BPH 3
BPH 3
BPH 3
Yüksel & Deveci Özkan (2021) Comm. J. Biol. 5(1), 84-89. e-ISSN 2602-456X
DOI: 10.31594/commagene.895415
Research Article / Araştırma Makalesi
Received: 11.03.2021 Accepted: 15.06.2021 Published online: 24.06.2021 Issue published: 30.06.2021
Abstract: Nobiletin (NOB) is a polymethoxylated flavone. It has multiple biologic activities that can modulate oxidative stress
in many cancer types. However, there is no study in the literature that has examined the effects of NOB on oxidative stress
levels in Metastatic Castration-Resistant Prostate Cancer (MCRPC) yet. Motivated from this gap, we investigated the impact
of NOB on oxidative stress and superoxide dismutase (SOD) enzyme activities in MCRPC as a preliminary study. For this
purpose, PC-3 and HUVEC cells were used to determine the effects of NOB on the amount of Malondialdehyde (MDA),
hydrogen peroxide (H2O2), and proline as well as SOD enzyme activities. NOB potentially induced SOD enzyme activities but
the level of MDA, H2O2, and proline decreased after incubation with NOB in PC-3 cells (p<.05 and p<.001 were considered
statistically significant). Our results confirmed that NOB acted as a protective agent for cancer cells and could selectively
regulate oxidant status in MCRPC cells. Consequently, these preliminary findings provide better insight into the role of citrus
NOB on oxidative stress levels and antioxidant enzyme activities in MCRPC. Additionally, there is a need to elucidate the
molecular mechanisms of this cytoprotective effect of NOB as a potential chemotherapeutic agent.
Keywords: Antioxidant effect, cancer, flavanoid, malondialdehyde, proline.
Öz: Nobiletin (NOB) polimetoksile bir flavondur ve birçok kanser türünde oksidatif stresi modüle edebilen çok sayıda
biyolojik aktiviteye sahiptir. Bununla birlikte, literatürde, MCRPC'de Metastatik Kastrasyona Dirençli Prostat Kanserinde
(MCRPC) NOB'nin oksidatif stres seviyeleri üzerindeki etkilerine dair henüz bir çalışma bulunmamaktadır. Bu nedenle, ön
çalışma olarak MCRPC'de NOB'nin oksidatif stres ve süperoksit dismutaz (SOD) enzim aktiviteleri üzerindeki etkilerini
belirlemeyi amaçladık. Bu amaçla, çalışmada NOB'nin Malondialdehit (MDA), hidrojen peroksit (H2O2) ve prolin miktarı ile
SOD enzim aktiviteleri üzerindeki etkilerini belirlemek için PC-3 ve HUVEC hücreleri kullanıldı. NOB’un potansiyel olarak
SOD enzim aktivitelerini indüklediği, ancak PC-3 hücrelerinde NOB ile inkübasyondan sonra MDA, H2O2 ve prolin
seviyesinin azaldığı tespit edildi (p<.05 ve p <.001 istatistiksel olarak anlamlı kabul edildi). Elde edilen veriler, NOB'nin kanser
hücreleri için koruyucu bir ajan olarak hareket ettiğini ve MCRPC hücrelerinde oksidan durumunu seçici olarak
düzenleyebildiğini doğruladı. Sonuç olarak, bu ön bulgular, MCRPC'de turunçgil NOB'nin oksidatif stres seviyeleri ve
antioksidan enzim aktiviteleri üzerindeki rolü hakkında daha iyi fikir vermektedir. Ek olarak, potansiyel bir kemoterapötik
ajan olarak NOB'nin bu sitoprotektif etkisinin moleküler mekanizmalarının aydınlatılmasına ihtiyaç vardır.
Anahtar kelimeler: Antioksidan etki, flavonoid, kanser, malondialdehyde, proline.
Nobiletin (NOB) is a bioactive polymethoxylated 5% CO2. The optimal treatment concentration and times
flavone (5,6,7,8,3’,4’‐hexamethoxyflavone) which was for NOB in PC-3 and HUVEC cell lines were determined
found in citrus peels and had multiple biologic activities in our previous studies (Deveci Ozkan et al., 2020).
