Anti-EGFR treatment effects on laryngeal cancer stem cells
Laryngeal cancer (LC) is one of the common head and neck neoplasms and is characterized by resistance to conventional therapy and poor prognosis. This may result from the presence of cancer stem cells (CSCs), which form a small population in tumors with metastatic potential, high invasive capacity,...
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creator | Fernandes, Glaucia Maria de Mendonça Galbiatti-Dias, Ana Lívia Silva Ferreira, Leticia Antunes Muniz Serafim Junior, Vilson Rodrigues-Fleming, Gabriela Helena de Oliveira-Cucolo, Juliana Garcia Biselli-Chicote, Patrícia Matos Kawasaki-Oyama, Rosa Sayoko Maniglia, José Victor Pavarino, Érika Cristina Goloni-Bertollo, Eny Maria |
description | Laryngeal cancer (LC) is one of the common head and neck neoplasms and is characterized by resistance to conventional therapy and poor prognosis. This may result from the presence of cancer stem cells (CSCs), which form a small population in tumors with metastatic potential, high invasive capacity, self-renewal, and differentiation. This study aimed to evaluate the effectiveness of 5-fluorouracil and cisplatin individually, as well as the combination of cetuximab and paclitaxel in a CSC subpopulation separated with biomarkers related to tumoral growth (CD44, CD117, and CD133). In addition, expression of
and
-A genes and proteins related to cell proliferation were evaluated in this subpopulation. The CD44, CD133, and CD117 biomarkers were used to analyze the identification and separation of both subpopulations using FACSAria Fusion. Subpopulations positive for CD44, CD133, and CD117 or lacking these biomarkers were classified as laryngeal cancer stem cells (LCSCs) or laryngeal cancer non-stem cells (non-LCSCs), respectively. Matrigel invasion and colony forming assays were performed to confirm CSC presence. Subpopulations were cultured and exposed to 5-fluorouracil, cisplatin, and cetuximab/paclitaxel drugs for 24 h. Cell proliferation was determined using MTS assay.
and
gene expression levels were evaluated using quantitative real time PCR with TaqMan
Assay in both subpopulations. The non-LCSC subpopulation was considered as the control for relative expression. We found that the LCSC subpopulation demonstrated more resistance to cetuximab and paclitaxel combination chemotherapy when compared with the non-LCSC subpopulation of the cell line. These LCSC subpopulations presented up-regulated expression of
and
genes and proteins and no
gene expression, but TrkB protein expression was up-regulated in the LC cell line when compared to the non-CSC subpopulation. "In conclusion, the combination of CD44, CD133, and CD117 biomarkers has stem cell properties. Moreover, LCSCs, are capable of resisting treatment and present high
and
gene expression". |
format | Article |
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and
-A genes and proteins related to cell proliferation were evaluated in this subpopulation. The CD44, CD133, and CD117 biomarkers were used to analyze the identification and separation of both subpopulations using FACSAria Fusion. Subpopulations positive for CD44, CD133, and CD117 or lacking these biomarkers were classified as laryngeal cancer stem cells (LCSCs) or laryngeal cancer non-stem cells (non-LCSCs), respectively. Matrigel invasion and colony forming assays were performed to confirm CSC presence. Subpopulations were cultured and exposed to 5-fluorouracil, cisplatin, and cetuximab/paclitaxel drugs for 24 h. Cell proliferation was determined using MTS assay.
