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...
Gespeichert in:
Veröffentlicht in: | International journal of cancer 2022-05, Vol.150 (10), p.1640-1653 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2612733528</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2639933847</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3535-835cfa40c677b75492a2de1b67d71ec209c55aff58a530b0c027f4a458e829b93</originalsourceid><addsrcrecordid>eNp10ctu1DAUBmALgehQWPACyBIbWKT1JR4n7KoRl6JKbMo6OvGcdDxy7GA7LbPjEfoGfTeeBE-nZYHEypL9-ZePf0Jec3bCGROndmtOpGy5ekIWnLW6YoKrp2RRzliluVwekRcpbRnjXLH6OTmSdSsVl_WC3F1GhDyizzQMdIMT5GDQudlBpAaisT6MQG9s3lCYc3DhKsyJTg4yOsyJojcwpcKz9Vc0hQgDetvTEKlDf73ftv0HekZ9uEZH8wYjTDuKPycX7P2dPI8h_v51-5hJrc8FmWyDTy_JswFcwlcP6zH5_unj5epLdfHt8_nq7KIyUklVNVKZAWpmllr3WtWtALFG3i_1WnM0grVGKRgG1YCSrGeGCT3UUKsGG9H2rTwm7w65Uww_Zky5G23afwR4LAN3YsmFllKJptC3_9BtmKMvrytKtq2UTa2Len9QJoaUIg7dFO0Icddx1u1b60pr3X1rxb55SJz7Edd_5WNNBZwewI11uPt_Unf-dXWI_APBhaYV</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2639933847</pqid></control><display><type>article</type><title>Treatment of hepatocellular carcinoma with autologous platelets encapsulating sorafenib or lenvatinib: A novel therapy exploiting tumor‐platelet interactions</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><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</creator><creatorcontrib>Tanaka, Hiroki ; Horioka, Kie ; Hasebe, Takumu ; Sawada, Koji ; Nakajima, Shunsuke ; Konishi, Hiroaki ; Isozaki, Shotaro ; Goto, Masanori ; Fujii, Yumiko ; Kamikokura, Yuki ; Ogawa, Katsuhiro ; Nishikawa, Yuji</creatorcontrib><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.</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 & 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. 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><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Cancer</subject><subject>Carcinoma, Hepatocellular - drug therapy</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Drug delivery</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - pathology</subject><subject>Growth factors</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Inhibitor drugs</subject><subject>Intravenous administration</subject><subject>lenvatinib</subject><subject>Liquid chromatography</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - pathology</subject><subject>Mass spectroscopy</subject><subject>Medical research</subject><subject>Phenylurea Compounds - pharmacology</subject><subject>Phenylurea Compounds - therapeutic use</subject><subject>platelet</subject><subject>Platelets</subject><subject>Protein-tyrosine kinase</subject><subject>Quinolines - pharmacology</subject><subject>Quinolines - therapeutic use</subject><subject>Rats</subject><subject>sorafenib</subject><subject>Sorafenib - pharmacology</subject><subject>Sorafenib - therapeutic use</subject><subject>Targeted cancer therapy</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10ctu1DAUBmALgehQWPACyBIbWKT1JR4n7KoRl6JKbMo6OvGcdDxy7GA7LbPjEfoGfTeeBE-nZYHEypL9-ZePf0Jec3bCGROndmtOpGy5ekIWnLW6YoKrp2RRzliluVwekRcpbRnjXLH6OTmSdSsVl_WC3F1GhDyizzQMdIMT5GDQudlBpAaisT6MQG9s3lCYc3DhKsyJTg4yOsyJojcwpcKz9Vc0hQgDetvTEKlDf73ftv0HekZ9uEZH8wYjTDuKPycX7P2dPI8h_v51-5hJrc8FmWyDTy_JswFcwlcP6zH5_unj5epLdfHt8_nq7KIyUklVNVKZAWpmllr3WtWtALFG3i_1WnM0grVGKRgG1YCSrGeGCT3UUKsGG9H2rTwm7w65Uww_Zky5G23afwR4LAN3YsmFllKJptC3_9BtmKMvrytKtq2UTa2Len9QJoaUIg7dFO0Icddx1u1b60pr3X1rxb55SJz7Edd_5WNNBZwewI11uPt_Unf-dXWI_APBhaYV</recordid><startdate>20220515</startdate><enddate>20220515</enddate><creator>Tanaka, Hiroki</creator><creator>Horioka, Kie</creator><creator>Hasebe, Takumu</creator><creator>Sawada, Koji</creator><creator>Nakajima, Shunsuke</creator><creator>Konishi, Hiroaki</creator><creator>Isozaki, Shotaro</creator><creator>Goto, Masanori</creator><creator>Fujii, Yumiko</creator><creator>Kamikokura, Yuki</creator><creator>Ogawa, Katsuhiro</creator><creator>Nishikawa, Yuji</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><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>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0011-3454</orcidid></search><sort><creationdate>20220515</creationdate><title>Treatment