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3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma

Microscopic analysis of tumor vasculature plays an important role in understanding the progression and malignancy of colorectal carcinoma. However, due to the geometry of blood vessels and their connections, standard microtome-based histology is limited in providing the spatial information of the va...

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Autores principales: Liu, Yuan-An, Pan, Shien-Tung, Hou, Yung-Chi, Shen, Ming-Yin, Peng, Shih-Jung, Tang, Shiue-Cheng, Chung, Yuan-Chiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843693/
https://www.ncbi.nlm.nih.gov/pubmed/24324559
http://dx.doi.org/10.1371/journal.pone.0081857
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author Liu, Yuan-An
Pan, Shien-Tung
Hou, Yung-Chi
Shen, Ming-Yin
Peng, Shih-Jung
Tang, Shiue-Cheng
Chung, Yuan-Chiang
author_facet Liu, Yuan-An
Pan, Shien-Tung
Hou, Yung-Chi
Shen, Ming-Yin
Peng, Shih-Jung
Tang, Shiue-Cheng
Chung, Yuan-Chiang
author_sort Liu, Yuan-An
collection PubMed
description Microscopic analysis of tumor vasculature plays an important role in understanding the progression and malignancy of colorectal carcinoma. However, due to the geometry of blood vessels and their connections, standard microtome-based histology is limited in providing the spatial information of the vascular network with a 3-dimensional (3-D) continuum. To facilitate 3-D tissue analysis, we prepared transparent human colorectal biopsies by optical clearing for in-depth confocal microscopy with CD34 immunohistochemistry. Full-depth colons were obtained from colectomies performed for colorectal carcinoma. Specimens were prepared away from (control) and at the tumor site. Taking advantage of the transparent specimens, we acquired anatomic information up to 200 μm in depth for qualitative and quantitative analyses of the vasculature. Examples are given to illustrate: (1) the association between the tumor microstructure and vasculature in space, including the perivascular cuffs of tumor outgrowth, and (2) the difference between the 2-D and 3-D quantitation of microvessels. We also demonstrate that the optically cleared mucosa can be retrieved after 3-D microscopy to perform the standard microtome-based histology (H&E staining and immunohistochemistry) for systematic integration of the two tissue imaging methods. Overall, we established a new tumor histological approach to integrate 3-D imaging, illustration, and quantitation of human colonic microvessels in normal and cancerous specimens. This approach has significant promise to work with the standard histology to better characterize the tumor microenvironment in colorectal carcinoma.
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spelling pubmed-38436932013-12-09 3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma Liu, Yuan-An Pan, Shien-Tung Hou, Yung-Chi Shen, Ming-Yin Peng, Shih-Jung Tang, Shiue-Cheng Chung, Yuan-Chiang PLoS One Research Article Microscopic analysis of tumor vasculature plays an important role in understanding the progression and malignancy of colorectal carcinoma. However, due to the geometry of blood vessels and their connections, standard microtome-based histology is limited in providing the spatial information of the vascular network with a 3-dimensional (3-D) continuum. To facilitate 3-D tissue analysis, we prepared transparent human colorectal biopsies by optical clearing for in-depth confocal microscopy with CD34 immunohistochemistry. Full-depth colons were obtained from colectomies performed for colorectal carcinoma. Specimens were prepared away from (control) and at the tumor site. Taking advantage of the transparent specimens, we acquired anatomic information up to 200 μm in depth for qualitative and quantitative analyses of the vasculature. Examples are given to illustrate: (1) the association between the tumor microstructure and vasculature in space, including the perivascular cuffs of tumor outgrowth, and (2) the difference between the 2-D and 3-D quantitation of microvessels. We also demonstrate that the optically cleared mucosa can be retrieved after 3-D microscopy to perform the standard microtome-based histology (H&E staining and immunohistochemistry) for systematic integration of the two tissue imaging methods. Overall, we established a new tumor histological approach to integrate 3-D imaging, illustration, and quantitation of human colonic microvessels in normal and cancerous specimens. This approach has significant promise to work with the standard histology to better characterize the tumor microenvironment in colorectal carcinoma. Public Library of Science 2013-11-29 /pmc/articles/PMC3843693/ /pubmed/24324559 http://dx.doi.org/10.1371/journal.pone.0081857 Text en © 2013 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Liu, Yuan-An
Pan, Shien-Tung
Hou, Yung-Chi
Shen, Ming-Yin
Peng, Shih-Jung
Tang, Shiue-Cheng
Chung, Yuan-Chiang
3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma
title 3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma
title_full 3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma
title_fullStr 3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma
title_full_unstemmed 3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma
title_short 3-D Visualization and Quantitation of Microvessels in Transparent Human Colorectal Carcinoma
title_sort 3-d visualization and quantitation of microvessels in transparent human colorectal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843693/
https://www.ncbi.nlm.nih.gov/pubmed/24324559
http://dx.doi.org/10.1371/journal.pone.0081857
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