Chemopreventive Potential of Green Tea Catechins in Hepatocellular Carcinoma

Abstract

Hepatocellular carcinoma (HCC), which is a common malignancy worldwide, usually develops in a cirrhotic liver due to hepatitis virus infection. Metabolic syndrome, which is frequently complicated by obesity and diabetes mellitus, is also a critical risk factor for liver carcinogenesis. Green tea catechins (GTCs) may possess potent anticancer and chemopreventive properties for a number of different malignancies, including liver cancer. Antioxidant and anti-inflammatory activities are key mechanisms through which GTCs prevent the development of neoplasms, and they also exert cancer chemopreventive effects by modulating several signaling transduction and metabolic pathways. Furthermore, GTCs are considered to be useful for the prevention of obesity- and metabolic syndrome-related carcinogenesis by improving metabolic disorders. Several interventional trials in humans have shown that GTCs may ameliorate metabolic abnormalities and prevent the development of precancerous lesions. The purpose of this article is to review the key mechanisms by which GTCs exert chemopreventive effects in liver carcinogenesis, focusing especially on their ability to inhibit receptor tyrosine kinases and improve metabolic abnormalities. We also review the evidence for GTCs acting to prevent metabolic syndrome-associated liver carcinogenesis.

1. Introduction

Hepatocellular carcinoma (HCC) is one of the most common malignancies and results in high mortality; an estimated 748,300 new cases and 695,900 deaths occur worldwide in a single year as a result [1]. HCC usually develops in the livers of patients with chronic hepatitis and liver cirrhosis caused by persistent infection with hepatitis viruses, indicating that these patients are at high risk of liver carcinogenesis [2,3]. In addition to hepatitis virus infection, metabolic syndrome, which is strongly associated with obesity and diabetes mellitus, has been identified as a major risk factor for the development of HCC [4,5,6]. These findings strongly suggest that cirrhotic patients, especially those who are obese and have diabetes mellitus, are at high risk of developing HCC and, therefore, may be good candidates for chemoprevention strategies [7,8,9].

Tea, produced from dried leaves of the plant Camellia sinensis, is one of the most popular beverages worldwide. The possible beneficial effects of tea polyphenols (catechins), including cancer chemoprevention in humans, have been extensively investigated [10,11,12]. Among tea catechins, green tea catechins (GTCs) have been most extensively studied for their cancer chemopreventive and anti-cancer properties. In addition, the ability of GTCs to improve metabolic abnormalities and reduce body weight has been reported by a number of basic and clinical studies [13,14,15]. These reports indicate that GTCs, which can exert both chemopreventive and anti-metabolic syndrome effects, are promising agents to prevent the development of HCC, especially in obese liver cirrhotic patients with metabolic disorders.

In this article, we provide an overview of the clinical characteristics and molecular pathogenesis of HCC, focusing on the role of obesity and its related metabolic abnormalities. We also review the evidence that GTCs might prevent obesity- and metabolic syndrome-related liver carcinogenesis.

2. Clinical Characteristics and Molecular Pathogenesis of HCC

As described above, HCC development is frequently associated with chronic inflammation and subsequent cirrhosis of the liver induced by hepatitis virus infection. The annual rate of HCC development is approximately 7% in cirrhotic patients, and the recurrence rate for this malignancy 5 years after curative treatment may exceed 70% [16,17,18]. The high incidence of HCC development in the cirrhotic liver is associated with its characteristic mode of carcinogenesis, i.e., “multicentric carcinogenesis” [19,20]. Liver cirrhosis is caused by continuous inflammation leading to severe fibrosis, and is regarded as a precancerous field that contains multiple, independent premalignant lesions (clones). As a result, curative treatment of HCC is extremely difficult once these clones or HCC develop in the cirrhotic liver. This is one of the reasons why the prognosis of patients with cirrhosis and HCC is poor; therefore, there is an urgent need to develop more effective strategies for the chemoprevention of HCC.

