiator. Lymphatic drug delivery into the accessory axillary LN was used to treat PALN. In vivo bioluminescence imaging, high‐frequency ultrasound, and histology showed that combination therapy using TBI (total dose 1.0 Gy once) and the LDDS suppressed tumor growth in LNs and lung metastases and was more effective than using LDDS or TBI alone. Quantitative RT‐PCR of spleens after combination therapy revealed increased expression of CD4, CD8, and IL‐12b, indicating an activated immune response. The results show that combination therapy with TBI and LDDS is a method to improve the efficacy of LN metastases and distant metastases therapy and is a promising novel approach to treat cancer patients.
Lymphatic drug delivery system (LDDS) targeting early stage lymph node (LN) metastasis. Middle ‐dose (1.0 Gy) total body irradiation (M‐TBI) was combined with LDDS. Antitumor effects were evaluated using in vivo bioluminescence imaging, high‐frequency ultrasound, histology, and quantitative RT‐PCR. Combination therapy with M‐TBI and LDDS is a promising novel approach to enhance the treatment of micrometastases in early metastatic LNs and distant organs. |
doi_str_mv | 10.1111/cas.15562 |
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Lymphatic drug delivery system (LDDS) targeting early stage lymph node (LN) metastasis. Middle ‐dose (1.0 Gy) total body irradiation (M‐TBI) was combined with LDDS. Antitumor effects were evaluated using in vivo bioluminescence imaging, high‐frequency ultrasound, histology, and quantitative RT‐PCR. Combination therapy with M‐TBI and LDDS is a promising novel approach to enhance the treatment of micrometastases in early metastatic LNs and distant organs.</description><identifier>ISSN: 1347-9032</identifier><identifier>EISSN: 1349-7006</identifier><identifier>DOI: 10.1111/cas.15562</identifier><identifier>PMID: 36056924</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Animals ; Antitumor activity ; Bioluminescence ; Cancer ; CD4 antigen ; CD8 antigen ; Chemotherapy ; cisplatin ; Drug delivery ; Drug Delivery Systems ; Drug dosages ; Drugs ; Experiments ; Health aspects ; Immune response ; Inoculation ; Lung ; Lung Neoplasms - drug therapy ; Lung Neoplasms - radiotherapy ; lymph node metastasis ; Lymph nodes ; Lymph Nodes - pathology ; lymphatic drug delivery system ; Lymphatic system ; Metastases ; Metastasis ; Mice ; Original ; ORIGINAL ARTICLES ; Radiation ; Radiation therapy ; radiotherapy ; Retention ; Tumor cells ; Tumor Microenvironment ; Tumor necrosis factor-TNF ; Vehicles ; Viscosity ; Whole-Body Irradiation</subject><ispartof>Cancer science, 2023-01, Vol.114 (1), p.227-235</ispartof><rights>2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.</rights><rights>2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.</rights><rights>COPYRIGHT 2023 John Wiley & Sons, Inc.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5612-26e4ed0e0659640a74f919eb4dfe042d8abbda0f120b56dd5445cb714c57728e3</citedby><cites>FETCH-LOGICAL-c5612-26e4ed0e0659640a74f919eb4dfe042d8abbda0f120b56dd5445cb714c57728e3</cites><orcidid>0000-0003-4727-9558 ; 0000-0003-0588-6376 ; 0000-0001-9137-2966</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807513/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807513/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36056924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sora, Shota</creatorcontrib><creatorcontrib>Sukhbaatar, Ariunbuyan</creatorcontrib><creatorcontrib>Fukushige, Shinichi</creatorcontrib><creatorcontrib>Mori, Shiro</creatorcontrib><creatorcontrib>Sakamoto, Maya</creatorcontrib><creatorcontrib>Kodama, Tetsuya</creatorcontrib><title>Combination therapy of lymphatic drug delivery and total body irradiation in a metastatic lymph node and lung mouse model</title><title>Cancer science</title><addtitle>Cancer Sci</addtitle><description>Chemotherapy using a lymphatic drug delivery system (LDDS) targeting lymph nodes (LNs) in the early stage of metastasis has a superior antitumor effect to systemic chemotherapy. An LDDS produces a higher drug retention rate and tissue selectivity in LNs. To expand the therapeutic coverage of LDDS from local treatment of metastatic LNs to prevention of distant metastases, the combination of treatment with therapies that enhance systemic tumor immune effects is an important therapeutic strategy. Recently, total body irradiation (TBI) has been shown to activate immune responses and alter the tumor microenvironment. Here we show that combination therapy with TBI and LDDS improves the antitumor effect of metastatic LNs and lung metastasis. Tumor cells were inoculated into the subiliac LN (SiLN) to induce metastasis into the proper axillary LN (PALN) and lung in a mouse model. TBI was carried out on day 4 after inoculation using a gamma irradiator. Lymphatic drug delivery into the accessory axillary LN was used to treat PALN. In vivo bioluminescence imaging, high‐frequency ultrasound, and histology showed that combination therapy using TBI (total dose 1.0 Gy once) and the LDDS suppressed tumor growth in LNs and lung metastases and was more effective than using LDDS or TBI alone. Quantitative RT‐PCR of spleens after combination therapy revealed increased expression of CD4, CD8, and IL‐12b, indicating an activated immune response. The results show that combination therapy with TBI and LDDS is a method to improve the efficacy of LN metastases and distant metastases therapy and is a promising novel approach to treat cancer patients.
