TITLE

Increased microvascular blood content is an early event in colon carcinogenesis

AUTHOR(S)
Wali, R. K.; Roy, H. K.; Kim, Y. L.; Liu, Y.; Koetsier, J. L.; Kunte, D. P.; Goldberg, M. J.; Turzhitsky, V.; Backman, V.
PUB. DATE
May 2005
SOURCE
Gut;May2005, Vol. 54 Issue 5, p654
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Background: Increased premalignant epithelial microvascular blood content is a common theme in neoplastic transformation; however, demonstration of this phenomenon in colon carcinogenesis has been stymied by methodological limitations. Our group has recently developed a novel optics technology, four dimensional elastic light scattering fingerprinting (40-ELF), which allows examination of the colonic mucosal architecture with unprecedented accuracy. In this study, we utilised 40-ELF to probe the preneoplastic colonic microvasculature. Methods: Colonic mucosal blood content was assessed by 4D-ELF at serial preneoplastic time points from azoxymethane (AOM) treated Fisher 344 rots and age matched control animals. We also examined the pretumorigenic intestinal mucosa of the MIN mouse, and compared with wild-type mice. Finally, in a pilot study, we examined superficial blood content from the endoscopically normal mid transverse colon in 37 patients undergoing screening colonoscopy. Results: In the AOM treated rat model, augmentation of superficial mucosal and total mucosal/superficial submucosal blood supply preceded the appearance of aberrant crypt foci (ACF) and temporally and spatially correlated with future ACF occurrence. These findings were replicated in MIN mice. The 40-ELF based results were corroborated with immunoblot analysis for haemoglobin on mucosal scrapings from AOM treated rats. Moreover, 40-ELF analysis of normal human colonic mucosa indicated that there was a threefold increase in superficial blood in patients who harboured advanced adenomas. Conclusion: We report, for the first time, that blood content is increased in the colonic microvasculature at the earliest stages of colon carcinogenesis. These findings may provide novel insights into early biological events in colorectal carcinogenesis and have potential applicability for screening.
ACCESSION #
16886339

 

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