Imaging and Therapy Against Hypoxic Tumors with 64Cu-ATSM

  • Yasuhisa FujibayashiEmail author
  • Yukie Yoshii
  • Takako Furukawa
  • Mitsuyoshi Yoshimoto
  • Hiroki Matsumoto
  • Tsuneo Saga
Open Access
Conference paper


Hypoxia in tumors is known to contribute to the malignant characteristics such as therapy resistance and metastatic potential. Cu-diacetyl-bis (N4-methylthiosemicarbazone) (Cu-ATSM), labeled with several Cu radioisotopes (60Cu, 62Cu and 64Cu) is a potential PET imaging agent that targets tumor hypoxia with over-reduced conditions. Clinical studies of Cu-ATSM PET has been conducted worldwide in recent years and the usefulness of this agent is being recognized. Multicenter clinical study of 62Cu-ATSM PET has been conducted in Japan. Among Cu-ATSM tracers, 64Cu-ATSM can be used not only as a PET imaging agent but also as a therapeutic agent, because 64Cu emits β particle and Auger electron, which can damage the cells. Here, we will discuss the present status and future prospects of Cu-ATSM.


Cu-ATSM Hypoxia Internal radiotherapy PET 

29.1 Radiolabeled Cu-ATSM as a Hypoxia Imaging Agent for PET

In tumors, hypoxia frequently occurs due to poor vascularization and tight packing of cancer cells. Tumor hypoxia is associated with adverse prognosis due to failures in radiotherapy and chemotherapy and to tumor metastasis (Brown 1999). It is thus important to develop methods for diagnosis and therapy of hypoxic tumors. Noninvasive methods to detect hypoxic tumor have been intensively developed (Padhani et al. 2007).

We have developed a novel positron emission tomography (PET) imaging agent, Cu-diacetyl-bis (N4-methylthiosemicarbazone) (Cu-ATSM), which can target tumor hypoxia with over-reduced conditions. Cu-ATSM can be labeled with several Cu radioisotopes, such as 60Cu, 62Cu and 64Cu (Dehdashti et al. 2008; Fujibayashi et al. 1997, 1999; Lewis et al. 2001; Obata et al. 2001, 2005; Yoshii et al. 2012). Cu-ATSM is reported to accumulate in hypoxic environments in many kinds of tumor cells in vitro (Obata et al. 2005; Lewis et al. 1999; Burgman et al. 2005). Distribution of Cu-ATSM in tumor tissues differs from that of 18F-fluorodeoxyglucose (18FDG), a commonly used PET imaging tracer of glucose uptake (Obata et al. 2003; Tanaka et al. 2006). Cu-ATSM shows its high uptake in regions that are hypovascular, undergoing cell cycle arrest but little necrosis, while 18FDG accumulates regions of hypervascularity and cell proliferation going to necrosis (Obata et al. 2003; Tanaka et al. 2006). The mechanism of Cu-ATSM accumulation in hypoxic regions has been reported (Fujibayashi et al. 1997; Obata et al. 2001; Burgman et al. 2005; Dearling et al. 2002; Holland et al. 2009). Cu-ATSM, a rigid complex of Cu(II) and ATSM, is easily divided by reduction of Cu(II) to Cu(I) and trapped into the cells under highly reduced intracellular conditions such as hypoxia (Fujibayashi et al. 1997; Obata et al. 2001; Burgman et al. 2005; Dearling et al. 2002). Cu-ATSM rapidly diffuses into cells and tissues even in low perfusion areas and is trapped within cells under highly reduced conditions such as hypoxia (Fujibayashi et al. 1997, 1999; Obata et al. 2001; Yoshii et al. 2012; Holland et al. 2009; Bowen et al. 2011). Preclinical studies have revealed that Cu-ATSM uptake increases with higher intracellular levels of the biological reductant NAD(P)H, which is associated with hypoxia and mitochondrial dysfunction, and activity of NAD(P)H-dependent reductive enzymes, rather than oxygenic conditions (Obata et al. 2001; Yoshii et al. 2012; Holland et al. 2009; Bowen et al. 2011).

In recent years, clinical PET studies using radiolabeled Cu-ATSM have been conducted for many types of cancers throughout the world. In Japan, our institute produced a generator system of 62Cu and multicenter clinical studies of 62Cu-ATSM PET have been conducted using our system. These clinical studies have shown that Cu-ATSM uptake is associated with therapeutic resistance, metastatic potential, and poor prognosis in several types of cancer (Dehdashti et al. 2008; Dietz et al. 2008; Lewis et al. 2008; Sato et al. 2014; Tateishi et al. 2013). Cu-ATSM uptake is correlated with high HIF-1α expression in patients’ glioma (Tateishi et al. 2013). These clinical studies have demonstrated that tumor hypoxia assessed by Cu-ATSM uptake is associated with the tumors’ malignant behaviors (Dehdashti et al. 2003, 2008; Dietz et al. 2008; Grigsby et al. 2007).

