Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer

Gastric cancer, one of the most common disease, has become a major public health problem worldwide. Cisplatin (DDP) has been a widely used drug for the treatment of cancer, also usually applied in gastric cancer in clinic. However, the side effects including toxicity and drug-resistance restricted t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pathology, research and practice research and practice, 2019-04, Vol.215 (4), p.755-760
Hauptverfasser: Qian, Keyang, Qian, Hanqing, Cai, Juan, Yue, Wuheng, Yu, Xiaoxiao, Liu, Baorui
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 760
container_issue 4
container_start_page 755
container_title Pathology, research and practice
container_volume 215
creator Qian, Keyang
Qian, Hanqing
Cai, Juan
Yue, Wuheng
Yu, Xiaoxiao
Liu, Baorui
description Gastric cancer, one of the most common disease, has become a major public health problem worldwide. Cisplatin (DDP) has been a widely used drug for the treatment of cancer, also usually applied in gastric cancer in clinic. However, the side effects including toxicity and drug-resistance restricted the usage of DDP in clinic, so we prepared a DDP-complexed hydrogel (DDP-Gel) and investigated its efficacy in gastric cancer. For in vivo studies, MKN45-Luc cells were injected into BLAB/C node mice subcutaneously to establish gastric cancer with orthotopically grown tumors. Mice bearing tumors were treated with normal saline, DDP and DDP-Gel. Body weight and survival condition were observed and recorded. The treatment efficacy in vivo was detected by luciferase imaging and histological evaluation was performed by H&E staining of different organs. Additionally, normal ICR mice were treated with different doses of DDP/DDP-Gel to calculate their LD50 in vivo. The results showed that DDP-Gel prolonged survival time and ameliorated body weight changes of mice bearing tumors. DDP-Gel exhibited higher efficacy to inhibit tumor growth and metastasis, compared to DDP. Besides, LD50 of DDP-Gel was 166.0 mg/kg, 13.2 folds higher than DDP. As a conclusion, DDP-Gel showed a more effective and safer function than DDP in gastric cancer, which indicating that DDP-Gel might be a novel strategy for gastric cancer therapy.
doi_str_mv 10.1016/j.prp.2019.01.005
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2179525496</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S034403381831570X</els_id><sourcerecordid>2179525496</sourcerecordid><originalsourceid>FETCH-LOGICAL-c353t-ea8e7ecdd2d5a3f4a98bd01b9007be846ab02b07a245541bceca4d59155502e3</originalsourceid><addsrcrecordid>eNp9kE1v1DAQhi1ERbcfP4AL8pFLwkxs50OcUFUoUiUuvVaWY08Wr5I42MlKy6_H1RaOnEYz886rdx7G3iOUCFh_OpRLXMoKsCsBSwD1hu2wxraAWuBbtgMhZQFCtJfsKqUDADQg8R27FNBgC127Y8_3RzNuZvVh5mHg1qdlzN1c_Dy5GPY08iFE7qclhqOf93wM1oz-Nzlu5tWv25S3NAzeGnvifuZ7k9boLbdmthRv2MVgxkS3r_WaPX29f7p7KB5_fPt-9-WxsEKJtSDTUkPWucopIwZpurZ3gH2XA_fUytr0UPXQmEoqJbG3ZI10qkOlFFQkrtnHs21O-WujtOrJJ0vjaGYKW9IVNp2qlOzqLMWz1MaQUqRBL9FPJp40gn6Bqg95sugXqBpQZ6j55sOr_dZP5P5d_KWYBZ_PAso_Hj1FnaynDMD5SHbVLvj_2P8B9J-Jjg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2179525496</pqid></control><display><type>article</type><title>Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Qian, Keyang ; Qian, Hanqing ; Cai, Juan ; Yue, Wuheng ; Yu, Xiaoxiao ; Liu, Baorui</creator><creatorcontrib>Qian, Keyang ; Qian, Hanqing ; Cai, Juan ; Yue, Wuheng ; Yu, Xiaoxiao ; Liu, Baorui</creatorcontrib><description>Gastric cancer, one of the most common disease, has become a major public health problem worldwide. Cisplatin (DDP) has been a widely used drug for the treatment of cancer, also usually applied in gastric cancer in clinic. However, the side effects including