Effect of β-sitosterol against methyl nitrosourea-induced mammary gland carcinoma in albino rats
© The Author(s). 2016
Received: 17 February 2016
Accepted: 23 July 2016
Published: 29 July 2016
The present study was in quested to study the effects of β-sitosterol on methyl nitrosourea (MNU) induced mammary gland carcinoma in albino wistar rats.
Animals were randomized and divided into four groups of eight animals each. Group I (sham control 1 % CMC in normal saline p.o.); Group II (toxic control, MNU 47 mg/kg, i.v); Group III (MNU 47 mg/kg, i.v + β-sitosterol, 10 mg/kg, p.o); Group IV (MNU 47 mg/kg, i.v + β-sitosterol, 20 mg/kg, p.o). Toxicity was induced by single i.v. injection of MNU followed by β-sitosterol supplementation therapy for 115 days at the dose mentioned above.
Treatment with β-sitosterol evidenced decrease in the alveolar bud and lobule score in the whole mount of the mammary gland. β-sitosterol exhibited diminishing effect on oxidative stress through synchronizing lipid and enzymatic antioxidant defense. A significant decrease in the saturated and unsaturated fatty acid was evident with the MNU treatment and β-sitosterol demonstrated a marked effect on it. Pgp 9.5 expression was dose dependently upregulated by β-sitosterol treatment in comparison to MNU treatment. On the contrary, downregulated NF-kB expression was perceived, when β-sitosterol was concomitantly administered with MNU.
β-sitosterol afforded significant protection against the deleterious effects of MNU.
Keywordsβ-sitosterol Mammary gland P-glycoprotein Oxidative stress Inflammation FAME
Cancer is a one of the most life-threatening disease worldwide. Mammary gland cancer constitutes about 10 % of the total cancer population . However alteration in cell membrane integrity, dysregulated apoptotic pathway along with other inflammatory changes are reported to play a crucial role [2, 3].
Recent findings have demonstrated that the dietary factors including fat and other phytochemicals may offer protection against mammary gland carcinoma, infact, controlled dietary preclinical studies are suggestive that the phytosterols may offer protection from a wide array of cancers including mammary gland carcinoma [4–7]. The phytosterols are the cholesterol-like compounds exclusively synthesized by plants, and it is hypothesized that phytosterols can induce apoptosis/programmed cell death in highly proliferating tumor cells [8–10]. Henceforth, β-sitosterol has been evaluated against a variety of cancers using preclinical experimental models [11, 12]. The studies have suggested potential efficacy of β-sitosterol particularly towards colon cancer, prostate cancer and leukemia [13–16]. On the same line, few preliminary studies have also demonstrated that β-sitosterol can induce apoptosis by activating fatty acid synthase (FAS) signaling in MCF-7 cells .
Additionally, Pgp-9.5 (ubiquitin COOH-terminal esterase L1 or UCHL-1) is an ubiquitin COOH terminal hydrolase that is widely expressed in different type of cancer cells . Recent study demonstrated that Pgp-9.5 is highly overexpressed at many non-neuronal tumors, including breast, colorectal and pancreatic tumors .
Considering the same, the present study was undertaken to study the effect of β-sitosterol on Pgp expression and cellular lipids in methyl nitrosourea (MNU) induced mammary gland carcinoma in female albino rats. The study also extends its horizon towards elucidating the biochemical and inflammatory paradigms as markers for efficacy of β-sitosterol against MNU induced mammary gland carcinoma.
Drugs and chemicals
MNU was purchased from Sigma-Aldrich Co. St. Louise Mo 63103 USA. β-sitosterol was purchased from Cayman Chemical Company, Michigan, USA. All other chemicals were of analytical grade and obtained from Himedia Laboratories, Mumbai, India, else otherwise stated in the text.
Albino wistar female rats of 100–120 g body weight were used for the study. The rats were procured from the central animal house facility. The animals were housed in propylene cages under controlled conditions (23 °C, 12 h light/ dark cycle) with free access to commercial pellet diet and water. Animals were acclimatized for two weeks before the commencement of the experiment. Animals were randomized and divided into 4 groups of 8 animals each. Group I (sham control 1 % CMC in normal saline p.o.); Group II (toxic control, MNU 47 mg/kg, i.v); Group III (MNU 47 mg/kg, i.v + β-sitosterol, 10 mg/kg, p.o); Group IV (MNU 47 mg/kg, i.v + β-sitosterol, 20 mg/kg, p.o). Toxicity was induced by single i.v. injection of MNU followed by β-sitosterol supplementation therapy for 115 days at the dose mentioned above. The blood samples were collected under chloroform anesthesia through retro-orbital plexus in centrifugation tubes. The blood samples were incubated at 37 °C for 1 h and centrifuged at 10,000 rpm for 15 min to collect serum. The serum samples were stored at −20°C till further use. Animals were sacrificed on the 116th day and subjected to the following estimation.
