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Diffusion parameters of the extracellular space in human gliomas
Tumor cell migration through the extracellular space (ECS) might be affected by its pore size and extracellular matrix molecule content. ECS volume fraction α (α = ECS volume/total tissue volume), tortuosity λ (λ2 = free/apparent diffusion coefficient) and nonspecific uptake k′ were studied by the r...
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Published in: | Glia 2003-04, Vol.42 (1), p.77-88 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
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Online Access: | Get full text |
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Summary: | Tumor cell migration through the extracellular space (ECS) might be affected by its pore size and extracellular matrix molecule content. ECS volume fraction α (α = ECS volume/total tissue volume), tortuosity λ (λ2 = free/apparent diffusion coefficient) and nonspecific uptake k′ were studied by the real‐time tetramethylammonium method in acute slices of human tissue. The diffusion parameters in temporal cortical tissue resected during surgical treatment of temporal lobe epilepsy (control) were compared with those in brain tumors. Subsequently, tumor slices were histopathologically classified according to the grading system of the World Health Organization (WHO), and proliferative activity was assessed. The average values of α, λ, and k′ in control cortex were 0.24, 1.55, and 3.66 × 10−3s−1, respectively. Values of α, λ, and k′ in oligodendrogliomas did not significantly differ from controls. In pilocytic astrogliomas (WHO grade I) as well as in ependymomas (WHO grade II), α was significantly higher, while λ and k′ were unchanged. Higher values of α as well as λ were found in low‐grade diffuse astrocytomas (WHO grade II). In cellular regions of high‐grade astrocytomas (WHO grade III and IV), α and λ were further increased, and k′ was significantly larger than in controls. Classic medulloblastomas (WHO grade IV) had an increased α, but not λ or k′, while in the desmoplastic type α and k′ remained unchanged, but λ was greatly increased. Tumor malignancy grade strongly corresponds to an increase in ECS volume, which is accompanied by a change in ECS structure manifested by an increase in diffusion barriers for small molecules. GLIA 42:77–88, 2003. © 2003 Wiley‐Liss, Inc. |
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ISSN: | 0894-1491 1098-1136 |
DOI: | 10.1002/glia.10204 |