Expression and prognostic significance of placental growth factor in hepatocellular carcinoma and peritumoral liver tissue
Vascular endothelial growth factor‐targeted therapy is a promising treatment for hepatocellular carcinoma (HCC), but its clinical benefit is often accompanied by acquired resistance. In animal studies, antiplacental growth factor therapy is effective with less resistance. The role of placental growt...
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Veröffentlicht in: | International journal of cancer 2011-04, Vol.128 (7), p.1559-1569 |
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creator | Xu, Hua‐Xiang Zhu, Xiao‐Dong Zhuang, Peng‐Yuan Zhang, Ju‐Bo Zhang, Wei Kong, Ling‐Qun Wang, Wen‐Quan Liang, Ying Wu, Wei‐Zhong Wang, Lu Fan, Jia Tang, Zhao‐You Sun, Hui‐Chuan |
description | Vascular endothelial growth factor‐targeted therapy is a promising treatment for hepatocellular carcinoma (HCC), but its clinical benefit is often accompanied by acquired resistance. In animal studies, antiplacental growth factor therapy is effective with less resistance. The role of placental growth factor (PlGF) in the progression of HCC is not clear. In our study, we used immunohistochemistry in tissue microarrays to investigate PlGF expression in tumor and peritumoral liver tissues from 105 patients with HCC. Intratumoral and peritumoral PlGF mRNA expression was analyzed in another cohort of 37 patients. Peritumoral PlGF expression was significantly higher than intratumoral PlGF expression (p < 0.001). Intratumoral PlGF expression was not associated with patients' overall survival (OS) or time to recurrence (TTR). However, peritumoral PlGF expression, which was associated with tumor size, presence of intrahepatic metastasis, TNM stage and Barcelona Clinic Liver Cancer stage, was an independent risk factor for OS (p = 0.026) and TTR (p = 0.041). The prognostic value of peritumoral PlGF expression was further validated in a validation cohort (n = 394). We inferred that the elevation of PlGF in peritumoral liver might be induced by hypoxia. We found that peritumoral PlGF expression was associated with hypoxia‐inducible factor‐1α (p = 0.017). PlGF expression was elevated in L02, a hepatic cell line, under hypoxic conditions in vitro. These findings indicate that high peritumoral PlGF expression is associated with tumor recurrence and survival after resection of HCC. PlGF could be a target of adjuvant therapy and deserves further investigations. |
doi_str_mv | 10.1002/ijc.25492 |
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In animal studies, antiplacental growth factor therapy is effective with less resistance. The role of placental growth factor (PlGF) in the progression of HCC is not clear. In our study, we used immunohistochemistry in tissue microarrays to investigate PlGF expression in tumor and peritumoral liver tissues from 105 patients with HCC. Intratumoral and peritumoral PlGF mRNA expression was analyzed in another cohort of 37 patients. Peritumoral PlGF expression was significantly higher than intratumoral PlGF expression (p < 0.001). Intratumoral PlGF expression was not associated with patients' overall survival (OS) or time to recurrence (TTR). However, peritumoral PlGF expression, which was associated with tumor size, presence of intrahepatic metastasis, TNM stage and Barcelona Clinic Liver Cancer stage, was an independent risk factor for OS (p = 0.026) and TTR (p = 0.041). The prognostic value of peritumoral PlGF expression was further validated in a validation cohort (n = 394). We inferred that the elevation of PlGF in peritumoral liver might be induced by hypoxia. We found that peritumoral PlGF expression was associated with hypoxia‐inducible factor‐1α (p = 0.017). PlGF expression was elevated in L02, a hepatic cell line, under hypoxic conditions in vitro. These findings indicate that high peritumoral PlGF expression is associated with tumor recurrence and survival after resection of HCC. PlGF could be a target of adjuvant therapy and deserves further investigations.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.25492</identifier><identifier>PMID: 20521248</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Carcinoma, Hepatocellular - diagnosis ; Carcinoma, Hepatocellular - metabolism ; Carcinoma, Hepatocellular - surgery ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Gene Expression Regulation, Neoplastic ; hepatocellular carcinoma ; Humans ; Immunohistochemistry - methods ; Ligands ; Liver - metabolism ; Liver Neoplasms - diagnosis ; Liver Neoplasms - metabolism ; Liver Neoplasms - surgery ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Neovascularization, Pathologic - metabolism ; Oligonucleotide Array Sequence Analysis ; peritumoral liver tissue ; Placenta Growth Factor ; placental growth factor ; Pregnancy Proteins - biosynthesis ; Prognosis ; Tumors ; vascular endothelial growth factor</subject><ispartof>International journal of cancer, 2011-04, Vol.128 (7), p.1559-1569</ispartof><rights>Copyright © 2010 