Mammary gland whole mount
The fourth abdominal mammary glands obtained were dissected, stretched onto a slide, placed in a fixative solution and stained with a carmine aluminum solution to prepare whole mounts . Whole mounts were examined under the 4X microscope and evaluated to assess the number of alveolar buds/terminal end buds (AB/TEB). The whole mounts were also evaluated for ductal elongation and differentiation. Ductal elongation was measured, using a ruler, as the distance (in cm) from the nipple to the end of the epithelial tree. Mammary gland differentiation was assessed by scoring the number of alveolar buds (ABs) type 1 and type 2. The score values (0–5) from AB1 and AB2 were added for a final differentiation score (0–10). The average rating values (0–5) from AB1 and AB2 were added to the lobule score values (0–5) for a final differentiation score (0–10) .
The mammary gland tissues (10 % w/v) were homogenized in 0.15 M KCl and centrifuged at 10,000 rpm. The supernatants were scrutinized for biochemical parameters including thiobarbituric acid reactive substances (TBARs), superoxide dismutase (SOD), catalase and glutathione (GSH) using the methods established in our laboratory [21–24].
Determination of Nitric Oxide (NO) level in serum
Generation of NO in the serum samples was arbitrated by measuring nitrite accumulation, using Griess reagent [1 % sulphanilamide, 0.1 % N-(1-napthyl)-ethylenediamine dihydrochloride in 5 % H3P04].
Equal quantity (500 μl) of serum and Griess reagent were mixed and incubated at 37 °C for 5 min. The test mixture was subsequently read on the UV-Visible spectrophotometer (Cary60, Agilent Technologies, CA95051, US) at 540 nm .
Enzymatic activity of COX and LOX
A 10 % mammary gland tissue homogenate in TRIS buffer (50 mM) was centrifuged at 5000 rpm for 5 min followed by sonication. The tissue supernatant (10 μl) was incubated for 5 min with TRIS buffer (160 μl). A 10 μl each of TMPD reagent and arachidonic acid (AA) solution were added and read at 630 nm using a multiplate reader (ALERE Microplate Reader, AM-2100) at 0 and 30 s interval. AA solution was prepared by mixing 50 μl of 40 mM AA with 50 μl of 0.1 N potassium hydroxide using vortexing and subsequently 900 μl of double distilled water. TMPD stock solution was prepared by dissolving 0.3 mg in 1 ml of distilled water and subsequent 1:10 dilution was prepared for the assay [26, 27].
For LOX assay, 25 μl of AA solution was added to the 475 μl supernatant (as prepared for COX assay) and incubated for 6 min. A 500 μl of ferrithiocyanate (FTC) reagent was added and read at 480 nm using U V spectrophotometer (Cary 60, Agilent Technologies International Private Limited, CA United States) after 5 min. FTC reagent was prepared by mixing the reagent 1 (4.5 mM FeSO4 in 0.2 M HCl) and reagent 2 (3 % NH4SCN methanolic solution) in 1:1 ratio .
Fatty acid methyl ester (FAME) analysis of mammary gland tissue
Mammary gland tissue homogenate (0.5 %) was prepared in the mixture of chloroform: methanol (2:1) by using tissue homogenizer followed by sonication at 4 °C for 5 min. The homogenate was subsequently filtered using a whatmann filter paper and final volume made up by methanol. The filtrate was mixed thoroughly with 0.2 ml volume of double distilled water for removal of non-lipid contaminants. The mixture was kept for 30 min and centrifuged at 5000 rpm for 5 min.; upper phase was removed, and lower phase was collected with mammary gland lipids. Methyl esters for the lipid samples were prepared by stirring 0.5 gm of samples with hexane (2 ml). Methanolic KOH (2 N) (0.2 ml) was added to the above mixture and vortexed for 15 min. The phases were allowed to settle down, and the upper layer containing the FAME was collected .
The FAME samples were filtered using 0.2 μm syringe filters and subjected to the gas chromatographic analysis (Perkin Elmer GC- clarus 480; Column : Elite-5 Length-30 mt, Internal diameter- 0.25 mm) using Flame ionization detector(250 °C; carrier gas: nitrogen (10 psi); volume of injection 1 μl; Oven temperature: 150 (1 min), ramp 1–5 °C/min to 230 °C (5 min), ramp 2–150 °C /min to 245 for 12 min; internal standard : cetyl alchohol .
