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Novel radionuclides to kill cancer

机译:新型放射性核素可杀死癌症

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A new radiolabelled molecule obtained by the association of a ~(177)Lu isotope and a somatostatin-analogue peptide is showing potential as a cancer killer for certain types of tumour. It is being developed by Advanced Accelerator Applications (AAA), a radiopharmaceutical company that was set up in 2002 by Stefano Buono, a former CERN scientist. With its roots in the nuclear-physics expertise acquired at CERN, AAA started its commejcial activity with the production of radiotracers for medical imaging. The successful commercial activity made it possible for AAA to invest in nuclear research to produce innovative radiopharmaceuticals. ~(177)Lu emits both a β particle, which can kill cancerous cells, and a γ ray, which can be useful for SPECT (Single-Photon Emission Computed Tomography) imaging. Advanced neuroendocrine tumours can be inoperable, and for many patients there are no therapeutic options. However, about 80% of all neuroendocrine tumours overexpress somatostatin receptors, and the radiolabelled molecule is able to selectively target those receptors. The new radiopharmaceutical acts by releasing the high-energy electrons after internalization in the tumour cells through the receptors. The tumour cells are destroyed by the radiation, and the drug is rapidly cleared from the body via urine. A complete treatment consists of only four injections, one every six to eight weeks.
机译:通过〜(177)Lu同位素与生长抑素-类似物肽缔合而获得的一种新的放射性标记分子,显示出对某些类型的肿瘤具有作为癌症杀手的潜力。它是由Advanced Accelerator Applications(AAA)开发的,AAA是一家放射性药物公司,由前CERN科学家Stefano Buono于2002年成立。 AAA凭借在CERN获得的核物理专业知识而扎根,开始了其商业活动,生产了用于医学成像的放射性示踪剂。成功的商业活动使AAA可以投资于核研究以生产创新的放射性药物。 〜(177)Lu发射可杀死癌细胞的β粒子和可用于SPECT(单光子发射计算机断层扫描)成像的γ射线。晚期神经内分泌肿瘤可能无法手术,而且对于许多患者而言,尚无治疗选择。但是,所有神经内分泌肿瘤中约有80%过表达生长抑素受体,并且放射性标记的分子能够选择性地靶向那些受体。新的放射性药物的作用是通过受体使肿瘤细胞内化后释放高能电子。肿瘤细胞被辐射破坏,药物通过尿液迅速从体内清除。完整的治疗仅需四次注射,每六至八周一次。

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    《CERN courier》 |2015年第9期|10-10|共1页
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