Literature DB >> 7691427

Growth inhibition and differentiation of HT-29 cells in vitro by inositol hexaphosphate (phytic acid).

K Sakamoto1, G Venkatraman, A M Shamsuddin.   

Abstract

Inositol hexaphosphate (InsP6 or phytic acid) has been shown to have antineoplastic action in in vivo models of colon carcinogenesis. We therefore investigated its effect on proliferation and differentiation of the human colon cancer cell line HT-29 in vitro. Proliferation was evaluated by neutral red incorporation assay, and differentiation was assessed by expression of the markers, cytokeratin, carcinoembryonic antigen (CEA) and beta-D-galactose-[1-->3]-N-acetyl-galactosamine (Gal-GalNAc). InsP6 in the culture media (0.66-10 mM) inhibited cell proliferation in a dose-dependent manner (P < 0.001), while inositol or inositol hexasulfate used as controls or media without InsP6 did not show any suppressive effect. The expression of the tumor marker, Gal-GalNac, was augmented (100.7% increase) by low dose (0.66 mM) of InsP6 but was subsequently suppressed with higher concentrations of InsP6. The expression of cytokeratin and CEA were both augmented by either InsP6 or inositol at all concentrations tested, although the degree of augmentation was milder with inositol than with InsP6. The combination of InsP6 and inositol (both 0.66 mm) resulted in augmentation (P < 0.001) of cytokeratin expression, while that of CEA remained unchanged. The inhibitory effect of InsP6 on cell proliferation was not altered by combination with additional inositol at any concentrations tested. Our results show that InsP6 inhibits cell proliferation and concomitantly increases differentiation and is therefore a candidate chemopreventive and chemotherapeutic agent for human large intestinal cancer.

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Year:  1993        PMID: 7691427     DOI: 10.1093/carcin/14.9.1815

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  7 in total

1.  Effects of cellular redox balance on induction of apoptosis by eicosapentaenoic acid in HT29 colorectal adenocarcinoma cells and rat colon in vivo.

Authors:  P Latham; E K Lund; J C Brown; I T Johnson
Journal:  Gut       Date:  2001-07       Impact factor: 23.059

2.  Inositol hexaphosphate-induced enhancement of natural killer cell activity correlates with suppression of colon carcinogenesis in rats.

Authors:  Zheng Zhang; Yang Song; Xiu-Li Wang
Journal:  World J Gastroenterol       Date:  2005-08-28       Impact factor: 5.742

3.  Expression of a marker for colonic crypt base cells is correlated with poor prognosis in human colorectal cancer.

Authors:  A A van der Wurff; J ten Kate; P T Marx; E P van der Linden; C C Beek; F J Bovelander; J Dekker; W N Dinjens; M F von Meyenfeldt; J W Arends; F T Bosman
Journal:  Gut       Date:  1998-01       Impact factor: 23.059

4.  Apoptotic effect of IP(6) was not enhanced by co-treatment with myo-inositol in prostate carcinoma PC3 cells.

Authors:  Hyun-Jung Kim; Yu-Mi Jang; Harriet Kim; Young Hye Kwon
Journal:  Nutr Res Pract       Date:  2007-09-30       Impact factor: 1.926

5.  Molecular mechanism of inositol hexaphosphate-mediated apoptosis in human malignant glioblastoma T98G cells.

Authors:  Surajit Karmakar; Naren L Banik; Swapan K Ray
Journal:  Neurochem Res       Date:  2007-07-07       Impact factor: 3.996

Review 6.  Broad Spectrum Anticancer Activity of Myo-Inositol and Inositol Hexakisphosphate.

Authors:  Mariano Bizzarri; Simona Dinicola; Arturo Bevilacqua; Alessandra Cucina
Journal:  Int J Endocrinol       Date:  2016-10-04       Impact factor: 3.257

7.  Phytate and Butyrate Differently Influence the Proliferation, Apoptosis and Survival Pathways in Human Cancer and Healthy Colonocytes.

Authors:  Lidia Hanna Markiewicz; Anna Maria Ogrodowczyk; Wiesław Wiczkowski; Barbara Wróblewska
Journal:  Nutrients       Date:  2021-05-31       Impact factor: 5.717

  7 in total

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