Technetium-99m sestamibi single photon emission computed tomography findings correlated with P-glycoprotein expression, encoded by the multidrug resistance gene-1 messenger ribonucleic acid, in intracranial meningiomas

被引:8
|
作者
Kunishio, K
Morisaki, K
Matsumoto, Y
Nagao, S
Nishiyama, Y
机构
[1] Kagawa Med Univ, Dept Neurol Surg, Kagawa, Japan
[2] Kagawa Med Univ, Dept Radiol, Kagawa, Japan
关键词
meningioma; technetium-99m sestamibi; single photon emission computed tomography; multidrug resistance gene; P-glycoprotein;
D O I
10.2176/nmc.43.573
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The present study evaluated whether technetium-99m sestamibi (Tc-99m-MIBI) single photon emission computed tomography (SPECT) characteristics of intracranial meningioma are correlated with the histological malignancy, proliferative potential, and P-glycoprotein (Pgp) expression, encoded by the multidrug resistance gene-1 (MDR-1) messenger ribonucleic acid (mRNA). Twenty-one patients with intracranial meningiomas, including 17 benign and four nonbenign meningiomas, underwent Tc-99m-MIBI SPECT imaging at 15 minutes (early) and 3 hours (delayed) after injection. The tumor-to-normal pituitary gland ratio was calculated on both early (ER) and delayed (DR) images. Retention index (RI) was calculated using the following formula: (DR - ER)/ER X 100%. Meningioma specimens were examined by immunohistochemistry using anti-Pgp and MIB-1 monoclonal antibody. MDR-1 mRNA expression was also investigated using reverse transcription-polymerase chain reaction assay. Tc-99m-MIBI was highly accumulated and retained in the tumors. 99-Tc-MIBI SPECT findings were not related to MIB-1 labeling index. Tc-99m-MIBI SPECT RI of the Pgp-positive group (-9.12 +/- 22.27%) was significantly lower than that of the Pgp-negative group (28.79 +/- 22.80%) (p = 0.0016). No significant difference was seen in ER and DR between the positive and negative groups. These results show that Tc-99m-MIBI may not be useful for determining proliferative potential and histological malignancy, but could predict anticancer drug resistance related to the expression of MDR-1 mRNA and its gene product Pgp in patients with intracranial meningiomas.
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收藏
页码:573 / 580
页数:8
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