Editorial
Copyright ©The Author(s) 1999. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Dec 15, 1999; 5(6): 461-464
Published online Dec 15, 1999. doi: 10.3748/wjg.v5.i6.461
Update of preclinical and human studies of calcium and colon cancer prevention
Martin Lipkin
Martin Lipkin, Strang Cancer Research Laboratory at the Rockefeller University and Weil l Medical College of Cornell University, New York, NY 10021, USA
Author contributions: All authors contributed equally to the work.
Correspondence to: Martin Lipkin, Strang Cancer Research Laborat ory at the Rockefeller University and Weill Medical College of Cornell University, New York, NY 10021, USA. lipkin@rockvax.rockefeller.edu
Telephone: +1-212-5342024 Fax: +1-212-8799371
Received: September 28, 1999
Revised: October 22, 1999
Accepted: November 6, 1999
Published online: December 15, 1999

Abstract
Key Words: headings calcium/metabolism, colonic neoplasms/prevent ion and control, vitamin D



TEXT

Many articles on the subject of colon cancer begin by noting that the disease continues to be a major cause of tumor mortality in the United States and other countries. Despite attempts at reduction, the incidence of this disease is still high in Western populations and is increasing in some Eastern countries. Chemoprevention of this disease therefore continues to be an important public health objective. Among recent chemopreventive approaches, an increased intake of calcium and vitamin D continues to be evaluated in both preclinical and clinical studies. Many experimental findings, as described below, have indicated real associatio ns between high calcium and vitamin D intake and decreased risk for colorectal c ancer.

BASIC STUDIES OF CALCIUM METABOLISM

Calcium is both an essential structural body component and a critical functional element in living cells. It is a key component for maintaining cell structure, membrane viscosity or rigidity, and the related membrane permeability is partly dependent on local calcium concentration. Calcium is also a pivotal regulator of a wide variety of cell functions in its role as a major second messenger[1].

Among the numerous cell properties modulated by calcium, its participation in cell division and the regulation of cell proliferation and differentiation are particularly important[2]. Low levels of intracellular ionized calcium contribute to cell proliferation, and increasing calcium concentration in cell and organ culture media decreased cell proliferation; and induced cell differentiation in rat esophageal epithelial cells[3], murine epidermal cells[4], mammary cells[5,6], and colon cells[7].

The absorption and metabolism of calcium are carefully regulated, 1, 25-dihydroxyvitamin D3 is an important calcium modulator that can become deficient as a consequence of inappropriate diet or inadequate exposure to sunlight. Therefore vitamin D3 also may have a role in the regulation of cell proliferation and differentiation while modulating calcium metabolism. It has also been shown to directly inhibit the proliferation of several malignant cell lines in vitro[8-10], and to induce the differentiation of human colonic cells[11], human myeloid leukemia cells[12], and other cell lines in vitro[13,14]. A role of vitamin D as a chemopreventive agent has also been studied in rodent models[15-19], and the tumor growth and promotional stag e of chemical carcinogenesis have been inhibited by vitamin D. On the other hand, vitamin D3 enhanced chemically-induced transformation of cultured cells in vitro[20,21] and promoted skin tumor formation in mice[22].

PRECLINICAL AND EARLY HUMAN INTERVENTION STUDIES OF EFFECTS OF INCREASED DIETARY CALCIUM
Preclinical studies

The results of direct experimental studies of calcium intake and colon cancer development are summarized in Table 1. The results of many individual studies are further described in Tables 2, 3, 4 and 5. In many preclinical experimental models, calcium effects on colon cancer development and on cellular processes associated with colon cancer have been remarkably consistent: (1) decreasing and normalizing excessive proliferation of colonic epithelial cells, reducing the susceptibility of proliferating epithelial cells to accumulate abnormalities in their DNA; (2) reducing the cytotoxicity of fecal water; (3) increasing the differentiation and maturation of colonic epithelial cells; and (4) decreasing the end-stage development of colon cancer itself.

