Nuclear heat shock protein 110 expression is associated with poor prognosis and hyperthermo-chemotherapy resistance in gastric cancer patients with peritoneal metastasis

AIM To investigate the significance of heat shock protein 110(HSP110) in gastric cancer(GC) patients with peritoneal metastasis undergoing hyperthermochemotherapy.METHODS Primary GC patients(n = 14) with peritoneal metastasis or positive peritoneal lavage cytology who underwent distal or total gastr...

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Veröffentlicht in:World journal of gastroenterology : WJG 2017-11, Vol.23 (42), p.7541-7550
Hauptverfasser: Kimura, Akiharu, Ogata, Kyoichi, Altan, Bolag, Yokobori, Takehiko, Mochiki, Erito, Yanai, Mitsuhiro, Kogure, Norimichi, Yanoma, Toru, Suzuki, Masaki, Bai, Tuya, Kuwano, Hiroyuki
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container_end_page 7550
container_issue 42
container_start_page 7541
container_title World journal of gastroenterology : WJG
container_volume 23
creator Kimura, Akiharu
Ogata, Kyoichi
Altan, Bolag
Yokobori, Takehiko
Mochiki, Erito
Yanai, Mitsuhiro
Kogure, Norimichi
Yanoma, Toru
Suzuki, Masaki
Bai, Tuya
Kuwano, Hiroyuki
description AIM To investigate the significance of heat shock protein 110(HSP110) in gastric cancer(GC) patients with peritoneal metastasis undergoing hyperthermochemotherapy.METHODS Primary GC patients(n = 14) with peritoneal metastasis or positive peritoneal lavage cytology who underwent distal or total gastrectomy between April 2000 and December 2011 were enrolled in this study. The patients underwent postoperative intraperitoneal hyperthermo-chemotherapy using a Thermotron RF-8 heating device two weeks after surgery. We analyzed nuclear HSP110 expression in surgically resected tumors using immunohistochemistry. Additionally, the effect of HSP110 suppression on hyptherthermochemosensitivity was assessed in vitro in the MKN45 GC cell line using the HSP inhibitor KNK437. RESULTS HSP110 immnohistochemical staining in 14 GC patients showed that five(35.7%) samples belonged to the low expression group, and nine(64.3%) samples belonged to the high expression group. Progression-free survival was significantly shorter in the HSP110 high-expression group than in the low-expression group(P = 0.0313). However, no significant relationships were identified between HSP110 expression and the clinicopathological characteristics of patients. Furthermore, high HSP110 expression was not an independent prognostic factor in GC patients with peritoneal metastasis(P = 0.0625). HSP110 expression in MKN45 cells was suppressed by KNK437 at the hyperthermic temperature of 43 ℃ in vitro. Comparison of MKN45 cell proliferation in the presence and absence of KNK437 at 43 ℃, revealed that proliferation was significantly decreased when HSP110 was inhibited by KNK437. Additionally, HSP110 suppression via HSP inhibitor treatment increased cellular sensitivity to hyperthermo-chemotherapy in vitro.CONCLUSION The expression of nuclear HSP110 in GC patients might be a new marker of chemosensitivity and a therapeutic target for patients who are tolerant to existing hyperthermo-chemotherapies.
doi_str_mv 10.3748/wjg.v23.i42.7541
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The patients underwent postoperative intraperitoneal hyperthermo-chemotherapy using a Thermotron RF-8 heating device two weeks after surgery. We analyzed nuclear HSP110 expression in surgically resected tumors using immunohistochemistry. Additionally, the effect of HSP110 suppression on hyptherthermochemosensitivity was assessed in vitro in the MKN45 GC cell line using the HSP inhibitor KNK437. RESULTS HSP110 immnohistochemical staining in 14 GC patients showed that five(35.7%) samples belonged to the low expression group, and nine(64.3%) samples belonged to the high expression group. Progression-free survival was significantly shorter in the HSP110 high-expression group than in the low-expression group(P = 0.0313). However, no significant relationships were identified between HSP110 expression and the clinicopathological characteristics of patients. Furthermore, high HSP110 expression was not an independent prognostic factor in GC patients with peritoneal metastasis(P = 0.0625). HSP110 expression in MKN45 cells was suppressed by KNK437 at the hyperthermic temperature of 43 ℃ in vitro. Comparison of MKN45 cell proliferation in the presence and absence of KNK437 at 43 ℃, revealed that proliferation was significantly decreased when HSP110 was inhibited by KNK437. Additionally, HSP110 suppression via HSP inhibitor treatment increased cellular sensitivity to hyperthermo-chemotherapy in vitro.CONCLUSION The expression of nuclear HSP110 in GC patients might be a new marker of chemosensitivity and a therapeutic target for patients who are tolerant to existing hyperthermo-chemotherapies.