adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment
Chemotherapeutic resistance is a major problem in effective cancer treatment. Cancer cells engage various cells or mechanisms to resist anti-cancer therapeutics, which results in metastasis and the recurrence of disease. Considering the cellular heterogeneity of cancer stroma, the involvement of ste...
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doaj-953aac4fdfc74a5d9830fcc5e30c93202021-06-30T23:48:24ZengMDPI AGBioengineering2306-53542021-06-018838310.3390/bioengineering8060083adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma TreatmentBanani Kundu0Virginia Brancato1Joaquim Oliveira2Vitor M. Correlo3Rui L. Reis4Subhas C. Kundu53B’s Research Group, I3Bs—Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Guimarães, Portugal3B’s Research Group, I3Bs—Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Guimarães, Portugal3B’s Research Group, I3Bs—Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Guimarães, Portugal3B’s Research Group, I3Bs—Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Guimarães, Portugal3B’s Research Group, I3Bs—Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Guimarães, Portugal3B’s Research Group, I3Bs—Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Guimarães, PortugalChemotherapeutic resistance is a major problem in effective cancer treatment. Cancer cells engage various cells or mechanisms to resist anti-cancer therapeutics, which results in metastasis and the recurrence of disease. Considering the cellular heterogeneity of cancer stroma, the involvement of stem cells is reported to affect the proliferation and metastasis of osteosarcoma. Hence, the duo (osteosarcoma: Saos 2 and human adipose-derived stem cells: ASCs) is co-cultured in present study to investigate the therapeutic response using a nonadherent, concave surface. Staining with a cell tracker allows real-time microscopic monitoring of the cell arrangement within the sphere. Cell–cell interaction is investigated by means of E-cadherin expression. Comparatively high expression of E-cadherin and compact organization is observed in heterotypic tumorspheres (Saos 2–ASCs) compared to homotypic ones (ASCs), limiting the infiltration of chemotherapeutic compound doxorubicin into the heterotypic tumorsphere, which in turn protects cells from the toxic effect of the chemotherapeutic. In addition, genes known to be associated with drug resistance, such as SOX2, OCT4, and CD44 are overexpressed in heterotypic tumorspheres post-chemotherapy, indicating that the duo collectively repels the effect of doxorubicin. The interaction between ASCs and Saos 2 in the present study points toward the growing oncological risk of using ASC-based regenerative therapy in cancer patients and warrants further investigation.https://www.mdpi.com/2306-5354/8/6/83heterotypic tumorspheresnonadherent surfaceosteosarcomahuman adipose-derived stem cellsdrug response |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Banani Kundu Virginia Brancato Joaquim Oliveira Vitor M. Correlo Rui L. Reis Subhas C. Kundu |
spellingShingle |
Banani Kundu Virginia Brancato Joaquim Oliveira Vitor M. Correlo Rui L. Reis Subhas C. Kundu adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment Bioengineering heterotypic tumorspheres nonadherent surface osteosarcoma human adipose-derived stem cells drug response |
author_facet |
Banani Kundu Virginia Brancato Joaquim Oliveira Vitor M. Correlo Rui L. Reis Subhas C. Kundu |
author_sort |
Banani Kundu |
title |
adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment |
title_short |
adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment |
title_full |
adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment |
title_fullStr |
adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment |
title_full_unstemmed |
adipoSIGHT in Therapeutic Response: Consequences in Osteosarcoma Treatment |
title_sort |
adiposight in therapeutic response: consequences in osteosarcoma treatment |
publisher |
MDPI AG |
series |
Bioengineering |
issn |
2306-5354 |
publishDate |
2021-06-01 |
description |
Chemotherapeutic resistance is a major problem in effective cancer treatment. Cancer cells engage various cells or mechanisms to resist anti-cancer therapeutics, which results in metastasis and the recurrence of disease. Considering the cellular heterogeneity of cancer stroma, the involvement of stem cells is reported to affect the proliferation and metastasis of osteosarcoma. Hence, the duo (osteosarcoma: Saos 2 and human adipose-derived stem cells: ASCs) is co-cultured in present study to investigate the therapeutic response using a nonadherent, concave surface. Staining with a cell tracker allows real-time microscopic monitoring of the cell arrangement within the sphere. Cell–cell interaction is investigated by means of E-cadherin expression. Comparatively high expression of E-cadherin and compact organization is observed in heterotypic tumorspheres (Saos 2–ASCs) compared to homotypic ones (ASCs), limiting the infiltration of chemotherapeutic compound doxorubicin into the heterotypic tumorsphere, which in turn protects cells from the toxic effect of the chemotherapeutic. In addition, genes known to be associated with drug resistance, such as SOX2, OCT4, and CD44 are overexpressed in heterotypic tumorspheres post-chemotherapy, indicating that the duo collectively repels the effect of doxorubicin. The interaction between ASCs and Saos 2 in the present study points toward the growing oncological risk of using ASC-based regenerative therapy in cancer patients and warrants further investigation. |
topic |
heterotypic tumorspheres nonadherent surface osteosarcoma human adipose-derived stem cells drug response |
url |
https://www.mdpi.com/2306-5354/8/6/83 |
work_keys_str_mv |
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1721350458904150016 |