Cancer gene panel analysis of cultured circulating tumor cells and primary tumor tissue from patients with breast cancer
Although numerous effective therapies have improved the survival rate of patients with breast cancer, a number of patients present with tumor recurrence and metastasis. A liquid biopsy of circulating tumor cells (CTC) is a non-invasive method to obtain tumor cells and may be used as substitute for a...
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Veröffentlicht in: | Oncology letters 2017-06, Vol.13 (6), p.4627-4632 |
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creator | Hwang, Eunjoo Uh, Ji-Hyun Lee, Hye Seon Lee, Cham Han Lee, Soo Jeong Ahn, Sei Hyun Son, Byung Ho Lee, Jong Won Yu, Jong Han Kwon, Nak-Jung Lee, Woo Chung Yang, Kap-Seok Choi, Sung Ho Kim, Myoung Shin Lee, Jinseon Jeon, Byung Hee |
description | Although numerous effective therapies have improved the survival rate of patients with breast cancer, a number of patients present with tumor recurrence and metastasis. A liquid biopsy of circulating tumor cells (CTC) is a non-invasive method to obtain tumor cells and may be used as substitute for a tumor tissue biopsy. The present study focuses on determining whether CTC culture is an optimal method of obtaining sufficient amounts of CTCs for molecular analysis. The current study demonstrates a method of isolating and culturing CTCs from patients with breast cancer and the construction of a molecular profile of cultured cells using the Ion AmpliSeq Cancer Gene Panel V2. Gene mutations that were observed in cultured CTCs were compared with those observed in primary tumor tissues. CTCs were isolated and cultured from the blood of six patients with breast cancer. Mutations from the Catalogue Of Somatic Mutation In Cancer (COSMIC) were detected in Platelet-Derived Growth Factor Receptor Alpha, MET (also known as Hepatocyte Growth Factor Receptor), Phosphatase and Tensin Homolog, Harvey Rat Sarcoma Viral Oncogene Homolog, SWI/SNF Related, Matrix Associated, Actin Dependent Regulator of Chromatin Subfamily B Member 1, Cyclin Dependent Kinase Inhibitor 2A and MutL Homolog 1 genes in 5/6 samples. A comparison between mutations detected in cultured CTCs and mutations detected in primary tumor tissues demonstrated that a large number of mutations that were identified in CTCs were also detected in primary tumor tissues. The results from the current study describe a novel cell culture approach that may be used to obtain an optimal number of CTCs for molecular analysis. This novel approach is able to be used as a tool for liquid biopsy during breast cancer treatment. |
doi_str_mv | 10.3892/ol.2017.6077 |
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A liquid biopsy of circulating tumor cells (CTC) is a non-invasive method to obtain tumor cells and may be used as substitute for a tumor tissue biopsy. The present study focuses on determining whether CTC culture is an optimal method of obtaining sufficient amounts of CTCs for molecular analysis. The current study demonstrates a method of isolating and culturing CTCs from patients with breast cancer and the construction of a molecular profile of cultured cells using the Ion AmpliSeq Cancer Gene Panel V2. Gene mutations that were observed in cultured CTCs were compared with those observed in primary tumor tissues. CTCs were isolated and cultured from the blood of six patients with breast cancer. Mutations from the Catalogue Of Somatic Mutation In Cancer (COSMIC) were detected in Platelet-Derived Growth Factor Receptor Alpha, MET (also known as Hepatocyte Growth Factor Receptor), Phosphatase and Tensin Homolog, Harvey Rat Sarcoma Viral Oncogene Homolog, SWI/SNF Related, Matrix Associated, Actin Dependent Regulator of Chromatin Subfamily B Member 1, Cyclin Dependent Kinase Inhibitor 2A and MutL Homolog 1 genes in 5/6 samples. A comparison between mutations detected in cultured CTCs and mutations detected in primary tumor tissues demonstrated that a large number of mutations that were identified in CTCs were also detected in primary tumor tissues. The results from the current study describe a novel cell culture approach that may be used to obtain an optimal number of CTCs for molecular analysis. This novel approach is able to be used as a tool for liquid biopsy during breast cancer treatment.