In vivo optical pathology of paclitaxel efficacy on the peritoneal metastatic xenograft model of gastric cancer using two-photon laser scanning microscopy
Background We previously visualized in vivo responses to chemotherapy in a colorectal liver metastatic xenograft model using in vivo real-time and time-series intravital two-photon laser scanning microscopy (TPLSM). In this study, we established the method for evaluating the response of peritoneal x...
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Veröffentlicht in: | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2015-01, Vol.18 (1), p.109-118 |
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container_title | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association |
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creator | Shimura, Tadanobu Tanaka, Koji Toiyama, Yuji Okigami, Masato Ide, Shozo Kitajima, Takahito Kondo, Satoru Saigusa, Susumu Ohi, Masaki Araki, Toshimitsu Inoue, Yasuhiro Uchida, Keiichi Mohri, Yasuhiko Mizoguchi, Akira Kusunoki, Masato |
description | Background
We previously visualized in vivo responses to chemotherapy in a colorectal liver metastatic xenograft model using in vivo real-time and time-series intravital two-photon laser scanning microscopy (TPLSM). In this study, we established the method for evaluating the response of peritoneal xenografts to chemotherapy of metastatic gastric cancer using intravital TPLSM.
Methods
Red fluorescent protein-expressing gastric cancer cells (NUGC4) were inoculated into the peritoneal cavity of green fluorescent protein nude mice.
Results
Laparotomy revealed that 2 weeks after inoculation, macroscopic peritoneal metastatic nodules were formed. The first intravital TPLSM session revealed that they were composed of red tumor cell clusters and green surrounding stroma. Paclitaxel was administered intraperitoneally after the first TPLSM three times a week for 7 days in the treatment group. At the second laparotomy, there were significantly fewer and smaller nodules in the treated mice than in the controls. The second intravital TPLSM session showed tumor cell fragmentation, swelling, and nuclear condensation in the metastatic nodules—a response to chemotherapy. There were multinuclear tumor cells in the paclitaxel-treated living mice.
Conclusions
Our method may become a powerful tool for evaluating the efficacy of novel anti-gastric cancer drugs in a preclinical murine model with minimum interindividual variation. |
doi_str_mv | 10.1007/s10120-013-0334-y |
format | Article |
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We previously visualized in vivo responses to chemotherapy in a colorectal liver metastatic xenograft model using in vivo real-time and time-series intravital two-photon laser scanning microscopy (TPLSM). In this study, we established the method for evaluating the response of peritoneal xenografts to chemotherapy of metastatic gastric cancer using intravital TPLSM.
Methods
Red fluorescent protein-expressing gastric cancer cells (NUGC4) were inoculated into the peritoneal cavity of green fluorescent protein nude mice.
Results
Laparotomy revealed that 2 weeks after inoculation, macroscopic peritoneal metastatic nodules were formed. The first intravital TPLSM session revealed that they were composed of red tumor cell clusters and green surrounding stroma. Paclitaxel was administered intraperitoneally after the first TPLSM three times a week for 7 days in the treatment group. At the second laparotomy, there were significantly fewer and smaller nodules in the treated mice than in the controls. The second intravital TPLSM session showed tumor cell fragmentation, swelling, and nuclear condensation in the metastatic nodules—a response to chemotherapy. There were multinuclear tumor cells in the paclitaxel-treated living mice.