Like other cancers, HCC development is significantly associated with the accumulation of genetic alterations, such as mutations in the p53 tumor suppressor gene and the CTNNB1 gene that encodes β-catenin [21,22,23]. Changes in several cell signaling and metabolic pathways also play a key role in liver carcinogenesis. In particular, abnormalities in the expression and function of receptor tyrosine kinases (RTKs) and their downstream signaling pathways, including the Ras/extracellular signal-regulated kinase (ERK) and phosphoinositide 3-kinase (PI3K)/Akt signaling pathways, are critically involved in the proliferation of HCC cells and tumor progression [24,25]. Among these pathways, the insulin-like growth factor-1 (IGF-1)/IGF-1 receptor (IGF-1R) axis, which is one of the most commonly deregulated signaling pathways contributing to the development of several types of human malignancies including HCC [25,26], seems to be particularly interesting because this axis plays a key role in metabolic syndrome-related liver carcinogenesis [7,8,9], as discussed in the next section.

3. Obesity, Metabolic Syndrome, and HCC

Obesity, a serious healthcare problem worldwide, and its related metabolic disorders, including diabetes mellitus and insulin resistance, which are collectively known as “metabolic syndrome” have been recognized as major risk factors for the development of HCC [4,5,6]. Several meta-analyses have shown a significant association between the risk of liver carcinogenesis and obesity- and diabetes mellitus-related complications [27,28,29]. Furthermore, a higher body mass index and diabetes mellitus have been shown to increase the risk of HCC in patients with decompensated cirrhosis [5]. Insulin resistance and hyperleptinemia, both of which are frequently observed in obese individuals, also contribute to the increased risk of HCC recurrence after curative treatment [6,30]. Nonalcoholic fatty liver disease (NAFLD) is commonly associated with metabolic syndrome and can progress to nonalcoholic steatohepatitis (NASH), which in turn leads to liver cirrhosis and HCC development [31,32].

Several pathophysiological mechanisms, including the emergence of insulin resistance, activation of the IGF/IGF-1R axis, development of adipokine imbalance, chronic inflammation, and induction of oxidative stress, link metabolic syndrome and hepatocarcinogenesis (Figure 1) [7,8,9]. Among these metabolic disorders, activation of the IGF/IGF-1R axis, which is caused by insulin resistance and hyperinsulinemia, is considered to play a key role in liver carcinogenesis in patients with metabolic syndrome [7,8,9]. Obese patients have been shown to have higher circulating levels of IGF-1 than non-obese patients in the presence of hyperinsulinemia [33], and animal studies have revealed that insulin resistance and activation of the IGF/IGF-1R axis are implicated in obesity- and diabetes-related liver carcinogenesis [34,35]. IGF-1R is overexpressed in vitro and in animal models of HCC [26,36,37], suggesting that activation of the IGF/IGF-1R axis and its related signaling pathways, such as the PI3K/Akt signaling pathway, significantly contribute to the stimulation of HCC cell growth and liver carcinogenesis, especially in the presence of metabolic disorders.

Figure 1.

Proposed mechanisms linking metabolic syndrome and liver carcinogenesis. The black arrows at the right corner mean the incidence of hepatocellular carcinoma (HCC) is up-regulated.

4. HCC Chemoprevention by Targeting Metabolic Disorders Caused by Metabolic Syndrome

Because metabolic abnormalities caused by metabolic syndrome have a great impact on liver carcinogenesis, we considered the possibility that metabolic disorders, such as insulin resistance and activation of the IGF/IGF-1R axis, might be effective targets in the prevention of HCC, and we tested this using animal models of obesity- and diabetes-related liver carcinogenesis.

We found that supplementation with branched-chain amino acids (BCAA), which improve protein malnutrition in patients with liver cirrhosis [38], significantly inhibited liver carcinogen diethylnitrosamine (DEN)-induced hepatocarcinogenesis as well as spontaneously occurring hepatic preneoplastic lesions in db/db obese and diabetic mice [34,39]. In these studies, BCAA supplementation suppressed liver carcinogenesis by reducing insulin resistance, ameliorating hepatic steatosis, inhibiting activation of the IGF/IGF-1R axis, and attenuating hepatic inflammation [34,39]. BCAA significantly inhibited the proliferation of HCC cells induced by visfatin, an adipokine, through the induction of apoptosis and cell-cycle arrest in G₀/G₁ phase [40]. Administration of acyclic retinoid, which can suppress the post-therapeutic recurrence of HCC and improve the survival rate of patients [41,42], also inhibited DEN-induced liver tumorigenesis in db/db mice, and this was associated with improved liver steatosis and insulin sensitivity [43]. In addition, pitavastatin, a drug widely used for the treatment of hyperlipidemia, inhibited the early phase of obesity-related liver tumorigenesis by improving liver steatosis, increasing serum levels of adiponectin, and attenuating chronic inflammation induced by excess fat deposition in the liver of db/db mice [44]. The possible chemopreventive properties of GTCs in metabolic syndrome-related liver carcinogenesis have also been investigated, and are described later.

