Showing papers on "7,12-Dimethylbenz[a]anthracene published in 2019"

Zingerone induced caspase-dependent apoptosis in MCF-7 cells and prevents 7,12-dimethylbenz(a)anthracene-induced mammary carcinogenesis in experimental rats.

Abstract: Breast cancer is a prevalent of tumoregenesis in women and reports for the maximum mortality and morbidity in the global. Ginger (Zingiber officinale) is the mainly widespread spice and herbal remedies used in the world. Since antique periods, ginger has been used in Greece, India and China for the curing of upset stomach, nausea, diarrhea, colds, and headaches. The current work was planned to explore the anticancer properties of zingerone (ZO) toward 7,12-dimethylbenz(a)anthracene (DMBA)-treated mammary carcinogenesis in Sprague-Dawley (SD) rats and MCF-7 mammary cancer cells. The mammary carcinogenesis was produced through a single dosage of DMBA (20 mg/kg bwt) mixed in soya oil (1 mL) administrated intragastrically with a gavage. We found improved concentrations of lipid peroxidation (LOOH and TBARS), carcinoembryonic antigen, lowered levels of enzymatic (CAT, GPx, and SOD), and nonenzymatic (vitamin E, GSH, and vitamin C) antioxidant in mammary tissues and plasma of DMBA-induced cancer bearing animals. Moreover, augmented concentrations of phase I (Cyt-b5 and CYP450 ) and reduced levels of phase II (GR and GST) detoxification microsomal proteins in mammary tissues were noticed. ZO administrations significantly reverted back to all these parameters in this way, showing efficient of anticancer effect. Furthermore, our in vitro study also supported the anticancer effect of the treatment of ZO were noticed loss of cell viability, improved reactive oxygen species formation, and reduced MMP. Furthermore, the status of apoptosis proteins such as Bcl-2, Bax, and Bid expressions was determined by using Western blot analysis techniques. Overall, these results proposed the anticancer effect of ZO toward DMBA-induced mammary cancer in SD animals and Michigan cancer foundation-7 mammary cancer cells.

Polydatin Encapsulated Poly [Lactic-co-glycolic acid] Nanoformulation Counteract the 7,12-Dimethylbenz[a] Anthracene Mediated Experimental Carcinogenesis through the Inhibition of Cell Proliferation.

Abstract: In the present study, the authors have attempted to fabricate Polydatin encapsulated Poly [lactic-co-glycolic acid] (POL-PLGA-NPs) to counteract 7,12-dimethyl benzyl anthracene (DMBA) promoted buccal pouch carcinogenesis in experimental animals. The bio-formulated POL-PLGA-NPs were characterized by dynamic light scattering (DLS), Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD) pattern analysis, and transmission electron microscope (TEM). In addition, the nano-chemopreventive potential of POL-PLGA-NPs was assessed by scrutinizing the neoplastic incidence and analyzing the status of lipid peroxidation, antioxidants, phase I, phase II detoxification status, and histopathological changes and in DMBA-treated animals. In golden Syrian hamsters, oral squamous cell carcinoma (OSCC) was generated by painting with 0.5% DMBA in liquid paraffin three times a week for 14 weeks. After 100% tumor formation was observed, high tumor volume, tumor burden, and altered levels of biochemical status were observed in the DMBA-painted hamsters. Intra-gastric administration of varying concentration of POL-PLGA-NPs (7.5, 15, and 30 mg/kg b.wt) to DMBA-treated hamsters assumedly prevents oncological incidences and restores the status of the biochemical markers. It also significantly enhances the apoptotic associated and inhibits the cancer cell proliferative markers expression (p53, Bax, Bcl-2, cleaved caspase 3, cyclin-D1). The present study reveals that POL-PLGA-NPs is a penitential candidate for nano-chemopreventive, anti-lipid peroxidative, and antioxidant potential, and also has a modulating effect on the phase I and Phase II detoxification system, which is associated with reduced cell proliferation and induced apoptosis in experimental oral carcinogenesis.