Conclusions
Our method may become a powerful tool for evaluating the efficacy of novel anti-gastric cancer drugs in a preclinical murine model with minimum interindividual variation.</description><identifier>ISSN: 1436-3291</identifier><identifier>EISSN: 1436-3305</identifier><identifier>DOI: 10.1007/s10120-013-0334-y</identifier><identifier>PMID: 24399494</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Abdominal Surgery ; Animals ; Antineoplastic Agents, Phytogenic - administration & dosage ; Antineoplastic Agents, Phytogenic - pharmacology ; Cancer Research ; Gastric cancer ; Gastroenterology ; Green Fluorescent Proteins - genetics ; Humans ; Luminescent Proteins - genetics ; Medicine ; Medicine & Public Health ; Mice, Nude ; Mice, Transgenic ; Microscopy, Confocal - methods ; Oncology ; Original Article ; Paclitaxel - administration & dosage ; Paclitaxel - pharmacology ; Peritoneal Neoplasms - drug therapy ; Peritoneal Neoplasms - secondary ; Red Fluorescent Protein ; Stomach Neoplasms - drug therapy ; Stomach Neoplasms - pathology ; Surgical Oncology ; Xenograft Model Antitumor Assays</subject><ispartof>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2015-01, Vol.18 (1), p.109-118</ispartof><rights>The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2014</rights><rights>The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c643t-2f6492a512a63ba4dcc97a923660aecb435295206ed88f300282b392872d86953</citedby><cites>FETCH-LOGICAL-c643t-2f6492a512a63ba4dcc97a923660aecb435295206ed88f300282b392872d86953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10120-013-0334-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10120-013-0334-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24399494$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimura, Tadanobu</creatorcontrib><creatorcontrib>Tanaka, Koji</creatorcontrib><creatorcontrib>Toiyama, Yuji</creatorcontrib><creatorcontrib>Okigami, Masato</creatorcontrib><creatorcontrib>Ide, Shozo</creatorcontrib><creatorcontrib>Kitajima, Takahito</creatorcontrib><creatorcontrib>Kondo, Satoru</creatorcontrib><creatorcontrib>Saigusa, Susumu</creatorcontrib><creatorcontrib>Ohi, Masaki</creatorcontrib><creatorcontrib>Araki, Toshimitsu</creatorcontrib><creatorcontrib>Inoue, Yasuhiro</creatorcontrib><creatorcontrib>Uchida, Keiichi</creatorcontrib><creatorcontrib>Mohri, Yasuhiko</creatorcontrib><creatorcontrib>Mizoguchi, Akira</creatorcontrib><creatorcontrib>Kusunoki, Masato</creatorcontrib><title>In vivo optical pathology of paclitaxel efficacy on the peritoneal metastatic xenograft model of gastric cancer using two-photon laser scanning microscopy</title><title>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</title><addtitle>Gastric Cancer</addtitle><addtitle>Gastric Cancer</addtitle><description>Background
We previously visualized in vivo responses to chemotherapy in a colorectal liver metastatic xenograft model using in vivo real-time and time-series intravital two-photon laser scanning microscopy (TPLSM). In this study, we established the method for evaluating the response of peritoneal xenografts to chemotherapy of metastatic gastric cancer using intravital TPLSM.
Methods
Red fluorescent protein-expressing gastric cancer cells (NUGC4) were inoculated into the peritoneal cavity of green fluorescent protein nude mice.
Results
Laparotomy revealed that 2 weeks after inoculation, macroscopic peritoneal metastatic nodules were formed. The first intravital TPLSM session revealed that they were composed of red tumor cell clusters and green surrounding stroma. Paclitaxel was administered intraperitoneally after the first TPLSM three times a week for 7 days in the treatment group. At the second laparotomy, there were significantly fewer and smaller nodules in the treated mice than in the controls. The second intravital TPLSM session showed tumor cell fragmentation, swelling, and nuclear condensation in the metastatic nodules—a response to chemotherapy. There were multinuclear tumor cells in the paclitaxel-treated living mice.
