Background PTEN is an anti-oncogene frequently inactivating in glioma. The previous study found that PTEN was closely related to cellular autophagy activity. The purpose of this paper is to study whether the inactivation of PTEN in glioma stem/progenitor cells (GSPCs) is correlativewith the low autophagic activity in GSPCs. Methods Wild-type PTEN genes were transferred into GSPCs mediated by adenovirus. The autophagic activity in GSPCs before or after the introduction of wild-type PTEN was detected by immunocytochemistry, electron microscopy, and Western blotting assay. Results After transfection of wild-type PTEN, a large number of microtuble-associated protein 1 light chain 3 (MAP1LC3)-positive granules could be found in the cytoplasm of ...
A patient diagnosed with a glioma, generally, has an average of 14 months year to live after impleme...
PTEN is a tumour suppressor frequently mutated in many types of cancers. Here we show that targeted ...
<p>A. Representative electron micrographs of U-87 MG glioma cells infected with Delta-24-RGD or ΔE1B...
PTEN (phosphatase and tensin homologue deleted on chromosome ten) is a tumor suppressor gene implica...
Two major mechanisms of intracellular protein degradation, autophagy and the ubiquitin-proteasome pa...
PTEN (phosphatase and tensin homologue deleted on chromosome ten) is a tumor suppressor gene implica...
To study the effects of wild-type PTEN on gene expressions of glioblastomas.Glioblastoma U87MG cells...
Objective More and more attention has been given to the presumption that glioma stem cells (GSCs) or...
Glioma stem/progenitor cells (GSPCs) are considered to be responsible for the initiation, propagatio...
Human bone marrow-derived mesenchymal stem cells (MSC) have been increasingly used as a vehicle for ...
Glioblastoma multiforme (GBM) is the most common and aggressive primary brain tumor featuring rapid ...
The carcinogenesis of glial tumors appears complex because of the many genetic and epigenetic phenom...
Autophagy is an evolutionarily conserved process regulating cellular homeostasis via digestion of dy...
<div><p>The term astrocytoma defines a quite heterogeneous group of neoplastic diseases that collect...
Autophagy is a physiological process by which various damaged or non-essential cytosolic components ...
A patient diagnosed with a glioma, generally, has an average of 14 months year to live after impleme...
PTEN is a tumour suppressor frequently mutated in many types of cancers. Here we show that targeted ...
<p>A. Representative electron micrographs of U-87 MG glioma cells infected with Delta-24-RGD or ΔE1B...
PTEN (phosphatase and tensin homologue deleted on chromosome ten) is a tumor suppressor gene implica...
Two major mechanisms of intracellular protein degradation, autophagy and the ubiquitin-proteasome pa...
PTEN (phosphatase and tensin homologue deleted on chromosome ten) is a tumor suppressor gene implica...
To study the effects of wild-type PTEN on gene expressions of glioblastomas.Glioblastoma U87MG cells...
Objective More and more attention has been given to the presumption that glioma stem cells (GSCs) or...
Glioma stem/progenitor cells (GSPCs) are considered to be responsible for the initiation, propagatio...
Human bone marrow-derived mesenchymal stem cells (MSC) have been increasingly used as a vehicle for ...
Glioblastoma multiforme (GBM) is the most common and aggressive primary brain tumor featuring rapid ...
The carcinogenesis of glial tumors appears complex because of the many genetic and epigenetic phenom...
Autophagy is an evolutionarily conserved process regulating cellular homeostasis via digestion of dy...
<div><p>The term astrocytoma defines a quite heterogeneous group of neoplastic diseases that collect...
Autophagy is a physiological process by which various damaged or non-essential cytosolic components ...
A patient diagnosed with a glioma, generally, has an average of 14 months year to live after impleme...
PTEN is a tumour suppressor frequently mutated in many types of cancers. Here we show that targeted ...
<p>A. Representative electron micrographs of U-87 MG glioma cells infected with Delta-24-RGD or ΔE1B...