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Notch signalling is a potential resistance mechanism of progenitor cells within patient‐derived prostate cultures following ROS‐inducing treatments
- Source :
- Febs Letters
- Publication Year :
- 2019
- Publisher :
- Wiley, 2019.
-
Abstract
- Low Temperature Plasma (LTP) generates reactive oxygen and nitrogen species, causing cell death, similarly to radiation. Radiation resistance results in tumour recurrence, however mechanisms of LTP resistance are unknown. LTP was applied to patient-derived prostate epithelial cells and gene expression assessed. A typical global oxidative response (AP-1 and Nrf2 signalling) was induced, whereas Notch signalling was activated exclusively in progenitor cells. Notch inhibition induced expression of prostatic acid phosphatase (PAP), a marker of prostate epithelial cell differentiation, whilst reducing colony forming ability and preventing tumour formation. Therefore, if LTP is to be progressed as a novel treatment for prostate cancer, combination treatments should be considered in the context of cellular heterogeneity and existence of cell type-specific resistance mechanisms.
- Subjects :
- Male
Plasma Gases
Cell
Radiation Tolerance
Biochemistry
Prostate cancer
Structural Biology
Prostate
Epithelial cell differentiation
reactive oxygen species
0303 health sciences
Cell Death
Receptors, Notch
Chemistry
Stem Cells
030302 biochemistry & molecular biology
Cell Differentiation
progenitor cells
prostate cancer
Reactive Nitrogen Species
Low temperature plasma
3. Good health
Gene Expression Regulation, Neoplastic
medicine.anatomical_structure
Prostatic acid phosphatase
Notch signalling
Signal Transduction
Programmed cell death
NF-E2-Related Factor 2
Acid Phosphatase
Biophysics
Notch signaling pathway
03 medical and health sciences
Cell Line, Tumor
Genetics
medicine
Humans
Progenitor cell
Molecular Biology
Cell Proliferation
030304 developmental biology
Therapy resistance
Prostatic Neoplasms
Epithelial Cells
Cell Biology
medicine.disease
Transcription Factor AP-1
Editor's Choice
Cancer research
Subjects
Details
- ISSN :
- 18733468 and 00145793
- Volume :
- 594
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....341d0f4e89b092696e428c035b64ce1c