5. Preventive and Therapeutic Potential of GTCs in Metabolic Syndrome

Beneficial effects of GTCs on metabolic syndrome-related parameters, including decreased body weight and adipose mass, as well as improved glucose homeostasis and dyslipidemia, have been found in a number of preclinical animal studies (for more detail, see reviews [13,14]). Administration of (−)-epigallocatechin gallate (EGCG), a major component of GTCs, through drinking water significantly decreased the amount of white adipose tissue and serum triglyceride levels in db/db mice [35,45]. In cell culture studies, treatment with GTCs inhibited preadipocyte differentiation, decreased adipocyte proliferation, induced adipocyte apoptosis, and suppressed cellular triglyceride accumulation [13,14]. Moreover, several human studies found that green tea administration was effective at preventing metabolic syndrome and controlling body weight [13,14,15]. The results of a cross sectional study in a Japanese population showed that green tea consumption was significantly associated with lower circulating levels of aminotransferases, triglycerides, and atherogenic lipoproteins [46]. Meta-analyses by Hursel et al. [47,48] also revealed that GTCs combined with caffeine had a significant effect on weight loss, weight maintenance, and energy expenditure.

GTCs also exert preventive and therapeutic effects on pathological changes in the liver associated with metabolic syndrome [49]. Treatment with EGCG improved hepatic histology, such as fibrosis and steatohepatitis, and attenuated oxidative stress and inflammation in an experimental rat model of NAFLD/NASH [50,51,52]. In a double-blind placebo-controlled study, drinking green tea containing high-density catechins reduced the percentage of body fat and hepatic fat infiltration, improved liver function, and attenuated oxidative stress in patients with NAFLD [53]. These findings strongly suggest that supplementation with GTCs is a potentially viable strategy for the treatment of NAFLD and, probably, for the prevention of its progression to NASH.

6. Molecular Mechanisms for Anti-Cancer Effects of GTCs and Chemopreventive Potential in Liver Carcinogenesis

Chemopreventive and anti-cancer effects of GTCs in HCC have been reported in several in vitro studies (for more detail, see review [54]). EGCG inhibits the growth and proliferation of human HCC-derived cells by inducing apoptosis [55,56,57]. EGCG also suppresses the growth of HepG2 human HCC cells by inhibiting the phosphorylation of IGF-1R, followed by decreased activation of its downstream signaling molecules, including ERK, Akt, STAT-3, and GSK-3β [58]. In the literature, it is shown that the levels of both IGF-1 and IGF-2 in cells and culture media are decreased by treatment with EGCG, while the levels of IGF binding protein-3 are increased. In addition, treatment of HuH7 human HCC cells with EGCG decreases the expression of both phosphorylated and non-phosphorylated vascular endothelial growth factor (VEGF) receptor-2 (VEGFR-2) proteins [59]. EGCG also inhibits HuH7 cell proliferation and down-regulated the levels of VEGF in culture media, suggesting that EGCG may be able to inhibit cell growth by disrupting the VEGF-VEGFR related autocrine loop existing in HCC cells. These two article, focusing on IGF-1R and VEGFR-2, indicate that certain types of RTKs and their downstream pathways are key targets of GTCs and hence mediators of their chemopreventive and anti-cancer properties. Moreover, EGCG suppresses platelet-derived growth factor (PDGF)-induced cell proliferation in human hepatic stellate cells by inhibiting the phosphorylation of PDGF receptor (PDGFR), another RTK [60]. Along with the direct effects of EGCG on certain types of RTKs at the cell surface, several studies have revealed that EGCG has indirect effects on RTKs by targeting the lipid organization of the plasma membrane, lipid rafts. EGCG treatment alters the lipid rafts of cancer cells and inhibits binding of the ligand epidermal growth factor (EGF) to the EGF receptor (EGFR), which is an RTK as well, and the subsequent receptor dimerization [61]. EGCG also decreases cell surface EGFR by inducing the internalization of EGFR into endosomal vesicles, leading to inhibiting the activation of the receptor and exerting anti-cancer effects [62]. Although only colon cancer cells are employed in these examinations, the indirect effects on cell surface RTKs appear to be one of the putative mechanisms of GTCs against liver cancer. Administration of EGCG through drinking water also prevented carbon tetrachloride (CCl₄)-induced rat hepatic fibrosis by inhibiting IGF-1R and PDGFR-β expression [63]. These findings may be particularly significant because, in addition to HCC cells, GTCs also target several types of RTKs in a variety of other cell types, and this might contribute to the prevention of liver fibrosis progression, a precancerous condition of HCC development.

