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Overcoming trastuzumab resistance in HER2‐positive breast cancer using combination therapy
Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. For many years, trastuzumab, a monoclonal antibody, has been used to inhibit the HER2 activity. Though, the main resistance to trastuzumab has...
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Published in: | Journal of cellular physiology 2020-04, Vol.235 (4), p.3142-3156 |
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creator | Derakhshani, Afshin Rezaei, Zohreh Safarpour, Hossein Sabri, Morteza Mir, Atefeh Sanati, Mohammad Amin Vahidian, Fatemeh Gholamiyan Moghadam, Ali Aghadoukht, Ali Hajiasgharzadeh, Khalil Baradaran, Behzad |
description | Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. For many years, trastuzumab, a monoclonal antibody, has been used to inhibit the HER2 activity. Though, the main resistance to trastuzumab has challenged the use of this drug in the management of HER2‐positive BC. Therefore, the determination of resistance mechanisms and the incorporation of new agents may lead to the development of a better blockade of the HER family receptor signaling. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. In this regard, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects.
Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. So, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects. |
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Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. So, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.29216</identifier><identifier>PMID: 31566722</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Antineoplastic Agents - pharmacology ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Combination therapy ; drug resistance ; Drug Resistance, Neoplasm - drug effects ; Epidermal growth factor ; ErbB-2 protein ; Growth factors ; HER2 positive ; Humans ; Immunotherapy ; Lapatinib - therapeutic use ; Monoclonal antibodies ; Receptor, ErbB-2 - drug effects ; Targeted cancer therapy ; Trastuzumab ; Trastuzumab - therapeutic use</subject><ispartof>Journal of cellular physiology, 2020-04, Vol.235 (4), p.3142-3156</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><rights>2020 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4196-3d84a632ae0f91908c96adde0e8c99865c3432a7c2bb1b52ed5cf836769e6b593</citedby><cites>FETCH-LOGICAL-c4196-3d84a632ae0f91908c96adde0e8c99865c3432a7c2bb1b52ed5cf836769e6b593</cites><orcidid>0000-0002-8642-6795 ; 0000-0002-3243-233X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31566722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Derakhshani, Afshin</creatorcontrib><creatorcontrib>Rezaei, Zohreh</creatorcontrib><creatorcontrib>Safarpour, Hossein</creatorcontrib><creatorcontrib>Sabri, Morteza</creatorcontrib><creatorcontrib>Mir, Atefeh</creatorcontrib><creatorcontrib>Sanati, Mohammad Amin</creatorcontrib><creatorcontrib>Vahidian, Fatemeh</creatorcontrib><creatorcontrib>Gholamiyan Moghadam, Ali</creatorcontrib><creatorcontrib>Aghadoukht, Ali</creatorcontrib><creatorcontrib>Hajiasgharzadeh, Khalil</creatorcontrib><creatorcontrib>Baradaran, Behzad</creatorcontrib><title>Overcoming trastuzumab resistance in HER2‐positive breast cancer using combination therapy</title><title>Journal of cellular physiology</title><addtitle>J Cell Physiol</addtitle><description>Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. For many years, trastuzumab, a monoclonal antibody, has been used to inhibit the HER2 activity. Though, the main resistance to trastuzumab has challenged the use of this drug in the management of HER2‐positive BC. Therefore, the determination of resistance mechanisms and the incorporation of new agents may lead to the development of a better blockade of the HER family receptor signaling. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. In this regard, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects.
Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. So, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Combination therapy</subject><subject>drug resistance</subject><subject>Drug Resistance, Neoplasm - drug effects</subject><subject>Epidermal growth factor</subject><subject>ErbB-2 protein</subject><subject>Growth factors</subject><subject>HER2 positive</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Lapatinib - therapeutic use</subject><subject>Monoclonal antibodies</subject><subject>Receptor, ErbB-2 - drug effects</subject><subject>Targeted cancer therapy</subject><subject>Trastuzumab</subject><subject>Trastuzumab - therapeutic