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Research ArticleBasic Science Investigations

Apoptosis Imaging Probe Predicts Early Chemotherapy Response in Preclinical Models: A Comparative Study with 18F-FDG PET

Shaoli Song, Chiyi Xiong, Wei Lu, Geng Ku, Gang Huang and Chun Li
Journal of Nuclear Medicine January 2013, 54 (1) 104-110; DOI: https://doi.org/10.2967/jnumed.112.109397
Shaoli Song
1Department of Nuclear Medicine, Renji Hospital, Shanghai Jiaotong University, School of Medicine, Shanghai, China
2Department of Experimental Diagnostic Imaging, University of Texas MD Anderson Cancer Center, Houston, Texas; and
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Chiyi Xiong
2Department of Experimental Diagnostic Imaging, University of Texas MD Anderson Cancer Center, Houston, Texas; and
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Wei Lu
2Department of Experimental Diagnostic Imaging, University of Texas MD Anderson Cancer Center, Houston, Texas; and
3Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, Rhode Island
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Geng Ku
2Department of Experimental Diagnostic Imaging, University of Texas MD Anderson Cancer Center, Houston, Texas; and
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Gang Huang
1Department of Nuclear Medicine, Renji Hospital, Shanghai Jiaotong University, School of Medicine, Shanghai, China
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Chun Li
2Department of Experimental Diagnostic Imaging, University of Texas MD Anderson Cancer Center, Houston, Texas; and
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    FIGURE 1.

    Design of study comparing γ-imaging using SAAC(99mTc)-PSBP-6 with small-animal PET using 18F-FDG in tumor-bearing mice after chemotherapy: TG (A) and N-TG (B). IHC = immunohistochemical.

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    FIGURE 2.

    Tumor growth delays after chemotherapy. (A) C3H/HeJ mice bearing murine 38C13 B-cell lymphoma were treated with intraperitoneal injection of cyclophosphamide at dose of 100 mg/kg. (B) Nude mice bearing B16/F10 melanoma were treated with intravenous injection of PG-TXL at equivalent paclitaxel dose of 80 mg/kg. *P < 0.01. IHC = immunohistochemical.

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    FIGURE 3.

    Representative images of 38C13 tumor–bearing mice before and 1 d after treatment with cyclophosphamide (intraperitoneal, 100 mg/kg). (A) Small-animal PET images acquired 1 h after 18F-FDG injection. (B) γ-images obtained 4 h after SAAC(99mTc)-PSBP-6 injection. SUV = standardized uptake value; T = tumors; T/M = tumor-to-muscle ratio.

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    FIGURE 4.

    Representative autoradiographs and photographs of H&E-, TUNEL-, and active caspase 3–stained slides of 38C13 tumors from nontreated mouse (A) and cyclophosphamide-treated mouse (B). Tumors were removed at 4 h after intravenous injection of SAAC(99mTc)-PSBP-6. Red in fluorescent microphotographs shows TUNEL-positive apoptotic cells; blue represents 6-diamidino-2-phenylindole (DAPI)–stained cells.

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    FIGURE 5.

    Representative images of B16/F10 tumor–bearing mice before and 1 d after treatment with PG-TXL (intravenous, equivalent TXL dose = 80 mg/kg). (A) Small-animal PET images acquired 1 h after 18F-FDG injection. (B) γ-images obtained 4 h after SAAC(99mTc)-PSBP-6 injection. SUV = standardized uptake value; T = tumors; T/M = tumor-to-muscle ratio.

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Journal of Nuclear Medicine: 54 (1)
Journal of Nuclear Medicine
Vol. 54, Issue 1
January 1, 2013
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Apoptosis Imaging Probe Predicts Early Chemotherapy Response in Preclinical Models: A Comparative Study with 18F-FDG PET
Shaoli Song, Chiyi Xiong, Wei Lu, Geng Ku, Gang Huang, Chun Li
Journal of Nuclear Medicine Jan 2013, 54 (1) 104-110; DOI: 10.2967/jnumed.112.109397

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Apoptosis Imaging Probe Predicts Early Chemotherapy Response in Preclinical Models: A Comparative Study with 18F-FDG PET
Shaoli Song, Chiyi Xiong, Wei Lu, Geng Ku, Gang Huang, Chun Li
Journal of Nuclear Medicine Jan 2013, 54 (1) 104-110; DOI: 10.2967/jnumed.112.109397
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Keywords

  • SAAC(99mTc)-PSBP-6
  • apoptosis imaging
  • 18F-FDG
  • PET
  • chemotherapy
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