fig3

Negative effects of tumor cell nitric oxide on anti-glioblastoma photodynamic therapy

Figure 3. Enhanced proliferation and invasion rate of glioblastoma cells that survive ALA/light treatment: iNOS/NO dependency. U87 cells were sensitized with ALA-induced PpIX as described in Figure 2, exposed to a light fluence of ~ 1 J/cm2, and then assessed for various post-irradiation parameters. 1400W(W), L-NAME (N), or cPTIO (cP) was either absent or present throughout. A: loss of viability (0-24 h post-hν) and subsequent proliferation of surviving cells (24-48 h post post-hν); DC: ALA-only dark control; B: surviving cell proliferation rate for selected conditions represented in panel (A); C: surviving cell invasiveness measured with a trans-well device; D: matrix metalloprotein-9 (MMP-9) activity measured by gelatin zymography 24 h after cells were ALA-light-treated. Plotted values are means ± SEM (n = 3); *P < 0.01 vs. ALA/hν (B); **P < 0.01 vs. ALA/hν (C); *P < 0.01 vs. ALA/hν (D). ALA: 5-Aminolevulinic acid; PpIX: protoporphyrin IX; NO: nitric oxide; iNOS: inducible NO synthase; post-hν: post-irradiation (Reproduced from Ref. 56 and 62, with permission)

Journal of Cancer Metastasis and Treatment
ISSN 2454-2857 (Online) 2394-4722 (Print)

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