Protein samples were prepared from the mammary gland tissue through acetone precipitation and quantified by using the Bradford reagent . SDS-PAGE analysis was performed following the principles of laemmli with slight modifications . Briefly, protein samples were mixed with sample buffer (125 mM Tris–HCl, pH6.8, 20 % glycerol, 4 % SDS, 0.05 % bromophenol blue, 10 % 2-mecaptoethanol). A 30 μg of protein sample was allowed to resolve through 12 % polyacrylamide gel using SDS-PAGE (GX-SCZ2+, Genetix Biotech Asia Pvt. Ltd, New Delhi). The proteins as resolved through SDS-PAGE were transferred to a PVDF membrane (IPVH 00010 Millipore, Bedford, MA USA) using semidry transfer (GX-ZY3, Genetix Biotech Asia Pvt. Ltd, New Delhi). Subsequently, membrane was blocked with 3 % BSA and 3 % not fat milk in TBST for 2 h and incubated overnight with primary antibody against Pgp 9.5(MA1-83428) (1:2000 dilution), NF-kBP65 (MA5-1616) (1:2000) and β-actin MA5-15739-HRP(1:3000 dilution) (Pierce, Thermo Scientific, USA). The membrane was washed with TBST thrice and incubated with HRP conjugated rat anti-mouse secondary antibody (31430, 1:5000 dilutions) (Pierce Thermo Scientific, USA) at room temperature for 2 h. The signals were detected using an enhanced chemiluminescence substrate (Wester Bright ECL HRP substrate, Advansta, Melanopark, California, US). The Quantification of protein was done through densiometric digital analysis of protein bands using Image J software [32, 33].
Effect of MNU and β-sitosterol on differentiation of mammary gland
AB1 + AB2
DF SCORE- 1 (AB1 + AB2 + LOBULES)
DF SCORE 2 (LOBULES/AB1 + AB2)
CONTROL (3 ml/kg)
685.75 ± 223.36
367.75 ± 79.88
1053.5 ± 302.45
1805.75 ± 460.39
2859.25 ± 756.67
1.76 ± 0.09
MNU (47 mg/kg)
786.5 ± 20.56
432.5 ± 36.60
1219 ± 57.17
2606 ± 243.72
3825 ± 300.89
2.13 ± 0.09
β-SITOSTEROL + MNU (10 mg/kg + 47 mg/kg)
532 ± 178.53
201.5 ± 48.64*
733.5 ± 227.17
1774.5 ± 417.74
2508 ± 644.92
2.48 ± 0.19
β-SITOSTEROL + MNU (20 mg/kg + 47 mg/kg)
380.5 ± 111.83
143 ± 2.00**
523.5 ± 113.83
1390.5 ± 142.92
1914 ± 256.76
2.72 ± 0.31
Effect of β-sitosterol upon various in-vivo antioxidant markers
TBARs (nM of MDA/μg of protein)
GSH (mg %)
SOD (Units of SOD/mg of protein)
Catalase (nM of H2O2/min/mg of protein)
CONTROL (3 ml/kg)
86.08 ± 5.00***
2.30 ± 0.12
1.92 ± 0
50.63 ± 7.81*
MNU (47 mg/kg)
118.84 ± 4.65
2.00 ± 0.16
1.81 ± 0.02
31.76 ± 2.59
β-SITOSTEROL + MNU (10 mg/kg + 47 mg/kg)
147.93 ± 6.67**
1.03 ± 0.14**
1.82 ± 0.03
26.90 ± 3.06
β-SITOSTEROL + MNU (20 mg/kg + 47 mg/kg)
105.51 ± 2.35
1.24 ± 0.21*
1.80 ± 0.03
51.75 ± 3.31*
Fatty acid profiling of mammary gland tissue treated with MNU and β-Sitosterol
Type of fatty acid
MNU (47 mg/kg)
β-sitosterol (10 mg/kg)
β-sitosterol (20 mg/kg)
Linoleic acid (ω-6)
Total fatty acid
Saturated fatty acid
Unsaturated fatty acid
The present study perceived critical protection by β-sitosterol to combat the deleterious effects of MNU on the mammary gland. The whole mount preparations are frequently used as a convenient method for the examination of small proliferative lesions as represented by an increase in the number of terminal end buds (TEBs) . The AB/TEB is the morphologic structure reported to be the target of carcinogenic outcome in the rat mammary gland carcinoma and also the structure from which premalignant pathologies changes in ductal carcinoma . We considered it primary to determine whether the vascularisation and angiogenesis of TEBs was affected by MNU administration. If angiogenesis was increased, then a decrease in vascularity of TEB by a cancer preventive agent is expected. Therefore, TEBs/AB is potentially used as an early positive marker of antiangiogenic cancer preventive activity . The MNU treatment was evident with a rise in AB/TEBs count and differentiation score, and can be closely linked to increased risk of mammary tumourigenesis. These identical mammary structures are the sites of malignant transformation in the rat mammary gland  and the corresponding structures in the human breast are the terminal ductal lobular units . Studies have shown that higher number of AB/TEBs correlates with greater risk of mammary cancer . Treatment with MNU was evident with an increase in some alveolar bud score and differentiation score which was counteracted by β-sitosterol to the sizable amount in a dose-dependent manner.