and
gene expression levels were evaluated using quantitative real time PCR with TaqMan
Assay in both subpopulations. The non-LCSC subpopulation was considered as the control for relative expression. We found that the LCSC subpopulation demonstrated more resistance to cetuximab and paclitaxel combination chemotherapy when compared with the non-LCSC subpopulation of the cell line. These LCSC subpopulations presented up-regulated expression of
and
genes and proteins and no
gene expression, but TrkB protein expression was up-regulated in the LC cell line when compared to the non-CSC subpopulation. "In conclusion, the combination of CD44, CD133, and CD117 biomarkers has stem cell properties. Moreover, LCSCs, are capable of resisting treatment and present high
and
gene expression".</description><identifier>ISSN: 1943-8141</identifier><identifier>EISSN: 1943-8141</identifier><identifier>PMID: 33527014</identifier><language>eng</language><publisher>United States: e-Century Publishing Corporation</publisher><subject>Original</subject><ispartof>American journal of translational research, 2021-01, Vol.13 (1), p.143-155</ispartof><rights>AJTR Copyright © 2021.</rights><rights>AJTR Copyright © 2021 2021</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847503/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847503/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33527014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fernandes, Glaucia Maria de Mendonça</creatorcontrib><creatorcontrib>Galbiatti-Dias, Ana Lívia Silva</creatorcontrib><creatorcontrib>Ferreira, Leticia Antunes Muniz</creatorcontrib><creatorcontrib>Serafim Junior, Vilson</creatorcontrib><creatorcontrib>Rodrigues-Fleming, Gabriela Helena</creatorcontrib><creatorcontrib>de Oliveira-Cucolo, Juliana Garcia</creatorcontrib><creatorcontrib>Biselli-Chicote, Patrícia Matos</creatorcontrib><creatorcontrib>Kawasaki-Oyama, Rosa Sayoko</creatorcontrib><creatorcontrib>Maniglia, José Victor</creatorcontrib><creatorcontrib>Pavarino, Érika Cristina</creatorcontrib><creatorcontrib>Goloni-Bertollo, Eny Maria</creatorcontrib><title>Anti-EGFR treatment effects on laryngeal cancer stem cells</title><title>American journal of translational research</title><addtitle>Am J Transl Res</addtitle><description>Laryngeal cancer (LC) is one of the common head and neck neoplasms and is characterized by resistance to conventional therapy and poor prognosis. This may result from the presence of cancer stem cells (CSCs), which form a small population in tumors with metastatic potential, high invasive capacity, self-renewal, and differentiation. This study aimed to evaluate the effectiveness of 5-fluorouracil and cisplatin individually, as well as the combination of cetuximab and paclitaxel in a CSC subpopulation separated with biomarkers related to tumoral growth (CD44, CD117, and CD133). In addition, expression of
and
-A genes and proteins related to cell proliferation were evaluated in this subpopulation. The CD44, CD133, and CD117 biomarkers were used to analyze the identification and separation of both subpopulations using FACSAria Fusion. Subpopulations positive for CD44, CD133, and CD117 or lacking these biomarkers were classified as laryngeal cancer stem cells (LCSCs) or laryngeal cancer non-stem cells (non-LCSCs), respectively. Matrigel invasion and colony forming assays were performed to confirm CSC presence. Subpopulations were cultured and exposed to 5-fluorouracil, cisplatin, and cetuximab/paclitaxel drugs for 24 h. Cell proliferation was determined using MTS assay.
and
gene expression levels were evaluated using quantitative real time PCR with TaqMan
Assay in both subpopulations. The non-LCSC subpopulation was considered as the control for relative expression. We found that the LCSC subpopulation demonstrated more resistance to cetuximab and paclitaxel combination chemotherapy when compared with the non-LCSC subpopulation of the cell line. These LCSC subpopulations presented up-regulated expression of
and
genes and proteins and no
gene expression, but TrkB protein expression was up-regulated in the LC cell line when compared to the non-CSC subpopulation. "In conclusion, the combination of CD44, CD133, and CD117 biomarkers has stem cell properties. Moreover, LCSCs, are capable of resisting treatment and present high
and
