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Published on: April 16, 2018
5-Aminolevulinic acid-mediated photodynamic therapy can target human glioma stem-like cells refractory to
Takahiro Fujishiro1, Naosuke Nonoguchi1, Marat Pavliukov2
1Department of Neurosurgery, Osaka Medical College, Takatsuki, Osaka, Japan.
Background:
Glioblastoma (GBM) is a highly malignant lethal brain cancer. Accumulated evidence suggests that elevated resistance of GBM to both chemo- and radio-therapy is, at least in part, due to the presence of a small population of glioma stem cells (GSC). In the present study, we aimed to determine the sensitivity of GSCs to 5-aminolevulinic acid-mediated photodynamic therapy (ALA-PDT).
Methods:
For this purpose, we established GSC-enriched cell cultures (termed glioma stem-like cells or GSLCs) from A172 human GBM cell line. Under our cultivation conditions, GSLCs formed floating spheroid clusters that contained increased population of CD133/Sox2 expressing cells. Firstly, to compare the activity of protoporphyrin IX (PpIX) biosynthesis in the GSLCs and the parental A172 glioma cells, we examined the expression levels of biosynthesis enzymes and transporters for PpIX using qRT-PCR, and investigated the intracellular levels of PpIX with use of flow cytometry analysis. Then, we evaluated the sensitivity of these cells to ALA-PDT in vitro. Finally, to confirm the therapeutic impact of ALA-PDT on GSLCs with more clinically relevant model, we performed the same experiment using three different patient-derived glioma sphere lines, which cultivated them either in stem cell media or under differentiation conditions in the presence of serum.
Results And Conclusion:
GSLCs expressed higher mRNA levels of PpIX biosynthesis enzymes and its transporters PEPT1/2 and ABCB6, when compared to the parental A172 glioma cells. Consistently, flow cytometry analysis revealed that upon incubation with ALA, GSLCs accumulate a higher level of PpIX. Finally, we showed that GSLCs were more sensitive to ALA-PDT than the original A172 cells, and confirmed that all patient-derived glioma sphere lines also showed significantly increased sensitivity to ALA-PDT if cultivated under the pro-stem cell condition. Our data indicate that ALA-PDT has potential as a novel clinically useful treatment that might eliminate GBM stem cells that are highly resistant to current chemo- and radio-therapy.
Insights
5-aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) effectively targets therapy-resistant glioblastoma stem cells (GSCs). This novel approach shows promise for eliminating these resilient cancer cells, offering a potential new treatment strategy.
Area of Science:
- Oncology
- Biochemistry
- Cell Biology
Background:
- Glioblastoma (GBM) exhibits resistance to conventional chemo- and radio-therapy, partly due to glioma stem cells (GSCs).
- Investigating novel therapeutic strategies targeting GSCs is crucial for improving GBM treatment outcomes.
Purpose of the Study:
- To determine the sensitivity of GSCs to 5-aminolevulinic acid-mediated photodynamic therapy (ALA-PDT).
- To compare the efficacy of ALA-PDT against GSC-enriched cultures and patient-derived glioma spheres.
Main Methods:
- Established GSC-enriched cultures (GSLCs) from A172 human GBM cell line.
- Quantified protoporphyrin IX (PpIX) biosynthesis enzyme expression and intracellular PpIX levels.
- Assessed cellular sensitivity to ALA-PDT in vitro using GSLCs and patient-derived glioma spheres.
Main Results:
- GSLCs exhibited higher mRNA levels of PpIX biosynthesis enzymes and transporters (PEPT1/2, ABCB6) compared to parental A172 cells.
- GSLCs accumulated higher intracellular PpIX levels after ALA incubation.
- GSLCs and patient-derived glioma spheres under pro-stem cell conditions showed increased sensitivity to ALA-PDT.
Conclusions:
- Glioma stem cells show enhanced PpIX accumulation and sensitivity to ALA-PDT.
- ALA-PDT demonstrates potential for eliminating therapy-resistant GBM stem cells.
- This therapy may offer a novel clinical approach to overcome GBM treatment resistance.
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