Detection of metastatic lymph node and sentinel lymph node mapping ​using mannose receptor targeting in in vivo mouse footpad tumor models and rabbit uterine cancer models.

Autor: Jeong S; Department of Obstetrics and Gynecology, Korea University Guro Hospital., Jeon OH; Department of Thoracic and Cardiovascular Surgery, Korea University Guro Hospital, Korea University College of Medicine.; Department of Biomedical Sciences, Korea University College of Medicine., Hong JH; Department of Obstetrics and Gynecology, Korea University Guro Hospital., Kim K; Department of Thoracic and Cardiovascular Surgery, Korea University Guro Hospital, Korea University College of Medicine.; Department of Biomedical Sciences, Korea University College of Medicine., Kim BM; Department of Bio-Convergence, Korea University., Park JY; Department of Nuclear Medicine, College of Medicine, Seoul National University., Kim K; Cellbion Co., Ltd., Seoul, Republic of Korea., Cho HW; Department of Obstetrics and Gynecology, Korea University Guro Hospital., Kim HK; Department of Thoracic and Cardiovascular Surgery, Korea University Guro Hospital, Korea University College of Medicine.; Department of Biomedical Sciences, Korea University College of Medicine.
Jazyk: angličtina
Zdroj: International journal of surgery (London, England) [Int J Surg] 2024 May 01; Vol. 110 (5), pp. 2692-2700. Date of Electronic Publication: 2024 May 01.
DOI: 10.1097/JS9.0000000000001227
Abstrakt: Background: This study aimed to evaluate the effectiveness of neo-mannosyl human serum albumin-indocyanine green (MSA-ICG) for detecting metastatic lymph node (LN) and mapping sentinel lymph node (SLN) using mouse footpad uterine tumor models. Additionally, the authors assessed the feasibility of MSA-ICG in SLN mapping in rabbit uterine cancer models.
Materials and Methods: The authors compared the LN targeting ability of MSA-ICG with ICG. Six mouse footpad tumor models and two normal mice were each assigned to MSA-ICG and ICG, respectively. After the assigned tracers were injected, fluorescence images were taken, and the authors compared the signal-to-background ratio (SBR) of the tracers. A SLN biopsy was performed to confirm LN metastasis status and CD206 expression level. Finally, an intraoperative SLN biopsy was performed in rabbit uterine cancer models using MSA-ICG.
Results: The authors detected 14 groin LNs out of 16 in the MSA-ICG and ICG groups. The SBR of the MSA-ICG group was significantly higher than that of the ICG group. The metastatic LN subgroup of MSA-ICG showed a significantly higher SBR than that of ICG. CD206 was expressed at a high level in metastatic LN, and the signal intensity difference increased as the CD206 expression level increased. SLN mapping was successfully performed in two of the three rabbit uterine cancer models.
Conclusions: MSA-ICG was able to distinguish metastatic LN for an extended period due to its specific tumor-associated macrophage-targeting property. Therefore, it may be a more distinguishable tracer for identifying metastatic LNs and SLNs during uterine cancer surgery. Further research is needed to confirm these results.
(Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.)
Databáze: MEDLINE
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