(Bernini et al., 2011; Zheng et al., 2019; Dusabimana et al., Therefore, all cells were treated with NOB (80 µM for PC-
2019). Flavonoids exhibit anti-carcinogenic characteristics 3 and HUVEC, respectively) for 48 h in all experiments.
in vitro and reduce cancer risk by protecting cells from Additionally, cells were grown in a culture medium
oxidation or inflammation by changing the level of sex without NOB used as a negative control.
hormones, reducing angiogenesis or cell proliferation, and
2.2. Antioxidant enzyme activity and oxidative stress
regulating apoptosis (Gates et al., 2009). NOB is anti-
assays
apoptotic, anti-inflammatory, anti-tumor, and antioxidant
and an effective inhibitor against human prostate cancer 2.2.1. Preparation of cell lysate
cells and melanoma cells (Kunimasa et al., 2010; Lee et al.,
To determine the effects of NOB on antioxidant enzyme
2013; Xiao et al., 2016; Huang et al., 2016; Surichana et al.,
activity and oxidative stress level, the cells (5x10 5) were
2018). Additionally, studies have shown that NOB has an
seeded six-well plates and treated with indicated
anti-inflammatory effect and exhibit an inhibiting effect on
concentrations (80 µM for PC-3 and HUVEC, respectively)
tumor invasion, proliferation, and metastasis and inhibit
of NOB for 48h. After incubation, the cells were treated
the creation of reactive oxygen species (ROS) by increasing
with RIPA lysis and extraction buffer (Sigma Aldrich,
the superoxide dismutase (SOD) and glutathione (GSH)
USA), centrifuged for 10 min at 10.000 rpm at 4°C. After
activity and reduction in the making of malondialdehyde
centrifugation, obtained supernatant was used for the
(MDA) and H2O2‐induced PC12 cells (Luo et al., 2008; Lu
analysis of antioxidant enzyme activity and oxidative
et al., 2010; Güney Eskiler et al.; 2018; Liu et al., 2019;
stress.
Deveci Ozkan et al., 2020). In addition, researchers
reported that nobiletin impeded cell proliferation both 2.2.2. Determination of Superoxide Dismutase (SOD)
depending on the dose and duration and prevented cell activity
cycle progression in G1 (Morley et al., 2007). Nobiletin can
SOD activity was established phytochemically according
induce DNA damage that contributes to apoptosis by
to the proposed method of Beauchamp and Fridovich
regulating polymerase activity in cancer cells (Zhang et al.,
(1971). SOD accelerates superoxide radicals' degradation
2020). It has been suggested that NOB may be a pathway
(O2-), H2O2, and molecular oxygen formed during
that triggers pyroptosis associated with apoptosis by
oxidative energy production. SOD activity is determined
inducing IL-1β expression (He et al., 2015). NOB is
by the inhibition of NBT (nitrobluetetrazolium) and
hypothesized to inhibit metastasis by impeding the
formazan (blue crystals) formation. The blue-purple color
activity of activator protein-1, a dimeric protein,
formation from NBT with the effect of light is inversely
preventing DNA binding (Kawabata et al., 2005; Goh et al.,
proportional to the activity of the SOD enzyme. One unit
2019). Another suggestion proposes that NOB functions
of SOD activity was determined as the quantity of enzyme
through the Nuclear Factor-kappa B route and
needed to reduce 50% of the NBT kept under light at 560
differentiates gene expression via regulating its promoter
nm. Therefore, SOD enzyme activity was calculated
regions (Xiong et al., 2015; Park et al., 2016). As a food
according to the formula below.
ingredient, nobiletin may be a favorable new anti-prostate
cancer functional food component that can generate ROS- %Inhibition = [(Blank OD – Sample OD)/Blank OD] x 100
mediated apoptosis in prostate cancer cells.
2.2.3. Determination of Malondialdehyde (MDA) level
No study has been conducted in the literature that
MDA level was verified by the proposed method of
shows the effects of NOB on oxidative stress levels and
Ohkawa et al. (1979). According to this method, the
antioxidant enzyme activities in MCRPC. Therefore, in this
thiocarboxylic acid (TBA) test, which accepts MDA as the
study, we aimed to determine the effects of NOB on
final product of lipid peroxidation, was used. The
oxidative stress in MCRPC (PC-3) and control cells
formation of MDA content resulting from the TBA reaction
(HUVEC). To clarify if NOB affects oxidative stress, we
is accepted as a lipid peroxidation measure. The amount of
measured the amount of Malondialdehyde (MDA),
MDA in 1 ml of solution was calculated according to the
hydrogen peroxide (H2O2), and proline as well as SOD
formula below and the results were given as MDA
(superoxide dismutase) enzyme activities. Thus, it is
(nmol/gram tissue) (Ananieva et al., 2002).
aimed to obtain information that will contribute to the
potential of NOB as a functionally unique and possible MDA (nmol/g): [(A532-A600)/155000] x 106
chemopreventive agent in inflammation-related tumor
2.2.4. Determination of Proline Level
formation such as MCRPC.
