Pharmacognosy Magazine

ORIGINAL ARTICLE
Year
: 2018  |  Volume : 14  |  Issue : 54  |  Page : 186--190

Biochemical evidence for the antitumor potential of Garcinia mangostana Linn. On diethylnitrosamine-induced hepatic carcinoma


V Vishnu Priya1, Mallika Jainu2, Surapaneni Krishna Mohan3,  
1 Department of Biochemistry, Saveetha Dental College and Hospital, Saveetha University, Velappanchavadi, Chennai, Tamil Nadu, India
2 Department of Biochemistry, Biogen Care Research Center, Chennai, Tamil Nadu, India
3 Department of Biochemistry, College of Medicine, Texila American University, Guyana, South America

Correspondence Address:
Mallika Jainu
Department of Biochemistry, Biogen Care Research Center, 32/285, Royapettah High Road, Chennai - 600 014, Tamil Nadu
India

Abstract

Background: Garcinia mangostana is extensively used in most of the Indian herbal pharmaceuticals and nutraceuticals. Objective: The objective of this study was to elucidate the underlying biochemical protective mechanism of G. Mangostana Linn. fruit extract (GME) in deterioration of diethylnitrosamine (DEN)-induced hepatic carcinoma (HCC) in rats. Materials and Methods: The cancer was induced using DEN to the experimental rats and treated with GME (200, 400, and 600 mg/kg) to find its anticancer property. The cancer biomarkers such as alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), hepatic hydroxyl proline, total tissue protein, and tumor necrosis factor-alpha levels were measured using ELISA. The vascular endothelial growth factor expressions were also seen in liver tissues using immunohistochemistry. Results: In addition, there was a significant increase in serum AFP, CEA, hepatic hydroxylproline, and total tissue protein levels in HCC group versus the negative control group. In contrast, the groups with HCC subjected to either high or low dose of GME elicited significant reduction of AFP, CEA, hepatic hydroxylproline, and increase in total protein in serum compared to the untreated HCC rats. Interestingly, treatment with GME elicited marked improvement in the liver histological feature and downregulation of tumor necrosis factor-alpha levels in HCC groups. GME extract may have chemopreventive benefits by reducing the tumor promoting growth factor levels in HCC-induced group. Conclusion: To sum up, all findings on curative groups had proved clearly that the GME has anticarcinogenic effect on the development of liver cancer induced by DEN in rats. Abbreviations used: TNF-α: Tumor necrosis factor-alpha, PBS: Phosphate buffered saline, ROS: Reactive oxygen species, DNA: Deoxyribonucleic acid, GSH: Glutathione, VEGF: Vascular endothelial growth factor.



How to cite this article:
Priya V V, Jainu M, Mohan SK. Biochemical evidence for the antitumor potential of Garcinia mangostana Linn. On diethylnitrosamine-induced hepatic carcinoma.Phcog Mag 2018;14:186-190


How to cite this URL:
Priya V V, Jainu M, Mohan SK. Biochemical evidence for the antitumor potential of Garcinia mangostana Linn. On diethylnitrosamine-induced hepatic carcinoma. Phcog Mag [serial online] 2018 [cited 2019 Dec 12 ];14:186-190
Available from: http://www.phcog.com/text.asp?2018/14/54/186/229685


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SUMMARY

Garcinia mangostana Linn. (GME) may have chemopreventive property by reducing the tumor promoting growth factor and tumor necrosis factor-alpha levels in diethylnitrosamine (DEN)-induced hepatic cancerThe suppression in the levels of cancer biomarkers by GME due to the presence of anticancer phytoconstituentsThe histological studies proved the effective dose of GME against DEN-induced experimental hepatic cancer.

