中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2009年
48期
3420-3424
,共5页
徐文贵%戴东%房娜%宋秀宇%王健%朱研佳%门晓媛
徐文貴%戴東%房娜%宋秀宇%王健%硃研佳%門曉媛
서문귀%대동%방나%송수우%왕건%주연가%문효원
基因探针%~(18)F-FHBG%PET-CT显像%HSV1-tk基因%乳腺癌
基因探針%~(18)F-FHBG%PET-CT顯像%HSV1-tk基因%乳腺癌
기인탐침%~(18)F-FHBG%PET-CT현상%HSV1-tk기인%유선암
Reporter gene probe%~(18)F-FHBG%PET-CT imaging%HSV1-tk%Breast carcinoma
目的 对~(18)F-FHBG体外摄取、体内分布及荷瘤裸鼠PET-CT显像等方面进行研究.方法 利用γ井型计数器测定体外肿瘤细胞T47D和T47D-tk对~(18)F-FHBG的摄取、正常昆明小鼠和移植瘤裸鼠~(18)F-FHBG体内分布;并进行荷皮下移植瘤裸鼠~(18)F-FHBG PET-CT显像.结果 体外肿瘤细胞摄取实验显示T47D-tk细胞摄取~(18)F-FHBG的程度明显高于正常的T47D细胞,120 min时T47D-tk细胞对~(18)F-FHBG的摄取为T47D细胞的64倍(P<0.001).正常小鼠注射~(18)F-FHBG后,主要分布于肝脏、肠道、肾脏和膀胱,而脑部未见明显放射性分布.荷皮下移植瘤裸鼠PET-CT显像显示,T47D-tk肿瘤浓聚~(18)F-FHBG的程度明显高于T47D肿瘤,且2 h显像效果较好.结论 体外T47D-tk细胞摄取~(18)F-FHBG的程度明显高于正常的T47D细胞;在小鼠体内~(18)F-FHBG主要经肠道和泌尿系统排泄.~(18)F-FHBG报告基因探针可以有效的定位于HSV1-tk基因表达的部位且与移植瘤裸鼠体内分布研究结果一致.这可为进一步开展~(18)F-FHBG报告基因显像与肿瘤基因治疗的监测提供有效手段和科学依据.
目的 對~(18)F-FHBG體外攝取、體內分佈及荷瘤裸鼠PET-CT顯像等方麵進行研究.方法 利用γ井型計數器測定體外腫瘤細胞T47D和T47D-tk對~(18)F-FHBG的攝取、正常昆明小鼠和移植瘤裸鼠~(18)F-FHBG體內分佈;併進行荷皮下移植瘤裸鼠~(18)F-FHBG PET-CT顯像.結果 體外腫瘤細胞攝取實驗顯示T47D-tk細胞攝取~(18)F-FHBG的程度明顯高于正常的T47D細胞,120 min時T47D-tk細胞對~(18)F-FHBG的攝取為T47D細胞的64倍(P<0.001).正常小鼠註射~(18)F-FHBG後,主要分佈于肝髒、腸道、腎髒和膀胱,而腦部未見明顯放射性分佈.荷皮下移植瘤裸鼠PET-CT顯像顯示,T47D-tk腫瘤濃聚~(18)F-FHBG的程度明顯高于T47D腫瘤,且2 h顯像效果較好.結論 體外T47D-tk細胞攝取~(18)F-FHBG的程度明顯高于正常的T47D細胞;在小鼠體內~(18)F-FHBG主要經腸道和泌尿繫統排洩.~(18)F-FHBG報告基因探針可以有效的定位于HSV1-tk基因錶達的部位且與移植瘤裸鼠體內分佈研究結果一緻.這可為進一步開展~(18)F-FHBG報告基因顯像與腫瘤基因治療的鑑測提供有效手段和科學依據.
목적 대~(18)F-FHBG체외섭취、체내분포급하류라서PET-CT현상등방면진행연구.방법 이용γ정형계수기측정체외종류세포T47D화T47D-tk대~(18)F-FHBG적섭취、정상곤명소서화이식류라서~(18)F-FHBG체내분포;병진행하피하이식류라서~(18)F-FHBG PET-CT현상.결과 체외종류세포섭취실험현시T47D-tk세포섭취~(18)F-FHBG적정도명현고우정상적T47D세포,120 min시T47D-tk세포대~(18)F-FHBG적섭취위T47D세포적64배(P<0.001).정상소서주사~(18)F-FHBG후,주요분포우간장、장도、신장화방광,이뇌부미견명현방사성분포.하피하이식류라서PET-CT현상현시,T47D-tk종류농취~(18)F-FHBG적정도명현고우T47D종류,차2 h현상효과교호.결론 체외T47D-tk세포섭취~(18)F-FHBG적정도명현고우정상적T47D세포;재소서체내~(18)F-FHBG주요경장도화비뇨계통배설.~(18)F-FHBG보고기인탐침가이유효적정위우HSV1-tk기인표체적부위차여이식류라서체내분포연구결과일치.저가위진일보개전~(18)F-FHBG보고기인현상여종류기인치료적감측제공유효수단화과학의거.
Objective To study the in vitro accumulation of ~(18)F-FHBG, its in vivo distribution and ~(18)F-FHBG PET-CT imaging for reporter gene (HSVl-tk) in nude mice with a xenograft of breast adenocarcinoma Methods The in vitro uptake of ~(18)F-FHBG in tumor cells of T47D and T47D-tk and the distribution of ~(18)F-FHBG in normal Kunming mice and nude mice with breast adenocarcinoma xenograft were detected by well-type γ counter. Reporter gene PET-CT imaging with ~(18)F-FHBG was performed in nude mice with a xenograft of breast adenocarcinoma. And the expression location of HSVl-tk gene could be monitored by observing the in vitro and in vivo accumulation of ~(18)F-FHBG. Results The in vitro uptake of ~(18)F-FHBG in T47D-tk cells (143. 67 dpm/10~4 ± 5. 82 dpm/10~4 cells) was significantly higher than that in T47D cells (2.23 dpm/10~4 ± 0.23 dpm/10~4 cells) at 60 and 120 min post-injection ( P < 0. 001 ) and reaches a plateau at 60 min. In normal Kunming mice, ~(l8)F-FHBG was mainly distributed in liver, intestine, kidney and bladder while there was no obvious radioactive accumulation in brain. F-FHBG accumulated at a significantly higher level in T47D-tk tumors than in T47D tumors and its accumulation yielded the best image effect at 2 h by PET-CT imaging in nude mice. Conclusion The in vitro uptake of ~(18)F-FHBG in T47D-tk cells is significantly higher than that in T47D cells. ~(18)F-FHBG is mainly excreted by digestive tract and urinary tract in mice. It agrees with the expression pattern of HSVl-tk gene. ~(18)F-FHBG can determine the localization of HSVl-tk gene expression in an efficient way. This study will offer a monitoring method and scientific base for ~(18)F-FHBG reporter gene imaging and HSV1 -tk gene therapy in tumors.