Chronic inflammation and release of NO results in DNA damage and nitrosylation of proteins which has been implicated in carcinogenesis. The COX and LOX inhibitors have been deliberated to have anticancer activity since long . Infact, over expression of COX and LOX in progression and neo-angiogenesis of human cancer has been supported by large body of scientific literature [39, 40]. A recent finding also affirmed that the COX-2 over expression can induce mammary gland carcinogenesis by reducing the proapoptotic (BAX and BCL-XL) and inflating the antiapoptotic proteins (BCL-2) expression in the mammary gland tissue [41, 42]. Overexpression of LOX has also been reported in variety of tumors including breast, colorectal and prostate cancer [43, 44]. In line with the previous reports upregulated COX levels were perceived after MNU treatment and β-sitosterol afforded a marked reduction of the same. However, MNU treatment downregulated LOXs in the course of tumor development suggesting that LOX exhibit antitumorigenic rather protumorigenic effects. Infact decreased LOX activity has been reported in the prostate cancer, high-grade prostatic intraepithelial neoplasia and human colon cancer and therefore represent a research question which needs to be addressed to its full [45–47].
NF-kB is a group of sequence-specific transcription factor and is best known as a key regulator of inflammatory responses . Elevated NF-kB DNA binding activity is detected in both mammary carcinoma cell lines and primary human breast cancer tissues. In fact, NF-kB is reported to contribute expansion of breast tumor stem cells and enhancement of vasculogenesis  and, therefore, has emerged as a viable target for cancer progression. In the same line, we perceived significant up-regulation of the levels of NF-kB in MNU treated animals, which subsided to a significant amount by β-sitosterol treatment. The efficacy of β-sitosterol to nudge down NF-kB is in agreement with the previous findings . Prima faci it appears that β-sitosterol can impart a noticeable effect against the MNU induced carcinogenesis.
The link between MNU induced carcinogenesis and oxidative stress regulators is well established [50, 51]. The oxidative stress is defined as an imbalance in the production of reactive oxygen species (ROS) and reactive nitrogen species (RNS) leading to impaired cellular metabolism and changes in the intra and extracellular environmental conditions. ROS and RNS can further lead to DNA damage such as mutations, deletions, amplifications and rearrangements which can lead to cancer initiation and progression. The effects of ROS and RNS are balanced by the exogenous/endogenous antioxidants acting through enzymatic or non-enzymatic mechanisms. Treatment with MNU deliberated significant rise in TBARs with noticeable downturn in the enzymatic defense of SOD/catalase/GSH. The NO levels were also curtailed down subsequent to MNU treatment. The drop in the oxidative defense and up-regulation of the lipid peroxidation products is a clear testimony of oxidative stress and is in line with the previous reports about MNU induced carcinogenesis [52, 53]. Treatment with β-sitosterol demarcated significant restoration of the oxidative stress markers at a higher dose. Interestingly, β-sitosterol at lower dose deteriorated the markers of oxidative stress, in particular, TBARs, GSH and enzymatic levels of catalase. Authors would not like to mention that the results scrutinized with the low dose of β-sitosterol are neither in line with the previous reports, nor in consonance with the findings elaborated by us in the preceding section of the manuscript. All in all, one can conclude that β-sitosterol can impart a demarcating biochemical effect on the MNU induced carcinogenesis through modifying the inflammatory signaling and regulating the oxidative stress markers at higher dose.
Pgp-9.5 (ubiquitin COOH-terminal esterase L1 or UCHL-1) is an ubiquitin COOH terminal hydrolase that is widely expressed in different type of cancer cells . Recent study demonstrated that Pgp-9.5 is highly overexpressed at many non-neuronal tumors, including breast, colorectal and pancreatic tumors . There are very few studies, carried out in the particular subtype of ER positive breast cancers and result are also non-conclusive . PGP-9.5 expression is significantly associated with higher MVD (intratumoral microvessel density) in ER negative breast cancer . Their actual role and underlying mechanism is not properly understood in case of ER or PR receptor positive breast cancer produced by MNU treatment . In this particular study the toxic group showed elevated expression in comparison with control, which ensures overexpression of Pgp-9.5 in MNU induced toxicant group. Pgp-9.5 overexpression in the primary cancerous tissues is due to biological transformations, imparting it the status of oncogenic marker [56–58]. UCHL-1 encodes two opposite characteristic pattern in the ubiquitin pathway. When ubiquitin COOH terminus hydrolase to generate another single ubiquitin, the other end show ligase activity which lead to multiple ubiquitination. Different animal studied showed that on application of apoptotic stimuli, UCHL-1 overexpression does not happen . The previous results suggest that Pgp-9.5 is more likely to be act as a tumor suppressor molecule, which is in line with our experimental outcome [60–62]. The dose dependent increase in Pgp-9.5 expression was observed after β-sitosterol treatment.