of hepatocellular carcinoma with autologous platelets encapsulating sorafenib or lenvatinib: A novel therapy exploiting tumor‐platelet interactions</title><author>Tanaka, Hiroki ; Horioka, Kie ; Hasebe, Takumu ; Sawada, Koji ; Nakajima, Shunsuke ; Konishi, Hiroaki ; Isozaki, Shotaro ; Goto, Masanori ; Fujii, Yumiko ; Kamikokura, Yuki ; Ogawa, Katsuhiro ; Nishikawa, Yuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-835cfa40c677b75492a2de1b67d71ec209c55aff58a530b0c027f4a458e829b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Cancer</topic><topic>Carcinoma, Hepatocellular - drug therapy</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Drug delivery</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - pathology</topic><topic>Growth factors</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Inhibitor drugs</topic><topic>Intravenous administration</topic><topic>lenvatinib</topic><topic>Liquid chromatography</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - pathology</topic><topic>Mass spectroscopy</topic><topic>Medical research</topic><topic>Phenylurea Compounds - pharmacology</topic><topic>Phenylurea Compounds - therapeutic use</topic><topic>platelet</topic><topic>Platelets</topic><topic>Protein-tyrosine kinase</topic><topic>Quinolines - pharmacology</topic><topic>Quinolines - therapeutic use</topic><topic>Rats</topic><topic>sorafenib</topic><topic>Sorafenib - pharmacology</topic><topic>Sorafenib - therapeutic use</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanaka, Hiroki</au><au>Horioka, Kie</au><au>Hasebe, Takumu</au><au>Sawada, Koji</au><au>Nakajima, Shunsuke</au><au>Konishi, Hiroaki</au><au>Isozaki, Shotaro</au><au>Goto, Masanori</au><au>Fujii, Yumiko</au><au>Kamikokura, Yuki</au><au>Ogawa, Katsuhiro</au><au>Nishikawa, Yuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment of hepatocellular carcinoma with autologous platelets encapsulating sorafenib or lenvatinib: A novel therapy exploiting tumor‐platelet interactions</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2022-05-15</date><risdate>2022</risdate><volume>150</volume><issue>10</issue><spage>1640</spage><epage>1653</epage><pages>1640-1653</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><abstract>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.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & 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> |
fulltext | fulltext |
identifier | ISSN: 0020-7136 |
ispartof | International journal of cancer, 2022-05, Vol.150 (10), p.1640-1653 |
issn | 0020-7136 1097-0215 |
language | eng |
recordid | cdi_proquest_miscellaneous_2612733528 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T06%3A03%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Treatment%20of%20hepatocellular%20carcinoma%20with%20autologous%20platelets%20encapsulating%20sorafenib%20or%20lenvatinib:%20A%20novel%20therapy%20exploiting%20tumor%E2%80%90platelet%20interactions&rft.jtitle=International%20journal%20of%20cancer&rft.au=Tanaka,%20Hiroki&rft.date=2022-05-15&rft.volume=150&rft.issue=10&rft.spage=1640&rft.epage=1653&rft.pages=1640-1653&rft.issn=0020-7136&rft.eissn=1097-0215&rft_id=info:doi/10.1002/ijc.33915&rft_dat=%3Cproquest_cross%3E2639933847%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2639933847&rft_id=info:pmid/34935134&rfr_iscdi=true |