HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels
Abstract Chemotherapy plays a significant role in glioma treatment; however, it has limited effectiveness in extending the life expectancies of glioma patients. Traditional studies have attributed this lack of efficacy to glioma stem cells (GSCs) and their high resistance to chemotherapy, and hypoxi...
Guardado en:
Autores principales: | , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/6a5b57193964410488125334d895996d |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:6a5b57193964410488125334d895996d |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:6a5b57193964410488125334d895996d2021-12-02T15:05:41ZHIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels10.1038/s41598-017-06086-22045-2322https://doaj.org/article/6a5b57193964410488125334d895996d2017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-06086-2https://doaj.org/toc/2045-2322Abstract Chemotherapy plays a significant role in glioma treatment; however, it has limited effectiveness in extending the life expectancies of glioma patients. Traditional studies have attributed this lack of efficacy to glioma stem cells (GSCs) and their high resistance to chemotherapy, and hypoxia worsens this issue. In contrast, hyperoxia effectively alleviates hypoxia in glioma and sensitizes glioma cells to chemotherapy. In a summary of traditional studies, the majority of researchers overlooked the influence of hypoxia on differentiated cells because they only focused on the maintenance of GSCs stemness, which thus resulted in chemoresistance. Because of this background, we hypothesized that GSCs may be induced through dedifferentiation under hypoxic conditions, and hypoxia maintains GSCs stemness, which thus leads to resistance to chemotherapy. In contrast, hyperoxia inhibits the dedifferentiation process and promotes GSCs differentiation, which increases the sensitization of glioma cells to chemotherapy. Hypoxia-inducible factor-1α (HIF1α) contributes substantially to the stemness maintenance of GSCs and resistance of glioma to chemotherapy; thus, we investigated whether HIF1α regulates the resistance or sensitization of glioma cells to chemotherapy in different oxygen levels. It highlights a novel viewpoint on glioma chemosensitivity from the transformation between dedifferentiation and differentiation in different oxygen levels.Pan WangWenwu WanShuanglong XiongJunwei WangDewei ZouChuan LanShuangjiang YuBin LiaoHua FengNan WuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-16 (2017) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Pan Wang Wenwu Wan Shuanglong Xiong Junwei Wang Dewei Zou Chuan Lan Shuangjiang Yu Bin Liao Hua Feng Nan Wu HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
description |
Abstract Chemotherapy plays a significant role in glioma treatment; however, it has limited effectiveness in extending the life expectancies of glioma patients. Traditional studies have attributed this lack of efficacy to glioma stem cells (GSCs) and their high resistance to chemotherapy, and hypoxia worsens this issue. In contrast, hyperoxia effectively alleviates hypoxia in glioma and sensitizes glioma cells to chemotherapy. In a summary of traditional studies, the majority of researchers overlooked the influence of hypoxia on differentiated cells because they only focused on the maintenance of GSCs stemness, which thus resulted in chemoresistance. Because of this background, we hypothesized that GSCs may be induced through dedifferentiation under hypoxic conditions, and hypoxia maintains GSCs stemness, which thus leads to resistance to chemotherapy. In contrast, hyperoxia inhibits the dedifferentiation process and promotes GSCs differentiation, which increases the sensitization of glioma cells to chemotherapy. Hypoxia-inducible factor-1α (HIF1α) contributes substantially to the stemness maintenance of GSCs and resistance of glioma to chemotherapy; thus, we investigated whether HIF1α regulates the resistance or sensitization of glioma cells to chemotherapy in different oxygen levels. It highlights a novel viewpoint on glioma chemosensitivity from the transformation between dedifferentiation and differentiation in different oxygen levels. |
format |
article |
author |
Pan Wang Wenwu Wan Shuanglong Xiong Junwei Wang Dewei Zou Chuan Lan Shuangjiang Yu Bin Liao Hua Feng Nan Wu |
author_facet |
Pan Wang Wenwu Wan Shuanglong Xiong Junwei Wang Dewei Zou Chuan Lan Shuangjiang Yu Bin Liao Hua Feng Nan Wu |
author_sort |
Pan Wang |
title |
HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
title_short |
HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
title_full |
HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
title_fullStr |
HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
title_full_unstemmed |
HIF1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
title_sort |
hif1α regulates glioma chemosensitivity through the transformation between differentiation and dedifferentiation in various oxygen levels |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/6a5b57193964410488125334d895996d |
work_keys_str_mv |
AT panwang hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT wenwuwan hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT shuanglongxiong hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT junweiwang hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT deweizou hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT chuanlan hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT shuangjiangyu hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT binliao hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT huafeng hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels AT nanwu hif1aregulatesgliomachemosensitivitythroughthetransformationbetweendifferentiationanddedifferentiationinvariousoxygenlevels |
_version_ |
1718388708986585088 |