Abstract

BackgroundColon carcinogenesis is a multistep process and it emanates from a series of molecular and histopathological alterations. Glycyrrhizic acid (GA) is a natural and major pentacyclic triterpenoid glycoside of licorice roots extracts. It has several pharmacological and biological properties such as anti-inflammatory, anti-viral, and anti-cancer. In the present study, we investigated the chemopreventive potential of GA against 1,2-dimethyhydrazine (DMH)-induced precancerous lesions i.e., aberrant crypt foci (ACF) and mucin depleted foci (MDF), and its role in regulating the hyperproliferation, inflammation, angiogenesis and apoptosis in the colon of Wistar rats.MethodsAnimals were divided into 5 groups. In group III, IV and V, GA was administered at the dose of 15 mg/kg b. wt. orally while in group II, III and IV, DMH was administered subcutaneously in the groin at the dose of 20 mg/kg b.wt once a week for first 5 weeks and animals were euthanized after 9 weeks.ResultsGA supplementation suppressed the development of precancerous lesions and it also reduced the infiltration of mast cells, suppressed the immunostaining of Ki-67, NF-kB-p65, COX-2, iNOS and VEGF while enhanced the immunostaining of p53, connexin-43, caspase-9 and cleaved caspase-3. GA treatment significantly attenuated the level of TNF-α and it also reduced the depletion of the mucous layer as well as attenuated the shifting of sialomucin to sulphomucin.ConclusionOur findings suggest that GA has strong chemopreventive potential against DMH-induced colon carcinogenesis but further studies are warranted to elucidate the precise mechanism of action of GA.

Highlights

  • Colon cancer is one of the most common, best-understood neoplasms from a genetic point of view, yet it remains the leading cause of cancer-related mortality in men and women [1,2]

  • It thought to arise by the accretion of genetic alterations involving a variety of oncogenes and tumor suppressor genes that transform normal colonic epithelium into an invasive carcinoma, with aberrant crypt foci (ACF) and mucin depleted foci (MDF) as putative preneoplastic lesions in this transformation process [3,4,5]

  • ACF were first discovered in the colon of carcinogen treated rodent [6] and they have been observed in patients with sporadic colorectal cancer (CRC) and with familial adenomatous polyposis (FAP) [7,8,9]

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Summary

Introduction

Colon cancer is one of the most common, best-understood neoplasms from a genetic point of view, yet it remains the leading cause of cancer-related mortality in men and women [1,2]. ACF were first discovered in the colon of carcinogen treated rodent [6] and they have been observed in patients with sporadic colorectal cancer (CRC) and with familial adenomatous polyposis (FAP) [7,8,9]. They are identified by their elevated crypts, thicker colonic epithelial cell lining and increased pericryptal zone comparative to normal crypts [6]. We investigated the chemopreventive potential of GA against 1,2-dimethyhydrazine (DMH)-induced precancerous lesions i.e., aberrant crypt foci (ACF) and mucin depleted foci (MDF), and its role in regulating the hyperproliferation, inflammation, angiogenesis and apoptosis in the colon of Wistar rats

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