toxicity and drug-resistance restricted the usage of DDP in clinic, so we prepared a DDP-complexed hydrogel (DDP-Gel) and investigated its efficacy in gastric cancer. For in vivo studies, MKN45-Luc cells were injected into BLAB/C node mice subcutaneously to establish gastric cancer with orthotopically grown tumors. Mice bearing tumors were treated with normal saline, DDP and DDP-Gel. Body weight and survival condition were observed and recorded. The treatment efficacy in vivo was detected by luciferase imaging and histological evaluation was performed by H&amp;E staining of different organs. Additionally, normal ICR mice were treated with different doses of DDP/DDP-Gel to calculate their LD50 in vivo. The results showed that DDP-Gel prolonged survival time and ameliorated body weight changes of mice bearing tumors. DDP-Gel exhibited higher efficacy to inhibit tumor growth and metastasis, compared to DDP. Besides, LD50 of DDP-Gel was 166.0 mg/kg, 13.2 folds higher than DDP. As a conclusion, DDP-Gel showed a more effective and safer function than DDP in gastric cancer, which indicating that DDP-Gel might be a novel strategy for gastric cancer therapy.</description><identifier>ISSN: 0344-0338</identifier><identifier>EISSN: 1618-0631</identifier><identifier>DOI: 10.1016/j.prp.2019.01.005</identifier><identifier>PMID: 30718098</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Animals ; Antineoplastic Agents - administration &amp; dosage ; Antineoplastic Agents - therapeutic use ; Apoptosis - drug effects ; Cell Proliferation - drug effects ; Cisplatin ; Cisplatin - administration &amp; dosage ; Cisplatin - therapeutic use ; Disease Models, Animal ; Drug Delivery Systems ; Drug Resistance, Neoplasm - drug effects ; Gastric cancer ; Hydrogel ; Hydrogels - administration &amp; dosage ; Hydrogels - therapeutic use ; Mice ; Mice, Inbred ICR ; Orthotopic ; Stomach Neoplasms - drug therapy ; Stomach Neoplasms - pathology ; Toxicity ; Treatment Outcome</subject><ispartof>Pathology, research and practice, 2019-04, Vol.215 (4), p.755-760</ispartof><rights>2019</rights><rights>Copyright © 2019. Published by Elsevier GmbH.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-ea8e7ecdd2d5a3f4a98bd01b9007be846ab02b07a245541bceca4d59155502e3</citedby><cites>FETCH-LOGICAL-c353t-ea8e7ecdd2d5a3f4a98bd01b9007be846ab02b07a245541bceca4d59155502e3</cites><orcidid>0000-0002-7743-6019</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.prp.2019.01.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30718098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qian, Keyang</creatorcontrib><creatorcontrib>Qian, Hanqing</creatorcontrib><creatorcontrib>Cai, Juan</creatorcontrib><creatorcontrib>Yue, Wuheng</creatorcontrib><creatorcontrib>Yu, Xiaoxiao</creatorcontrib><creatorcontrib>Liu, Baorui</creatorcontrib><title>Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer</title><title>Pathology, research and practice</title><addtitle>Pathol Res Pract</addtitle><description>Gastric cancer, one of the most common disease, has become a major public health problem worldwide. Cisplatin (DDP) has been a widely used drug for the treatment of cancer, also usually applied in gastric cancer in clinic. However, the side effects including toxicity and drug-resistance restricted the usage of DDP in clinic, so we prepared a DDP-complexed hydrogel (DDP-Gel) and investigated its efficacy in gastric cancer. For in vivo studies, MKN45-Luc cells were injected into BLAB/C node mice subcutaneously to establish gastric cancer with orthotopically grown tumors. Mice bearing tumors were treated with normal saline, DDP and DDP-Gel. Body weight and survival condition were observed and recorded. The treatment efficacy in vivo was detected