29.2 64Cu-ATSM as a Theranostic Agent

64Cu-ATSM can be used as a “theranostic” agent. Namely, this agent can be applied not only as a PET imaging agent but also as an internal radiotherapy agent against tumors, since 64Cu shows β+ decay (0.653 MeV, 17.4%) as well as β decay (0.574 MeV, 40%) and electron capture (42.6%). The photons from electron-positron annihilation can be detected by PET, while the β particles and Auger electrons emitted from this nuclide can damage tumor cells (Lewis et al. 2001; Obata et al. 2005; Yoshii et al. 2011; Yoshii et al. 2016). In addition, the half-life of 64Cu (t1/2 = 12.7 h) is appropriate for both diagnostic and therapeutic use. 64Cu is a practical nuclide for the use of both diagnosis and therapy, because it can be readily produced with an in-hospital small cyclotron. The therapeutic effect of 64Cu-ATSM has been demonstrated in both in vitro (Obata et al. 2005) and in vivo studies (Lewis et al. 2001; Aft et al. 2003). 64Cu-ATSM reduces the clonogenic survival of tumor cells under hypoxia by inducing post-mitotic apoptosis (Obata et al. 2005). This is caused by heavy damage to DNA via high-linear energy transfer (LET) Auger electrons emitted from 64Cu (McMillan et al. 2015). An in vivo study using tumor-bearing hamsters demonstrated that 64Cu-ATSM treatment increased survival time without severe toxicity (Lewis et al. 2001). These previous studies supported the feasibility of 64Cu-ATSM treatment against hypoxic tumors with high-LET radiation.

29.3 64Cu-ATSM Theranostics for Cancer Stem Cells

We have demonstrated that 64Cu-ATSM preferentially localizes in intratumoral regions with a high density of CD133+ cells, which show characteristics of cancer stem cells or cancer stem cell-like cells (CSCs) and showed therapeutic effect against CSCs in a mouse colon carcinoma (Colon-26) and human colon carcinoma (HT-29) models (Yoshii et al. 2011; Yoshii et al. 2016; Yoshii et al. 2010). In these studies, 64Cu-ATSM treatment inhibited tumor growth, and the percentage of CD133+ cells and metastatic ability in 64Cu-ATSM treated tumors were decreased compared to that in non-treated control tumors. 64Cu-ATSM accumulated in the cells under hypoxic conditions and incorporation of 64Cu-ATSM under hypoxia caused cell death in both CD133+ and CD133 cells. We have demonstrated that the intratumoral 64Cu-ATSM high-uptake regions exhibited upregulation of DNA repair, which results in therapeutic resistance. 64Cu-ATSM high-uptake regions showed upregulation of pathways related to DNA repair along with nucleic acid incorporation (bromodeoxyuridine uptake). In addition, combination use of nucleic acid antimetabolites, such as a pyrimidine analog 5-fluorouracil, a purine analog 6-thioguanine, and a folate analog pemetrexed, enhanced the efficacy of 64Cu-ATSM internal radiotherapy by inhibiting DNA repair and effectively reduced %CD133+ CSCs. Therefore, our study suggested that co-administration of 64Cu-ATSM and nucleic acid antimetabolites could have a potential to cure tumor malignant environment and CSCs.

29.4 Biodistribution and Dosimetry of 64Cu-ATSM

We have examined biodistribution of 64Cu-ATSM using mice and performed dosimetry analysis. Relatively high accumulation of 64Cu was observed in the liver, small intestine, and large intestine among normal organs. 64Cu were mainly excreted in the feces, but little urinary excretion was observed. Our dosimetry analysis demonstrated that the liver, ovaries, and red marrow should be considered as dose-limiting organs in 64Cu-ATSM internal radiotherapy. For clinical applications, we have developed a strategy to reduce radiation doses to these critical organs while preserving tumor radiation doses by the appropriately scheduled administration of copper chelator penicillamine during 64Cu-ATSM internal radiotherapy (Yoshii et al. 2014). In this method, penicillamine was orally administered at 1 h after 64Cu-ATSM injection, when radioactivity was almost cleared from the blood and tumor uptake had plateaued. Using this method, penicillamine decreased 64Cu accumulation in the critical organs, while maintaining tumor uptake.

