Cargando…

Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma

Receptor tyrosine kinases (RTKs) are membrane receptors that play a vital role in various biological processes, in particular, cell survival, cell proliferation, and cell differentiation. These cellular processes are composed of multitiered signaling cascades of kinases starting from ligand binding...

Descripción completa

Detalles Bibliográficos
Autores principales: Chaiyawat, Parunya, Klangjorhor, Jeerawan, Settakorn, Jongkolnee, Champattanachai, Voraratt, Phanphaisarn, Areerak, Teeyakasem, Pimpisa, Svasti, Jisnuson, Pruksakorn, Dumnoensun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587873/
https://www.ncbi.nlm.nih.gov/pubmed/28881260
http://dx.doi.org/10.1016/j.tranon.2017.08.005
_version_ 1783262075737341952
author Chaiyawat, Parunya
Klangjorhor, Jeerawan
Settakorn, Jongkolnee
Champattanachai, Voraratt
Phanphaisarn, Areerak
Teeyakasem, Pimpisa
Svasti, Jisnuson
Pruksakorn, Dumnoensun
author_facet Chaiyawat, Parunya
Klangjorhor, Jeerawan
Settakorn, Jongkolnee
Champattanachai, Voraratt
Phanphaisarn, Areerak
Teeyakasem, Pimpisa
Svasti, Jisnuson
Pruksakorn, Dumnoensun
author_sort Chaiyawat, Parunya
collection PubMed
description Receptor tyrosine kinases (RTKs) are membrane receptors that play a vital role in various biological processes, in particular, cell survival, cell proliferation, and cell differentiation. These cellular processes are composed of multitiered signaling cascades of kinases starting from ligand binding to extracellular domains of RTKs that activate the entire pathways through tyrosine phosphorylation of the receptors and downstream effectors. A previous study reported that, based on proteomics data, RTKs were a major candidate target for osteosarcoma. In this study, activation profiles of six candidate RTKs, including c-Met, c-Kit, VEGFR2, HER2, FGFR1, and PDGFRα, were directly examined from chemonaive fresh frozen tissues of 32 osteosarcoma patients using a multiplex immunoassay. That examination revealed distinct patterns of tyrosine phosphorylation of RTKs in osteosarcoma cases. Unsupervised hierarchical clustering was calculated using Pearson uncentered correlation coefficient to classify RTKs into two groups—Group A (c-Met, c-Kit, VEGFR2, and HER2) and Group B (FGFR1 and PDGFRα)—based on tyrosine phosphorylation patterns. Nonactivation of all Group A RTKs was associated with shorter overall survival in stage IIB osteosarcoma patients. Percentages of tumor necrosis in patients with inactive Group A RTKs were significantly lower than those in patients with at least one active Group A RTK. Paired primary osteosarcoma cells with fresh osteosarcoma tissue were extracted and cultured for cytotoxicity testing. Primary cells with active Group A RTKs tended to be sensitive to doxorubicin and cisplatin. We also found that osteosarcoma cells with active Group A RTKs were more proliferative than cells with inactive Group A RTKs. These findings indicate that the activation pattern of Group A RTKs is a potential risk stratification and chemoresponse predictor and might be used to guide the optimum chemotherapy regimen for osteosarcoma patients.
format Online
Article
Text
id pubmed-5587873
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Neoplasia Press
record_format MEDLINE/PubMed
spelling pubmed-55878732017-09-15 Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma Chaiyawat, Parunya Klangjorhor, Jeerawan Settakorn, Jongkolnee Champattanachai, Voraratt Phanphaisarn, Areerak Teeyakasem, Pimpisa Svasti, Jisnuson Pruksakorn, Dumnoensun Transl Oncol Original article Receptor tyrosine kinases (RTKs) are membrane receptors that play a vital role in various biological processes, in particular, cell survival, cell proliferation, and cell differentiation. These cellular processes are composed of multitiered signaling cascades of kinases starting from ligand binding to extracellular domains of RTKs that activate the entire pathways through tyrosine phosphorylation of the receptors and downstream effectors. A previous study reported that, based on proteomics data, RTKs were a major candidate target for osteosarcoma. In this study, activation profiles of six candidate RTKs, including c-Met, c-Kit, VEGFR2, HER2, FGFR1, and PDGFRα, were directly examined from chemonaive fresh frozen tissues of 32 osteosarcoma patients using a multiplex immunoassay. That examination revealed distinct patterns of tyrosine phosphorylation of RTKs in osteosarcoma cases. Unsupervised hierarchical clustering was calculated using Pearson uncentered correlation coefficient to classify RTKs into two groups—Group A (c-Met, c-Kit, VEGFR2, and HER2) and Group B (FGFR1 and PDGFRα)—based on tyrosine phosphorylation patterns. Nonactivation of all Group A RTKs was associated with shorter overall survival in stage IIB osteosarcoma patients. Percentages of tumor necrosis in patients with inactive Group A RTKs were significantly lower than those in patients with at least one active Group A RTK. Paired primary osteosarcoma cells with fresh osteosarcoma tissue were extracted and cultured for cytotoxicity testing. Primary cells with active Group A RTKs tended to be sensitive to doxorubicin and cisplatin. We also found that osteosarcoma cells with active Group A RTKs were more proliferative than cells with inactive Group A RTKs. These findings indicate that the activation pattern of Group A RTKs is a potential risk stratification and chemoresponse predictor and might be used to guide the optimum chemotherapy regimen for osteosarcoma patients. Neoplasia Press 2017-09-04 /pmc/articles/PMC5587873/ /pubmed/28881260 http://dx.doi.org/10.1016/j.tranon.2017.08.005 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Chaiyawat, Parunya
Klangjorhor, Jeerawan
Settakorn, Jongkolnee
Champattanachai, Voraratt
Phanphaisarn, Areerak
Teeyakasem, Pimpisa
Svasti, Jisnuson
Pruksakorn, Dumnoensun
Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma
title Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma
title_full Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma
title_fullStr Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma
title_full_unstemmed Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma
title_short Activation Status of Receptor Tyrosine Kinases as an Early Predictive Marker of Response to Chemotherapy in Osteosarcoma
title_sort activation status of receptor tyrosine kinases as an early predictive marker of response to chemotherapy in osteosarcoma
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587873/
https://www.ncbi.nlm.nih.gov/pubmed/28881260
http://dx.doi.org/10.1016/j.tranon.2017.08.005
work_keys_str_mv AT chaiyawatparunya activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT klangjorhorjeerawan activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT settakornjongkolnee activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT champattanachaivoraratt activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT phanphaisarnareerak activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT teeyakasempimpisa activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT svastijisnuson activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma
AT pruksakorndumnoensun activationstatusofreceptortyrosinekinasesasanearlypredictivemarkerofresponsetochemotherapyinosteosarcoma