Proline level was determined by the proposed method of
2. Material and Methods
Myara et al. (1982). According to this method, the proline
2.1. Cell culture and NOB treatment level was determined by measuring absorbance in a
spectrophotometer. Absorbance values were obtained
In this study, the PC-3 (prostate cancer) cell line was used
from an ultraviolet spectrophotometer (Shimadzu UV
as MCRPC cells and human umbilical vein endothelial
mini-1240 spectrophotometer) at 520 nm wavelength.
cells (HUVEC) were evaluated as a control cell line. All
Proline concentration was calculated as μmol/g according
cells were bought from American Type Culture Collection
to the proline standard curve.
(ATCC). PC-3 was cultured in RPMI-1640 (Thermo Fisher,
USA) and HUVEC cells were grown in DMEM medium 2.2.5. Determination of Hydrogen Peroxide (H2O2) level
(Thermo Fisher, USA) supplemented with 0.1% penicillin
H2O2 level was determined by the proposed method of
and streptomycin, 10% FBS, and incubated at 37°C with
85
Yüksel & Deveci Özkan (2021) Comm. J. Biol. 5(1), 84–89.
Jana and Choudhuri (1981). According to this method, the a similar significant increase was observed in HUVEC cells
H2O2 level was determined by measuring absorbance in a treated with NOB compared to the control group level in
spectrophotometer. Absorbance values were obtained both treatment times (*p<.05, **p<.001, Table 1 and Fig. 1).
from an ultraviolet spectrophotometer (Shimadzu UV As we expect that a significant decrease was observed in
mini-1240 spectrophotometer) at 410 nm wavelength. MDA levels of the PC-3 cells treated with NOB (0.19 ± 0.03)
H2O2 concentration was calculated according to the compared to the control (0.37 ± 0.06) for 48 h but a
proline standard curve. significant increase was determined in HUVEC cells
treated with NOB (0.69 ± 0.28) compared to the control
2.3. Statistical analysis
(0.60 ± 0.47) for 48h (*p<.05, **p<.001, Table 1 and Fig. 2).
Statistical analyses were carried out via Graph pad Prism Additionally, a similar significant decrease was observed
v9.0 (Software, CA) and showed the mean ± standard for in H2O2 concentration of the PC-3 cells treated with
deviation of three independent experiments. One-way NOB for 24 and 48h (0.21 ± 0.08 and 0.34 ± 0.01,
analysis of variance (ANOVA) and Tukey's test was respectively) compared to the control (1.49 ± 0.05 and 0.12
utilized to obtain multiple comparisons (p<.05 and p<.001 ± 0.05, respectively) but a significant increase was
were taken as statistically significant). determined in HUVEC cells treated with NOB compared
to the control for both 24 and 48h (*p<.05, **p<.001, Table 1
3. Results
and Fig. 3). Besides, the proline level of the cells incubated
Our results showed that the SOD activities of the cells with NOB showed a statistically non-significant decrease
incubated with NOB for 24 and 48 h showed a significant in PC-3 and HUVEC cells compared to the control cells for
increase in PC-3 cells (9.71 ± 2.04 and 9.36 ± 2.32, 48h (Table 1 and Fig. 4). Therefore, according to our
respectively) compared to the control cells not treated with results, MDA and H2O2 levels were significantly lower
NOB (7.98 ± 0.41 and 6.87 ± 0.13, respectively). Moreover, whereas SOD activity was significantly higher in the
MCRPC cells treated with NOB.
Table 1. Comparison of the oxidative stress levels and antioxidant enzyme activities according to the control group and NOB treated
group in PC-3 and HUVEC for 24 and 48h.
