Treatment of hepatocellular carcinoma with autologous platelets encapsulating sorafenib or lenvatinib: A novel therapy exploiting tumor‐platelet interactions

Hepatocellular carcinoma (HCC) activates platelets through the action of adjacent sinusoidal cells. Activated platelets bind to tumor‐associated endothelial cells and release growth factors that promote tumor progression. We hypothesized that platelets encapsulated with tumor inhibitors would functi...

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Veröffentlicht in:International journal of cancer 2022-05, Vol.150 (10), p.1640-1653
Hauptverfasser: Tanaka, Hiroki, Horioka, Kie, Hasebe, Takumu, Sawada, Koji, Nakajima, Shunsuke, Konishi, Hiroaki, Isozaki, Shotaro, Goto, Masanori, Fujii, Yumiko, Kamikokura, Yuki, Ogawa, Katsuhiro, Nishikawa, Yuji
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container_end_page 1653
container_issue 10
container_start_page 1640
container_title International journal of cancer
container_volume 150
creator Tanaka, Hiroki
Horioka, Kie
Hasebe, Takumu
Sawada, Koji
Nakajima, Shunsuke
Konishi, Hiroaki
Isozaki, Shotaro
Goto, Masanori
Fujii, Yumiko
Kamikokura, Yuki
Ogawa, Katsuhiro
Nishikawa, Yuji
description Hepatocellular carcinoma (HCC) activates platelets through the action of adjacent sinusoidal cells. Activated platelets bind to tumor‐associated endothelial cells and release growth factors that promote tumor progression. We hypothesized that platelets encapsulated with tumor inhibitors would function as drug carriers for tumor therapy. We propose a therapeutic strategy for HCC using autologous platelets encapsulating multiple tyrosine kinase inhibitors in a rat chemically induced HCC model. Sorafenib or lenvatinib was encapsulated in platelets isolated from tumor‐bearing rats in vitro. The rats were divided into groups that received repeated intravenous injections (twice a week for 10 weeks) of the following materials: placebo, sorafenib (SOR), lenvatinib (LEN), autologous platelets, autologous platelets encapsulating sorafenib (SOR‐PLT) and autologous platelets encapsulating lenvatinib (LEN‐PLT). The therapeutic effect was then analyzed by ultrasonography (US) and histopathological analysis. Histopathological and US analysis demonstrated extensive tumor necrosis in the tumor tissue of SOR‐PLT or LEN‐PLT, but not in other experimental groups. By liquid chromatography‐mass spectrometry, more abundant sorafenib was detected in tumor tissues after SOR‐PLT administration than in surrounding normal tissues, but no such difference in sorafenib level was observed with SOR administration. Therefore, the use of autologous platelets encapsulating drugs might be a novel therapeutic strategy for HCC. What's new? Hepatocellular carcinoma activates platelets, which in turn bind to tumour‐associated endothelial cells and release growth factors that promote tumour progression. Here, the authors hypothesise that it may be possible to harness platelets as drug carriers for tumour therapy. Using a chemically‐induced hepatocellular carcinoma rat model, they demonstrate that autologous platelets encapsulating multiple tyrosine kinase inhibitors can be used to efficiently deliver the anticancer drugs to tumour tissues. The findings point to a novel potential therapeutic approach for hepatocellular carcinoma.
doi_str_mv 10.1002/ijc.33915
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Activated platelets bind to tumor‐associated endothelial cells and release growth factors that promote tumor progression. We hypothesized that platelets encapsulated with tumor inhibitors would function as drug carriers for tumor therapy. We propose a therapeutic strategy for HCC using autologous platelets encapsulating multiple tyrosine kinase inhibitors in a rat chemically induced HCC model. Sorafenib or lenvatinib was encapsulated in platelets isolated from tumor‐bearing rats in vitro. The rats were divided into groups that received repeated intravenous injections (twice a week for 10 weeks) of the following materials: placebo, sorafenib (SOR), lenvatinib (LEN), autologous platelets, autologous platelets encapsulating sorafenib (SOR‐PLT) and autologous platelets encapsulating lenvatinib (LEN‐PLT). The therapeutic effect was then analyzed by ultrasonography (US) and histopathological analysis. Histopathological and US analysis demonstrated extensive tumor necrosis in the tumor tissue of SOR‐PLT or LEN‐PLT, but not in other experimental groups. By liquid chromatography‐mass spectrometry, more abundant sorafenib was detected in tumor tissues after SOR‐PLT administration than in surrounding normal tissues, but no such difference in sorafenib level was observed with SOR administration. Therefore, the use of autologous platelets encapsulating drugs might be a novel therapeutic strategy for HCC. What's new? Hepatocellular carcinoma activates platelets, which in turn bind to tumour‐associated endothelial cells and release growth factors that promote tumour progression. Here, the authors hypothesise that it may be possible to harness platelets as drug carriers for tumour therapy. Using a chemically‐induced hepatocellular carcinoma rat model, they demonstrate that autologous platelets encapsulating multiple tyrosine kinase inhibitors can be used to efficiently deliver the anticancer drugs to tumour tissues. The findings point to a novel potential therapeutic approach for hepatocellular carcinoma.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.33915</identifier><identifier>PMID: 34935134</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - therapeutic use ; Cancer ; Carcinoma, Hepatocellular - drug therapy ; Carcinoma, Hepatocellular - pathology ; Drug delivery ; Endothelial cells ; Endothelial Cells - pathology ; Growth factors ; Hepatocellular carcinoma ; Humans ; Inhibitor drugs ; Intravenous administration ; lenvatinib ; Liquid chromatography ; Liver cancer ; Liver Neoplasms - drug therapy ; Liver Neoplasms - pathology ; Mass spectroscopy ; Medical research ; Phenylurea Compounds - pharmacology ; Phenylurea Compounds - therapeutic use ; platelet ; Platelets ; Protein-tyrosine kinase ; Quinolines - pharmacology ; Quinolines - therapeutic use ; Rats ; sorafenib ; Sorafenib - pharmacology ; Sorafenib - therapeutic use ; Targeted cancer therapy</subject><ispartof>International journal of cancer, 2022-05, Vol.150 (10), p.1640-1653</ispartof><rights>2021 UICC.