Author/Authors :
Jung, Ki-Hye Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Park, Ji-Ae Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Kim, Jung Young Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Kim, Mi Hyun Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Oh, Seyoung Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Kim, Hee-Kyung School of Medicine - Kyungpook National University - Daegu, Republic of Korea , Choi, Eun-Ji Konkuk University - Seoul, Republic of Korea , Kim, Han-Jun Konkuk University - Seoul, Republic of Korea , Do, Sun Hee Konkuk University - Seoul, Republic of Korea , Lee, Kyo Chul Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Kim, Kyeong Min Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Lee, Yong Jin Korea Institute of Radiological and Medical Science - Seoul, Republic of Korea , Chang, Yongmin Department of Radiology - Kyungpook National University Hospital - Daegu, Republic of Korea
Abstract :
Gadolinium-neutron capture therapy (Gd-NCT) is based on the nuclear capture reaction that occurs when 157Gd is irradiated with
low energy thermal neutrons to primarily produce gamma photons. Herein, we investigated the efiect of neutron capture therapy
(NCT) using a small molecular gadolinium complex, Gd-DO3A-benzothiazole (Gd-DO3A-BTA), which could be a good candidate
for use as an NCT drug due to its ability to enter the intracellular nuclei of tumor cells. Furthermore, MRI images of Gd-DO3A-BTA
showed a clear signal enhancement in the tumor, and the images also played a key role in planning NCT by providing accurate
information on the in vivo uptake time and duration of Gd-DO3A-BTA. We injected Gd-DO3A-BTA into MDA-MB-231 breast
tumor-bearing mice and irradiated the tumors with cyclotron neutrons at the maximum accumulation time (postinjection 6 h); then,
we observed the size of the growing tumor for 60 days. Gd-DO3A-BTA showed good therapeutic efiects of chemo-Gd-NCTfor the in
vivo tumor models. Simultaneously, the Gd-DO3A-BTA groups ([Gd-DO3A-BTA(+), NCT(+)]) showed a signi¢cant reduction in
tumor size (p < 0.05), and the inhibitory efiect on tumor growth was exhibited in the following order: [Gd-DO3A-BTA(+), NCT(+)]
> [Gd-DO3A-BTA(+), NCT(−)] > [Gd-DO3A-BTA(−), NCT(+)] > [Gd-DO3A-BTA(−), NCT(−)]. On day 60, the [Gd-DO3A-BTA
(+), NCT(+)] and [Gd-DO3A-BTA(−), NCT(−)] groups exhibited an approximately 4.5-fold difierence in tumor size. Immunohistochemistry studies demonstrated that new combinational therapy with chemo-Gd-NCT could treat breast cancer by both the
inhibition of tumor cell proliferation and induction of apoptosis-related proteins, with in vivo tumor monitoring by MRI.
Keywords :
Gd-DO3A , Treatment , NCT , MRI