Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells

Autores
Homann, Luana Micaela; Calvo, Natalia Graciela
Año de publicación
2022
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
Tumor angiogenesis plays a crucial role in cervical cancer (CC) from early stages. Research for potential biomarkers and therapeutictargets has been hampered by heterogeneity, plasticity, and molecular differences of the endothelial cells that form the tumor vasculature.This is due, in part, to the effect of factors released by tumor cells. The aim of this work was to investigate the early effects of factorsreleased by CC-derived tumor cells on the morphology and protein profile of endothelial cells. Treatment with CC-derived HeLa cellsconditioned medium (TCM) for 3 h increased the number of HMEC-1 endothelial cells with cytoplasmic processes and a more elongatedshape. Furthermore, qRT-PCR analysis revealed that HMEC-1 cells exposed to TCM decreased VE-cadherin endothelial marker mRNAand increased α-smooth muscle actin mRNA, a cancer-associated fibroblast marker. These findings could be associated with early stagesof tumor angiogenesis characterized by increased cell migration and a partial transition from endothelial to mesenchymal phenotype(EndoMT). Next, the proteome response of HMEC-1 cells was studied under these experimental conditions, performing a Label-Freequantitative (LFQ) mass spectrometry (MS) (CEQUIBIEM Proteomics Center). Proteins were identified and quantified with theProteome Discoverer software and the Uniprot database. Using the Perseus software, 9 negatively regulated proteins and 24 positivelyregulated proteins were obtained in HMEC-1 cells treated with TCM (P ≤ 0.05 and fold change > 1.5), where clusterin (CLU) presentedthe highest fold change. CLU is a glycoprotein with a key role in cellular stress response and cancer, regulating processes such as cellmigration. In addition, the classification of positively regulated proteins, according to their class, with the PANTHER bioinformaticstool, showed 2 cytoskeletal proteins, actin alpha cardiac muscle 1 (ACTC1) and tubulin beta-8 chain (TUBB8). ACTC1 can promotecell migration and modulate the length of actin tension fibers. qRT-PCR additional analysis also revealed an increased mRNA expressionof CLU and ACTC1 in HMEC-1 cells treated with TCM. These results suggest that the recently identified proteins are involved in theearly stages of biological processes leading to angiogenesis or EndoMT in CC and could be considered as potential biomarkers.
Fil: Homann, Luana Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Ciencias Biológicas y Biomédicas del Sur. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia. Instituto de Ciencias Biológicas y Biomédicas del Sur; Argentina
Fil: Calvo, Natalia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Ciencias Biológicas y Biomédicas del Sur. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia. Instituto de Ciencias Biológicas y Biomédicas del Sur; Argentina
XXIII Annual Meeting of the Argentinean Biology Society
Argentina
Sociedad Argentina de Biología
Materia
CERVICAL CANCER
ENDOTHELIAL CELLS
CELL PLASTICITY
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/243510

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network_name_str CONICET Digital (CONICET)
spelling Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cellsHomann, Luana MicaelaCalvo, Natalia GracielaCERVICAL CANCERENDOTHELIAL CELLSCELL PLASTICITYhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Tumor angiogenesis plays a crucial role in cervical cancer (CC) from early stages. Research for potential biomarkers and therapeutictargets has been hampered by heterogeneity, plasticity, and molecular differences of the endothelial cells that form the tumor vasculature.This is due, in part, to the effect of factors released by tumor cells. The aim of this work was to investigate the early effects of factorsreleased by CC-derived tumor cells on the morphology and protein profile of endothelial cells. Treatment with CC-derived HeLa cellsconditioned medium (TCM) for 3 h increased the number of HMEC-1 endothelial cells with cytoplasmic processes and a more elongatedshape. Furthermore, qRT-PCR analysis revealed that HMEC-1 cells exposed to TCM decreased VE-cadherin endothelial marker mRNAand increased α-smooth muscle actin mRNA, a cancer-associated fibroblast marker. These findings could be associated with early stagesof tumor angiogenesis characterized by increased cell migration and a partial transition from endothelial to mesenchymal phenotype(EndoMT). Next, the proteome response of HMEC-1 cells was studied under these experimental conditions, performing a Label-Freequantitative (LFQ) mass spectrometry (MS) (CEQUIBIEM Proteomics Center). Proteins were identified and quantified with theProteome Discoverer software and the Uniprot database. Using the Perseus software, 9 negatively regulated proteins and 24 positivelyregulated proteins were obtained in HMEC-1 cells treated with TCM (P ≤ 0.05 and fold change > 1.5), where clusterin (CLU) presentedthe highest fold change. CLU is a glycoprotein with a key role in cellular