Paeonol exhibits anti-tumor effects by apoptotic and anti-inflammatory activities in 7,12-dimethylbenz(a)anthracene induced oral carcinogenesis.

Abstract: We investigated the preventive potential of paeonol on 7,12-dimethylbenz(a)anthracene (DMBA) induced oral carcinogenesis. Oral tumors were developed in the buccal pouches of Syrian golden hamsters using topical application of 0.5% DMBA three times/week for 10 weeks. DMBA treated hamsters developed hyperplasia, dysplasia and well-differentiated squamous cell carcinoma. The animals also exhibited increased lipid oxidation, decreased antioxidant status and altered levels of detoxification agents. Paeonol treatment of DMBA treated hamsters for 14 weeks decreased tumor incidence, volume and burden Paeonol treatment also increased antioxidant activity and decreased lipid oxidation to near normal levels. Histomorphology and the expression patterns of mutant p53, cyclo-oxygenase (COX-2) and caspase-9 were investigated in the oral buccal mucosa. Paeonol exhibited protective effects against DMBA induced oral carcinogenesis owing to its antitumor, antioxidant, anti-inflammatory and apoptosis inducing properties.

Effects of the Cell Debris and Supernatant of Saccharomyces boulardii on 7,12-Dimethylbenz(a) Anthracene-Induced Breast Cancer in Rats

Abstract: Background: Saccharomyces boulardii is a probiotic yeast with a demonstrated ability to inhibit different cancer cell lines. Objectives: The present study was conducted to evaluate the protective effects of the cell debris and supernatant of Saccharomyces boulardii on breast cancer induced by 7,12-Dimethylbenz(a) anthracene (DMBA) in rats. Methods: After culturing Saccharomyces boulardii on dextrose agar, the cell debris and supernatant were collected. The present study was conducted on 32 rats weighing 150 ± 20 g in four groups, including the injection control group, the cancer group, the group treated with the cell debris of Saccharomyces boulardii and the group treated with the supernatant. Hematological factors were evaluated after the treatment. Histopathological changes and concentrations of BAX and Bcl-2 were also assessed in the tumors. Results: Significant changes were observed in all the blood factors in the cancer compared to control group, whereas no significant changes were observed in the two groups treated with the supernatant and cell debris of Saccharomyces boulardii compared to in the control group except for a significant increase in MCV. Deformed mammary acini and an increased volume of milk glands confirmed the duct carcinoma. Although fewer pathological carcinogenic changes were observed in the two groups treated with the supernatant and cell debris of Saccharomyces boulardii, the appearance of the tissues was still inflamed. The concentration of BAX significantly increased and that of BCL-2 significantly decreased in the group treated with the Saccharomyces boulardii supernatant compared to in the cancer group. Conclusions: Saccharomyces boulardii and its supernatant could reduce the size of the tumor and inhibited its spread to other parts of the body by inducing apoptosis in the tumor cells.

7,12-dimethylbenz(a)anthracene induced breast cancer in Sprague Dawley rats proved by ultrasound imaging

Abstract: Many studies have shown that some of cancer animal models have been established to study various aspects of cancer biology, including breast cancer. Substantial evidence has shown that administration of 7,12-dimethylbenz(a)anthracene (DMBA) in animal models can mimic human breast cancer in many ways. This preliminary research aimed to develop rat breast cancer models that will be used for a further study on phytotherapy as the alternative medicine for breast cancer. Four young Sprague Dawley female rats, aged 60 days, received a single subcutaneous injection of 25 mg DMBA mixed with 0.5 mL sunflower oil and 0.5 mL sodium chloride 0.9%. Control group received 0.5 ml of sunflower oil and 0.5 ml of saline only. Tumor detection by palpation and rats’ body weight measurement were performed every week after DMBA induction. At 10-weeks after DMBA induction, the tumor development was examined by ultrasound imaging. No significant differences were observed in the body weight between DMBA-induced rats and non-induced rats during 8-weeks after induction. Starting from week ninth, the body weight of the DMBA group significantly decreased (p=0.02) compared to the counterpart. A solid mass on the breast area was firstly detected at week seventh in one rat. Three weeks later the solid masses were detected in all DMBA-induced rats that proved by the ultrasound images showing hypoechoic lesions with irregular margin and calcification indicating malignancies. DMBA induced malignant lesions in female rats that demonstrated by ultrasound imaging.

