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胶质母细胞瘤中使用缺氧放射性示踪剂(18)F-FRP170进行正电子发射断层扫描时的高摄取区域包括在缺氧条件下保持增殖活性的区域。

High-uptake areas on positron emission tomography with the hypoxic radiotracer (18)F-FRP170 in glioblastomas include regions retaining proliferative activity under hypoxia.

作者信息

Beppu Takaaki, Sasaki Toshiaki, Terasaki Kazunori, Saura Hiroaki, Mtsuura Hideki, Ogasawara Kuniaki, Sasaki Makoto, Ehara Shigeru, Iwata Ren, Takai Yoshihiro

机构信息

Department of Neurosurgery, Iwate Medical University, Uchimaru 19-1, Morioka, 020-8505, Japan,

出版信息

Ann Nucl Med. 2015 May;29(4):336-41. doi: 10.1007/s12149-015-0951-0. Epub 2015 Jan 25.

Abstract

OBJECTIVE

The aim was to evaluate the proliferative activity of high-uptake areas on positron emission tomography (PET) with the hypoxic cell radiotracer, 1-(2-[(18)F]fluoro-1-[hydroxymethyl]ethoxy)methyl-2-nitroimidazole (FRP170).

METHODS

Thirteen patients with glioblastoma underwent FRP170 PET before tumor resection. During surgery, tumor specimens were stereotaxically obtained from regions corresponding to high (high-uptake areas, HUAs) and relatively low (low-uptake areas, LUAs) accumulation of FRP170. We compared immunohistochemical staining for Ki-67 and hypoxia-inducible factor (HIF)-1α between HUA and LUA.

RESULTS

HIF-1α index was significantly higher in HUAs than in LUAs. In contrast, mean Ki-67 indices did not differ significantly between HUAs and LUAs.

CONCLUSIONS

Findings for HIF-1α index clearly indicated that HUAs on FRP170 PET represented hypoxic regions in glioblastoma. However, findings of Ki-67 index suggest that HUAs on FRP170 PET include regions retaining proliferative activity regardless of tissue hypoxia.

摘要

目的

旨在使用乏氧细胞放射性示踪剂1-(2-[(18)F]氟-1-[羟甲基]乙氧基)甲基-2-硝基咪唑(FRP170)评估正电子发射断层扫描(PET)上高摄取区域的增殖活性。

方法

13例胶质母细胞瘤患者在肿瘤切除前接受了FRP170 PET检查。手术过程中,从与FRP170高积聚区域(高摄取区域,HUAs)和相对低积聚区域(低摄取区域,LUAs)对应的部位立体定向获取肿瘤标本。我们比较了HUA和LUA之间Ki-67和缺氧诱导因子(HIF)-1α的免疫组织化学染色情况。

结果

HUA中的HIF-1α指数显著高于LUA。相比之下,HUA和LUA之间的平均Ki-67指数没有显著差异。

结论

HIF-1α指数的结果清楚地表明,FRP170 PET上的HUA代表胶质母细胞瘤中的乏氧区域。然而,Ki-67指数的结果表明,FRP170 PET上的HUA包括无论组织缺氧情况仍保留增殖活性的区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c8d/4661197/6fd2a5a9aa79/12149_2015_951_Fig1_HTML.jpg

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