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Synergistic antitumor activity of regorafenib and lapatinib in preclinical models of human colorectal cancer
Abstract Regorafenib significantly prolongs overall survival in patients with metastatic colorectal cancer (mCRC), but the overall clinical efficacy of regorafenib remains quite limited. Combination chemotherapy is a potentially promising approach to enhance anticancer activity, overcome drug resist...
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Published in: | Cancer letters 2017-02, Vol.386, p.100-109 |
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container_title | Cancer letters |
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creator | Zhang, Wen-Ji Li, Yong Wei, Meng-Ning Chen, Yao Qiu, Jian-Ge Jiang, Qi-Wei Yang, Yang Zheng, Di-Wei Qin, Wu-Ming Huang, Jia-Rong Wang, Kun Zhang, Wen-Juan Wang, Yi-Jun Yang, Dong-Hua Chen, Zhe-Sheng, MD, PhD Shi, Zhi, MD, PhD |
description | Abstract Regorafenib significantly prolongs overall survival in patients with metastatic colorectal cancer (mCRC), but the overall clinical efficacy of regorafenib remains quite limited. Combination chemotherapy is a potentially promising approach to enhance anticancer activity, overcome drug resistance, and improve disease-free and overall survival. The current study investigates the antitumor activity of regorafenib in combination with lapatinib in preclinical models of human CRC. Our results show improved antitumor efficacy when regorafenib is combined with lapatinib both in vitro and in vivo . Furthermore, pharmacokinetic analyses revealed that regorafenib and lapatinib do not influence on each plasma concentration. The finding that regorafenib in combination with lapatinib have synergistic activity warrants further clinical investigation of this beneficial combination as a potential treatment strategy for CRC patients. |
doi_str_mv | 10.1016/j.canlet.2016.11.011 |
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Combination chemotherapy is a potentially promising approach to enhance anticancer activity, overcome drug resistance, and improve disease-free and overall survival. The current study investigates the antitumor activity of regorafenib in combination with lapatinib in preclinical models of human CRC. Our results show improved antitumor efficacy when regorafenib is combined with lapatinib both in vitro and in vivo . Furthermore, pharmacokinetic analyses revealed that regorafenib and lapatinib do not influence on each plasma concentration. The finding that regorafenib in combination with lapatinib have synergistic activity warrants further clinical investigation of this beneficial combination as a potential treatment strategy for CRC patients.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2016.11.011</identifier><identifier>PMID: 27864115</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Angiogenesis Inhibitors - pharmacokinetics ; Angiogenesis Inhibitors - pharmacology ; Animals ; Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Apoptosis ; Apoptosis - drug effects ; Cancer therapies ; Cell cycle ; Cell Cycle Checkpoints - drug effects ; Cell growth ; Cell Proliferation - drug effects ; Colorectal cancer ; Colorectal Neoplasms - blood ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - pathology ; Combination chemotherapy ; Conflicts of interest ; Dose-Response Relationship, Drug ; Drug dosages ; Drug Synergism ; FDA approval ; Female ; Growth factors ; HCT116 Cells ; Hematology, Oncology and Palliative Medicine ; HT29 Cells ; Humans ; Immunoglobulins ; Inhibitory Concentration 50 ; Lapatinib ; Mice, Inbred BALB C ; Mice, Nude ; Molecular Targeted Therapy ; Neovascularization, Pathologic ; Phenylurea Compounds - pharmacokinetics ; Phenylurea Compounds - pharmacology ; Protein Kinase Inhibitors - pharmacokinetics ; Protein Kinase Inhibitors - pharmacology ; Pyridines - pharmacokinetics ; Pyridines - pharmacology ; Quinazolines - pharmacokinetics ; Quinazolines - pharmacology ; Regorafenib ; Science ; Software ; Targeted therapy ; Tumor Burden - drug effects ; Xenograft Model Antitumor Assays</subject><ispartof>Cancer letters, 2017-02, Vol.386, p.100-109</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Feb 1, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-21f96138dc8652a4aead88ae38ef54776d29fa23f141ac7cb75541bbcd9d34753</citedby><cites>FETCH-LOGICAL-c478t-21f96138dc8652a4aead88ae38ef54776d29fa23f141ac7cb75541bbcd9d34753</cites><orcidid>0000-0003-3462-6055</orcidid></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/27864115$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Wen-Ji</creatorcontrib><creatorcontrib>Li, Yong</creatorcontrib><creatorcontrib>Wei, Meng-Ning</creatorcontrib><creatorcontrib>Chen, Yao</creatorcontrib><creatorcontrib>Qiu, Jian-Ge</creatorcontrib><creatorcontrib>Jiang, Qi-Wei</creatorcontrib><creatorcontrib>Yang, Yang</creatorcontrib><creatorcontrib>Zheng, Di-Wei</creatorcontrib><creatorcontrib>Qin, Wu-Ming</creatorcontrib><creatorcontrib>Huang, Jia-Rong</creatorcontrib><creatorcontrib>Wang, Kun</creatorcontrib><creatorcontrib>Zhang, Wen-Juan</creatorcontrib><creatorcontrib>Wang, Yi-Jun</creatorcontrib><creatorcontrib>Yang, Dong-Hua</creatorcontrib><creatorcontrib>Chen, Zhe-Sheng, MD, PhD</creatorcontrib><creatorcontrib>Shi, Zhi, MD, PhD</creatorcontrib><title>Synergistic antitumor activity of regorafenib and lapatinib in preclinical models of human colorectal cancer</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Abstract Regorafenib significantly prolongs overall survival in patients with metastatic colorectal cancer (mCRC), but the overall clinical efficacy of regorafenib remains quite limited. Combination chemotherapy is a potentially promising approach to enhance anticancer activity, overcome drug resistance, and improve disease-free and overall survival. The current study investigates the antitumor activity of regorafenib in combination with lapatinib in preclinical models of human CRC. Our results show improved antitumor efficacy when regorafenib is combined with lapatinib both in vitro and in vivo . Furthermore, pharmacokinetic analyses revealed that regorafenib and lapatinib do not influence on each plasma concentration. The finding that regorafenib in combination with lapatinib have synergistic activity warrants further clinical investigation of this beneficial combination as a potential treatment strategy for CRC patients.</description><subject>Angiogenesis Inhibitors - pharmacokinetics</subject><subject>Angiogenesis Inhibitors - pharmacology</subject><subject>Animals</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Cell Cycle Checkpoints - drug effects</subject><subject>Cell growth</subject><subject>Cell Proliferation - drug effects</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - blood</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Combination chemotherapy</subject><subject>Conflicts of interest</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug dosages</subject><subject>Drug Synergism</subject><subject>FDA approval</subject><subject>Female</subject><subject>Growth factors</subject><subject>HCT116 Cells</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>HT29 Cells</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Inhibitory Concentration 50</subject><subject>Lapatinib</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Molecular Targeted Therapy</subject><subject>Neovascularization, Pathologic</subject><subject>Phenylurea Compounds - pharmacokinetics</subject><subject>Phenylurea Compounds - pharmacology</subject><subject>Protein Kinase Inhibitors - pharmacokinetics</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Pyridines - pharmacokinetics</subject><subject>Pyridines - pharmacology</subject><subject>Quinazolines - pharmacokinetics</subject><subject>Quinazolines - pharmacology</subject><subject>Regorafenib</subject><subject>Science</subject><subject>Software</subject><subject>Targeted therapy</subject><subject>Tumor Burden - drug effects</subject><subject>Xenograft Model Antitumor Assays</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkkFv1DAQhSMEotvCP0AoEhcuCR7bie0LEqqAIlXiUDhbjj0pXpJ4sZ1K--9xtC1IvcDJGvmbsd97U1WvgLRAoH-3b61ZJswtLVUL0BKAJ9UOpKCNUJI8rXaEEd4wybqz6jylPSGk46J7Xp1RIXsO0O2q6ea4YLz1KXtbmyX7vM4h1sZmf-fzsQ5jHfE2RDPi4odCuHoyB5P9VvmlPkS0Uymsmeo5OJzS1vJjnc1S2zCFcp3LVfmqxfiiejaaKeHL-_Oi-v7p47fLq-b66-cvlx-uG8uFzA2FUfXApLOy76jhBo2T0iCTOBYBondUjYayETgYK-wguo7DMFinHCsC2UX19jT3EMOvFVPWs08Wp8ksGNakQXaKKyU7-R8oB6FUca6gbx6h-7DGpQjZBlIlKRekUPxE2RhSijjqQ_SziUcNRG_B6b0-Bae34DSALsGVttf3w9dhRven6SGpArw_AcVivPMYdbIei6vObx5rF_y_Xng84CG4n3jE9FeLTlQTfbMtz7Y70DPSKyHZb5mOwNs</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Zhang, Wen-Ji</creator><creator>Li, Yong</creator><creator>Wei, Meng-Ning</creator><creator>Chen, Yao</creator><creator>Qiu, Jian-Ge</creator><creator>Jiang, Qi-Wei</creator><creator>Yang, Yang</creator><creator>Zheng, Di-Wei</creator><creator>Qin, Wu-Ming</creator><creator>Huang, Jia-Rong</creator><creator>Wang, Kun</creator><creator>Zhang, Wen-Juan</creator><creator>Wang, Yi-Jun</creator><creator>Yang, Dong-Hua</creator><creator>Chen, Zhe-Sheng, MD, PhD</creator><creator>Shi, Zhi, MD, PhD</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Limited</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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3462-6055</orcidid></search><sort><creationdate>20170201</creationdate><title>Synergistic antitumor activity of regorafenib and lapatinib in preclinical models of human colorectal cancer</title><author>Zhang, Wen-Ji ; Li, Yong ; Wei, Meng-Ning ; Chen, Yao ; Qiu, Jian-Ge ; Jiang, Qi-Wei ; Yang, Yang ; Zheng, Di-Wei ; Qin, Wu-Ming ; Huang, Jia-Rong ; Wang, Kun ; Zhang, Wen-Juan ; Wang, Yi-Jun ; Yang, Dong-Hua ; Chen, Zhe-Sheng, MD, PhD ; Shi, Zhi, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-21f96138dc8652a4aead88ae38ef54776d29fa23f141ac7cb75541bbcd9d34753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Angiogenesis Inhibitors - pharmacokinetics</topic><topic>Angiogenesis Inhibitors - pharmacology</topic><topic>Animals</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Cancer therapies</topic><topic>Cell cycle</topic><topic>Cell Cycle Checkpoints - drug effects</topic><topic>Cell growth</topic><topic>Cell Proliferation - drug effects</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - blood</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Combination chemotherapy</topic><topic>Conflicts of interest</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug dosages</topic><topic>Drug Synergism</topic><topic>FDA approval</topic><topic>Female</topic><topic>Growth factors</topic><topic>HCT116 Cells</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>HT29 Cells</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Inhibitory Concentration 50</topic><topic>Lapatinib</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Molecular Targeted Therapy</topic><topic>Neovascularization, Pathologic</topic><topic>Phenylurea Compounds - pharmacokinetics</topic><topic>Phenylurea Compounds - pharmacology</topic><topic>Protein Kinase Inhibitors - pharmacokinetics</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Pyridines - pharmacokinetics</topic><topic>Pyridines - pharmacology</topic><topic>Quinazolines - pharmacokinetics</topic><topic>Quinazolines - pharmacology</topic><topic>Regorafenib</topic><topic>Science</topic><topic>Software</topic><topic>Targeted therapy</topic><topic>Tumor Burden - drug