Division of Endocrine, Diabetes and Metabolism, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE, 68198, USA.
Radiat Environ Biophys. 2020 Mar;59(1):99-109. doi: 10.1007/s00411-019-00820-2. Epub 2019 Nov 14.
Treatment of differentiated thyroid cancer often involves administration of radioactive iodine (I-131) for remnant ablation or adjuvant therapy. However, there is morbidity associated with I-131 therapy, which can result in both acute and chronic complications. Currently, there are no approved radioprotectors that can be used in conjunction with I-131 to reduce complications in thyroid cancer therapy. It is well known that the damaging effects of ionizing radiation are mediated, in part, by the formation of reactive oxygen species (ROS). A potent scavenger of ROS, Mn(III)meso-tetrakis(N-n-butoxyethylpyridinium-2-yl)porphyrin (MnTnBuOE-2-PyP), has radioprotective and anti-tumor effects in various cancer models including head and neck, prostate, and brain tumors exposed to external beam radiation therapy. Female C57BL/6 mice were administered I-131 orally at doses of 0.0085-0.01 mCi/g (3.145 × 10 to 3.7 × 10 Bq) of body weight with or without MnTnBuOE-2-PyP. We measured acute external inflammation, blood cell counts, and collected thyroid tissue and salivary glands for histological examination. We found oral administration of I-131 caused an acute decrease in platelets and white blood cells, caused facial swelling, and loss of thyroid and salivary tissues. However, when MnTnBuOE-2-PyP was given during and after I-131 administration, blood cell counts remained in the normal range, less facial inflammation was observed, and the salivary glands were protected from radiation-induced killing. These data indicate that MnTnBuOE-2-PyP may be a potent radioprotector of salivary glands in thyroid cancer patients receiving I-131 therapy.
分化型甲状腺癌的治疗通常包括给予放射性碘(I-131)进行残余消融或辅助治疗。然而,I-131 治疗存在一定的发病率,可导致急性和慢性并发症。目前,尚无批准的放射防护剂可与 I-131 联合使用,以减少甲状腺癌治疗的并发症。众所周知,电离辐射的损伤作用部分是由活性氧(ROS)的形成介导的。Mn(III)meso-四(N-正丁氧基乙基吡啶-2-基)卟啉(MnTnBuOE-2-PyP)是一种有效的 ROS 清除剂,在各种癌症模型中具有放射防护和抗肿瘤作用,包括头颈部、前列腺和脑肿瘤,这些肿瘤在接受外照射放疗时。雌性 C57BL/6 小鼠经口给予 I-131,剂量为 0.0085-0.01 mCi/g(3.145×10 至 3.7×10 Bq)体重,给予或不给予 MnTnBuOE-2-PyP。我们测量了急性外炎症、血细胞计数,并收集甲状腺组织和唾液腺进行组织学检查。我们发现,口服 I-131 可导致血小板和白细胞急性减少、面部肿胀以及甲状腺和唾液腺组织丧失。然而,当在给予 I-131 期间和之后给予 MnTnBuOE-2-PyP 时,血细胞计数保持在正常范围内,观察到较少的面部炎症,并且唾液腺免受辐射诱导的杀伤。这些数据表明,MnTnBuOE-2-PyP 可能是接受 I-131 治疗的甲状腺癌患者唾液腺的有效放射防护剂。