Protective Effect of Madhuca longifolia Leaves in 7, 12-Dimethylbenz(a)anthracene Induced Mammary Carcinoma in Sprague Dawley Rat model

Abstract: Objectives: To evaluate the pretreatment with Madhuca longifolia leaves on 7, 12-Dimethylbenz(a)anthracene (DMBA)-induced mammary carcinoma in Sprague Dawley rat. Materials and Methods: Thirty female Sprague Dawley rats were divided into five groups, and each group is having six rats. Group I rats received vehicle (1 mL of emulsion of sunflower oil and physiological saline) subcutaneously and 1 mL of 2% dimethyl sulfoxide per orally. Groups II, III, IV, and V were induced mammary carcinogenesis by giving single dose of subcutaneous injection of 25 mg of DMBA. Group III, IV, and V rats were administered with MEML 100, 200 mg/kg and Vincristine 0.5 mg/kg dissolved in 1 ml of 2% dimethylsulfoxide given 1 week before the administration of the carcinogen, respectively, and continued for 16 weeks. At the end of experiment, the animals were sacrificed and biochemical estimations were done in all groups. Mammary tissues in all groups were dissected out and used for histopathological studies. Results: Oral administration of 200 mg/kg of MEML to DMBA-treated rats effectively prevented the tumor incidence, total number of tumors, and tumor volume and brought back the biochemical markers to normal, which was comparable with standard group. In lower dose 100 mg/kg, the effect was very less compared to normal and standard groups. Our data showed that MEML 200 mg/kg significantly restored the breast tissue biochemically and histologically which was comparable with standard. Conclusion: Our results concluded that the leaves of Madhuca longifolia may be used in the treatment of mammary carcinoma.

Pre-Exposure to Chronic Unpredictable Stress Suppresses the Chemopreventive Potential of Aloe Vera (Av) Leaf Gel Against 7,12-Dimethylbenz(a)anthracene (DMBA) Induced Carcinogenesis.

Abstract: The present study evaluates the topical application of aloe vera (Av) leaf gel as a protective natural product against 7,12-dimethylbenz(a)anthracene (DMBA)-induced skin lesions in Swiss albino mice and as an antioxidant for the systemic toxicity of DMBA in the presence and absence of chronic unpredictable stress (CUS). Animals were randomized into seven groups and sacrificed after 16 weeks of treatment. Av gel application along with DMBA + 12-O-tetradecanoylphorbol-13-acetate (TPA) was found to be effective in reducing tumor incidence, cumulative number of papillomas, tumor burden and tumor yield when compared to untreated groups. Furthermore, topical treatment with Av gel significantly increased the overall in vivo antioxidant status of mice. Conversely, lipid peroxidation levels were significantly decreased in skin and circulation. However, pre-exposure to CUS followed by DMBA + TPA + Av gel application reduced the chemopreventive efficacy of Av gel as evidenced by increased tumor incidence, tumor burden, tumor yield and MDA levels accompanied by decrease in the enzymatic and nonenzymatic antioxidants. These observations were further supported by the results of fluorescent studies and comet assay. The study demonstrates a reduction in the antioxidant and antitumor potential of Av gel in presence of CUS thereby, signifying the need of stress reduction during cancer chemopreventive trials.

A rat model of serous borderline ovarian tumors induced by 7,12-dimethylbenz[a]anthracene.

