Literature DB >> 15504245

Histological and immunohistochemical observations of mucin-depleted foci (MDF) stained with Alcian blue, in rat colon carcinogenesis induced with 1,2-dimethylhydrazine dihydrochloride.

Naoki Yoshimi1, Takamitsu Morioka, Tatsuya Kinjo, Morihiko Inamine, Tatsuya Kaneshiro, Takahiro Shimizu, Masumi Suzui, Yasuhiro Yamada, Hideki Mori.   

Abstract

The usefulness of mucin-depleted foci (MDF), which have recently been proposed as a new preneoplastic biomarker in rat colon carcinogenesis, was histologically investigated in rat colonic tissues treated with 1,2-dimethylhydrazine dihydrochloride (DMH). The relationship among aberrant crypt foci (ACF), MDF and beta-catenin accumulated crypts (BCAC) was examined by comparing the corresponding computer-captured images. Twelve male F344 rats were given DMH s.c. at a dose of 40 mg/kg body weight, once a week for 2 weeks, and randomly divided into two groups. Rats in group 1 were given normal drinking water, while those in group 2 were given drinking water containing indomethacin (IND) at 16 ppm for 6 weeks. All animals were sacrificed 8 weeks after the first DMH treatment. The resected colons were fixed in 10% formalin, and stained with Alcian blue for observation of ACF and MDF. Histological and immunohistochemical analysis revealed that the numbers of ACF, MDF and overlapping lesions in group 2 (treated with IND) were significantly decreased, compared with those in group 1. The number of BCAC in group 2 was also significantly lower than that in group 1. The reduction (61.5%) of MDF by IND was much greater than that (29.3%) of ACF. Analyses of the computer-captured images indicated that MDF had more frequent dysplastic changes and overexpression of beta-catenin than did ACF. MDF having over 4 crypts or MDF with the appearance of ACF corresponded well to BCAC. These results suggest that MDF may be useful as an early biomarker in colon carcinogenesis.

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Year:  2004        PMID: 15504245     DOI: 10.1111/j.1349-7006.2004.tb02183.x

Source DB:  PubMed          Journal:  Cancer Sci        ISSN: 1347-9032            Impact factor:   6.716


  12 in total

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Journal:  Environ Mol Mutagen       Date:  2016-01-06       Impact factor: 3.216

3.  Abberant crypt foci -- importance in colorectal carcinogenesis and expression of p53 and mdm2: a changing concept.

Authors:  Prasenjit Das; Deepali Jain; Kim Vaiphei; J D Wig
Journal:  Dig Dis Sci       Date:  2007-12-14       Impact factor: 3.199

Review 4.  Morphological and molecular alterations in 1,2 dimethylhydrazine and azoxymethane induced colon carcinogenesis in rats.

Authors:  Martina Perše; Anton Cerar
Journal:  J Biomed Biotechnol       Date:  2010-12-28

5.  A method for serial tissue processing and parallel analysis of aberrant crypt morphology, mucin depletion, and Beta-catenin staining in an experimental model of colon carcinogenesis.

Authors:  John N McGinley; Matthew D Thompson; Henry J Thompson
Journal:  Biol Proced Online       Date:  2010-05-18       Impact factor: 3.244

6.  Time course of the incidence/multiplicity and histopathological features of murine colonic dysplasia, adenoma and adenocarcinoma induced by benzo[a]pyrene and dextran sulfate sodium.

Authors:  Jiro Sonoda; Yuki Seki; Atsushi Hakura; Satoru Hosokawa
Journal:  J Toxicol Pathol       Date:  2015-03-01       Impact factor: 1.628

7.  Deletion of glutathione peroxidase-2 inhibits azoxymethane-induced colon cancer development.

Authors:  Mike F Müller; Simone Florian; Stefanie Pommer; Martin Osterhoff; R Steven Esworthy; Fong-Fong Chu; Regina Brigelius-Flohé; Anna P Kipp
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8.  Post-initiation chlorophyllin exposure does not modulate aflatoxin-induced foci in the liver and colon of rats.

Authors:  Gayle A Orner; Bill D Roebuck; Roderick H Dashwood; George S Bailey
Journal:  J Carcinog       Date:  2006-02-06

Review 9.  Colon preneoplastic lesions in animal models.

Authors:  Masumi Suzui; Takamitsu Morioka; Naoki Yoshimi
Journal:  J Toxicol Pathol       Date:  2013-12-26       Impact factor: 1.628

10.  Newly defined aberrant crypt foci as a marker for dysplasia in the rat colon.

Authors:  Masako Ochiai; Yoshitaka Hippo; Masashi Izumiya; Masatoshi Watanabe; Hitoshi Nakagama
Journal:  Cancer Sci       Date:  2014-07-12       Impact factor: 6.716

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