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Photoimmunotheranostics of epithelioid sarcoma by targeting CD44 or EGFR
被引:1
|作者:
Jin, Jiefu
[1
]
Barnett, James D.
[1
]
Mironchik, Yelena
[1
]
Gross, John
[4
]
Kobayashi, Hisataka
[6
]
Levin, Adam
[5
]
Bhujwalla, Zaver M.
[1
,2
,3
,7
]
机构:
[1] Johns Hopkins Univ, Sch Med, Russell Morgan Dept Radiol & Radiol Sci H, Div Canc Imaging Res, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Radiat Oncol & Mol Radiat Sci, Baltimore, MD USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Orthopaed Oncol, Baltimore, MD USA
[6] NCI, Mol Imaging Branch, Lab Mol Theranost, NIH, Bethesda, MD USA
[7] Johns Hopkins Univ, Sch Med, Dept Radiol, Div Canc Imaging Res, Rm 208C Traylor Bldg,720 Rutland Ave, Baltimore, MD 21205 USA
来源:
TRANSLATIONAL ONCOLOGY
|
2024年
/
45卷
关键词:
Epithelioid sarcoma;
Photoimmunotheranostics;
CD44;
EGFR;
Targeted therapy;
NEAR-INFRARED PHOTOIMMUNOTHERAPY;
GROWTH-FACTOR RECEPTOR;
SOFT-TISSUE;
CANCER;
D O I:
10.1016/j.tranon.2024.101966
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Epithelioid sarcoma (ES) is a rare soft tissue neoplasm with high recurrence rates. Wide surgical resection remains the only potential curative treatment. ES presents most commonly on the fingers, hands and forearm, making light-based cancer cell-targeted therapies such as near-infrared photoimmunotherapy (NIR-PIT) that is target-specific, but with limited penetration depth, suitable for ES treatment. We established that CD44 and EGFR were overexpressed in ES patient samples and in the VA-ES-BJ human ES cell line. NIR-PIT of VA-ES-BJ cells using antibody photosensitizer conjugates, prepared by conjugating a CD44 or EGFR monoclonal antibody to the photosensitizer IR700, confirmed that NIR-PIT with both conjugates resulted in cell death. Neither treatment with NIR light alone nor treatment with the conjugates but without NIR light were effective. CD44IR700-PIT resulted in greater cell death than EGFR-IR700-PIT, consistent with the increased expression of CD44 by VA-ES-BJ cells. In tumors, EGFR-IR700 exhibited a higher tumor-to-normal ratio, as determined by in vivo fluorescence imaging, and a higher anti-tumor growth effect, compared to CD44-IR700. No antitumor effect of the EGFR antibody or the photosensitizer conjugate alone was observed in vivo. Our data support evaluating the use of EGFR-IR700-PIT in the management of ES for detecting and eliminating ES cells in surgical margins, and in the treatment of superficial recurrent tumors.
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