stress response and cancer, regulating processes such as cellmigration. In addition, the classification of positively regulated proteins, according to their class, with the PANTHER bioinformaticstool, showed 2 cytoskeletal proteins, actin alpha cardiac muscle 1 (ACTC1) and tubulin beta-8 chain (TUBB8). ACTC1 can promotecell migration and modulate the length of actin tension fibers. qRT-PCR additional analysis also revealed an increased mRNA expressionof CLU and ACTC1 in HMEC-1 cells treated with TCM. These results suggest that the recently identified proteins are involved in theearly stages of biological processes leading to angiogenesis or EndoMT in CC and could be considered as potential biomarkers.Fil: Homann, Luana Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Ciencias Biológicas y Biomédicas del Sur. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia. Instituto de Ciencias Biológicas y Biomédicas del Sur; ArgentinaFil: Calvo, Natalia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Ciencias Biológicas y Biomédicas del Sur. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia. Instituto de Ciencias Biológicas y Biomédicas del Sur; ArgentinaXXIII Annual Meeting of the Argentinean Biology SocietyArgentinaSociedad Argentina de BiologíaTech Science Press2022info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/243510Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells; XXIII Annual Meeting of the Argentinean Biology Society; Argentina; 2021; 1-31667-5746CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.biologia.org.ar/wp-content/uploads/2022/11/BIOCELL-Vol.-46-Suppl.-4-2022_Jornada-Anual-SAB-2021.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:47:43Zoai:ri.conicet.gov.ar:11336/243510instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:47:43.543CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
title Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
spellingShingle Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
Homann, Luana Micaela
CERVICAL CANCER
ENDOTHELIAL CELLS
CELL PLASTICITY
title_short Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
title_full Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
title_fullStr Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
title_full_unstemmed Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
title_sort Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells
dc.creator.none.fl_str_mv Homann, Luana Micaela
Calvo, Natalia Graciela
author Homann, Luana Micaela
author_facet Homann, Luana Micaela
Calvo, Natalia Graciela
author_role author
author2 Calvo, Natalia Graciela
author2_role author
dc.subject.none.fl_str_mv CERVICAL CANCER
ENDOTHELIAL CELLS
CELL PLASTICITY
topic CERVICAL CANCER
ENDOTHELIAL CELLS
CELL PLASTICITY
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Tumor angiogenesis plays a crucial role in cervical cancer (CC) from early stages. Research for potential biomarkers and therapeutictargets has been hampered by heterogeneity, plasticity, and molecular differences of the endothelial cells that form the tumor vasculature.This is due, in part, to the effect of factors released by tumor cells. The aim of this work was to investigate the early effects of factorsreleased by CC-derived tumor cells on the morphology and protein profile of endothelial cells. Treatment with CC-derived HeLa cellsconditioned medium (TCM) for 3 h increased the number of HMEC-1 endothelial cells with cytoplasmic processes and a more elongatedshape. Furthermore, qRT-PCR analysis revealed that HMEC-1 cells exposed to TCM decreased VE-cadherin endothelial marker mRNAand increased α-smooth muscle actin mRNA, a cancer-associated fibroblast marker. These findings could be associated with early stagesof tumor angiogenesis characterized by increased cell migration and a partial transition from endothelial to mesenchymal phenotype(EndoMT). Next, the proteome response of HMEC-1 cells was studied under these experimental conditions, performing a Label-Freequantitative (LFQ) mass spectrometry (MS) (CEQUIBIEM Proteomics Center). Proteins were identified and quantified with theProteome Discoverer software and the Uniprot database. Using the Perseus software, 9 negatively regulated proteins and 24 positivelyregulated proteins were obtained in HMEC-1 cells treated with TCM (P ≤ 0.05 and fold change > 1.5), where clusterin (CLU) presentedthe highest fold change. CLU is a glycoprotein with a key role in cellular stress response and cancer, regulating processes such as cellmigration. In addition, the classification of positively regulated proteins, according to their class, with the PANTHER bioinformaticstool, showed 2 cytoskeletal proteins, actin alpha cardiac muscle 1 (ACTC1) and tubulin beta-8 chain (TUBB8). ACTC1 can promotecell migration and modulate the length of actin tension fibers. qRT-PCR additional analysis also revealed an increased mRNA expressionof CLU and ACTC1 in HMEC-1 cells treated with TCM. These results suggest that the recently identified proteins are involved in theearly stages of biological processes leading to angiogenesis or EndoMT in CC and could be considered as potential biomarkers.
