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Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model
Purpose Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclona...
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Published in: | Surgery today (Tokyo, Japan) Japan), 2010-09, Vol.40 (9), p.851-857 |
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container_title | Surgery today (Tokyo, Japan) |
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creator | Imaizumi, Takuya Aoyagi, Keishiro Miyagi, Motoshi Shirouzu, Kazuo |
description | Purpose
Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclonal antibody against VEGF, had a suppressive effect on peritoneal dissemination from gastric cancer, in an experimental nude mouse model of peritoneal metastasis.
Methods
Each mouse was treated with a single intraperitoneal (i.p.) injection of bevacizumab. Five mice were killed, and we measured their body weight, the mean number of tumor nodules, and the volume of ascites. We also extracted retroperitoneal tissues for histological examination, to count the frequency of mitosis, and to calculate the mitotic index. Another five mice were monitored until death, and their mean survival duration was calculated.
Results
The volume of ascites and the mitotic index were significantly lower in the therapy group than in the nontherapy group (
P
= 0.042 and
P
< 0.01, respectively). The survival curve of the therapy group was significantly higher than that of the nontherapy group (
P
= 0.005).
Conclusion
Bevacizumab may suppress peritoneal dissemination from gastric cancer. |
doi_str_mv | 10.1007/s00595-009-4154-y |
format | article |
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Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclonal antibody against VEGF, had a suppressive effect on peritoneal dissemination from gastric cancer, in an experimental nude mouse model of peritoneal metastasis.
Methods
Each mouse was treated with a single intraperitoneal (i.p.) injection of bevacizumab. Five mice were killed, and we measured their body weight, the mean number of tumor nodules, and the volume of ascites. We also extracted retroperitoneal tissues for histological examination, to count the frequency of mitosis, and to calculate the mitotic index. Another five mice were monitored until death, and their mean survival duration was calculated.
Results
The volume of ascites and the mitotic index were significantly lower in the therapy group than in the nontherapy group (
P
= 0.042 and
P
< 0.01, respectively). The survival curve of the therapy group was significantly higher than that of the nontherapy group (
P
= 0.005).
Conclusion
Bevacizumab may suppress peritoneal dissemination from gastric cancer.</description><identifier>ISSN: 0941-1291</identifier><identifier>EISSN: 1436-2813</identifier><identifier>DOI: 10.1007/s00595-009-4154-y</identifier><identifier>PMID: 20740349</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Angiogenesis Inhibitors - administration & dosage ; Animals ; Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal, Humanized ; Ascites - pathology ; Bevacizumab ; Cell Line, Tumor ; Injections, Intraperitoneal ; Male ; Medicine ; Medicine & Public Health ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Mitotic Index ; Neoplasm Transplantation ; Original Article ; Peritoneal Neoplasms - pathology ; Peritoneal Neoplasms - prevention & control ; Peritoneal Neoplasms - secondary ; Stomach Neoplasms - pathology ; Surgery ; Surgical Oncology ; Vascular Endothelial Growth Factor A - immunology</subject><ispartof>Surgery today (Tokyo, Japan), 2010-09, Vol.40 (9), p.851-857</ispartof><rights>Springer 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-b63b8b163ba4fa96b07aadc8ef7d752006d1fe8f5b5184b4bcae0b0506eda98f3</citedby><cites>FETCH-LOGICAL-c396t-b63b8b163ba4fa96b07aadc8ef7d752006d1fe8f5b5184b4bcae0b0506eda98f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20740349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Imaizumi, Takuya</creatorcontrib><creatorcontrib>Aoyagi, Keishiro</creatorcontrib><creatorcontrib>Miyagi, Motoshi</creatorcontrib><creatorcontrib>Shirouzu, Kazuo</creatorcontrib><title>Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model</title><title>Surgery today (Tokyo, Japan)</title><addtitle>Surg Today</addtitle><addtitle>Surg Today</addtitle><description>Purpose
Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclonal antibody against VEGF, had a suppressive effect on peritoneal dissemination from gastric cancer, in an experimental nude mouse model of peritoneal metastasis.
Methods
Each mouse was treated with a single intraperitoneal (i.p.) injection of bevacizumab. Five mice were killed, and we measured their body weight, the mean number of tumor nodules, and the volume of ascites. We also extracted retroperitoneal tissues for histological examination, to count the frequency of mitosis, and to calculate the mitotic index. Another five mice were monitored until death, and their mean survival duration was calculated.
Results
The volume of ascites and the mitotic index were significantly lower in the therapy group than in the nontherapy group (
P
= 0.042 and
P
< 0.01, respectively). The survival curve of the therapy group was significantly higher than that of the nontherapy group (
P
= 0.005).