Fatty acids are important modifiers of the mammary gland carcinoma risk and are composed of complex mixtures including the saturated, monounsaturated and polyunsaturated fatty acids. Modifying the fatty acid profile has been found to be closely associated with mammary gland cancer risk in rodent models and humans [63–65]. Plethoras of scientific studies are available pointing the positive association between saturated/monounsaturated fatty acid and progression of mammary gland carcinoma, with a negative modulation by polyunsaturated fatty acid. Similar framework of decreased total polyunsaturated fats and increased saturated/monounsaturated fat in the mammary gland was scrutinized after the MNU treatment. β-sitosterol afforded to curtail down the upraised saturated/monounsaturated fats profile in the mammary gland tissue dose-dependently without much affecting the total PUFA concentration. It would be appropriate to mention that total fat in a cancerous tissue has been directly correlated drug resistance and subsequently Pgp expression. In fact inhibition of the multidrug resistance, MDR1/P-gp has been postulated as one of the mechanism through which polyunsaturated fatty acids exert a synergetic effect in the response of tumor cells to anticancer drugs . In the present study, we contemplated overexpressed Pgp and diminished unsaturated fatty acid after the MNU treatment and vice versa results after the β-sitosterol administration. The up-regulated PUFA levels after the β-sitosterol treatment also strengthens the previous observations that β-sitosterol can promote apoptosis through activating FAS enzyme.
With all above one can conclude that β-sitosterol can impart significant protection against the MNU induced mammary gland carcinogenesis through modifying the pathological, biochemical and inflammatory markers, which authors would like to attribute to its modulatory activity towards Pgp and fatty acid profile of the mammary gland. Authors would also like to hypothesize that the same could be attributed to its potential to activate FAS and thereby promote apoptosis. However, because FAS is primarily regulated through the hypoxia-inducible factor and subsequently prolyl hydroxylase, it would interest to investigate the effect of β-sitosterol on the same.
AA, arachidonic acid; AB/TEB, alveolar buds/terminal end buds; CAT, catalase; COX, cyclooxygenase; FAME, fatty acid methyl ester; FAS, fatty acid synthase; FTC, ferrithiocynate; GSH, glutathione; LOX, lipoxygenase; MNU, methyl nitrosourea; MVD, intratumoral microvessel density; NO, nitric oxide; RNS, reactive nitrogen species; ROS, reactive oxygen species; SOD, superoxide dismutase; TBARs, thiobarbituric acid reactive substances; TMPD, N, N, N’, N’-tetramethyl-p-phenylenediamine
The author would like to thanks, University Grants Commission for providing Fellowship to MS, JKR, SG, and RKY.
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Availability of data and materials
The datasets supporting the conclusions of this article are included within the article.
CM: Carried out the bench work; SG, SR & MS: Contributed towards bench work and statistical analysis; RKY, JKY & UD: Compiled the data, statistical analysis and organized the manuscript. MNA and ASS: performed the statistical studies and compiled the data; GK: perceived the idea, designed and supervised the study, prepared and proofread the final manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
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Ethics approval and consent to participate
The experiment was performed according to the CPCSEA guidelines for laboratory Animals and Ethics, Department of Animal Welfare, Government of India and approved by the institutional ethics committee (SDCOP & VS/AH/CPCSEA/01/0037).
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- Prasad L. Burden of oral cancer: An Indian scenario. J Orofac Sci. 2014;6(2):77.View ArticleGoogle Scholar
- Abdulkareem IH. Aetio-pathogenesis of breast cancer. Niger Med J. 2013;54(6):371.View ArticlePubMedPubMed CentralGoogle Scholar
- Chapa J, Bourgo RJ, Greene GL, Kulkarni S, An G. Examining the pathogenesis of breast cancer using a novel agent-based model of mammary ductal epithelium dynamics. PLoS ONE. 2013;8(5):e64091.View ArticlePubMedPubMed CentralGoogle Scholar