A number of in vivo preclinical studies, including chemically induced models, tumor xenograft models, and spontaneous models, have found that GTCs have chemopreventive effects in liver carcinogenesis [54]. Supplementation with GTCs significantly suppressed the development of glutathione S-transferase placental form (GST-P)-positive (GST-P⁺) foci, a hepatic preneoplastic lesion, induced by DEN via reduction of oxidative stress [64]. The growth of HCC xenografts was suppressed by administration of EGCG in drinking water, and this was associated with the induction of apoptosis [56]. EGCG also suppressed the growth of HuH7 xenografts in nude mice by preventing activation of the VEGF/VEGFR signaling axis [59]. Furthermore, EGCG administration also reduced the incidence of spontaneous HCC development in mice [65]. The results of these preclinical studies demonstrate that GTCs can potentially prevent the early phase of liver carcinogenesis and inhibit the growth of existing HCC.

7. Chemopreventive Potential of GTCs in Metabolic Syndrome-Related Liver Carcinogenesis

In order to evaluate the potential of GTCs to act as chemopreventive agents for metabolic syndrome-related liver carcinogenesis, we have performed a number of animal studies [35,51,52]. In the first of these, we examined the effects of EGCG on the development of DEN-induced liver tumorigenesis in db/db mice. In this study, drinking EGCG significantly inhibited the development of liver cell adenomas compared to the control group (EGCG-untreated), and this was associated with reduced phosphorylation of IGF-1R, ERK, and Akt proteins in the liver, improvement of liver steatosis, and activation of AMP-activated kinase protein in the liver. Interestingly, the serum levels of insulin, IGF-1, IGF-2, free fatty acid, and tumor necrosis factor (TNF)-α, and the hepatic expression levels of TNF-α, interleukin (IL)-6, IL-1β, and IL-18 mRNAs, were decreased after the administration of EGCG in drinking water [35].

Next, we investigated whether EGCG could inhibit liver tumorigenesis using a novel rat model that shows histopathological and pathophysiological characteristics of NASH. We found that the liver of Sprague-Dawley rats treated with DEN and a high-fat diet (HFD) exhibited marked development of GST-P⁺ foci associated with severe hepatic steatosis and inflammation, increased levels of oxidative stress, and enhancement of hepatocyte proliferation. EGCG administration in drinking water significantly inhibited the development of GST-P⁺ foci by reducing hepatic triglyceride content and hepatic fibrosis, lowering oxidative stress, attenuating inflammation, and inhibiting excessive hepatocyte proliferation in these rats [51].

Recently, we have also developed a novel NASH-related liver tumorigenesis model using SHRSP.Z-Lepr^fa/IzmDmcr (SHRSP-ZF) rats, which present with obesity, diabetes, and hypertension and thus mimic human metabolic syndrome; we examined whether EGCG inhibited the development of GST-P⁺ foci in these rats. When treated with CCl₄ and HFD, SHRSP-ZF rats showed liver dysfunction, obesity, insulin resistance, dyslipidemia, adipokine imbalance in the serum, and hepatic steatosis significantly more frequently than control non-obese and normotensive rats. The development of GST-P⁺ foci and liver fibrosis was markedly accelerated in SHRSP-ZF rats compared to control rats, and this was associated with activation of the renin-angiotensin system (RAS) and induction of inflammation and oxidative stress. However, administration of EGCG in drinking water significantly suppressed the development of GST-P⁺ foci by improving liver fibrosis, inhibiting RAS activation, and attenuating inflammation and oxidative stress in CCl₄- and HFD-treated SHRSP-ZF rats [52]. The results of these animal studies suggest that administering GTCs, which possess preventive and therapeutic properties against metabolic disorders, might serve as an effective chemoprevention modality for obesity- and metabolic syndrome-related liver tumorigenesis (Figure 2) [35,51,52].