Lymphatic drug delivery system (LDDS) targeting early stage lymph node (LN) metastasis. Middle ‐dose (1.0 Gy) total body irradiation (M‐TBI) was combined with LDDS. Antitumor effects were evaluated using in vivo bioluminescence imaging, high‐frequency ultrasound, histology, and quantitative RT‐PCR. 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An LDDS produces a higher drug retention rate and tissue selectivity in LNs. To expand the therapeutic coverage of LDDS from local treatment of metastatic LNs to prevention of distant metastases, the combination of treatment with therapies that enhance systemic tumor immune effects is an important therapeutic strategy. Recently, total body irradiation (TBI) has been shown to activate immune responses and alter the tumor microenvironment. Here we show that combination therapy with TBI and LDDS improves the antitumor effect of metastatic LNs and lung metastasis. Tumor cells were inoculated into the subiliac LN (SiLN) to induce metastasis into the proper axillary LN (PALN) and lung in a mouse model. TBI was carried out on day 4 after inoculation using a gamma irradiator. Lymphatic drug delivery into the accessory axillary LN was used to treat PALN. In vivo bioluminescence imaging, high‐frequency ultrasound, and histology showed that combination therapy using TBI (total dose 1.0 Gy once) and the LDDS suppressed tumor growth in LNs and lung metastases and was more effective than using LDDS or TBI alone. Quantitative RT‐PCR of spleens after combination therapy revealed increased expression of CD4, CD8, and IL‐12b, indicating an activated immune response. The results show that combination therapy with TBI and LDDS is a method to improve the efficacy of LN metastases and distant metastases therapy and is a promising novel approach to treat cancer patients.
Lymphatic drug delivery system (LDDS) targeting early stage lymph node (LN) metastasis. Middle ‐dose (1.0 Gy) total body irradiation (M‐TBI) was combined with LDDS. Antitumor effects were evaluated using in vivo bioluminescence imaging, high‐frequency ultrasound, histology, and quantitative RT‐PCR. Combination therapy with M‐TBI and LDDS is a promising novel approach to enhance the treatment of micrometastases in early metastatic LNs and distant organs.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>36056924</pmid><doi>10.1111/cas.15562</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-4727-9558</orcidid><orcidid>https://orcid.org/0000-0003-0588-6376</orcidid><orcidid>https://orcid.org/0000-0001-9137-2966</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antitumor activity Bioluminescence Cancer CD4 antigen CD8 antigen Chemotherapy cisplatin Drug delivery Drug Delivery Systems Drug dosages Drugs Experiments Health aspects Immune response Inoculation Lung Lung Neoplasms - drug therapy Lung Neoplasms - radiotherapy lymph node metastasis Lymph nodes Lymph Nodes - pathology lymphatic drug delivery system Lymphatic system Metastases Metastasis Mice Original ORIGINAL ARTICLES Radiation Radiation therapy radiotherapy Retention Tumor cells Tumor Microenvironment Tumor necrosis factor-TNF Vehicles Viscosity Whole-Body Irradiation |
title | Combination therapy of lymphatic drug delivery and total body irradiation in a metastatic lymph node and lung mouse model |
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