- Awad A, Fink C, Williams H, Kim U. In vitro and in vivo (SCID mice) effects of phytosterols on the growth and dissemination of human prostate cancer PC-3 cells. Eur J Cancer Prev. 2001;10(6):507–13.View ArticlePubMedGoogle Scholar
- Awad A, Chinnam M, Fink C, Bradford P. Targeting ceramide by dietary means to stimulate apoptosis in tumor cells. Curr Top Nutraceutical Res. 2004;2:93–100.Google Scholar
- Awad AB, Fink CS. Phytosterols as anticancer dietary components: evidence and mechanism of action. J Nutr. 2000;130(9):2127–30.PubMedGoogle Scholar
- Woyengo T, Ramprasath V, Jones P. Anticancer effects of phytosterols. Eur J Clin Nutr. 2009;63(7):813–20.View ArticlePubMedGoogle Scholar
- Hardman WE. Walnuts have potential for cancer prevention and treatment in mice. J Nutr. 2014;144(4):555S–60.View ArticlePubMedPubMed CentralGoogle Scholar
- Jones PJ, AbuMweis SS. Phytosterols as functional food ingredients: linkages to cardiovascular disease and cancer. Curr Opin Clin Nutr Metab Care. 2009;12(2):147–51.View ArticlePubMedGoogle Scholar
- Ramprasath VR, Awad AB. Role of Phytosterols in Cancer Prevention and Treatment. J AOAC Int. 2015;98(3):735–8.PubMedGoogle Scholar
- Park C, Moon D-O, Rhu C-H, Choi BT, Lee WH, Kim G-Y, Choi YH. BETA.-Sitosterol Induces Anti-proliferation and Apoptosis in Human Leukemic U937 Cells through Activation of Caspase-3 and Induction of Bax/Bcl-2 Ratio. Biol Pharm Bull. 2007;30(7):1317–23.View ArticlePubMedGoogle Scholar
- Baskar AA, Ignacimuthu S, Paulraj GM, Numair KS. Chemopreventive potential of β-sitosterol in experimental colon cancer model-an in vitro and in vivo study. BMC Complement Altern Med. 2010;10(1):1.View ArticleGoogle Scholar
- Awad A, Chen Y, Fink C, Hennessey T. beta-Sitosterol inhibits HT-29 human colon cancer cell growth and alters membrane lipids. Anticancer Res. 1995;16(5A):2797–804.Google Scholar
- Von Holtz RL, Fink CS, Awad AB. β-sitosterol activates the sphingomyelin cycle and induces apoptosis in LNCaP human prostate cancer cells. 1998; 32(1):8–12.Google Scholar
- Paniagua-Pérez R, Madrigal-Bujaidar E, Reyes-Cadena S, Alvarez-González I, Sánchez-Chapul L, Pérez-Gallaga J, Hernández N, Flores-Mondragón G, Velasco O. Cell protection induced by beta-sitosterol: inhibition of genotoxic damage, stimulation of lymphocyte production, and determination of its antioxidant capacity. Arch Toxicol. 2008;82(9):615–22.View ArticlePubMedGoogle Scholar
- Awad A, Chinnam M, Fink C, Bradford P. β-Sitosterol activates Fas signaling in human breast cancer cells. Phytomedicine. 2007;14(11):747–54.View ArticlePubMedGoogle Scholar
- Chai J, Kuppusamy U, Kanthimathi M. Beta-sitosterol induces apoptosis in MCF-7 cells. Malays J Biochem Mol Biol. 2008;16(2):28–30.Google Scholar
- Brichory F, Beer D, LeNaour F, Giordano T, Hanash S. Proteomics-based identification of protein gene product 9.5 as a tumor antigen that induces a humoral immune response in lung cancer. Cancer Res. 2001;61(21):7908–12.PubMedGoogle Scholar
- Hurst-Kennedy J, Chin L-S, Li L, Ubiquitin C-terminal hydrolase l1 in tumorigenesis. Biochem Res Int. 2012; Article ID 123706. 10 Pages.Google Scholar
- De Assis S, Warri A, Cruz MI, Hilakivi-Clarke L. Changes in mammary gland morphology and breast cancer risk in rats. JoVE (Journal of Visualized Experiments). 2010;44:e2260–0.Google Scholar
- Kaithwas G, Dubey K, Bhtia D, Sharma AD, Pillai K. Reversal of sodium nitrite induced impairment of spontaneous alteration by Aloe vera gel: involvement of cholinergic system. Pharmacologyonline. 2007;3:428–37.Google Scholar
- Kaithwas G, Dubey K, Pillai K. Effect of aloe vera (Aloe barbadensis Miller) gel on doxorubicin-induced myocardial oxidative stress and calcium overload in albino rats. Indian J Exp Biol. 2011;49(4):260.PubMedGoogle Scholar
- Kaithwas G, Majumdar DK. In vitro antioxidant and in vivo antidiabetic, antihyperlipidemic activity of linseed oil against streptozotocin‐induced toxicity in albino rats. Eur J Lipid Sci Technol. 2012;114(11):1237–45.View ArticleGoogle Scholar
- Reznick AZ, Packer L. Oxidative damage to proteins: spectrophotometric method for carbonyl assay. Methods Enzymol. 1994;233:357–63.View ArticlePubMedGoogle Scholar
- Rossi R, Tsikas D. S-Nitrosothiols in blood: does photosensitivity explain a 4-order-of-magnitude concentration range? Clin Chem. 2009;55(5):1036–8.View ArticlePubMedGoogle Scholar
- Cullen L, Kelly L, Connor SO, Fitzgerald DJ. Selective cyclooxygenase-2 inhibition by nimesulide in man. J Pharmacol Exp Ther. 1998;287(2):578–82.PubMedGoogle Scholar