Conclusion
Bevacizumab may suppress peritoneal dissemination from gastric cancer.</description><subject>Angiogenesis Inhibitors - administration & dosage</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antibodies, Monoclonal, Humanized</subject><subject>Ascites - pathology</subject><subject>Bevacizumab</subject><subject>Cell Line, Tumor</subject><subject>Injections, Intraperitoneal</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Mitotic Index</subject><subject>Neoplasm Transplantation</subject><subject>Original Article</subject><subject>Peritoneal Neoplasms - pathology</subject><subject>Peritoneal Neoplasms - prevention & control</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Stomach Neoplasms - pathology</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Vascular Endothelial Growth Factor A - immunology</subject><issn>0941-1291</issn><issn>1436-2813</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kMFO3TAQRS0EglfKB7CpvGOVdpw4ib1EqEAlpC7ari3bGSOjJE49CdLr12P0oOqqm5nFnHulOYxdCvgsAPovBNDqtgLQlRStrPZHbCdk01W1Es0x24GWohK1FmfsA9ETQC0VwCk7q6GX0Ei9Y_nHtiwZieIzcgwB_cpT4A6frY9_tsk6nma-YI5rmtGOfIhEOMXZrrEcQk4Tf7S05ui5t7PHzOPM7b-JCdcCWIrEpzTg-JGdBDsSXrztc_br9uvPm_vq4fvdt5vrh8o3ulsr1zVOOVGmlcHqzkFv7eAVhn7o2xqgG0RAFVrXCiWddN4iOGihw8FqFZpzdnXoXXL6vSGtZorkcRztjGkj00ulteykKqQ4kD4noozBLDlONu-NAPNq2hxMm2LavJo2-5L59Na-uQmHv4l3tQWoDwCV0_yI2TylLc_l4_-0vgDWgo1D</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Imaizumi, Takuya</creator><creator>Aoyagi, Keishiro</creator><creator>Miyagi, Motoshi</creator><creator>Shirouzu, Kazuo</creator><general>Springer Japan</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></search><sort><creationdate>20100901</creationdate><title>Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model</title><author>Imaizumi, Takuya ; Aoyagi, Keishiro ; Miyagi, Motoshi ; Shirouzu, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-b63b8b163ba4fa96b07aadc8ef7d752006d1fe8f5b5184b4bcae0b0506eda98f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Angiogenesis Inhibitors - administration & dosage</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Antibodies, Monoclonal, Humanized</topic><topic>Ascites - pathology</topic><topic>Bevacizumab</topic><topic>Cell Line, Tumor</topic><topic>Injections, Intraperitoneal</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Mitotic Index</topic><topic>Neoplasm Transplantation</topic><topic>Original Article</topic><topic>Peritoneal Neoplasms - pathology</topic><topic>Peritoneal Neoplasms - prevention & control</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Stomach Neoplasms - pathology</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Vascular Endothelial Growth Factor A - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Imaizumi, Takuya</creatorcontrib><creatorcontrib>Aoyagi, Keishiro</creatorcontrib><creatorcontrib>Miyagi, Motoshi</creatorcontrib><creatorcontrib>Shirouzu, Kazuo</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>Surgery today (Tokyo, Japan)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imaizumi, Takuya</au><au>Aoyagi, Keishiro</au><au>Miyagi, Motoshi</au><au>Shirouzu, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model</atitle><jtitle>Surgery today (Tokyo, Japan)</jtitle><stitle>Surg Today</stitle><addtitle>Surg Today</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>40</volume><issue>9</issue><spage>851</spage><epage>857</epage><pages>851-857</pages><issn>0941-1291</issn><eissn>1436-2813</eissn><abstract>Purpose
Vascular endothelial growth factor (VEGF) has been reported to enhance vascular permeability and angiogenesis in the abdominal wall, thereby contributing to peritoneal dissemination with malignant ascites. We conducted this experimental study to find out if bevacizumab, a humanized monoclonal antibody against VEGF, had a suppressive effect on peritoneal dissemination from gastric cancer, in an experimental nude mouse model of peritoneal metastasis.
Methods
Each mouse was treated with a single intraperitoneal (i.p.) injection of bevacizumab. Five mice were killed, and we measured their body weight, the mean number of tumor nodules, and the volume of ascites. We also extracted retroperitoneal tissues for histological examination, to count the frequency of mitosis, and to calculate the mitotic index. Another five mice were monitored until death, and their mean survival duration was calculated.
Results
The volume of ascites and the mitotic index were significantly lower in the therapy group than in the nontherapy group (
P
= 0.042 and
P
< 0.01, respectively). The survival curve of the therapy group was significantly higher than that of the nontherapy group (
P
= 0.005).
Conclusion
Bevacizumab may suppress peritoneal dissemination from gastric cancer.</abstract><cop>Japan</cop><pub>Springer Japan</pub><pmid>20740349</pmid><doi>10.1007/s00595-009-4154-y</doi><tpages>7</tpages></addata></record> |
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language | eng |
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source | Springer Nature |
subjects | Angiogenesis Inhibitors - administration & dosage Animals Antibodies, Monoclonal - administration & dosage Antibodies, Monoclonal, Humanized Ascites - pathology Bevacizumab Cell Line, Tumor Injections, Intraperitoneal Male Medicine Medicine & Public Health Mice Mice, Inbred BALB C Mice, Nude Mitotic Index Neoplasm Transplantation Original Article Peritoneal Neoplasms - pathology Peritoneal Neoplasms - prevention & control Peritoneal Neoplasms - secondary Stomach Neoplasms - pathology Surgery Surgical Oncology Vascular Endothelial Growth Factor A - immunology |
title | Suppressive effect of bevacizumab on peritoneal dissemination from gastric cancer in a peritoneal metastasis model |
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