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Early Detection in a Mouse Model of Pancreatic Cancer by Imaging DNA Damage Response Signaling.
- Source :
-
Journal of nuclear medicine : official publication, Society of Nuclear Medicine [J Nucl Med] 2020 Jul; Vol. 61 (7), pp. 1006-1013. Date of Electronic Publication: 2019 Dec 20. - Publication Year :
- 2020
-
Abstract
- Despite its widespread use in oncology, the PET radiotracer <superscript>18</superscript> F-FDG is ineffective for improving early detection of pancreatic ductal adenocarcinoma (PDAC). An alternative strategy for early detection of pancreatic cancer involves visualization of high-grade pancreatic intraepithelial neoplasias (PanIN-3s), generally regarded as the noninvasive precursors of PDAC. The DNA damage response is known to be hyperactivated in late-stage PanINs. Therefore, we investigated whether the SPECT imaging agent <superscript>111</superscript> In-anti-γH2AX-TAT allows visualization of the DNA damage repair marker γH2AX in PanIN-3s in an engineered mouse model of PDAC, to facilitate early detection of PDAC. Methods: Genetically engineered KPC (KRas <superscript>LSL.G12D/+</superscript> ; p53 <superscript>LSL.R172H/+</superscript> ; PdxCre) mice were imaged with <superscript>18</superscript> F-FDG and <superscript>111</superscript> In-anti-γH2AX-TAT. The presence of PanIN/PDAC as visualized by histologic examination was compared with autoradiography and immunofluorescence. Separately, the survival of KPC mice imaged with <superscript>111</superscript> In-anti-γH2AX-TAT was evaluated. Results: In KPC mouse pancreata, γH2AX expression was increased in high-grade PanINs but not in PDAC, corroborating earlier results obtained from human pancreas sections. Uptake of <superscript>111</superscript> In-anti-γH2AX-TAT, but not <superscript>111</superscript> In-IgG-TAT or <superscript>18</superscript> F-FDG, within the pancreas correlated positively with the age of KPC mice, which correlated with the number of high-grade PanINs. <superscript>111</superscript> In-anti-γH2AX-TAT localizes preferentially in high-grade PanIN lesions but not in established PDAC. Younger, non-tumor-bearing KPC mice that show uptake of <superscript>111</superscript> In-anti-γH2AX-TAT in the pancreas survive for a significantly shorter time than mice with physiologic <superscript>111</superscript> In-anti-γH2AX-TAT uptake. Conclusion: <superscript>111</superscript> In-anti-γH2AX-TAT imaging allows noninvasive detection of DNA damage repair signaling upregulation in preinvasive PanIN lesions and is a promising new tool to aid in the early detection and staging of pancreatic cancer.<br /> (© 2020 by the Society of Nuclear Medicine and Molecular Imaging.)
Details
- Language :
- English
- ISSN :
- 1535-5667
- Volume :
- 61
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Journal of nuclear medicine : official publication, Society of Nuclear Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 31862800
- Full Text :
- https://doi.org/10.2967/jnumed.119.234708