Table 1 Summary of studies on calcium and colon cancer.
·Majority of epidemiologic studies suggest protective effect
·In vitro studies: decreased proliferation and increased differentiation and maturation of many types of epithelial cells
·In vivo rodent studies: numerous studies demonstrated inhibition of colonic tumor development preceded by decreased hyperproliferation, ODC and ras mutations, binding of bile and fatty acids into insoluble complexes reducing irritant and hyperproliferative effects, reduced cytotoxicity of fecal water
·Human studies: decreased hyperproliferation in most studies, increased differentiation and maturation of colonic epithelial cells, binding of bile and fatty acids into insoluble complexes, decreased cytotoxicity of fecal water
·Decreased recurrence of human adenomas
Table 2 Dietary calcium effects on epithelial cells in the colon and other organs of rodents.
Cell proliferationReferences*
Calcium decreased hyperproliferation Gover et al 1994
Calcium: decreased hyperproliferation when induced by doxycholic acidWargovich et al 1983
Decreased hyperproliferation when induced by fatty acidsWargovich et al 1984
Decreased hyperproliferation when induced by cholic acidBird et al 1986
Decreased hyperproliferation induced by partial enteric resectionAppleton et al 1986
Decreased deoxycholic acid-induced hyperproliferationHu et al 1989
Decreased MNNG-induced hyperproliferation on diet low in fat and calciumReshef et al 1990
Decreased hyperproliferation induced by Western-style dietNewmark et al 1991
Decreased AOM-induced ODC and Tyr KArlow et al 1989
Decreased ODC induced by bile acidsBaer et al 1989
Decreased hyperproliferation when induced by Western-style dietRichter et al[24] 1995
Decreased hyperproliferation in other organs when induced by Western-style dietXue et al[25] 1999
Table 3 Dietary calcium effects on colonic epithelial cells of rodents.
Tumor developmentReferences*
Calcium: decreased tumors induced by partial enteric resection and carcinogenAppleton et al 1987
Decreased proliferation and tumor formation induced by dietary fat and carcinogenPence et al 1988
Decreased intestinal tumors after AMOSkrypec et al 1988
Decreased colonic tumors induced by AMOWargovich et al 1990
Decreased the number of invasive carcinomas after MNU and cholic acidMcSherr y et al 1989
Decreased the number of rats with multiple tumors after DMHSitrin et al 1991
Decreased K-ras mutationsLlor et al 1990
Unchanged tumor incidence after DMHKarkara et al 1989
Unchanged tumor incidence after DMHKaup et al 1989
Decreased late-stage precancerous lesion of whole colonic crypt dysplasiaRi sio et al[26] 1996
Table 4 Calcium effects on colonic cell proliferation, differentia tion and cytotoxicity in human subjects.
In vitroReferences*
Decreased proliferation (2 mM)Buset et al 1986
Decreased proliferation (2-4 mM)Appleton et al 1988
Decreased proliferation (2 mM)Arlow et al 1988
Decreased proliferation (2 mM)Buset et al 1987
Decreased proliferation (2 mM)Friedman et al 1989
Protected colonic cells against toxicity of bile acids and fatty acids (5 mM)Buset et al 1989
Decreased growth of human colon cancer cell linesGuo et al[27] 1990
Increased histone acetylation: cell differentiation (1-2 mM)Boffa et al 1989
Table 5 Calcium effects on colonic cell proliferation, differentiati on and cytotoxicity of fecal water in human subjects.
In vivoReferences*
Decreased hyperproliferationLipkin et al[28] 1985
Decreased hyperproliferationLipkin et al 1989
Decreased hyperproliferationRozen et al 1989
Decreased proliferationLynch et al 1991
Decreased proliferationBerger et al 1991
Decreased proliferationWargovich et al 1992
Decreased proliferationBarsoum et al 1992
Decreased proliferationO’Sullivan et al 1993
Decreased proliferationBostick et al 1995
Unchanged proliferationGregoire et al 1989
Unchanged proliferationCats et al 1995
Decreased ODCLans et al[29] 1991
Normalized differentiation-associated lectin bindingYang et al[30] 1991
Decreased cytotoxicity of fecal waterGovers et al[31] 1996
Increased maturation of colonic epithelial cellsHolt et al[43] 1998
Decreased adenoma recurrenceBaron et al[32] 1999

In animal models (Tables 2 and 3), oral calcium supplementation decreased epithelial cell hyperproliferation when it was induced by several factors that stimulate tumor promotion: the administration of bile acids and fatty acids, dietary fat, a Western-style diet, and partial enteric resection. Of further importance colonic carcinogenesis itself, when induced by chemical carcinogens, decreased with increasing dietary calcium intake, with almost all studies showing a decrease in the number of tumors induced, the percent of invasive carcinomas, or the number of animals with multiple tumors.

