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...

Full description

Bibliographic Details
Main Authors: Banani Kundu, Virginia Brancato, Joaquim Oliveira, Vitor M. Correlo, Rui L. Reis, Subhas C. Kundu
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Bioengineering
Subjects:
Online Access:https://www.mdpi.com/2306-5354/8/6/83
id doaj-953aac4fdfc74a5d9830fcc5e30c9320
record_format Article
spelling 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 AT bananikundu adiposightintherapeuticresponseconsequencesinosteosarcomatreatment
AT virginiabrancato adiposightintherapeuticresponseconsequencesinosteosarcomatreatment
AT joaquimoliveira adiposightintherapeuticresponseconsequencesinosteosarcomatreatment
AT vitormcorrelo adiposightintherapeuticresponseconsequencesinosteosarcomatreatment
AT ruilreis adiposightintherapeuticresponseconsequencesinosteosarcomatreatment
AT subhasckundu adiposightintherapeuticresponseconsequencesinosteosarcomatreatment
_version_ 1721350458904150016