29.5 This Project

Anti-VEGF antibody bevacizumab is an antiangiogenic agent in widespread clinical use for cancer. Despite the initial positive effect of this treatment, continued use of bevacizumab induces hypoxia and makes tumors malignant. Thus, additional strategies to treat the hypoxia during bevacizumab therapy are needed. In this project, we are developing a method to detect and treat tumors that became malignant by acquiring decreased vascularity and hypoxia, during antiangiogenic bevacizumab treatment, with 64Cu-ATSM.

29.6 Development of a Method to Detect Vascularity and Hypoxia In Vivo

Recently, an imaging technology with single-photon emission computed tomography/positron emission tomography/computed tomography (SPECT/PET/CT) to obtain simultaneous images using two different tracers labeled with SPECT and PET nuclides with CT has been developed. By applying the SPECT/PET/CT technology, we developed a method to simultaneously visualize vascularity and hypoxia with 99mTc-labeled human serum albumin (99mTc-HSA) to detect blood pool, and 64Cu-ATSM to detect hypoxia (Adachi et al. 2016). In this study, we performed in vivo imaging experiments using the VECTor SPECT/PET/CT small-animal scanner (MILabs) with HT-29 tumor-bearing mice. 64Cu-ATSM (37 MBq) and 99mTc-HSA (18.5 MBq) were intravenously injected into a mouse at 1 h and 10 min, respectively, before scanning for 20 min. The 99mTc/64Cu dual-isotope SPECT/PET/CT images were then obtained. In vivo SPECT/PET/CT imaging with 64Cu-ATSM and 99mTc-HSA visualized distribution of each probe and showed that 64Cu-ATSM high-uptake regions barely overlapped with 99mTc-HSA high-uptake regions within non-treated HT-29 tumors (Fig. 29.1).
Fig. 29.1

In vivo SPECT/PET/CT imaging with 64Cu-ATSM and 99mTc-HSA

To obtain a bevacizumab-treated tumor model, HT-29 tumor-bearing mice were treated with bevacizumab (5 mg/kg twice a week) for 3 weeks. Using this model, dual-isotope SPECT/PET/CT imaging with 99mTc-HSA and 64Cu-ATSM was performed to check tumor vascularity and hypoxia. For comparison, un-treated tumors that showed similar size to bevacizumab-treated tumor model, were used. From imaging study, bevacizumab-treated tumors showed reduced vascularity and increased proportion of hypoxic areas within tumors.

29.7 64Cu-ATSM Therapy

For treatment study, 64Cu-ATSM (37 MBq) or saline was intravenously injected into mice with bevacizumab-treated mice (bevacizumab+64Cu-ATSM or bevacizumab group). For comparison, a group without bevacizumab-treatment (64Cu-ATSM alone) and un-treated control were also examined. Bevacizumab+64Cu-ATSM group showed the greater inhibition of tumor growth, compared with bevacizumab group, 64Cu-ATSM alone group, and un-treated control, without side effect. Therefore, our data demonstrated that 64Cu-ATSM therapy effectively inhibited tumor growth in bevacizumab-treated HT-29 tumors. 64Cu-ATSM therapy could be a novel approach as an add-on to antiangiogenic therapy with bevacizumab (Fig. 29.2).
Fig. 29.2

64Cu-ATSM therapy as an add-on to antiangiogenic therapy with bevacizumab

29.8 Conclusion

We have seen that 64Cu-ATSM is a promising theranostic agent targeting tumor hypoxia, which is related to tumor malignant behaviors, such as therapy resistance, metastatic potential, existence of cancer stem cells. 64Cu-ATSM has unique characteristics to target tumor malignant behaviors. Therefore, 64Cu-ATSM would be useful to cure malignant tumors due to hypoxia.

Supplementary material

Video S3-9

(MP4 465091 kb)


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Authors and Affiliations

  • Yasuhisa Fujibayashi
    • 1
    Email author
  • Yukie Yoshii
    • 1
  • Takako Furukawa
    • 2
  • Mitsuyoshi Yoshimoto
    • 3
  • Hiroki Matsumoto
    • 4
  • Tsuneo Saga
    • 5
  1. 1.National Institute of Radiological SciencesNational Institutes for Quantum and Radiological Science and TechnologyChibaJapan
  2. 2.Department of Radiological and Medical Laboratory SciencesNagoya University Graduate School of MedicineNagoyaJapan
  3. 3.Division of Functional ImagingNational Cancer Center Hospital EastKashiwaJapan
  4. 4.Research CentreNihon Medi-Physics Co., Ltd.SodegauraJapan
  5. 5.Department of Diagnostic RadiologyKyoto University HospitalKyotoJapan

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