Abstract: Serous borderline ovarian tumors (SBOTs) behave between benign cystadenomas and carcinomas, and the effective detection and clinical management of SBOTs remain clinical challenges. Because it is difficult to isolate and enrich borderline tumor cells, a borderline animal model is in need. 7,12-dimethylbenz[a]anthracene (DMBA) is capable of inducing the initiation, promotion, and progression of serous ovarian tumors. This study aims to investigate the proper dosage and induction time of DMBA for rat models of SBOTs, and explore their morphological features demonstrated by magnetic resonance (MR) imaging and molecular genetic characteristics. Rats were randomly divided into six groups (1 mg/70 D, 2 mg/70 D, 3 mg/70 D, 2 mg/50 D, 2 mg/90 D, and 2 mg/110 D). The 3 mg/70 D group induced the most SBOTs (50.0%, 12/24). The micropapillary projections were shown on MR imaging, which was the characteristic of SBOTs. The Cyclin D1 characterizing an early pathogenetic event strongly expressed in induced serous benign tumors (SBTs). The immunoreactivity staining scores of P53 expression significantly increased from SBTs, SBOTs to serous ovarian carcinomas (SCAs), which elucidate that P53 might be a promising biomarker to grade serous ovarian tumors. Based on morphological and molecular genetic similarities, this rodent SBOT model was suitable for investigating the pathogenesis of serous ovarian tumors and developing an early detection strategy.

RETRACTED ARTICLE: Inhibition of Tumor Progression by NG-Nitro-L-arginine Methyl Ester in 7,12- dimethylbenz(a)anthracene Induced Breast Cancer: Nitric Oxide Synthase Inhibition as an Antitumor Prevention

Abstract: Breast cancer has high mortality rates among the women in the Republic of Armenia. It is now evident that nitric oxide plays important roles in various stages of carcinogenesis such as oncogene activation, tumor suppressor genes, modulation of apoptosis and metastasis. Advances in our understanding of the metabolism and molecular functions of arginine alterations in cancer have led to resurgence in the interest of targeting arginine catabolism, as an anticancer strategy. NOS inhibitors have been proposed, as a way to treat cancer. We have been researching the anti-tumor potential of the NOS inhibition by NG-Nitro-L-arginine methyl ester treatment (30 mg/kg/day, i.p.), administered for 5 weeks (parallelly to tumors development, every 3th day) against 7,12-dimethylbenz(a)anthracene induced mammary carcinogenesis in rats. Our treatment model results have shown the inhibition of NOS activity has influenced on development of carcinogenesis, which have been reflected in changes of rats’ tumors size and quantity, mortality rate, in alteration of breast histopathology, in decrease of polyamines, NO and malondialdeide concentrations in blood. Understanding dichotomy of NO has been a great challenge for researchers working in the field of cancer therapy.

Effect of Mushroom Extract on 7,12-Dimethylbenz[a]anthracene Induced Salivary Gland Pathosis in Albino Rats

Abstract: Salivary glands are essential structures for the wellbeing of an individual. Salivary gland tumors represent a diagnostic challenge. Following the treatment protocol for malignant salivary gland tumors, the majority of patients experience decreased salivation. Regeneration after the damage resulting from the treatment protocol, is believed to be through the transient activation of the Wnt/β-catenin pathway which preserve the stem/progenitor pool and allow for regeneration. Medicinal mushrooms have been tried in medicine for centuries. They have been reported to have anti-inflammatory, cardio-protective, hepatoprotective, and anticancer properties. Aim of the study: to evaluate the effect of mushrooms on the salivary glands of albino rats following DMBA induced pathological changes. Materials and methods: The study comprised three groups each of 12 albino rats. Group I was the control group, group II was given DMBA and group III was treated with mushrooms, following DMBA adminsteration. All groups were assessed histopathologically (H&E) and immunohistopathologically (PCNA). Results: Group II exhibited variable histopathological signs from apoptosis to inflammation, allergy and dysplasia. Group III showed absence of some of the previous signs and a significantly higher PCNA expression. Conclusion: mushrooms may help in the regeneration of acinar cells through the activation of the progenitor cells. It also may have a cancer- protective role.