UICC</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 UICC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3542-de95b832dccf69025d90454ac9b1f39f9c219ccff43d5a5f608b8b393c3b693</citedby><cites>FETCH-LOGICAL-c3542-de95b832dccf69025d90454ac9b1f39f9c219ccff43d5a5f608b8b393c3b693</cites></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.25492$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.25492$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23878747$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20521248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Hua‐Xiang</creatorcontrib><creatorcontrib>Zhu, Xiao‐Dong</creatorcontrib><creatorcontrib>Zhuang, Peng‐Yuan</creatorcontrib><creatorcontrib>Zhang, Ju‐Bo</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Kong, Ling‐Qun</creatorcontrib><creatorcontrib>Wang, Wen‐Quan</creatorcontrib><creatorcontrib>Liang, Ying</creatorcontrib><creatorcontrib>Wu, Wei‐Zhong</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Fan, Jia</creatorcontrib><creatorcontrib>Tang, Zhao‐You</creatorcontrib><creatorcontrib>Sun, Hui‐Chuan</creatorcontrib><title>Expression and prognostic significance of placental growth factor in hepatocellular carcinoma and peritumoral liver tissue</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Vascular endothelial growth factor‐targeted therapy is a promising treatment for hepatocellular carcinoma (HCC), but its clinical benefit is often accompanied by acquired resistance. In animal studies, antiplacental growth factor therapy is effective with less resistance. The role of placental growth factor (PlGF) in the progression of HCC is not clear. In our study, we used immunohistochemistry in tissue microarrays to investigate PlGF expression in tumor and peritumoral liver tissues from 105 patients with HCC. Intratumoral and peritumoral PlGF mRNA expression was analyzed in another cohort of 37 patients. Peritumoral PlGF expression was significantly higher than intratumoral PlGF expression (p < 0.001). Intratumoral PlGF expression was not associated with patients' overall survival (OS) or time to recurrence (TTR). However, peritumoral PlGF expression, which was associated with tumor size, presence of intrahepatic metastasis, TNM stage and Barcelona Clinic Liver Cancer stage, was an independent risk factor for OS (p = 0.026) and TTR (p = 0.041). The prognostic value of peritumoral PlGF expression was further validated in a validation cohort (n = 394). We inferred that the elevation of PlGF in peritumoral liver might be induced by hypoxia. We found that peritumoral PlGF expression was associated with hypoxia‐inducible factor‐1α (p = 0.017). PlGF expression was elevated in L02, a hepatic cell line, under hypoxic conditions in vitro. These findings indicate that high peritumoral PlGF expression is associated with tumor recurrence and survival after resection of HCC. PlGF could be a target of adjuvant therapy and deserves further investigations.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Hepatocellular - diagnosis</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Carcinoma, Hepatocellular - surgery</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>hepatocellular carcinoma</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>Ligands</subject><subject>Liver - metabolism</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - metabolism</subject><subject>Liver Neoplasms - surgery</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neovascularization, Pathologic - metabolism</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>peritumoral liver tissue</subject><subject>Placenta Growth Factor</subject><subject>placental growth factor</subject><subject>Pregnancy Proteins - biosynthesis</subject><subject>Prognosis</subject><subject>Tumors</subject><subject>vascular endothelial growth factor</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAURS0EoqUw8AeQFwaGtP6Im3hEVYEiJAbYI-fFbl25cWSnlPLrCaTAxPSGe9690kHokpIxJYRN7BrGTKSSHaEhJTJLCKPiGA27jCQZ5dMBOotxTQilgqSnaMCIYJSl-RB9zN-boGO0vsaqrnAT_LL2sbWAo13W1lhQNWjsDW6cAl23yuFl8Lt2hY2C1gdsa7zSjWo9aOe2TgUMKoCt_Ub1lTrYdrvxoft09k0H3NoYt_ocnRjlor443BF6uZu_zh6Sp-f7xez2KQEuUpZUWooy56wCMFNJmKgkSUWqQJbUcGkkMCq7zKS8EkqYKcnLvOSSAy-nko_QTd8KwccYtCmaYDcq7AtKii97RWev-LbXsVc922zLja5-yR9dHXB9AFQE5Uzo3Nj4x_E8y7M067hJz-2s0_v_F4vF46yf_gR42omX</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>Xu, Hua‐Xiang</creator><creator>Zhu, Xiao‐Dong</creator><creator>Zhuang, Peng‐Yuan</creator><creator>Zhang, Ju‐Bo</creator><creator>Zhang, Wei</creator><creator>Kong, Ling‐Qun</creator><creator>Wang, Wen‐Quan</creator><creator>Liang, Ying</creator><creator>Wu, Wei‐Zhong</creator><creator>Wang, Lu</creator><creator>Fan, Jia</creator><creator>Tang, Zhao‐You</creator><creator>Sun, Hui‐Chuan</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20110401</creationdate><title>Expression and prognostic significance of placental growth factor in hepatocellular carcinoma and peritumoral liver tissue</title><author>Xu, Hua‐Xiang ; Zhu, Xiao‐Dong ; Zhuang, Peng‐Yuan ; Zhang, Ju‐Bo ; Zhang, Wei ; Kong, Ling‐Qun ; Wang, Wen‐Quan ; Liang, Ying ; Wu, Wei‐Zhong ; Wang, Lu ; Fan, Jia ; Tang, Zhao‐You ; Sun, Hui‐Chuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3542-de95b832dccf69025d90454ac9b1f39f9c219ccff43d5a5f608b8b393c3b693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Hepatocellular - diagnosis</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Carcinoma, Hepatocellular - surgery</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>hepatocellular carcinoma</topic><topic>Humans</topic><topic>Immunohistochemistry - methods</topic><topic>Ligands</topic><topic>Liver - metabolism</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - metabolism</topic><topic>Liver Neoplasms - surgery</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neovascularization, Pathologic - metabolism</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>peritumoral liver tissue</topic><topic>Placenta Growth Factor</topic><topic>placental growth factor</topic><topic>Pregnancy Proteins - biosynthesis</topic><topic>Prognosis</topic><topic>Tumors</topic><topic>vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Hua‐Xiang</creatorcontrib><creatorcontrib>Zhu, Xiao‐Dong</creatorcontrib><creatorcontrib>Zhuang, Peng‐Yuan</creatorcontrib><creatorcontrib>Zhang, Ju‐Bo</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Kong, Ling‐Qun</creatorcontrib><creatorcontrib>Wang, Wen‐Quan</creatorcontrib><creatorcontrib>Liang, Ying</creatorcontrib><creatorcontrib>Wu, Wei‐Zhong</creatorcontrib><creatorcontrib>Wang, Lu</creatorcontrib><creatorcontrib>Fan, Jia</creatorcontrib><creatorcontrib>Tang, Zhao‐You</creatorcontrib><creatorcontrib>Sun, Hui‐Chuan</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Hua‐Xiang</au><au>Zhu, Xiao‐Dong</au><au>Zhuang, Peng‐Yuan</au><au>Zhang, Ju‐Bo</au><au>Zhang, Wei</au><au>Kong, Ling‐Qun</au><au>Wang, Wen‐Quan</au><au>Liang, Ying</au><au>Wu, Wei‐Zhong</au><au>Wang, Lu</au><au>Fan, Jia</au><au>Tang, Zhao‐You</au><au>Sun, Hui‐Chuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression and prognostic significance of placental growth factor in hepatocellular carcinoma and peritumoral liver tissue</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>128</volume><issue>7</issue><spage>1559</spage><epage>1569</epage><pages>1559-1569</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Vascular endothelial growth factor‐targeted therapy is a promising treatment for hepatocellular carcinoma (HCC), but its clinical benefit is often accompanied by acquired resistance. In animal studies, antiplacental growth factor therapy is effective with less resistance. The role of placental growth factor (PlGF) in the progression of HCC is not clear. In our study, we used immunohistochemistry in tissue microarrays to investigate PlGF expression in tumor and peritumoral liver tissues from 105 patients with HCC. Intratumoral and peritumoral PlGF mRNA expression was analyzed in another cohort of 37 patients. Peritumoral PlGF expression was significantly higher than intratumoral PlGF expression (p < 0.001). Intratumoral PlGF expression was not associated with patients' overall survival (OS) or time to recurrence (TTR). However, peritumoral PlGF expression, which was associated with tumor size, presence of intrahepatic metastasis, TNM stage and Barcelona Clinic Liver Cancer stage, was an independent risk factor for OS (p = 0.026) and TTR (p = 0.041). The prognostic value of peritumoral PlGF expression was further validated in a validation cohort (n = 394). We inferred that the elevation of PlGF in peritumoral liver might be induced by hypoxia. We found that peritumoral PlGF expression was associated with hypoxia‐inducible factor‐1α (p = 0.017). PlGF expression was elevated in L02, a hepatic cell line, under hypoxic conditions in vitro. These findings indicate that high peritumoral PlGF expression is associated with tumor recurrence and survival after resection of HCC. PlGF could be a target of adjuvant therapy and deserves further investigations.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20521248</pmid><doi>10.1002/ijc.25492</doi><tpages>11</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Biological and medical sciences Carcinoma, Hepatocellular - diagnosis Carcinoma, Hepatocellular - metabolism Carcinoma, Hepatocellular - surgery Female Gastroenterology. Liver. Pancreas. Abdomen Gene Expression Regulation, Neoplastic hepatocellular carcinoma Humans Immunohistochemistry - methods Ligands Liver - metabolism Liver Neoplasms - diagnosis Liver Neoplasms - metabolism Liver Neoplasms - surgery Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences Middle Aged Neovascularization, Pathologic - metabolism Oligonucleotide Array Sequence Analysis peritumoral liver tissue Placenta Growth Factor placental growth factor Pregnancy Proteins - biosynthesis Prognosis Tumors vascular endothelial growth factor |
title | Expression and prognostic significance of placental growth factor in hepatocellular carcinoma and peritumoral liver tissue |
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