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v23.i42.7541</identifier><identifier>PMID: 29204054</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Inc</publisher><subject>Basic Study</subject><ispartof>World journal of gastroenterology : WJG, 2017-11, Vol.23 (42), p.7541-7550</ispartof><rights>The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. 2017</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-628594b353a2cdbadf68f7d966dd0892ac6802cb78b16ee7789786fd4dd400dd3</citedby><cites>FETCH-LOGICAL-c440t-628594b353a2cdbadf68f7d966dd0892ac6802cb78b16ee7789786fd4dd400dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698247/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698247/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29204054$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kimura, Akiharu</creatorcontrib><creatorcontrib>Ogata, Kyoichi</creatorcontrib><creatorcontrib>Altan, Bolag</creatorcontrib><creatorcontrib>Yokobori, Takehiko</creatorcontrib><creatorcontrib>Mochiki, Erito</creatorcontrib><creatorcontrib>Yanai, Mitsuhiro</creatorcontrib><creatorcontrib>Kogure, Norimichi</creatorcontrib><creatorcontrib>Yanoma, Toru</creatorcontrib><creatorcontrib>Suzuki, Masaki</creatorcontrib><creatorcontrib>Bai, Tuya</creatorcontrib><creatorcontrib>Kuwano, Hiroyuki</creatorcontrib><title>Nuclear heat shock protein 110 expression is associated with poor prognosis and hyperthermo-chemotherapy resistance in gastric cancer patients with peritoneal metastasis</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM To investigate the significance of heat shock protein 110(HSP110) in gastric cancer(GC) patients with peritoneal metastasis undergoing hyperthermochemotherapy.METHODS Primary GC patients(n = 14) with peritoneal metastasis or positive peritoneal lavage cytology who underwent distal or total gastrectomy between April 2000 and December 2011 were enrolled in this study. The patients underwent postoperative intraperitoneal hyperthermo-chemotherapy using a Thermotron RF-8 heating device two weeks after surgery. We analyzed nuclear HSP110 expression in surgically resected tumors using immunohistochemistry. Additionally, the effect of HSP110 suppression on hyptherthermochemosensitivity was assessed in vitro in the MKN45 GC cell line using the HSP inhibitor KNK437. RESULTS HSP110 immnohistochemical staining in 14 GC patients showed that five(35.7%) samples belonged to the low expression group, and nine(64.3%) samples belonged to the high expression group. Progression-free survival was significantly shorter in the HSP110 high-expression group than in the low-expression group(P = 0.0313). However, no significant relationships were identified between HSP110 expression and the clinicopathological characteristics of patients. Furthermore, high HSP110 expression was not an independent prognostic factor in GC patients with peritoneal metastasis(P = 0.0625). HSP110 expression in MKN45 cells was suppressed by KNK437 at the hyperthermic temperature of 43 ℃ in vitro. Comparison of MKN45 cell proliferation in the presence and absence of KNK437 at 43 ℃, revealed that proliferation was significantly decreased when HSP110 was inhibited by KNK437. Additionally, HSP110 suppression via HSP inhibitor treatment increased cellular sensitivity to hyperthermo-chemotherapy in vitro.CONCLUSION The expression of nuclear HSP110 in GC patients might be a new marker of chemosensitivity and a therapeutic target for patients who are tolerant to existing hyperthermo-chemotherapies.</description><subject>Basic Study</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVkU1v1DAQhiMEokvhzgn5yCWLvxLbFyRU8SVVcIGz5bVnE5fETm1vy_4k_iUOXVYwlxl53vfxSG_TvCR4ywSXb-5vhu0dZVvP6VZ0nDxqNpQS1VLJ8eNmQzAWrWJUXDTPcr7BmDLW0afNBVUUc9zxTfPry8FOYBIawRSUx2h_oCXFAj4gQjCCn0uCnH0MyGdkco7WmwIO3fsyoiXGtMqHEPO6Dg6NxwVSGSHNsbUjzHGdzXJEFeNzMcECquzB5JK8RXZ9qAxTPISST1hIvsQAZkIzlKo01fq8ebI3U4YXp37ZfP_w_tvVp_b668fPV--uW8s5Lm1PZaf4jnXMUOt2xu17uRdO9b1zWCpqbC8xtTshd6QHEEIqIfu9485xjJ1jl83bB-5y2M3gbD0rmUkvyc8mHXU0Xv-_CX7UQ7zTXa8k5aICXp8AKd4eIBc9-2xhmkyAeMiaKMEwJYyQKsUPUptizgn2528I1mvCuiasa8K6JqzXhKvl1b_nnQ1_I60CdmKOMQy3PgxnjcJyLdVhLrnquo7-mWR1_QZd6Ljl</recordid><startdate>20171114</startdate><enddate>20171114</enddate><creator>Kimura, Akiharu</creator><creator>Ogata, Kyoichi</creator><creator>Altan, Bolag</creator><creator>Yokobori, Takehiko</creator><creator>Mochiki, Erito</creator><creator>Yanai, Mitsuhiro</creator><creator>Kogure, Norimichi</creator><creator>Yanoma, Toru</creator><creator>Suzuki, Masaki</creator><creator>Bai, Tuya</creator><creator>Kuwano, Hiroyuki</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20171114</creationdate><title>Nuclear