use</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKAzEUhoMoWi8LX0AG3Ohi2lwmmclSSr1RUER3QshkTjWlczGZqdSVj-Az-iSmtroQXJ0D_3c-Dj9ChwT3CcZ0MDVNn0pKxAbqESzTOBGcbqJeyEgseUJ20K73U4yxlIxtox1GuBAppT30eDMHZ-rSVk9R67Rvu7eu1HnkwFvf6spAZKvocnRHP98_mtrb1s4hyh0ENDLL3EWdX14HSW4r3dq6itpncLpZ7KOtiZ55OFjPPfRwProfXsbjm4ur4dk4NgmRImZFlmjBqAY8kUTizEihiwIwhE1mghuWhDQ1NM9JzikU3EwyJlIhQeRcsj10svI2rn7pwLeqtN7AbKYrqDuvKJUy4SnOlujxH3Rad64K3ynKGOOCYYIDdbqijKu9dzBRjbOldgtFsFpWrkLl6rvywB6tjV1eQvFL_nQcgMEKeLUzWPxvUtfD25XyC4ehi8o</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Derakhshani, Afshin</creator><creator>Rezaei, Zohreh</creator><creator>Safarpour, Hossein</creator><creator>Sabri, Morteza</creator><creator>Mir, Atefeh</creator><creator>Sanati, Mohammad Amin</creator><creator>Vahidian, Fatemeh</creator><creator>Gholamiyan Moghadam, Ali</creator><creator>Aghadoukht, Ali</creator><creator>Hajiasgharzadeh, Khalil</creator><creator>Baradaran, Behzad</creator><general>Wiley Subscription Services, Inc</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>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8642-6795</orcidid><orcidid>https://orcid.org/0000-0002-3243-233X</orcidid></search><sort><creationdate>202004</creationdate><title>Overcoming trastuzumab resistance in HER2‐positive breast cancer using combination therapy</title><author>Derakhshani, Afshin ; Rezaei, Zohreh ; Safarpour, Hossein ; Sabri, Morteza ; Mir, Atefeh ; Sanati, Mohammad Amin ; Vahidian, Fatemeh ; Gholamiyan Moghadam, Ali ; Aghadoukht, Ali ; Hajiasgharzadeh, Khalil ; Baradaran, Behzad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4196-3d84a632ae0f91908c96adde0e8c99865c3432a7c2bb1b52ed5cf836769e6b593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Combination therapy</topic><topic>drug resistance</topic><topic>Drug Resistance, Neoplasm - drug effects</topic><topic>Epidermal growth factor</topic><topic>ErbB-2 protein</topic><topic>Growth factors</topic><topic>HER2 positive</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Lapatinib - therapeutic use</topic><topic>Monoclonal antibodies</topic><topic>Receptor, ErbB-2 - drug effects</topic><topic>Targeted cancer therapy</topic><topic>Trastuzumab</topic><topic>Trastuzumab - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Derakhshani, Afshin</creatorcontrib><creatorcontrib>Rezaei, Zohreh</creatorcontrib><creatorcontrib>Safarpour, Hossein</creatorcontrib><creatorcontrib>Sabri, Morteza</creatorcontrib><creatorcontrib>Mir, Atefeh</creatorcontrib><creatorcontrib>Sanati, Mohammad Amin</creatorcontrib><creatorcontrib>Vahidian, Fatemeh</creatorcontrib><creatorcontrib>Gholamiyan Moghadam, Ali</creatorcontrib><creatorcontrib>Aghadoukht, Ali</creatorcontrib><creatorcontrib>Hajiasgharzadeh, Khalil</creatorcontrib><creatorcontrib>Baradaran, Behzad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Derakhshani, Afshin</au><au>Rezaei, Zohreh</au><au>Safarpour, Hossein</au><au>Sabri, Morteza</au><au>Mir, Atefeh</au><au>Sanati, Mohammad Amin</au><au>Vahidian, Fatemeh</au><au>Gholamiyan Moghadam, Ali</au><au>Aghadoukht, Ali</au><au>Hajiasgharzadeh, Khalil</au><au>Baradaran, Behzad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overcoming trastuzumab resistance in HER2‐positive breast cancer using combination therapy</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J Cell Physiol</addtitle><date>2020-04</date><risdate>2020</risdate><volume>235</volume><issue>4</issue><spage>3142</spage><epage>3156</epage><pages>3142-3156</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. For many years, trastuzumab, a monoclonal antibody, has been used to inhibit the HER2 activity. Though, the main resistance to trastuzumab has challenged the use of this drug in the management of HER2‐positive BC. Therefore, the determination of resistance mechanisms and the incorporation of new agents may lead to the development of a better blockade of the HER family receptor signaling. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. In this regard, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects.
Human epidermal growth factor receptor 2 (HER2)‐positive breast cancer (BC) comprises around 20–30% of all BC subtypes and is correlated with poor prognosis. During the last few years, some therapeutic drugs have been developed for treating patients with trastuzumab‐resistant HER2‐positive BC that have more effective influences in the management of this condition. So, the present study aimed at reviewing the mechanisms of trastuzumab resistance and the innovative therapies that have been investigated in trastuzumab‐resistant HER2‐positive BC subjects.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31566722</pmid><doi>10.1002/jcp.29216</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-8642-6795</orcidid><orcidid>https://orcid.org/0000-0002-3243-233X</orcidid></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Combination therapy drug resistance Drug Resistance, Neoplasm - drug effects Epidermal growth factor ErbB-2 protein Growth factors HER2 positive Humans Immunotherapy Lapatinib - therapeutic use Monoclonal antibodies Receptor, ErbB-2 - drug effects Targeted cancer therapy Trastuzumab Trastuzumab - therapeutic use |
title | Overcoming trastuzumab resistance in HER2‐positive breast cancer using combination therapy |
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