- Riendeau D, Percival M, Brideau C, Charleson S, Dube D, Ethier D, Falgueyret J-P, Friesen R, Gordon R, Greig G. Etoricoxib (MK-0663): preclinical profile and comparison with other agents that selectively inhibit cyclooxygenase-2. J Pharmacol Exp Ther. 2001;296(2):558–66.PubMedGoogle Scholar
- Lu W, Zhao X, Xu Z, Dong N, Zou S, Shen X, Huang J. Development of a new colorimetric assay for lipoxygenase activity. Anal Biochem. 2013;441(2):162–8.View ArticlePubMedGoogle Scholar
- Folch J, Lees M, Sloane-Stanley G. A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem. 1957;226(1):497–509.PubMedGoogle Scholar
- Kaithwas G, Mukerjee A, Kumar P, Majumdar DK. Linum usitatissimum (linseed/flaxseed) fixed oil: antimicrobial activity and efficacy in bovine mastitis. Inflammopharmacology. 2011;19(1):45–52.View ArticlePubMedGoogle Scholar
- Ahmad Y, Sharma N. An effective method for the analysis of Human Plasma Proteome using Two-dimensional Gel Electrophoresis. J Proteomics Bioinformatics. 2009;2(12):495–9.View ArticleGoogle Scholar
- Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227(5259):680–5.View ArticlePubMedGoogle Scholar
- Towbin H, Staehelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci. 1979;76(9):4350–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Russo IH, Russo J. Mammary gland neoplasia in long-term rodent studies. Environ Health Perspect. 1996;104(9):938.View ArticlePubMedPubMed CentralGoogle Scholar
- Russo J, Russo IH. Boundaries in mammary carcinogenesis. In: Boundaries between Promotion and Progression during Carcinogenesis. Springer/Humana Press; 1991;57:43–59.Google Scholar
- Thompson HJ, McGinley JN, Wolfe P, Spoelstra NS, Knott KK. Targeting angiogenesis for mammary cancer prevention: factors to consider in experimental design and analysis. Cancer Epidemiol Biomark Prev. 2004;13(7):1173–84.Google Scholar
- Russo J, Gusterson BA, Rogers AE, Russo IH, Wellings SR, Van Zwieten MJ. Comparative study of human and rat mammary tumorigenesis. Springer US. PressIn: Pathology Reviews• 1990. Springer; 1990:217–251.Google Scholar
- Romano M, Clària J. Cyclooxygenase-2 and 5-lipoxygenase converging functions on cell proliferation and tumor angiogenesis: implications for cancer therapy. FASEB J. 2003;17(14):1986–95.View ArticlePubMedGoogle Scholar
- Tuncer S, Banerjee S. Eicosanoid pathway in colorectal cancer: Recent updates. World J Gastroenterol. 2015;21(41):11748.View ArticlePubMedPubMed CentralGoogle Scholar
- Schneider C, Pozzi A. Cyclooxygenases and lipoxygenases in cancer. Cancer Metastasis Rev. 2011;30(3–4):277–94.View ArticlePubMedPubMed CentralGoogle Scholar
- Müller-Decker K, Berger I, Ackermann K, Ehemann V, Zoubova S, Aulmann S, Pyerin W, Fürstenberger G. Cystic duct dilatations and proliferative epithelial lesions in mouse mammary glands upon keratin 5 promoter-driven overexpression of cyclooxygenase-2. Am J Pathol. 2005;166(2):575–84.View ArticlePubMedPubMed CentralGoogle Scholar
- ZielińskaB A. Expression of Proapoptotic BAX and TP53 Genes and Antiapoptotic BCL-2 Gene in MCF-7 and T-47D Tumour Cell Cultures of the Mammary Gland After a Photodynamic Therapy with Photolon. Adv Clin Exp Med. 2015;24(1):37–46.View ArticleGoogle Scholar
- Ding XZ, Tong WG, Adrian TE. 12‐lipoxygenase metabolite 12 (S)‐HETE stimulates human pancreatic cancer cell proliferation via protein tyrosine phosphorylation and ERK activation. Int J Cancer. 2001;94(5):630–6.View ArticlePubMedGoogle Scholar
- Nie D, Hillman GG, Geddes T, Tang K, Pierson C, Grignon DJ, Honn KV. Platelet-type 12-lipoxygenase in a human prostate carcinoma stimulates angiogenesis and tumor growth. Cancer Res. 1998;58(18):4047–51.PubMedGoogle Scholar
- Shappell SB, Boeglin WE, Olson SJ, Kasper S, Brash AR. 15-lipoxygenase-2 (15-LOX-2) is expressed in benign prostatic epithelium and reduced in prostate adenocarcinoma. Am J Pathol. 1999;155(1):235–45.View ArticlePubMedPubMed CentralGoogle Scholar
- Jack GS, Brash AR, Olson SJ, Manning S, Coffey CS, Smith JA, Shappell SB. Reduced 15-lipoxygenase-2 immunostaining in prostate adenocarcinoma: correlation with grade and expression in high-grade prostatic intraepithelial neoplasia. Hum Pathol. 2000;31(9):1146–54.View ArticlePubMedGoogle Scholar
