Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.

Resistant cancer phenotype is a key obstacle in the successful therapy of prostate cancer. The primary aim of our study was to explore resistance mechanisms in the advanced type of prostate cancer cells (PC-3) and to clarify the role of autophagy in these processes. We performed time-lapse experimen...

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Main Authors: Jan Balvan, Jaromir Gumulec, Martina Raudenska, Aneta Krizova, Petr Stepka, Petr Babula, Rene Kizek, Vojtech Adam, Michal Masarik
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4679176?pdf=render
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author Jan Balvan
Jaromir Gumulec
Martina Raudenska
Aneta Krizova
Petr Stepka
Petr Babula
Rene Kizek
Vojtech Adam
Michal Masarik
author_facet Jan Balvan
Jaromir Gumulec
Martina Raudenska
Aneta Krizova
Petr Stepka
Petr Babula
Rene Kizek
Vojtech Adam
Michal Masarik
author_sort Jan Balvan
collection DOAJ
description Resistant cancer phenotype is a key obstacle in the successful therapy of prostate cancer. The primary aim of our study was to explore resistance mechanisms in the advanced type of prostate cancer cells (PC-3) and to clarify the role of autophagy in these processes. We performed time-lapse experiment (48 hours) with ROS generating plumbagin by using multimodal holographic microscope. Furthermore, we also performed the flow-cytometric analysis and the qRT-PCR gene expression analysis at 12 selected time points. TEM and confocal microscopy were used to verify the results. We found out that autophagy (namely mitophagy) is an important resistance mechanism. The major ROS producing mitochondria were coated by an autophagic membrane derived from endoplasmic reticulum and degraded. According to our results, increasing ROS resistance may be also accompanied by increased average cell size and polyploidization, which seems to be key resistance mechanism when connected with an escape from senescence. Many different types of cell-cell interactions were recorded including entosis, vesicular transfer, eating of dead or dying cells, and engulfment and cannibalism of living cells. Entosis was disclosed as a possible mechanism of polyploidization and enabled the long-term survival of cancer cells. Significantly reduced cell motility was found after the plumbagin treatment. We also found an extensive induction of pluripotency genes expression (NANOG, SOX2, and POU5F1) at the time-point of 20 hours. We suppose, that overexpression of pluripotency genes in the portion of prostate tumour cell population exposed to ROS leads to higher developmental plasticity and capability to faster respond to changes in the extracellular environment that could ultimately lead to an alteration of cell fate.
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spelling doaj.art-97d13d69b9f5426d8ce681cb3763bb602022-12-21T18:49:01ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011012e014501610.1371/journal.pone.0145016Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.Jan BalvanJaromir GumulecMartina RaudenskaAneta KrizovaPetr StepkaPetr BabulaRene KizekVojtech AdamMichal MasarikResistant cancer phenotype is a key obstacle in the successful therapy of prostate cancer. The primary aim of our study was to explore resistance mechanisms in the advanced type of prostate cancer cells (PC-3) and to clarify the role of autophagy in these processes. We performed time-lapse experiment (48 hours) with ROS generating plumbagin by using multimodal holographic microscope. Furthermore, we also performed the flow-cytometric analysis and the qRT-PCR gene expression analysis at 12 selected time points. TEM and confocal microscopy were used to verify the results. We found out that autophagy (namely mitophagy) is an important resistance mechanism. The major ROS producing mitochondria were coated by an autophagic membrane derived from endoplasmic reticulum and degraded. According to our results, increasing ROS resistance may be also accompanied by increased average cell size and polyploidization, which seems to be key resistance mechanism when connected with an escape from senescence. Many different types of cell-cell interactions were recorded including entosis, vesicular transfer, eating of dead or dying cells, and engulfment and cannibalism of living cells. Entosis was disclosed as a possible mechanism of polyploidization and enabled the long-term survival of cancer cells. Significantly reduced cell motility was found after the plumbagin treatment. We also found an extensive induction of pluripotency genes expression (NANOG, SOX2, and POU5F1) at the time-point of 20 hours. We suppose, that overexpression of pluripotency genes in the portion of prostate tumour cell population exposed to ROS leads to higher developmental plasticity and capability to faster respond to changes in the extracellular environment that could ultimately lead to an alteration of cell fate.http://europepmc.org/articles/PMC4679176?pdf=render
spellingShingle Jan Balvan
Jaromir Gumulec
Martina Raudenska
Aneta Krizova
Petr Stepka
Petr Babula
Rene Kizek
Vojtech Adam
Michal Masarik
Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.
PLoS ONE
title Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.
title_full Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.
title_fullStr Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.
title_full_unstemmed Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.
title_short Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating.
title_sort oxidative stress resistance in metastatic prostate cancer renewal by self eating
url http://europepmc.org/articles/PMC4679176?pdf=render
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