 Introduction



Carcinogenesis is a multistage process, by which a normal cell is transformed into a cancerous cell. Transformation involves initiation from typically deoxyribonucleic acid (DNA) damaging agents, promotion during which cell proliferation is increased and progression involving additional genetic alterations.[1] Diethylnitrosamine (DEN), a hepatocarcinogen, is known to cause perturbations in the nuclear enzymes involved in deoxyribonucleic acid (DNA) repair/replication and is normally used as a carcinogen to induce liver cancer in animal models.[2] DEN has been shown to be metabolized to its active ethyl radical metabolite, and the reactive product interacts with DNA causing mutation, which would lead to carcinogenesis.[3],[4] Experimental, clinical, and epidemiological studies have provided evidence supporting the role of reactive oxygen species in the etiology of cancer. DEN has been suggested to cause oxidative stress and cellular injury due to the enhanced formation of free radicals.[5]

Natural products once served humankind of as the source of all drugs and higher plants provided most of these therapeutic agents. The World Health Organization (WHO) estimates that 80% of the people in the developing countries of the world rely on traditional medicine for their health care and about 85% of the traditional medicine involves the use of plant extracts. Drug discovery from medicinal plants has played an important role in the treatment of cancer and indeed most new applications of plant secondary metabolites and their derivatives over the last half century have been applied toward combating cancer.[6] Mangosteen, Garcinia mangostana L. (Clusiaceae), is a tree fairly widespread in Southeast Asian countries, known for its medicinal properties. The edible fruit of this plant is considered to be one of the best of all tropical fruits. The fruit hulls have been in use in Thai folk medicine for the treatment of skin infections, wounds, and diarrhea.[7] Phytochemical studies have shown that these plant species are rich in a variety of prenylated xanthones,[8] and the constituents have demonstrated a number of bioactivities.

Xanthones and its derivatives have been reported to have neuroprotective activity,[9] antiulcer,[10] antioxidant activities,[11] antimalarial,[12] antimicrobial,[13] cytoprotective activity,[14] and anticancer.[15]Studies have been conducted to examine the anticancer properties of the extracts or xanthones obtained from the fruit hulls of this plant species against colon preneoplastic lesions,[16] human leukemia (HL60, K562, NB4, U937, and P3HR1),[14] hepatoma carcinoma (HCC36, TONG, HA22T, Hep 3B, HEpG2, and SK-HEp-1), lung (NCI-Hut 125, CH27-LC-1, H2981, and Calu-1), and gastric carcinomas (AZ521, NUGC-3, KATO-III, and AGS) and human breast cancer SKBR3 cells. The autofluorescence and Fourier transform–infrared spectral investigation on DEN-induced hepatocellular carcinoma treated with pericarp extract of Garcinia mangostana Linn. (GME) was evident in rats.[17]

The present study was designed with the aim to determine the chemopreventive effect of pericarp extract of GME which was evaluated in experimental model of DEN-induced hepatocellular carcinoma in rats. An in-depth study was conducted using the carcinogen to enlighten the hepatoprotective effect of pericarp extract of GME in combating the toxins mediated in the biomedical alterations in rats.

 Materials and Methods



Test drug and chemicals

G. mangostana pericarp extracts powder was obtained from Avesthagen Company, California, USA, as a compliment and was applied for the present investigation. All other chemicals used were of analytical grade.

Animals

Specific and pathogen-free Wistar strain rats were chosen for this study. They were obtained and acclimatized to the laboratory environment. They were housed in polypropylene cages with stainless steel grid covers and bedding material used is paddy or wheat husk. They were groomed in a controlled environment with feed and drinking water provided in polypropylene bottles. Experimental protocols were approved by the Institutional Animal Ethics Committee (IAEC), which follows the guidelines of Committee for the purpose of control and supervision of experiment on Animals and the Guide for the Care and Use of Laboratory Animals. The IAEC approval number for this study was Biochem: 005/2008 and 01/003/10.

Test compound and dose administration levels

Anticarcinogenic test is performed in accordance to the guidelines of WHO 2000 and the Organization of Economic Co-operation and Development (OECD) guideline for testing of chemicals (OECD, 2001). As the toxicity of the compound GME was determined in earlier studies, the drug dose was chosen accordingly.[18] Six groups of 6 rats each were used for the study. Group I-Normal rats received distilled water (1 ml/kg bwt); Group II-Rats induced with DEN (0.01% DEN through drinking water up to 16 weeks); Group III, IV, and V-Rats induced with DEN (0.01% DEN through drinking water up to 16 weeks and cotreated with G. mangostana extract (200, 400, and 600 mg/kg wt); and Group VI-Rats treated with G. mangostana extract (400 mg/kg wt) alone. Food and water were accessible ad libitum. Animals were sacrificed after 16 weeks, and livers were dissected and then excised samples of lobes for histological analysis.