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2017.6077</identifier><identifier>PMID: 28599463</identifier><language>eng</language><publisher>Greece: Spandidos Publications</publisher><subject>Biopsy ; Blood platelets ; Breast cancer ; Care and treatment ; Cell adhesion & migration ; Cell growth ; Deoxyribonucleic acid ; Development and progression ; DNA ; Genetic aspects ; Genetic testing ; Genotype ; Growth factors ; Innovations ; Kinases ; Medical prognosis ; Metastasis ; Molecular diagnostic techniques ; Mutation ; Patients ; Stem cells ; Testing ; Tumors</subject><ispartof>Oncology letters, 2017-06, Vol.13 (6), p.4627-4632</ispartof><rights>COPYRIGHT 2017 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2017</rights><rights>Copyright: © Hwang et al. 2017</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-c88f2824022aec6866319977e6d94f80aa6fe62c7ef160490d352055103781cd3</citedby><cites>FETCH-LOGICAL-c510t-c88f2824022aec6866319977e6d94f80aa6fe62c7ef160490d352055103781cd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452992/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452992/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28599463$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hwang, Eunjoo</creatorcontrib><creatorcontrib>Uh, Ji-Hyun</creatorcontrib><creatorcontrib>Lee, Hye Seon</creatorcontrib><creatorcontrib>Lee, Cham Han</creatorcontrib><creatorcontrib>Lee, Soo Jeong</creatorcontrib><creatorcontrib>Ahn, Sei Hyun</creatorcontrib><creatorcontrib>Son, Byung Ho</creatorcontrib><creatorcontrib>Lee, Jong Won</creatorcontrib><creatorcontrib>Yu, Jong Han</creatorcontrib><creatorcontrib>Kwon, Nak-Jung</creatorcontrib><creatorcontrib>Lee, Woo Chung</creatorcontrib><creatorcontrib>Yang, Kap-Seok</creatorcontrib><creatorcontrib>Choi, Sung Ho</creatorcontrib><creatorcontrib>Kim, Myoung Shin</creatorcontrib><creatorcontrib>Lee, Jinseon</creatorcontrib><creatorcontrib>Jeon, Byung Hee</creatorcontrib><title>Cancer gene panel analysis of cultured circulating tumor cells and primary tumor tissue from patients with breast cancer</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>Although numerous effective therapies have improved the survival rate of patients with breast cancer, a number of patients present with tumor recurrence and metastasis. A liquid biopsy of circulating tumor cells (CTC) is a non-invasive method to obtain tumor cells and may be used as substitute for a tumor tissue biopsy. The present study focuses on determining whether CTC culture is an optimal method of obtaining sufficient amounts of CTCs for molecular analysis. The current study demonstrates a method of isolating and culturing CTCs from patients with breast cancer and the construction of a molecular profile of cultured cells using the Ion AmpliSeq Cancer Gene Panel V2. Gene mutations that were observed in cultured CTCs were compared with those observed in primary tumor tissues. CTCs were isolated and cultured from the blood of six patients with breast cancer. Mutations from the Catalogue Of Somatic Mutation In Cancer (COSMIC) were detected in Platelet-Derived Growth Factor Receptor Alpha, MET (also known as Hepatocyte Growth Factor Receptor), Phosphatase and Tensin Homolog, Harvey Rat Sarcoma Viral Oncogene Homolog, SWI/SNF Related, Matrix Associated, Actin Dependent Regulator of Chromatin Subfamily B Member 1, Cyclin Dependent Kinase Inhibitor 2A and MutL Homolog 1 genes in 5/6 samples. A comparison between mutations detected in cultured CTCs and mutations detected in primary tumor tissues demonstrated that a large number of mutations that were identified in CTCs were also detected in primary tumor tissues. The results from the current study describe a novel cell culture approach that may be used to obtain an optimal number of CTCs for molecular analysis. This novel approach is able to be used as a tool for liquid biopsy during breast cancer treatment.</description><subject>Biopsy</subject><subject>Blood platelets</subject><subject>Breast cancer</subject><subject>Care and treatment</subject><subject>Cell adhesion & migration</subject><subject>Cell growth</subject><subject>Deoxyribonucleic acid</subject><subject>Development and progression</subject><subject>DNA</subject><subject>Genetic aspects</subject><subject>Genetic testing</subject><subject>Genotype</subject><subject>Growth factors</subject><subject>Innovations</subject><subject>Kinases</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Molecular diagnostic techniques</subject><subject>Mutation</subject><subject>Patients</subject><subject>Stem