Conclusions
Our method may become a powerful tool for evaluating the efficacy of novel anti-gastric cancer drugs in a preclinical murine model with minimum interindividual variation.</description><subject>Abdominal Surgery</subject><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - administration & dosage</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Cancer Research</subject><subject>Gastric cancer</subject><subject>Gastroenterology</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Humans</subject><subject>Luminescent Proteins - genetics</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mice, Nude</subject><subject>Mice, Transgenic</subject><subject>Microscopy, Confocal - methods</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Paclitaxel - administration & dosage</subject><subject>Paclitaxel - pharmacology</subject><subject>Peritoneal Neoplasms - drug therapy</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Red Fluorescent Protein</subject><subject>Stomach Neoplasms - drug therapy</subject><subject>Stomach Neoplasms - pathology</subject><subject>Surgical Oncology</subject><subject>Xenograft Model Antitumor Assays</subject><issn>1436-3291</issn><issn>1436-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kc1u1TAUhC1ERUvLA7BBltiwCfVffOMlqgpUqsSGri1f5yQ3VWIH2ynNq_C0nOi2CCGx8s98M8fWEPKWs4-csd1l5owLVjEuKyalqtYX5IwrqSspWf3yeS8MPyWvc75njNeG61fkVChpjDLqjPy6CfRheIg0zmXwbqSzK4c4xn6lscODH4fiHmGk0HWoe7wOtByAzpCGEgOgZYLicnHop48QYp9cV-gUW3RhRo9aQsm74CHRJQ-hp-VnrOZDxAA6uozXGeWwKdPgU8w-zusFOencmOHN03pO7j5ff7_6Wt1--3Jz9em28lrJUolOKyNczYXTcu9U673ZOSOk1syB3ytZC1MLpqFtmk4yJhqxl0Y0O9E22tTynHw45s4p_lggFzsN2cM4ugBxyZZrqcSuUUYj-v4f9D4uKeDrNkrUnOMspPiR2n6SE3R2TsPk0mo5s1tx9licxeLsVpxd0fPuKXnZT9D-cTw3hYA4Ahml0EP6a_R_U38DT-il2w</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Shimura, Tadanobu</creator><creator>Tanaka, Koji</creator><creator>Toiyama, Yuji</creator><creator>Okigami, Masato</creator><creator>Ide, Shozo</creator><creator>Kitajima, Takahito</creator><creator>Kondo, Satoru</creator><creator>Saigusa, Susumu</creator><creator>Ohi, Masaki</creator><creator>Araki, Toshimitsu</creator><creator>Inoue, Yasuhiro</creator><creator>Uchida, Keiichi</creator><creator>Mohri, Yasuhiko</creator><creator>Mizoguchi, Akira</creator><creator>Kusunoki, Masato</creator><general>Springer Japan</general><general>Springer Nature B.V</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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20150101</creationdate><title>In vivo optical pathology of paclitaxel efficacy on the peritoneal metastatic xenograft model of gastric cancer using two-photon laser scanning microscopy</title><author>Shimura, Tadanobu ; Tanaka, Koji ; Toiyama, Yuji ; Okigami, Masato ; Ide, Shozo ; Kitajima, Takahito ; Kondo, Satoru ; Saigusa, Susumu ; Ohi, Masaki ; Araki, Toshimitsu ; Inoue, Yasuhiro ; Uchida, Keiichi ; Mohri, Yasuhiko ; Mizoguchi, Akira ; Kusunoki, Masato</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c643t-2f6492a512a63ba4dcc97a923660aecb435295206ed88f300282b392872d86953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Abdominal Surgery</topic><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - administration & dosage</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Cancer Research</topic><topic>Gastric cancer</topic><topic>Gastroenterology</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Humans</topic><topic>Luminescent Proteins - genetics</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mice, Nude</topic><topic>Mice, Transgenic</topic><topic>Microscopy, Confocal - methods</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Paclitaxel - administration & dosage</topic><topic>Paclitaxel - pharmacology</topic><topic>Peritoneal Neoplasms - drug therapy</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Red Fluorescent Protein</topic><topic>Stomach Neoplasms - drug therapy</topic><topic>Stomach Neoplasms - pathology</topic><topic>Surgical