1.School of Precision Instruments and Optoelectronics Engineering, Tianjin University, No.92, Weijin Road, Nankai District, 300072 Tianjin, China
2.Institute of Biological and Medical Imaging, Helmholtz Zentrum München, Ingolstädter Landstr. 1, D-85764 Neuherberg, Germany
3.Chair of Biological Imaging, TranslaTUM, Technische Universität München, Ismaningerstr. 22, D-81675 Munich, Germany
4.Department of Instrumentation and Applied Physics, Indian Institute of Science Bangalore, CV Raman Rd, Bengaluru 560012 Karnataka, India
Vasilis Ntziachristos (v.ntziachristos@tum.de)
纸质出版日期:2020,
网络出版日期:2020-04-13,
收稿日期:2019-08-28,
修回日期:2020-02-10,
录用日期:2020-03-19
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Spatial heterogeneity of oxygenation and haemodynamics in breast cancer resolved in vivo by conical multispectral optoacoustic mesoscopy[J]. LSA, 2020,9(3):595-609.
Li, J. et al. Spatial heterogeneity of oxygenation and haemodynamics in breast cancer resolved in vivo by conical multispectral optoacoustic mesoscopy. Light: Science & Applications, 9, 595-609 (2020).
Spatial heterogeneity of oxygenation and haemodynamics in breast cancer resolved in vivo by conical multispectral optoacoustic mesoscopy[J]. LSA, 2020,9(3):595-609. DOI: 10.1038/s41377-020-0295-y.
Li, J. et al. Spatial heterogeneity of oxygenation and haemodynamics in breast cancer resolved in vivo by conical multispectral optoacoustic mesoscopy. Light: Science & Applications, 9, 595-609 (2020). DOI: 10.1038/s41377-020-0295-y.
The characteristics of tumour development and metastasis relate not only to genomic heterogeneity but also to spatial heterogeneity
associated with variations in the intratumoural arrangement of cell populations
vascular morphology and oxygen and nutrient supply. While optical (photonic) microscopy is commonly employed to visualize the tumour microenvironment
it assesses only a few hundred cubic microns of tissue. Therefore
it is not suitable for investigating biological processes at the level of the entire tumour
which can be at least four orders of magnitude larger. In this study
we aimed to extend optical visualization and resolve spatial heterogeneity throughout the entire tumour volume. We developed an optoacoustic (photoacoustic) mesoscope adapted to solid tumour imaging and
in a pilot study
offer the first insights into cancer optical contrast heterogeneity in vivo at an unprecedented resolution of < 50 μm throughout the entire tumour mass. Using spectral methods
we resolve unknown patterns of oxygenation
vasculature and perfusion in three types of breast cancer and showcase different levels of structural and functional organization. To our knowledge
these results are the most detailed insights of optical signatures reported throughout entire tumours in vivo
and they position optoacoustic mesoscopy as a unique investigational tool linking microscopic and macroscopic observations.
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