Fil: Homann, Luana Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Ciencias Biológicas y Biomédicas del Sur. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia. Instituto de Ciencias Biológicas y Biomédicas del Sur; Argentina
Fil: Calvo, Natalia Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Ciencias Biológicas y Biomédicas del Sur. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia. Instituto de Ciencias Biológicas y Biomédicas del Sur; Argentina
XXIII Annual Meeting of the Argentinean Biology Society
Argentina
Sociedad Argentina de Biología
description Tumor angiogenesis plays a crucial role in cervical cancer (CC) from early stages. Research for potential biomarkers and therapeutictargets has been hampered by heterogeneity, plasticity, and molecular differences of the endothelial cells that form the tumor vasculature.This is due, in part, to the effect of factors released by tumor cells. The aim of this work was to investigate the early effects of factorsreleased by CC-derived tumor cells on the morphology and protein profile of endothelial cells. Treatment with CC-derived HeLa cellsconditioned medium (TCM) for 3 h increased the number of HMEC-1 endothelial cells with cytoplasmic processes and a more elongatedshape. Furthermore, qRT-PCR analysis revealed that HMEC-1 cells exposed to TCM decreased VE-cadherin endothelial marker mRNAand increased α-smooth muscle actin mRNA, a cancer-associated fibroblast marker. These findings could be associated with early stagesof tumor angiogenesis characterized by increased cell migration and a partial transition from endothelial to mesenchymal phenotype(EndoMT). Next, the proteome response of HMEC-1 cells was studied under these experimental conditions, performing a Label-Freequantitative (LFQ) mass spectrometry (MS) (CEQUIBIEM Proteomics Center). Proteins were identified and quantified with theProteome Discoverer software and the Uniprot database. Using the Perseus software, 9 negatively regulated proteins and 24 positivelyregulated proteins were obtained in HMEC-1 cells treated with TCM (P ≤ 0.05 and fold change > 1.5), where clusterin (CLU) presentedthe highest fold change. CLU is a glycoprotein with a key role in cellular stress response and cancer, regulating processes such as cellmigration. In addition, the classification of positively regulated proteins, according to their class, with the PANTHER bioinformaticstool, showed 2 cytoskeletal proteins, actin alpha cardiac muscle 1 (ACTC1) and tubulin beta-8 chain (TUBB8). ACTC1 can promotecell migration and modulate the length of actin tension fibers. qRT-PCR additional analysis also revealed an increased mRNA expressionof CLU and ACTC1 in HMEC-1 cells treated with TCM. These results suggest that the recently identified proteins are involved in theearly stages of biological processes leading to angiogenesis or EndoMT in CC and could be considered as potential biomarkers.
publishDate 2022
dc.date.none.fl_str_mv 2022
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info:eu-repo/semantics/conferenceObject
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http://purl.org/coar/resource_type/c_5794
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status_str publishedVersion
format conferenceObject
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/243510
Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells; XXIII Annual Meeting of the Argentinean Biology Society; Argentina; 2021; 1-3
1667-5746
CONICET Digital
CONICET
url http://hdl.handle.net/11336/243510
identifier_str_mv Early effects of factors released by tumor cells derived from cervical cancer on the morphology and protein profile of vascular endothelial cells; XXIII Annual Meeting of the Argentinean Biology Society; Argentina; 2021; 1-3
1667-5746
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
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