Thus, a wide variety of rodent studies (Tables 1, 2 and 3 with references) demonstrated that increasing dietary calcium intake reduced colonic tumor formation: mechanisms involved included decreased epithelial cell hyperproliferation; decreased or nithine decarboxylase activity; decreased ras mutations in colonic epithelial cells; and calcium-binding of bile acids, fatty acids and phosphate into insoluble complexes, reducing their direct irritant and hyperproliferative effects on colonic epithelial cells and reducing the cytotoxicity of fecal water.

Two recent series of studies also have evaluated the effects of calcium and vitamin D on colonic tumor development when these nutrients were fed to rodents on Western-style diets. The first group of studies utilized preclinical models of n ormal mice. In the colonic crypts of these normal mice hyperproliferation, hyper plasia, abnormal differentiation and maturation of colonic crypt epithelial cells, and the late-stage preneoplastic lesion of whole-colonic-crypt dysplasia developed when the mice were fed- Western-style diets containing low calcium and vitamin D[26,33,34].

The second series of studies utilized mice having targeted mutations that are relevant to human colon cancer, the targeted mutation causing adenomas and carcinomas to develop in the mice[35,36]. Recent studies demonstrated the Western-style diets increased the development of the neoplastic colonic lesions that were initiated by those mutations; and the neoplasms together with carcinomas were decreased by: increasing calcium and vitamin D together with lowering fat content of diet[37], or increasing dietary calcium and vitamin D alone (Yang et al unpublished data).

In other organs, Western-style diets also have induced epithelial cell hyperproliferation and hyperplasia in mammary gland[38,39], and hyperproliferati on in pancreas[40] and prostate gland[41] in short-term studies; increasing dietary calcium and vitamin D alone also inhibited the development of those lesions[25].

EARLY HUMAN CLINICAL TRIALS OF CALCIUM AND COLON CANCER CHEMOPREVENTION

Prior to most of the preclinical studies noted above, a first human study was carried out[28]which began to evaluate calcium’s chemopreventive effects on the human colon. That first study, and a majority of the human studies that followed demonstrated that increased dietary calcium could decrease hyperprolife ration of colonic epithelial cells in human subjects; and several studies further demonstrated calcium’s binding of bile acids and fatty acids into insoluble complexes in the colon, decreasing the cytotoxicity of fecal water, the latter co ntributing to the decreased colonic epithelial cell hyperproliferation observed in human subjects (Tables 4 and 5).

The first pilot study in this human series noted above, and several other that followed, demonstrated significant reduction of excessive colonic epithelial cell proliferation, or reduced size of the proliferative compartment in colonic crypts. However, other human studies of supplemental calcium administration did not show this effect[42]. Several of those studies were accompanied by experimental techniques that included extremely low initial baseline levels of colonic cell proliferation measured before calcium administration, very high amounts of calcium intake by subjects before calcium was given, and enemas given prior to colonic biopsies that likely perturbed the mucosa[42]. Because early positive results were found in humans where calcium reduced colonic epithelial cell proliferation[28], a further large randomized adenoma-recurrence clinical trial was developed and carried out, recently verifying that increased calcium intake caused a significant reduction in the development of actual tumors (recurrent adenomas) in the human colon[32]. A further human study was recently carried out increasing dietary calcium intake through low fat dairy foods: this caused increased maturation and decreased proliferation of colonic epithelial cells following the increased dietary calcium intake[43].

Footnotes

Edited by Jing-Yun Ma

Proofread by Qi-Hong Miao

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