Research Interest Statement:
My research is investigating the pathophysiology of multiple myeloma (MM), a B cell cancer characterized by proliferation of malignant plasma cells in the bone marrow, presence of monoclonal serum immunoglobulin, and osteolytic lesions. MM studies demonstrate that MM causes severe lytic bone lesions by enhancing osteoclast activity/suppressing osteoblast activity. We are studying the factors of bone metabolism that may influence MM growth. We are also interested in the early detection of MM induced bone disease (MMBD). The current methods focused on either MM cell activity or structural damage of bone. Our recent clinical observation demonstrated that a significant portion (43%) of MMBD patients heal the large bone lesions after therapy while the rest do not. It leads us to hypothesize that MMBD may be cured by the treatment when they are on the right stage, thus MMBD may need to define stages based on the status of osteolysis process. We employed a newly developed collagen hybridizing peptide (CHP) to detect collagen degradation that is an early stage on the process and demonstrated that in situ imaging with CHP detects MMBD and highly correlated with MM cell numbers. Currently, we are defining the MMBD stages that CHP detects during MM development. Additionally, we have been developing various Patient-Derived Xenograft (PDX) mouse models from MM, Lymphoma, and non-small cell lung cancer. We have developed a unique humanized mouse strain that is susceptible to human tumor cells/tissue. We have been successfully developing various PDX models.
“Study of Sigma Anti-Bonding Calcium (SAC) Role(s) in Multiple Myeloma and Erythropoietin-Induced Osteoporosis”
05/21/20 – 05/20/22
NIH/Office of the Director – 1R21OD026618
“In Situ Imaging of Collagen Degradation Activity in Multiple Myeloma and Fibrosis Murine Models - Resubmission”
08/15/19 – 07/31/21
Hildebrandt GC, Berno T, Gurule A, [et al., including Yoon D]. Effect of low-dose bortezomib on bone formation in smouldering multiple myeloma. British journal of haematology. 2019 184(2):308-310. PMID: 29574687.
Bennink LL, Li Y, Kim B, [et al., including Yoon D]. Visualizing collagen proteolysis by peptide hybridization: From 3D cell culture to in vivo imaging. Biomaterials. 2018 183:67-76. PMID: 30149231.
Zangari M, Yoo H, Shin IJ, [et al., including Yoon D]. Surgical thyroparathyroidectomy prevents progression of 5TGM1 murine multiple myeloma in vivo. Journal of bone oncology. 2018 12:19-22. PMID: 29556454. PMCID: PMC5854927.
Zangari M, Yoo H, Shin I, [et al., including Yoon D]. Thymic PTH Increases After Thyroparathyroidectomy in C57BL/KaLwRij Mice. Endocrinology. 2018 159(4):1561-1569. PMID: 29381784. PMCID: PMC5839736.
Johann DJ Jr, Steliga M, Shin IJ, [et al., including Yoon D]. Liquid biopsy and its role in an advanced clinical trial for lung cancer. Experimental biology and medicine (Maywood, N.J.). 2018 243(3):262-271. PMID: 29405770. PMCID: PMC5813874.
Mohan M, Samant RS, Yoon D, [et al.]. Extensive Remineralization of Large Pelvic Lytic Lesions Following Total Therapy Treatment in Patients With Multiple Myeloma. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 2017 32(6):1261-1266. PMID: 28240368. PMCID: PMC5466479.
Divoky V, Song J, Horvathova M, [et al., including Yoon D]. Delayed hemoglobin switching and perinatal neocytolysis in mice with gain-of-function erythropoietin receptor. Journal of molecular medicine (Berlin, Germany). 2016 94(5):597-608. PMID: 26706855. PMCID: PMC5083035.
Song J, Yoon D, Christensen RD, [et al.]. HIF-mediated increased ROS from reduced mitophagy and decreased catalase causes neocytolysis. Journal of molecular medicine (Berlin, Germany). 2015 93(8):857-66. PMID: 26017143.
Yoon DH, Yoon S, Kim D, [et al.]. Regulation of dopamine D2 receptor-mediated extracellular signal-regulated kinase signaling and spine formation by GABAA receptors in hippocampal neurons. Neuroscience letters. 2015 586:24-30. PMID: 25483619.