Histological examination

After the fixation of the second portion of the liver tissue in formal saline (10%) for 24 h, the tissue were subjected to dehydration using absolute 70% ethyl alcohol followed by embedding in paraffin wax at 56°C. After that, the wax tissue blocks were sectioned by sliding microtome and then prepared for the histological slide examination under the light electric microscope (Olympus Cx21 with attached digital camera) after staining with hematoxylin and eosin stain.

Biochemical analyses

Serum alpha-fetoprotein (AFP) was determined by ELISA using kit purchased from Glory Science Co., Ltd., (USA), according to the manufacturer's instructions provided with AFP assay kit. Serum carcinoembryonic antigen (CEA) was quantified by ELISA using kit purchased from Glory Science Co., Ltd (USA), according to the manufacturer's instructions provided with CEA assay kit. The total protein content of each serum sample was determined using the modified Lowry protein assay; the result was expressed in mg/g.

Determination of vascular endothelial growth factor

Deparaffinized sections were incubated with anti-vascular endothelial growth factor (VEGF) antibody (Santa Cruz Biotechnology, Santa Cruz, CA, USA) overnight at 4°C. After washing with PBS, the sections were incubated with multilink swine immunoglobulin followed by washing with PBS and incubation with avidin-biotin-peroxidase complex. Then placed in 0.02% 3,3′2-diaminobenzidine (DAB) and 0.3% nickel ammonium sulfate in 50 mM Tris-HCl buffer (pH 7.4). The color was developed by immersing in the DAB solution containing 0.005% H2O2 and examined using light microscope.

Estimation of tumor necrosis factor-alpha

Serum samples were collected and stored at −80°C. Highly specific quantitative “sandwich” ELISA kits for mouse TNF-α were purchased from Pierce Biotechnology, USA. In brief, plates were coated with anti-human TNF-α in PBS (pH 7.3), and nonspecific binding was blocked with 1% bovine serum albumin. Samples and reconstituted TNF-α standard in concentrations ranging from 15 to 1000 pg/ml were added to the wells. Biotinylated polyclonal TNF-α was used as the detection antibody, followed by addition of streptavidin-HRP in dilution buffer. Color was developed using TMB as substrate and OD was taken at 450 nm.

Statistical analysis

The results were expressed as mean ± standard error of mean Statistical significance was determined by one-way analysis of variance and post hoc least-significant difference test. P <0.05 was considered statistically significant.

 Results



Effect of Garcinia mangostana Linn. on Tumor markers

The significant (*P < 0.001) increase in AFP, CEA, and hydroxylproline levels were evaluated in DEN-administered rats (Group II) which indicates liver damage and preneoplastic lesion when compared with those in control rats (Group I), in which it was not detected. The total protein was decreased in DEN-administered rats compared with those in control rats (Group I). All the above adverse effects of DEN were gradually suppressed in GME-treated rats according to low-to-high dose. GME alone treated rats showed no detection of AFP and CEA levels as in control rats and the protein levels were significantly increased when compared to control rats [Figure 1].{Figure 1}

Effect of Garcinia mangostana Linn. on histological observation

The appearance of liver in control group [Figure 2]a showed normal architecture. The DEN-administered rats [Figure 2]b revealed liver damage with big tumor nodules. Interestingly, a mild reduction in proliferation of hepatic cells in GME (200 mg/kg bw) [Figure 2]c-treated rats when compared to DEN-administered rats, whereas 400 mg/kg bw GME-treated rats [Figure 2]d showed reduction of proliferated cells and normal central vein and shrunken nucleus is seen and 600 mg/kg bwt GME-treated rats [Figure 2]e showed very much reduced pathological alterations in hepatic cellular architecture. GME alone treated rats showed normal hepatocytes with no pathological changes [Figure 2]f.{Figure 2}

Effect of Garcinia mangostana Linn. on vascular endothelial growth factor expression

