4.6 Article

ImmunoPET of the differential expression of CD146 in breast cancer

期刊

AMERICAN JOURNAL OF CANCER RESEARCH
卷 11, 期 4, 页码 1586-+

出版社

E-CENTURY PUBLISHING CORP
DOI: 10.21566976/ajcr0127905

关键词

ImmunoPET; Mn-52; Zr-89; CD146; YY146; breast cancer; optical imaging

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资金

  1. University of WisconsinMadison
  2. National Institutes of Health [P30CA014520, T32CA009206]
  3. Brazilian Science without Borders Program (SwBCNPq)
  4. National Natural Science Foundation of China [81871385]
  5. State Key Laboratory of Biochemical Engineering [2020KF01]
  6. PKU medicineX Youth Program [PKU-2020LCXQ007, PKU2021LCXQ023]

向作者/读者索取更多资源

This study developed a CD146-specific monoclonal antibody for targeting breast tumors, demonstrating its non-invasive imaging capabilities. The results showed that the antibody bound to CD146 and significantly improved the accuracy of PET imaging in vivo, providing new possibilities for cancer diagnosis.
With advancement in antibody engineering, the development and characterization of new cancer-specific molecular targets are in the forefront of this PET-antibody combination revolution. Overexpression of CD146 in different types of tumors, including breast tumor, has been associated with tumor progression and poor prognosis. Non-invasive detection of CD146 with a monoclonal antibody may provide a noninvasive diagnostic tool with high specificity and accountability. Methods: Herein, we have developed a CD146-specific monoclonal antibody (YY146), radiolabeled it with Mn-52 and Zr-89 and identified its capability in acting as a non-invasive imaging agent that specific targets CD146 in different murine breast cancer models. CD146 expression was first screened in different breast tumor cell lines through Western Blot and confirmed its binding ability to YY146 using Flow Cytometry. Serial immunoPET images were carried out after intravenous administration of 52Mn or 89Zr labeled YY146. In addition, we also performed in vivo fluorescence imaging in animals injected with YY146 conjugated with Cy5.5. Results: Western Blot results show that MDA-MB-435 cell line had greater levels of CD146 expression when compared to the other cell lines investigated. Flow cytometry confirmed binding ability of YY146. PET images revealed well correlated uptake between tumor uptake and CD146 expression levels, confirmed by biodistribution studies and fluorescence imaging. Conclusion: PET imaging, for up to 7 days, of mice bearing three different breast tumors were carried out and revealed radiotracer uptake in tumors that strongly (r(2) = 0.98, P < 0.01), correlated with CD146 expression levels, as confirmed by in vitro and ex vivo studies.

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