Figure 2.

Mechanisms of action of GTCs in the inhibition of metabolic syndrome-related liver carcinogenesis. Metabolic syndrome significantly increases the risk of HCC development. Several pathophysiological mechanisms link metabolic syndrome and liver carcinogenesis, such as insulin resistance, activation of the IGF/IGF-1R axis, chronic inflammation, oxidative stress, and adipokine dysbalance. They appear to be followed by molecular abnormality, including activation of PI3K/Akt and MAPK/ERK signaling, down-regulated phosphorylated-AMPK, and increased pro-inflammatory cytokines. Administration of GTCs significantly reduces the risk of HCC development in obese patients, and this might be associated with decreased insulin resistance and hepatic steatosis, inhibition of the activation of the IGF/IGF-1R axis, and attenuation of oxidative stress and chronic inflammation. Up- and down-pointing solid arrows mean items are up- and down-regulated, respectively.

8. Clinical Trial Using GTCs and Future Directions

Several series of preclinical investigations using both cell cultures and rodent models have strongly indicated that GTCs have chemopreventive and therapeutic potential in human cancers. In a pilot study, we found that, compared to an untreated control group, oral supplementation with green tea extract (1.5 g/day for 1 year) significantly reduced the development of metachronous colorectal adenomas, the precancerous lesions for colorectal cancer, after polypectomy [66]. The results from a randomized, double-blinded, placebo-controlled study showed that oral administration of GTCs for 1 year also inhibited the progression of high grade prostate intraepithelial neoplasia to prostate cancer [67]. Moreover, oral administration of mixed tea products significantly decreased the size of leukoplakia, a precancerous lesion of the oral mucosa [68]. These findings suggest that an interventional approach using GTCs may be effective in the prevention of certain types of tumorigenesis, especially in early stages.

It is believed that consumption of green tea in its whole form provides greater anti-cancer effect than supplementation with EGCG alone. Indeed, several reports have indicated that EGCG exerts more significant cancer chemopreventive effect when administered in combination with other tea catechins [69,70,71]. Our findings have also shown that EGCG treatment combined with (−)-epicatechin (EC) results in synergistic inhibition of cell growth in the HT29 human colon cancer cell line [72]. According to the combination assay, the optimal ratio of EGCG to EC for effective anti-cancer activity is 60:7. The ratio reflects the relative concentration of EGCG to EC of Polyphenon E (PolyE), which contains 65% EGCG, 25% other catechins, and 0.6% caffeine, extracted from green tea. PolyE is reported to display anti-cancer effects almost equivalent to that of the same concentration of EGCG alone in in vitro study [72]. Other studies in rodents have also demonstrated greater efficacy from PolyE in inhibiting tumor development compared to GTCs [10,73]. These findings suggest that the anti-cancer effect of GTC may differ depending on its composition or combination with other agents.

The safety of GTCs as a chemopreventive agent has been demonstrated in several studies; no adverse events are observed with administration of tea polyphenols at doses ranging from 600 to 1800 mg/day [66,67,74,75]. In human interventional studies, relatively high doses of GTCs seem to be often used to achieve high concentrations of catechins in the blood and tissues. Therefore, a number of case reports of side effects related to administration of GTCs can be seen; these include excess gas, nausea, heartburn, abdominal pain, dizziness, headache, muscle pain, and hepatotoxicity [75,76]. These adverse reactions appear to be experienced in examinations with supplementation of high doses of GTCs in pills or capsules rather than drinking green tea [77]. Recent literature indicates that green tea extract, including GTCs, may inhibit certain types of microsomal cytochrome P450 (CYP), and may not lead to drug-induced liver injury when a drug and green tea are administered simultaneously [78].