gene expression".</description><subject>Original</subject><issn>1943-8141</issn><issn>1943-8141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkFFLwzAQx4Mobk6_guTRl0KaS9LUB2GMbQoDQfQ5pOllVtp0Npngt7filPl0B3f8fv-7EzLNSwGZzkV-etRPyEWMb4wpWSp-TiYAkhcsF1NyOw-pyZbr1RNNA9rUYUgUvUeXIu0Dbe3wGbZoW-pscDjQmLCjDts2XpIzb9uIV4c6Iy-r5fPiPts8rh8W802240ql0a9KUXuGThaOYw0Vc4pXwESlclC8cDWvhbda1lo4oQErryVYBqKQJXiYkbsf7m5fdVi7MeFgW7Mbmm4MZ3rbmP-T0Lyabf9hCj0SGIyAmwNg6N_3GJPpmvh9gg3Y76PhQkvJmWRqXL0-dv1Jfh8GX9kVaBQ</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Fernandes, Glaucia Maria de Mendonça</creator><creator>Galbiatti-Dias, Ana Lívia Silva</creator><creator>Ferreira, Leticia Antunes Muniz</creator><creator>Serafim Junior, Vilson</creator><creator>Rodrigues-Fleming, Gabriela Helena</creator><creator>de Oliveira-Cucolo, Juliana Garcia</creator><creator>Biselli-Chicote, Patrícia Matos</creator><creator>Kawasaki-Oyama, Rosa Sayoko</creator><creator>Maniglia, José Victor</creator><creator>Pavarino, Érika Cristina</creator><creator>Goloni-Bertollo, Eny Maria</creator><general>e-Century Publishing Corporation</general><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210101</creationdate><title>Anti-EGFR treatment effects on laryngeal cancer stem cells</title><author>Fernandes, Glaucia Maria de Mendonça ; Galbiatti-Dias, Ana Lívia Silva ; Ferreira, Leticia Antunes Muniz ; Serafim Junior, Vilson ; Rodrigues-Fleming, Gabriela Helena ; de Oliveira-Cucolo, Juliana Garcia ; Biselli-Chicote, Patrícia Matos ; Kawasaki-Oyama, Rosa Sayoko ; Maniglia, José Victor ; Pavarino, Érika Cristina ; Goloni-Bertollo, Eny Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-81694df0ec57c2ed3b0c62b304b613627cd2d4fa85d84c483ebf853a0347593f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Fernandes, Glaucia Maria de Mendonça</creatorcontrib><creatorcontrib>Galbiatti-Dias, Ana Lívia Silva</creatorcontrib><creatorcontrib>Ferreira, Leticia Antunes Muniz</creatorcontrib><creatorcontrib>Serafim Junior, Vilson</creatorcontrib><creatorcontrib>Rodrigues-Fleming, Gabriela Helena</creatorcontrib><creatorcontrib>de Oliveira-Cucolo, Juliana Garcia</creatorcontrib><creatorcontrib>Biselli-Chicote, Patrícia Matos</creatorcontrib><creatorcontrib>Kawasaki-Oyama, Rosa Sayoko</creatorcontrib><creatorcontrib>Maniglia, José Victor</creatorcontrib><creatorcontrib>Pavarino, Érika Cristina</creatorcontrib><creatorcontrib>Goloni-Bertollo, Eny Maria</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of translational research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernandes, Glaucia Maria de Mendonça</au><au>Galbiatti-Dias, Ana Lívia Silva</au><au>Ferreira, Leticia Antunes Muniz</au><au>Serafim Junior, Vilson</au><au>Rodrigues-Fleming, Gabriela Helena</au><au>de Oliveira-Cucolo, Juliana Garcia</au><au>Biselli-Chicote, Patrícia Matos</au><au>Kawasaki-Oyama, Rosa Sayoko</au><au>Maniglia, José Victor</au><au>Pavarino, Érika Cristina</au><au>Goloni-Bertollo, Eny Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-EGFR treatment effects on laryngeal cancer stem cells</atitle><jtitle>American journal of translational research</jtitle><addtitle>Am J Transl Res</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>13</volume><issue>1</issue><spage>143</spage><epage>155</epage><pages>143-155</pages><issn>1943-8141</issn><eissn>1943-8141</eissn><abstract>Laryngeal cancer (LC) is one of the common head and neck neoplasms and is characterized by resistance to conventional therapy and poor prognosis. This may result from the presence of cancer stem cells (CSCs), which form a small population in tumors with metastatic potential, high invasive capacity, self-renewal, and differentiation. This study aimed to evaluate the effectiveness of 5-fluorouracil and cisplatin individually, as well as the combination of cetuximab and paclitaxel in a CSC subpopulation separated with biomarkers related to tumoral growth (CD44, CD117, and CD133). In addition, expression of
and
-A genes and proteins related to cell proliferation were evaluated in this subpopulation. The CD44, CD133, and CD117 biomarkers were used to analyze the identification and separation of both subpopulations using FACSAria Fusion. Subpopulations positive for CD44, CD133, and CD117 or lacking these biomarkers were classified as laryngeal cancer stem cells (LCSCs) or laryngeal cancer non-stem cells (non-LCSCs), respectively. Matrigel invasion and colony forming assays were performed to confirm CSC presence. Subpopulations were cultured and exposed to 5-fluorouracil, cisplatin, and cetuximab/paclitaxel drugs for 24 h. Cell proliferation was determined using MTS assay.
and
gene expression levels were evaluated using quantitative real time PCR with TaqMan
Assay in both subpopulations. The non-LCSC subpopulation was considered as the control for relative expression. We found that the LCSC subpopulation demonstrated more resistance to cetuximab and paclitaxel combination chemotherapy when compared with the non-LCSC subpopulation of the cell line. These LCSC subpopulations presented up-regulated expression of
and
genes and proteins and no
gene expression, but TrkB protein expression was up-regulated in the LC cell line when compared to the non-CSC subpopulation. "In conclusion, the combination of CD44, CD133, and CD117 biomarkers has stem cell properties. Moreover, LCSCs, are capable of resisting treatment and present high
and
gene expression".</abstract><cop>United States</cop><pub>e-Century Publishing Corporation</pub><pmid>33527014</pmid><tpages>13</tpages></addata></record> |
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subjects | Original |
title | Anti-EGFR treatment effects on laryngeal cancer stem cells |
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