Targeted PET imaging strategy to differentiate malignant from inflamed lymph nodes in diffuse large B-cell lymphoma.
Jun TangDarin SalloumBrandon CarneyChristian BrandSusanne KossatzAhmad SadiqueJason S LewisWolfgang A WeberHans-Guido WendelThomas ReinerPublished in: Proceedings of the National Academy of Sciences of the United States of America (2017)
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.
Keyphrases
- pet imaging
- diffuse large b cell lymphoma
- positron emission tomography
- lymph node
- epstein barr virus
- computed tomography
- gene expression
- dna damage
- cancer therapy
- mouse model
- end stage renal disease
- high glucose
- pet ct
- endothelial cells
- neoadjuvant chemotherapy
- chronic kidney disease
- ejection fraction
- newly diagnosed
- sentinel lymph node
- prognostic factors
- magnetic resonance
- drug delivery
- contrast enhanced
- peritoneal dialysis
- early stage