Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2005 Feb 8;92(4):729–735. doi: 10.1038/sj.bjc.6602385

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2005 Cancer Research UK

This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

(A) Intravital microscopy images recorded 15 min after injection of fluorescent tumour cells into the spleen of a control liver and a liver after 2 h rh-E pretreatment. (B) Number of fluorescent tumour cells that are present in the liver per hpf as measured by intravital microscopy 15 min and 1 h after intrasplenic injection. Recombinant human endostatin reduced the number of arrested tumour cells in the liver by 56% (P<0.001). No differences were observed within either treatment group between the two time points (controls 15 min vs 1 h P=0.93; endostatin 15 min vs 1 h P=0.39).