Oncology</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimura, Tadanobu</creatorcontrib><creatorcontrib>Tanaka, Koji</creatorcontrib><creatorcontrib>Toiyama, Yuji</creatorcontrib><creatorcontrib>Okigami, Masato</creatorcontrib><creatorcontrib>Ide, Shozo</creatorcontrib><creatorcontrib>Kitajima, Takahito</creatorcontrib><creatorcontrib>Kondo, Satoru</creatorcontrib><creatorcontrib>Saigusa, Susumu</creatorcontrib><creatorcontrib>Ohi, Masaki</creatorcontrib><creatorcontrib>Araki, Toshimitsu</creatorcontrib><creatorcontrib>Inoue, Yasuhiro</creatorcontrib><creatorcontrib>Uchida, Keiichi</creatorcontrib><creatorcontrib>Mohri, Yasuhiko</creatorcontrib><creatorcontrib>Mizoguchi, Akira</creatorcontrib><creatorcontrib>Kusunoki, Masato</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimura, Tadanobu</au><au>Tanaka, Koji</au><au>Toiyama, Yuji</au><au>Okigami, Masato</au><au>Ide, Shozo</au><au>Kitajima, Takahito</au><au>Kondo, Satoru</au><au>Saigusa, Susumu</au><au>Ohi, Masaki</au><au>Araki, Toshimitsu</au><au>Inoue, Yasuhiro</au><au>Uchida, Keiichi</au><au>Mohri, Yasuhiko</au><au>Mizoguchi, Akira</au><au>Kusunoki, Masato</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo optical pathology of paclitaxel efficacy on the peritoneal metastatic xenograft model of gastric cancer using two-photon laser scanning microscopy</atitle><jtitle>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</jtitle><stitle>Gastric Cancer</stitle><addtitle>Gastric Cancer</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>18</volume><issue>1</issue><spage>109</spage><epage>118</epage><pages>109-118</pages><issn>1436-3291</issn><eissn>1436-3305</eissn><abstract>Background
We previously visualized in vivo responses to chemotherapy in a colorectal liver metastatic xenograft model using in vivo real-time and time-series intravital two-photon laser scanning microscopy (TPLSM). In this study, we established the method for evaluating the response of peritoneal xenografts to chemotherapy of metastatic gastric cancer using intravital TPLSM.
Methods
Red fluorescent protein-expressing gastric cancer cells (NUGC4) were inoculated into the peritoneal cavity of green fluorescent protein nude mice.
Results
Laparotomy revealed that 2 weeks after inoculation, macroscopic peritoneal metastatic nodules were formed. The first intravital TPLSM session revealed that they were composed of red tumor cell clusters and green surrounding stroma. Paclitaxel was administered intraperitoneally after the first TPLSM three times a week for 7 days in the treatment group. At the second laparotomy, there were significantly fewer and smaller nodules in the treated mice than in the controls. The second intravital TPLSM session showed tumor cell fragmentation, swelling, and nuclear condensation in the metastatic nodules—a response to chemotherapy. There were multinuclear tumor cells in the paclitaxel-treated living mice.
Conclusions
Our method may become a powerful tool for evaluating the efficacy of novel anti-gastric cancer drugs in a preclinical murine model with minimum interindividual variation.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>24399494</pmid><doi>10.1007/s10120-013-0334-y</doi><tpages>10</tpages></addata></record> |
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subjects | Abdominal Surgery Animals Antineoplastic Agents, Phytogenic - administration & dosage Antineoplastic Agents, Phytogenic - pharmacology Cancer Research Gastric cancer Gastroenterology Green Fluorescent Proteins - genetics Humans Luminescent Proteins - genetics Medicine Medicine & Public Health Mice, Nude Mice, Transgenic Microscopy, Confocal - methods Oncology Original Article Paclitaxel - administration & dosage Paclitaxel - pharmacology Peritoneal Neoplasms - drug therapy Peritoneal Neoplasms - secondary Red Fluorescent Protein Stomach Neoplasms - drug therapy Stomach Neoplasms - pathology Surgical Oncology Xenograft Model Antitumor Assays |
title | In vivo optical pathology of paclitaxel efficacy on the peritoneal metastatic xenograft model of gastric cancer using two-photon laser scanning microscopy |
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