heat shock protein 110 expression is associated with poor prognosis and hyperthermo-chemotherapy resistance in gastric cancer patients with peritoneal metastasis</title><author>Kimura, Akiharu ; Ogata, Kyoichi ; Altan, Bolag ; Yokobori, Takehiko ; Mochiki, Erito ; Yanai, Mitsuhiro ; Kogure, Norimichi ; Yanoma, Toru ; Suzuki, Masaki ; Bai, Tuya ; Kuwano, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-628594b353a2cdbadf68f7d966dd0892ac6802cb78b16ee7789786fd4dd400dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Basic Study</topic><toplevel>online_resources</toplevel><creatorcontrib>Kimura, Akiharu</creatorcontrib><creatorcontrib>Ogata, Kyoichi</creatorcontrib><creatorcontrib>Altan, Bolag</creatorcontrib><creatorcontrib>Yokobori, Takehiko</creatorcontrib><creatorcontrib>Mochiki, Erito</creatorcontrib><creatorcontrib>Yanai, Mitsuhiro</creatorcontrib><creatorcontrib>Kogure, Norimichi</creatorcontrib><creatorcontrib>Yanoma, Toru</creatorcontrib><creatorcontrib>Suzuki, Masaki</creatorcontrib><creatorcontrib>Bai, Tuya</creatorcontrib><creatorcontrib>Kuwano, Hiroyuki</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimura, Akiharu</au><au>Ogata, Kyoichi</au><au>Altan, Bolag</au><au>Yokobori, Takehiko</au><au>Mochiki, Erito</au><au>Yanai, Mitsuhiro</au><au>Kogure, Norimichi</au><au>Yanoma, Toru</au><au>Suzuki, Masaki</au><au>Bai, Tuya</au><au>Kuwano, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nuclear heat shock protein 110 expression is associated with poor prognosis and hyperthermo-chemotherapy resistance in gastric cancer patients with peritoneal metastasis</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2017-11-14</date><risdate>2017</risdate><volume>23</volume><issue>42</issue><spage>7541</spage><epage>7550</epage><pages>7541-7550</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM To investigate the significance of heat shock protein 110(HSP110) in gastric cancer(GC) patients with peritoneal metastasis undergoing hyperthermochemotherapy.METHODS Primary GC patients(n = 14) with peritoneal metastasis or positive peritoneal lavage cytology who underwent distal or total gastrectomy between April 2000 and December 2011 were enrolled in this study. The patients underwent postoperative intraperitoneal hyperthermo-chemotherapy using a Thermotron RF-8 heating device two weeks after surgery. We analyzed nuclear HSP110 expression in surgically resected tumors using immunohistochemistry. Additionally, the effect of HSP110 suppression on hyptherthermochemosensitivity was assessed in vitro in the MKN45 GC cell line using the HSP inhibitor KNK437. RESULTS HSP110 immnohistochemical staining in 14 GC patients showed that five(35.7%) samples belonged to the low expression group, and nine(64.3%) samples belonged to the high expression group. Progression-free survival was significantly shorter in the HSP110 high-expression group than in the low-expression group(P = 0.0313). However, no significant relationships were identified between HSP110 expression and the clinicopathological characteristics of patients. Furthermore, high HSP110 expression was not an independent prognostic factor in GC patients with peritoneal metastasis(P = 0.0625). HSP110 expression in MKN45 cells was suppressed by KNK437 at the hyperthermic temperature of 43 ℃ in vitro. Comparison of MKN45 cell proliferation in the presence and absence of KNK437 at 43 ℃, revealed that proliferation was significantly decreased when HSP110 was inhibited by KNK437. Additionally, HSP110 suppression via HSP inhibitor treatment increased cellular sensitivity to hyperthermo-chemotherapy in vitro.CONCLUSION The expression of nuclear HSP110 in GC patients might be a new marker of chemosensitivity and a therapeutic target for patients who are tolerant to existing hyperthermo-chemotherapies.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Inc</pub><pmid>29204054</pmid><doi>10.3748/wjg.v23.i42.7541</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source Baishideng "World Journal of" online journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
subjects Basic Study
title Nuclear heat shock protein 110 expression is associated with poor prognosis and hyperthermo-chemotherapy resistance in gastric cancer patients with peritoneal metastasis
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