cells</subject><subject>Testing</subject><subject>Tumors</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptks9vFCEUxydGY5vam2dDYmI8uCswDD8uJs3GX0kTL3omlHns0jBQgan2v5ex69o1woEX-Lzve3zzuu45weteKvo2hTXFRKw5FuJRd0qEoiuCJX18iAU76c5LucZtDZxIyZ92J1QOSjHen3Y_NyZayGgLEdCNiRCQiSbcFV9QcsjOoc4ZRmR9brGpPm5RnaeUkYUQSoNHdJP9ZPLd_r76UmZALqepCVYPsRb0w9cduspgSkX2d8Vn3RNnQoHz_XnWffvw_uvm0-ryy8fPm4vLlR0IrisrpaOSMkypAcsl5z1RSgjgo2JOYmO4A06tAEc4ZgqP_UDx0HJ7IYkd-7Pu3b3uzXw1wWhbO9kEve9ZJ-P18Uv0O71Nt3pgA1WKNoHXe4Gcvs9Qqp58WT7fzEpz0URhyVqLRDT05T_odZpzs3OhFGuOqx7_pbYmgPbRpVbXLqL6gikpeiYladT6P1TbI0zepgjOt_ujhFcPEnZgQt2VFObqUyzH4Jt70OZUSgZ3MINgvUyVTkEvU6WXqWr4i4cGHuA_M9T_AiEoxww</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Hwang, Eunjoo</creator><creator>Uh, Ji-Hyun</creator><creator>Lee, Hye Seon</creator><creator>Lee, Cham Han</creator><creator>Lee, Soo Jeong</creator><creator>Ahn, Sei Hyun</creator><creator>Son, Byung Ho</creator><creator>Lee, Jong Won</creator><creator>Yu, Jong Han</creator><creator>Kwon, Nak-Jung</creator><creator>Lee, Woo Chung</creator><creator>Yang, Kap-Seok</creator><creator>Choi, Sung Ho</creator><creator>Kim, Myoung Shin</creator><creator>Lee, Jinseon</creator><creator>Jeon, Byung Hee</creator><general>Spandidos Publications</general><general>Spandidos Publications UK Ltd</general><general>D.A. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hwang, Eunjoo</au><au>Uh, Ji-Hyun</au><au>Lee, Hye Seon</au><au>Lee, Cham Han</au><au>Lee, Soo Jeong</au><au>Ahn, Sei Hyun</au><au>Son, Byung Ho</au><au>Lee, Jong Won</au><au>Yu, Jong Han</au><au>Kwon, Nak-Jung</au><au>Lee, Woo Chung</au><au>Yang, Kap-Seok</au><au>Choi, Sung Ho</au><au>Kim, Myoung Shin</au><au>Lee, Jinseon</au><au>Jeon, Byung Hee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer gene panel analysis of cultured circulating tumor cells and primary tumor tissue from patients with breast cancer</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>13</volume><issue>6</issue><spage>4627</spage><epage>4632</epage><pages>4627-4632</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>Although numerous effective therapies have improved the survival rate of patients with breast cancer, a number of patients present with tumor recurrence and metastasis. A liquid biopsy of circulating tumor cells (CTC) is a non-invasive method to obtain tumor cells and may be used as substitute for a tumor tissue biopsy. The present study focuses on determining whether CTC culture is an optimal method of obtaining sufficient amounts of CTCs for molecular analysis. The current study demonstrates a method of isolating and culturing CTCs from patients with breast cancer and the construction of a molecular profile of cultured cells using the Ion AmpliSeq Cancer Gene Panel V2. Gene mutations that were observed in cultured CTCs were compared with those observed in primary tumor tissues. CTCs were isolated and cultured from the blood of six patients with breast cancer. Mutations from the Catalogue Of Somatic Mutation In Cancer (COSMIC) were detected in Platelet-Derived Growth Factor Receptor Alpha, MET (also known as Hepatocyte Growth Factor Receptor), Phosphatase and Tensin Homolog, Harvey Rat Sarcoma Viral Oncogene Homolog, SWI/SNF Related, Matrix Associated, Actin Dependent Regulator of Chromatin Subfamily B Member 1, Cyclin Dependent Kinase Inhibitor 2A and MutL Homolog 1 genes in 5/6 samples. A comparison between mutations detected in cultured CTCs and mutations detected in primary tumor tissues demonstrated that a large number of mutations that were identified in CTCs were also detected in primary tumor tissues. The results from the current study describe a novel cell culture approach that may be used to obtain an optimal number of CTCs for molecular analysis. This novel approach is able to be used as a tool for liquid biopsy during breast cancer treatment.</abstract><cop>Greece</cop><pub>Spandidos Publications</pub><pmid>28599463</pmid><doi>10.3892/ol.2017.6077</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Blood platelets Breast cancer Care and treatment Cell adhesion & migration Cell growth Deoxyribonucleic acid Development and progression DNA Genetic aspects Genetic testing Genotype Growth factors Innovations Kinases Medical prognosis Metastasis Molecular diagnostic techniques Mutation Patients Stem cells Testing Tumors |
title | Cancer gene panel analysis of cultured circulating tumor cells and primary tumor tissue from patients with breast cancer |
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