Journal of biomedical optics · 2025
In vivo 3D imaging of ovarian cancer outgrowth in transgenic mouse model with optical coherence tomography.
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Han Huan, Mukhamedjanova Aleese, Connolly Denise C, Iwanicki Marcin P, Wang Shang
Аннотация
SIGNIFICANCE: Peritoneal dissemination is the major mechanism of how ovarian cancer (OC) spreads. It features tumor outgrowths in the form of multicellular spheroids, their detachment from the primary site, and their implantation in the peritoneal cavity. To understand this process, analyzing the outgrowths at their native locations within the female reproductive system is essential. However, in vivo study of the OC outgrowths remains unattainable primarily due to the lack of in vivo imaging approaches to probe such small tumor structures at a high resolution.
AIM: We address this technical challenge by establishing in vivo high-resolution 3D imaging of the OC outgrowths in the mouse model.
APPROACH: This in vivo imaging approach relies on optical coherence tomography (OCT) for 3D label-free imaging and an intravital window to bypass the mouse skin and muscle layers. To demonstrate the imaging capability, we use TgMISIIR-TAg transgenic mice that develop spontaneous epithelial OC. The normalized surface lengths of the ovary and the OC outgrowth are measured from OCT images to characterize the tissue morphology. Immunohistochemistry staining is employed to confirm the presence of transgene-positive cells in OC and outgrowths.
RESULTS: We present the first in vivo high-resolution 3D image of the OC outgrowths in the mouse model. The tissue morphology and structure of OC outgrowths have striking differences from the normal ovary, which is quantitatively assessed and compared. We further show that OC outgrowths within and growing out of the ovarian bursa, revealing the difference in their surface morphologies. We also present the detached OC outgrowths and the fluid-filled chambers inside OC, both with 3D quantifications showing the heterogeneity of their volumes.
CONCLUSIONS: This in vivo OCT imaging approach in the mouse model enables high-resolution assessment of detailed 3D structures of OC outgrowths, paving the way for in vivo study of the OC dissemination process.
AIM: We address this technical challenge by establishing in vivo high-resolution 3D imaging of the OC outgrowths in the mouse model.
APPROACH: This in vivo imaging approach relies on optical coherence tomography (OCT) for 3D label-free imaging and an intravital window to bypass the mouse skin and muscle layers. To demonstrate the imaging capability, we use TgMISIIR-TAg transgenic mice that develop spontaneous epithelial OC. The normalized surface lengths of the ovary and the OC outgrowth are measured from OCT images to characterize the tissue morphology. Immunohistochemistry staining is employed to confirm the presence of transgene-positive cells in OC and outgrowths.
RESULTS: We present the first in vivo high-resolution 3D image of the OC outgrowths in the mouse model. The tissue morphology and structure of OC outgrowths have striking differences from the normal ovary, which is quantitatively assessed and compared. We further show that OC outgrowths within and growing out of the ovarian bursa, revealing the difference in their surface morphologies. We also present the detached OC outgrowths and the fluid-filled chambers inside OC, both with 3D quantifications showing the heterogeneity of their volumes.
CONCLUSIONS: This in vivo OCT imaging approach in the mouse model enables high-resolution assessment of detailed 3D structures of OC outgrowths, paving the way for in vivo study of the OC dissemination process.