- Shureiqi I, Wojno KJ, Poore JA, Reddy RG, Moussalli MJ, Spindler SA, Greenson JK, Normolle D, Hasan AA, Lawrence TS. Decreased 13-S-hydroxyoctadecadienoic acid levels and 15-lipoxygenase-1 expression in human colon cancers. Carcinogenesis. 1999;20(10):1985–95.View ArticlePubMedGoogle Scholar
- Cao Y, Karin M. NF-kB in mammary gland development and breast cancer. J Mammary Gland Biol Neoplasia. 2003;8(2):215–23.View ArticlePubMedGoogle Scholar
- Loizou S, Lekakis I, Chrousos GP, Moutsatsou P. β‐Sitosterol exhibits anti‐inflammatory activity in human aortic endothelial cells. Mol Nutr Food Res. 2010;54(4):551–8.View ArticlePubMedGoogle Scholar
- Sun Y. Free radicals, antioxidant enzymes, and carcinogenesis. Free Radic Biol Med. 1990;8(6):583–99.View ArticlePubMedGoogle Scholar
- Valko M, Rhodes C, Moncol J, Izakovic M, Mazur M. Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem Biol Interact. 2006;160(1):1–40.View ArticlePubMedGoogle Scholar
- Stoll BA. N-3 fatty acids and lipid peroxidation in breast cancer inhibition. Br J Nutr. 2002;87(3):193–8.View ArticlePubMedGoogle Scholar
- Mallikarjuna G, Dhanalakshmi S, Raisuddin S, Rao AR. Chemomodulatory influence of Ferula asafoetida on mammary epithelial differentiation, hepatic drug metabolizing enzymes, antioxidant profiles and N-methyl-N-nitrosourea-induced mammary carcinogenesis in rats. Breast Cancer Res Treat. 2003;81(1):1–10.View ArticlePubMedGoogle Scholar
- Zhao Q, Yang Y, Liang X, Du G, Liu L, Lu L, Dong J, Han H, Zhang G. The clinicopathological significance of neurogenesis in breast cancer. BMC Cancer. 2014;14(1):1.View ArticleGoogle Scholar
- Romon R, Adriaenssens E, Lagadec C, Germain E, Hondermarck H, Le Bourhis X. Nerve growth factor promotes breast cancer angiogenesis by activating multiple pathways. Mol Cancer. 2010;9(1):1.View ArticleGoogle Scholar
- Tokumaru Y, Yamashita K, Osada M, Nomoto S, Sun D-I, Xiao Y, Hoque MO, Westra WH, Califano JA, Sidransky D. Inverse correlation between cyclin A1 hypermethylation and p53 mutation in head and neck cancer identified by reversal of epigenetic silencing. Cancer Res. 2004;64(17):5982–7.View ArticlePubMedGoogle Scholar
- Tezel E, Hibi K, Nagasaka T, Nakao A. PGP9. 5 as a prognostic factor in pancreatic cancer. Clin Cancer Res. 2000;6(12):4764–7.PubMedGoogle Scholar
- Takase T, Hibi K, Yamazaki T, Nakayama H, Taguchi M, Kasai Y, Ito K, Akiyama S, Nagasaka T, Nakao A. PGP9. 5 overexpression in esophageal squamous cell carcinoma. Hepato-Gastroenterology. 2002;50(53):1278–80.Google Scholar
- Harada T, Harada C, Wang Y-L, Osaka H, Amanai K, Tanaka K, Takizawa S, Setsuie R, Sakurai M, Sato Y. Role of ubiquitin carboxy terminal hydrolase-L1 in neural cell apoptosis induced by ischemic retinal injury in vivo. Am J Pathol. 2004;164(1):59–64.View ArticlePubMedPubMed CentralGoogle Scholar
- Ishibashi Y, Takada K, Joh K, Ohkawa K, Aoki T, Matsuda M. Ubiquitin immunoreactivity in human malignant tumours. Br J Cancer. 1991;63(2):320.View ArticlePubMedPubMed CentralGoogle Scholar
- Osada T, Sakamoto M, Nishibori H, Iwaya K, Matsuno Y, Muto T, Hirohashi S. Increased ubiquitin immunoreactivity in hepatocellular carcinomas and precancerous lesions of the liver. J Hepatol. 1997;26(6):1266–73.View ArticlePubMedGoogle Scholar
- Ishibashi Y, Hanyu N, Suzuki Y, Yanai S, Tashiro K, Usuba T, Iwabuchi S, Takahashi T, Takada K, Ohkawa K. Quantitative analysis of free ubiquitin and multi-ubiquitin chain in colorectal cancer. Cancer Lett. 2004;211(1):111–7.View ArticlePubMedGoogle Scholar
- Fay MP, Freedman LS, Clifford CK, Midthune DN. Effect of different types and amounts of fat on the development of mammary tumors in rodents: a review. Cancer Res. 1997;57(18):3979–88.PubMedGoogle Scholar
- Chajès V, Thiébaut AC, Rotival M, Gauthier E, Maillard V, Boutron-Ruault M-C, Joulin V, Lenoir GM, Clavel-Chapelon F. Association between serum trans-monounsaturated fatty acids and breast cancer risk in the E3N-EPIC Study. Am J Epidemiol. 2008;167(11):1312–20.View ArticlePubMedPubMed CentralGoogle Scholar
- Sasaki S, Horacsek M, Kesteloot H. An ecological study of the relationship between dietary fat intake and breast cancer mortality. Prev Med. 1993;22(2):187–202.View ArticlePubMedGoogle Scholar
- Kuan C-Y, Walker TH, Luo PG, Chen C-F. Long-chain polyunsaturated fatty acids promote paclitaxel cytotoxicity via inhibition of the MDR1 gene in the human colon cancer Caco-2 cell line. J Am Coll Nutr. 2011;30(4):265–73.View ArticlePubMedGoogle Scholar