by luciferase imaging and histological evaluation was performed by H&amp;E staining of different organs. Additionally, normal ICR mice were treated with different doses of DDP/DDP-Gel to calculate their LD50 in vivo. The results showed that DDP-Gel prolonged survival time and ameliorated body weight changes of mice bearing tumors. DDP-Gel exhibited higher efficacy to inhibit tumor growth and metastasis, compared to DDP. Besides, LD50 of DDP-Gel was 166.0 mg/kg, 13.2 folds higher than DDP. As a conclusion, DDP-Gel showed a more effective and safer function than DDP in gastric cancer, which indicating that DDP-Gel might be a novel strategy for gastric cancer therapy.</description><subject>Animals</subject><subject>Antineoplastic Agents - administration &amp; dosage</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Apoptosis - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Cisplatin</subject><subject>Cisplatin - administration &amp; dosage</subject><subject>Cisplatin - therapeutic use</subject><subject>Disease Models, Animal</subject><subject>Drug Delivery Systems</subject><subject>Drug Resistance, Neoplasm - drug effects</subject><subject>Gastric cancer</subject><subject>Hydrogel</subject><subject>Hydrogels - administration &amp; dosage</subject><subject>Hydrogels - therapeutic use</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Orthotopic</subject><subject>Stomach Neoplasms - drug therapy</subject><subject>Stomach Neoplasms - pathology</subject><subject>Toxicity</subject><subject>Treatment Outcome</subject><issn>0344-0338</issn><issn>1618-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQhi1ERbcfP4AL8pFLwkxs50OcUFUoUiUuvVaWY08Wr5I42MlKy6_H1RaOnEYz886rdx7G3iOUCFh_OpRLXMoKsCsBSwD1hu2wxraAWuBbtgMhZQFCtJfsKqUDADQg8R27FNBgC127Y8_3RzNuZvVh5mHg1qdlzN1c_Dy5GPY08iFE7qclhqOf93wM1oz-Nzlu5tWv25S3NAzeGnvifuZ7k9boLbdmthRv2MVgxkS3r_WaPX29f7p7KB5_fPt-9-WxsEKJtSDTUkPWucopIwZpurZ3gH2XA_fUytr0UPXQmEoqJbG3ZI10qkOlFFQkrtnHs21O-WujtOrJJ0vjaGYKW9IVNp2qlOzqLMWz1MaQUqRBL9FPJp40gn6Bqg95sugXqBpQZ6j55sOr_dZP5P5d_KWYBZ_PAso_Hj1FnaynDMD5SHbVLvj_2P8B9J-Jjg</recordid><startdate>201904</startdate><enddate>201904</enddate><creator>Qian, Keyang</creator><creator>Qian, Hanqing</creator><creator>Cai, Juan</creator><creator>Yue, Wuheng</creator><creator>Yu, Xiaoxiao</creator><creator>Liu, Baorui</creator><general>Elsevier GmbH</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>7X8</scope><orcidid>https://orcid.org/0000-0002-7743-6019</orcidid></search><sort><creationdate>201904</creationdate><title>Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer</title><author>Qian, Keyang ; Qian, Hanqing ; Cai, Juan ; Yue, Wuheng ; Yu, Xiaoxiao ; Liu, Baorui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-ea8e7ecdd2d5a3f4a98bd01b9007be846ab02b07a245541bceca4d59155502e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - administration &amp; dosage</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Apoptosis - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Cisplatin</topic><topic>Cisplatin - administration &amp; dosage</topic><topic>Cisplatin - therapeutic use</topic><topic>Disease Models, Animal</topic><topic>Drug Delivery Systems</topic><topic>Drug Resistance, Neoplasm - drug effects</topic><topic>Gastric cancer</topic><topic>Hydrogel</topic><topic>Hydrogels - administration &amp; dosage</topic><topic>Hydrogels - therapeutic use</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Orthotopic</topic><topic>Stomach Neoplasms - drug therapy</topic><topic>Stomach Neoplasms - pathology</topic><topic>Toxicity</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qian, Keyang</creatorcontrib><creatorcontrib>Qian, Hanqing</creatorcontrib><creatorcontrib>Cai, Juan</creatorcontrib><creatorcontrib>Yue, Wuheng</creatorcontrib><creatorcontrib>Yu, Xiaoxiao</creatorcontrib><creatorcontrib>Liu, Baorui</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology, research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qian, Keyang</au><au>Qian, Hanqing</au><au>Cai, Juan</au><au>Yue, Wuheng</au><au>Yu, Xiaoxiao</au><au>Liu, Baorui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer</atitle><jtitle>Pathology, research and practice</jtitle><addtitle>Pathol Res Pract</addtitle><date>2019-04</date><risdate>2019</risdate><volume>215</volume><issue>4</issue><spage>755</spage><epage>760</epage><pages>755-760</pages><issn>0344-0338</issn><eissn>1618-0631</eissn><abstract>Gastric cancer, one of the most common disease, has become a major public health problem worldwide. Cisplatin (DDP) has been a widely used drug for the treatment of cancer, also usually applied in gastric cancer in clinic. However, the side effects including toxicity and drug-resistance restricted the usage of DDP in clinic, so we prepared a DDP-complexed hydrogel (DDP-Gel) and investigated its efficacy in gastric cancer. For in vivo studies, MKN45-Luc cells were injected into BLAB/C node mice subcutaneously to establish gastric cancer with orthotopically grown tumors. Mice bearing tumors were treated with normal saline, DDP and DDP-Gel. Body weight and survival condition were observed and recorded. The treatment efficacy in vivo was detected by luciferase imaging and histological evaluation was performed by H&amp;E staining of different organs. Additionally, normal ICR mice were treated with different doses of DDP/DDP-Gel to calculate their LD50 in vivo. The results showed that DDP-Gel prolonged survival time and ameliorated body weight changes of mice bearing tumors. DDP-Gel exhibited higher efficacy to inhibit tumor growth and metastasis, compared to DDP. Besides, LD50 of DDP-Gel was 166.0 mg/kg, 13.2 folds higher than DDP. As a conclusion, DDP-Gel showed a more effective and safer function than DDP in gastric cancer, which indicating that DDP-Gel might be a novel strategy for gastric cancer therapy.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>30718098</pmid><doi>10.1016/j.prp.2019.01.005</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-7743-6019</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0344-0338
ispartof Pathology, research and practice, 2019-04, Vol.215 (4), p.755-760
issn 0344-0338
1618-0631
language eng
recordid cdi_proquest_miscellaneous_2179525496
source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - therapeutic use
Apoptosis - drug effects
Cell Proliferation - drug effects
Cisplatin
Cisplatin - administration & dosage
Cisplatin - therapeutic use
Disease Models, Animal
Drug Delivery Systems
Drug Resistance, Neoplasm - drug effects
Gastric cancer
Hydrogel
Hydrogels - administration & dosage
Hydrogels - therapeutic use
Mice
Mice, Inbred ICR
Orthotopic
Stomach Neoplasms - drug therapy
Stomach Neoplasms - pathology
Toxicity
Treatment Outcome
title Evaluation of cisplatin-hydrogel for improving localized antitumor efficacy in gastric cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T19%3A15%3A10IST&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=Evaluation%20of%20cisplatin-hydrogel%20for%20improving%20localized%20antitumor%20efficacy%20in%20gastric%20cancer&rft.jtitle=Pathology,%20research%20and%20practice&rft.au=Qian,%20Keyang&rft.date=2019-04&rft.volume=215&rft.issue=4&rft.spage=755&rft.epage=760&rft.pages=755-760&rft.issn=0344-0338&rft.eissn=1618-0631&rft_id=info:doi/10.1016/j.prp.2019.01.005&rft_dat=%3Cproquest_cross%3E2179525496%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=2179525496&rft_id=info:pmid/30718098&rft_els_id=S034403381831570X&rfr_iscdi=true