The VEGF protein expression was weak in the intact normal liver tissue. DEN induction markedly increased its expression by more than threefold when compared with the normal hepatic tissue. DEN and GME (400 mg/kg bwt) cotreated liver tissue decreased the VEGF protein expression when compared with the respective DEN control group [Figure 3].{Figure 3}

Effect of Garcinia mangostana Linn. on tumor necrosis factor-alpha

The levels of anti-inflammatory cytokine TNF-α in DEN-induced rats on administration of GME are presented in [Figure 4]. Compared with the normal group, the serum levels of TNF-α was significantly (*P < 0.001) increased in the DEN-induced group. Administration with GME (400 mg/kg bwt) could reduce the levels of TNF-α even after the induction of DEN.{Figure 4}

 Discussion



In recent times, there is an increased risk of malignancy because of environmental pollution such as exposure to genotoxic and carcinogenic chemicals. This has created awareness to prevent the harmful effect of these chemical agents. This has led to the development of several preventive agents. These agents significantly reduce tumor incidence, delay tumor onset and also have minimal long-term toxicity.

Several investigations have provided convincing evidence that N-nitrosamines cause a wide range of tumors in all animal species. These compounds are considered to be effective health hazards to human. Exposure of human to preformed N-nitrosamines occurs through the diet, in certain occupational settings and also due to the use of tobacco products, cosmetics, pharmaceutical products, and agricultural chemicals.[19]

AFP, a tumor-associated fetal protein, has long been employed as a serum fetal tumor marker to monitor disease progression.[20] In this study, there was increase in serum AFP and CEA levels on DEN induction associated with increase in tumor growth. The decrease in tumor markers after GME administration might be due to decrease in the production rate of tumors.[21] CEA levels can be elevated in about half of patients with small cell lung cancer and other malignant melanomas.[22] Hepatic hydroxyl proline content of HCC rats was found to be significantly higher than that of control group due to fibrotic activity.[23] GME treatment significantly reduced this increase in the hepatic hydroxyl proline content to the levels that were close to control rats.

The plasma proteins were reduced in DEN-administered rats which occur as a consequence of decreased synthesis or excessive losses.[24] The most abundant xanthone from GME, alpha-mangostin was found to suppress the carcinogen-induced formation of adherent crypt foci in a short-term colon carcinogenesis model.[10] The histological observation showed the presence of tumor nodule, pleomorphism of nuclei, some cells exhibit multiple nucleoli, others are pyknotic, some cells possess intranuclear vacuole and cellular infiltration. Liver tissue of DEN and GME cotreated rats showed very much reduced number of tumor nodules, shrunken nucleus, and less damage to cellular architecture. Earlier studies prove that GME is a powerful drug against DEN-induced HCC by altering the levels of antioxidants and liver marker enzymes favorably at normal condition [25] which supports the current study.

It has been demonstrated by various investigators that circulating pro-inflammatory cytokines, such as TNF-α and interleukin 6 which triggers hepatic injury, were increased at least in part by a free-radical-mediated apoptotic mechanism.[26] Augmented production of ROS on DEN induction in GME-treated rats could have been established by the free-radical scavenging potential of alpha-mangostin in preventing the depletion of GSH, thereby contributing to the curtailment in TNF-α expression. Suppressed TNF-α expression by xanthones in the present study is concurrent with the earlier studies.[27]

The extensive hypervascularity associated HCC is thought to be driven in part by the pro-angiogenic factor known as VEGF.[28] In the current study, the DEN-induced carcinogenic rats showed increased expression of VEGF in liver tissues. The antiangiogenic properties of alpha-mangostin may be very important to the development of cancer therapies, particularly those involved with molecular targeting in neoplasms. The treatment with alpha-mangostin induces a significant increase in survival and suppression of tumor growth and lymph node metastasis in cancer model carrying a p53 mutation [29] which is the active constituent of G. Mangostana. In addition, GME may have chemopreventive benefits or as a complementary alternative medicine in the treatment of hepatic cancer by reducing the tumor promoting growth factor levels.

 Conclusion



The results of the current study shed light on the promising anticancer potential of GME on the hepatocellular carcinoma-induced experimental model through its reduction of growth promoting factor levels and inhibition of cancer marker proteins.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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