| Literature DB >> 28827325 |
Jun Tang1, Darin Salloum2, Brandon Carney1,3,4, Christian Brand1, Susanne Kossatz1, Ahmad Sadique1, Jason S Lewis1, Wolfgang A Weber1,5, Hans-Guido Wendel2, Thomas Reiner6,7.
Abstract
Diffuse large B-cell lymphoma (DLBCL) is the most common lymphoma in adults. DLBCL exhibits highly aggressive and systemic progression into multiple tissues in patients, particularly in lymph nodes. Whole-body 18F-fluodeoxyglucose positron emission tomography ([18F]FDG-PET) imaging has an essential role in diagnosing DLBCL in the clinic; however, [18F]FDG-PET often faces difficulty in differentiating malignant tissues from certain nonmalignant tissues with high glucose uptake. We have developed a PET imaging strategy for DLBCL that targets poly[ADP ribose] polymerase 1 (PARP1), the expression of which has been found to be much higher in DLBCL than in healthy tissues. In a syngeneic DLBCL mouse model, this PARP1-targeted PET imaging approach allowed us to discriminate between malignant and inflamed lymph nodes, whereas [18F]FDG-PET failed to do so. Our PARP1-targeted PET imaging approach may be an attractive addition to the current PET imaging strategy to differentiate inflammation from malignancy in DLBCL.Entities:
Keywords: PARP1; PET/CT; [18F]PARPi; diffuse large B-cell lymphoma; inflammation
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Year: 2017 PMID: 28827325 PMCID: PMC5594659 DOI: 10.1073/pnas.1705013114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205