A randomized, double-blind, placebo-controlled phase IIa chemoprevention trial demonstrated that GTCs have antioxidant effects in individuals who have several risk factors for HCC, and this may suggest that chemoprevention with GTCs is an effective strategy for diminishing oxidative DNA damage [79]. Conversely, Jin et al. [80] reported that GTCs did not significantly reduce HCC incidence or HCC-related mortality in a review of four clinical studies. The authors found that there were major limitations that needed to be taken into account when interpreting the results of these studies, including an improper comparison of control and treatment groups, possible selection bias, and a lack of randomization. In addition, the dosage and duration of GTC administration varied between studies, and this might have affected the results of these studies. Therefore, large-scale, randomized, double-blinded, placebo-controlled studies should be conducted to clarify the chemopreventive effects of GTCs on HCC development in chronic liver disease patients, especially those who have metabolic syndrome or are obese. Interestingly, the serum levels of IGF-1, VEGF, and prostate-specific antigen were significantly decreased following the administration of a green tea mixture to prostate cancer patients [81]. Therefore, appropriate biomarkers, including HCC-related tumor markers and several types of growth factors associated with liver carcinogenesis and fibrosis, should be measured when evaluating the chemopreventive effects of GTCs on liver tumorigenesis in future clinical trials.

9. Concluding Remarks

Finally, we would like to discuss the interesting findings of our recent studies showing that specific agents may be able to prevent colorectal carcinogenesis associated with obesity and metabolic syndrome, both of which also increase the risk of colorectal cancer [82,83]. Specifically, we have reported that supplementation with both EGCG and BCAA suppresses obesity-related colorectal carcinogenesis in db/db mice by reducing serum levels of insulin and inhibiting activation of the IGF/IGF-1R signaling pathway in the colonic mucosa [45,84]. Supplementation with curcumin, a component of turmeric, also inhibits the development of chemically induced colonic premalignant lesions in db/db mice by attenuating chronic inflammation and reducing adipokine imbalance [85]. The results of these studies [45,84,85], together with the evidence summarized in this review, may indicate that a nutraceutical approach for targeting metabolic abnormalities could effectively prevent the development of certain types of cancers associated with obesity and metabolic syndrome [9,77,86]. In addition, as reviewed in this article, GTCs are one of the most practical agents to use with this treatment approach.

When considering current social and medical circumstances, there is a great concern that the number of patients with metabolic syndrome-associated HCC will continue to increase. GTCs are considered one of the most promising phytochemicals for the prevention of cancer and the treatment of metabolic disorders. From the present review, it is particularly noteworthy that the administration of GTCs is an effective strategy to prevent the development of metabolic syndrome-related liver tumorigenesis. In order to clarify the effectiveness of GTCs in suppressing metabolic syndrome-related liver tumorigenesis, further extensive study is needed, including an active intervention trial.

Abbreviations

AMPK

adenosine monophosphate-activated protein kinase

BCAA

branched-chain amino acids

CCl₄

carbon tetrachloride

CYP

cytochrome P450

DEN

N-diethylnitrosamine

EC

(−)-epicatechin

EGCG

(−)-epigallocatechin gallate

EGF

epidermal growth factor

EGFR

epidermal growth factor receptor

ERK

extracellular signal-regulated kinase

GSK

glycogen synthase kinase

GST-P

glutathione S-transferase placental form

GTCs

green tea catechins

HCC

hepatocellular carcinoma

HFD

high-fat diet

IGF-1

insulin-like growth factor-1

IGF-1R

insulin-like growth factor-1 receptor

IL-6

interleukin-6

MAPK

mitogen-activated protein kinase

NAFLD

non-alcoholic fatty liver disease

NASH

non-alcoholic steatohepatitis

PDGF

platelet-derived growth factor

PDGFR

platelet-derived growth factor receptor

PI3K

phosphoinositide 3-kinase

PolyE

Polyphenon E

RAS

renin-angiotensin system

RTKs

receptor tyrosine kinases

SHRSP-ZF

SHRSP.Z-Lepr^fa/IzmDmcr

STAT

signal transducer and activator of transcription TNF-α, tumor necrosis factor-α

VEGF

vascular endothelial growth factor

VEGFR

vascular endothelial growth factor receptor

Conflicts of Interest

The authors declare no conflict of interest.