</rights><rights>2022 UICC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-835cfa40c677b75492a2de1b67d71ec209c55aff58a530b0c027f4a458e829b93</citedby><cites>FETCH-LOGICAL-c3535-835cfa40c677b75492a2de1b67d71ec209c55aff58a530b0c027f4a458e829b93</cites><orcidid>0000-0003-0011-3454</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.33915$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.33915$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34935134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tanaka, Hiroki</creatorcontrib><creatorcontrib>Horioka, Kie</creatorcontrib><creatorcontrib>Hasebe, Takumu</creatorcontrib><creatorcontrib>Sawada, Koji</creatorcontrib><creatorcontrib>Nakajima, Shunsuke</creatorcontrib><creatorcontrib>Konishi, Hiroaki</creatorcontrib><creatorcontrib>Isozaki, Shotaro</creatorcontrib><creatorcontrib>Goto, Masanori</creatorcontrib><creatorcontrib>Fujii, Yumiko</creatorcontrib><creatorcontrib>Kamikokura, Yuki</creatorcontrib><creatorcontrib>Ogawa, Katsuhiro</creatorcontrib><creatorcontrib>Nishikawa, Yuji</creatorcontrib><title>Treatment of hepatocellular carcinoma with autologous platelets encapsulating sorafenib or lenvatinib: A novel therapy exploiting tumor‐platelet interactions</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Hepatocellular carcinoma (HCC) activates platelets through the action of adjacent sinusoidal cells. Activated platelets bind to tumor‐associated endothelial cells and release growth factors that promote tumor progression. We hypothesized that platelets encapsulated with tumor inhibitors would function as drug carriers for tumor therapy. We propose a therapeutic strategy for HCC using autologous platelets encapsulating multiple tyrosine kinase inhibitors in a rat chemically induced HCC model. Sorafenib or lenvatinib was encapsulated in platelets isolated from tumor‐bearing rats in vitro. The rats were divided into groups that received repeated intravenous injections (twice a week for 10 weeks) of the following materials: placebo, sorafenib (SOR), lenvatinib (LEN), autologous platelets, autologous platelets encapsulating sorafenib (SOR‐PLT) and autologous platelets encapsulating lenvatinib (LEN‐PLT). The therapeutic effect was then analyzed by ultrasonography (US) and histopathological analysis. 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Activated platelets bind to tumor‐associated endothelial cells and release growth factors that promote tumor progression. We hypothesized that platelets encapsulated with tumor inhibitors would function as drug carriers for tumor therapy. We propose a therapeutic strategy for HCC using autologous platelets encapsulating multiple tyrosine kinase inhibitors in a rat chemically induced HCC model. Sorafenib or lenvatinib was encapsulated in platelets isolated from tumor‐bearing rats in vitro. The rats were divided into groups that received repeated intravenous injections (twice a week for 10 weeks) of the following materials: placebo, sorafenib (SOR), lenvatinib (LEN), autologous platelets, autologous platelets encapsulating sorafenib (SOR‐PLT) and autologous platelets encapsulating lenvatinib (LEN‐PLT). The therapeutic effect was then analyzed by ultrasonography (US) and histopathological analysis. Histopathological and US analysis demonstrated extensive tumor necrosis in the tumor tissue of SOR‐PLT or LEN‐PLT, but not in other experimental groups. By liquid chromatography‐mass spectrometry, more abundant sorafenib was detected in tumor tissues after SOR‐PLT administration than in surrounding normal tissues, but no such difference in sorafenib level was observed with SOR administration. Therefore, the use of autologous platelets encapsulating drugs might be a novel therapeutic strategy for HCC. What's new? Hepatocellular carcinoma activates platelets, which in turn bind to tumour‐associated endothelial cells and release growth factors that promote tumour progression. Here, the authors hypothesise that it may be possible to harness platelets as drug carriers for tumour therapy. Using a chemically‐induced hepatocellular carcinoma rat model, they demonstrate that autologous platelets encapsulating multiple tyrosine kinase inhibitors can be used to efficiently deliver the anticancer drugs to tumour tissues. The findings point to a novel potential therapeutic approach for hepatocellular carcinoma.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>34935134</pmid><doi>10.1002/ijc.33915</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-0011-3454</orcidid></addata></record>
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subjects Animals
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Cancer
Carcinoma, Hepatocellular - drug therapy
Carcinoma, Hepatocellular - pathology
Drug delivery
Endothelial cells
Endothelial Cells - pathology
Growth factors
Hepatocellular carcinoma
Humans
Inhibitor drugs
Intravenous administration
lenvatinib
Liquid chromatography
Liver cancer
Liver Neoplasms - drug therapy
Liver Neoplasms - pathology
Mass spectroscopy
Medical research
Phenylurea Compounds - pharmacology
Phenylurea Compounds - therapeutic use
platelet
Platelets
Protein-tyrosine kinase
Quinolines - pharmacology
Quinolines - therapeutic use
Rats
sorafenib
Sorafenib - pharmacology
Sorafenib - therapeutic use
Targeted cancer therapy
title Treatment of hepatocellular carcinoma with autologous platelets encapsulating sorafenib or lenvatinib: A novel therapy exploiting tumor‐platelet interactions
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