effects</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Wen-Ji</creatorcontrib><creatorcontrib>Li, Yong</creatorcontrib><creatorcontrib>Wei, Meng-Ning</creatorcontrib><creatorcontrib>Chen, Yao</creatorcontrib><creatorcontrib>Qiu, Jian-Ge</creatorcontrib><creatorcontrib>Jiang, Qi-Wei</creatorcontrib><creatorcontrib>Yang, Yang</creatorcontrib><creatorcontrib>Zheng, Di-Wei</creatorcontrib><creatorcontrib>Qin, Wu-Ming</creatorcontrib><creatorcontrib>Huang, Jia-Rong</creatorcontrib><creatorcontrib>Wang, Kun</creatorcontrib><creatorcontrib>Zhang, Wen-Juan</creatorcontrib><creatorcontrib>Wang, Yi-Jun</creatorcontrib><creatorcontrib>Yang, Dong-Hua</creatorcontrib><creatorcontrib>Chen, Zhe-Sheng, MD, PhD</creatorcontrib><creatorcontrib>Shi, Zhi, MD, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Wen-Ji</au><au>Li, Yong</au><au>Wei, Meng-Ning</au><au>Chen, Yao</au><au>Qiu, Jian-Ge</au><au>Jiang, Qi-Wei</au><au>Yang, Yang</au><au>Zheng, Di-Wei</au><au>Qin, Wu-Ming</au><au>Huang, Jia-Rong</au><au>Wang, Kun</au><au>Zhang, Wen-Juan</au><au>Wang, Yi-Jun</au><au>Yang, Dong-Hua</au><au>Chen, Zhe-Sheng, MD, PhD</au><au>Shi, Zhi, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic antitumor activity of regorafenib and lapatinib in preclinical models of human colorectal cancer</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>386</volume><spage>100</spage><epage>109</epage><pages>100-109</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>Abstract Regorafenib significantly prolongs overall survival in patients with metastatic colorectal cancer (mCRC), but the overall clinical efficacy of regorafenib remains quite limited. Combination chemotherapy is a potentially promising approach to enhance anticancer activity, overcome drug resistance, and improve disease-free and overall survival. The current study investigates the antitumor activity of regorafenib in combination with lapatinib in preclinical models of human CRC. Our results show improved antitumor efficacy when regorafenib is combined with lapatinib both in vitro and in vivo . Furthermore, pharmacokinetic analyses revealed that regorafenib and lapatinib do not influence on each plasma concentration. The finding that regorafenib in combination with lapatinib have synergistic activity warrants further clinical investigation of this beneficial combination as a potential treatment strategy for CRC patients.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>27864115</pmid><doi>10.1016/j.canlet.2016.11.011</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3462-6055</orcidid></addata></record> |
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subjects | Angiogenesis Inhibitors - pharmacokinetics Angiogenesis Inhibitors - pharmacology Animals Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics Antineoplastic Combined Chemotherapy Protocols - pharmacology Apoptosis Apoptosis - drug effects Cancer therapies Cell cycle Cell Cycle Checkpoints - drug effects Cell growth Cell Proliferation - drug effects Colorectal cancer Colorectal Neoplasms - blood Colorectal Neoplasms - drug therapy Colorectal Neoplasms - pathology Combination chemotherapy Conflicts of interest Dose-Response Relationship, Drug Drug dosages Drug Synergism FDA approval Female Growth factors HCT116 Cells Hematology, Oncology and Palliative Medicine HT29 Cells Humans Immunoglobulins Inhibitory Concentration 50 Lapatinib Mice, Inbred BALB C Mice, Nude Molecular Targeted Therapy Neovascularization, Pathologic Phenylurea Compounds - pharmacokinetics Phenylurea Compounds - pharmacology Protein Kinase Inhibitors - pharmacokinetics Protein Kinase Inhibitors - pharmacology Pyridines - pharmacokinetics Pyridines - pharmacology Quinazolines - pharmacokinetics Quinazolines - pharmacology Regorafenib Science Software Targeted therapy Tumor Burden - drug effects Xenograft Model Antitumor Assays |
title | Synergistic antitumor activity of regorafenib and lapatinib in preclinical models of human colorectal cancer |
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