PC-3-Control PC-3-NOB HUVEC-Control HUVEC-NOB
Parameters
Mean ± SD (n=3) Mean ± SD (n=3) Mean ± SD (n=3) Mean ± SD (n=3)
24h 7.98 ± 0.41 9.71 ± 2.04* 8.36 ± 0.38 14.21 ± 1.29**
SOD (unit/mg)
48h 6.87 ± 0.13 9.36 ± 2.32* 3.38 ± 0.78 11.06 ± 0.86**
24h 0.53 ± 0.21 0.56 ± 0.15 0.42 ± 0.21 0.47 ± 0.08*
MDA (µM)
48h 0.37 ± 0.06 0.19 ± 0.03* 0.60 ± 0.47 0.69 ± 0.28**
24h 1.49 ± 0.05 0.21 ± 0.08** 0.16 ± 0.05 0.21 ± 0.01**
H2O2 (µM)
48h 0.12 ± 0.05 0.34 ± 0.01** 0.06 ± 0.01 0.10 ± 0.07**
24h 9.46 ± 1.83 6.68 ± 0.83 4.27 ± 0.57 6.85 ± 1.18
Prolin (µM)
48h 11.22 ± 1.22 7.63 ± 1.46 7.98 ± 0.08 7.27 ±1.07**
The results are expressed as mean ± SD of eight experiments. *p< .05 and **p< .001 significantly different compared to the controls.
Figure 1. Relative enzyme activity level of SOD in PC-3 and Figure 2. Relative level of MDA in PC-3 and HUVEC cells. To
HUVEC cells. To determine the enzyme activity level of SOD in determine the level of MDA in PC-3 and HUVEC cells were
PC-3 and HUVEC cells were treated with 80 mM NOB, for 24 and treated with 80 mM NOB, for 24 and 48 h. (*p<.05, **p<.001, NOB:
48 h. (*p<.05, **p<.001, NOB: Nobiletin). Nobiletin).
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Yüksel & Deveci Özkan (2021) Comm. J. Biol. 5(1), 84–89.
increased the H2O2 level in HUVEC cells. Our results Amaral, T.M.S., Macedo, D., Fernandes, I., & Costa, L. (2012). Castration-
resistant prostate cancer: mechanisms, targets, and treatment. Prostate
confirmed that NOB acted as a protective agent for cancer cancer, 2012, 1-11. https://doi.org/10.1155/2012/327253
cells and could selectively regulate oxidant status in Ananieva, E.A., Alexieva, V.S., & Popova, L.P. (2002). Treatment with
MCRPC cells. H2O2 activates the cellular or mitochondrial salicylic acid decreases the effects of paraquat on
apoptotic pathway (Cho et al., 2015). Considering all these
87
Yüksel & Deveci Özkan (2021) Comm. J. Biol. 5(1), 84–89.
photosynthesis. Journal of Plant Physiology, 159(7), 685-693. hypoxia/reoxygenation injury. European journal of pharmacology, 854, 48-
https://doi.org/10.1078/0176-1617-0706 53. https://doi.org/10.1016/j.ejphar.2019.03.056
Beauchamp, C., & Fridovich, I. (1971). Superoxide dismutase: improved Lu, Y.H., Su, M.Y., Huang, H.Y., & Yuan, C.G. (2010). Protective effects of
assays and an assay applicable to acrylamide gels. Analytical the citrus flavanones to PC12 cells against cytotoxicity induced by
Biochemistry, 44(1), 276-287. https://doi.org/10.1016/0003- hydrogen peroxide. Neuroscience Letters, 484(1), 6-11.
2697(71)90370-8 https://doi.org/10.1016/j.neulet.2010.07.078
Bernini, R., Crisante, F., & Ginnasi, M.C. (2011). A convenient and safe O- Luo, G., Guan, X., & Zhou, L. (2008). Apoptotic effect of citrus fruit extract
methylation of flavonoids with dimethyl carbonate (DMC). Molecules, nobiletin on lung cancer cell line A549 in vitro and in vivo. Cancer biology
16(2), 1418-1425. https://doi.org/10.3390/molecules16021418 & therapy, 7(6), 966-973. https://doi.org/10.4161/cbt.7.6.5967
Cho, H. W., Jung, S. Y., Lee, G. H., Cho, J. H., & Choi, I. Y. (2015). Ma, Q. (2010). Transcriptional responses to oxidative stress: pathological
Neuroprotective effect of Citrus unshiu immature peel and nobiletin and toxicological implications. Pharmacology & therapeutics, 125(3), 376-
inhibiting hydrogen peroxide-induced oxidative stress in HT22 murine 393. https://doi.org/10.1016/j.pharmthera.2009.11.004
hippocampal neuronal cells. Pharmacognosy Magazine, 11(2), 284. Malik, S., Bhatia, J., Suchal, K., Gamad, N., Dinda, A. K., Gupta, Y. K., &
https://dx.doi.org/10.4103%2F0973-1296.166047 Arya, D. S. (2015). Nobiletin ameliorates cisplatin-induced acute kidney
Cooke, M.S., Evans, M.D., Dizdaroglu, M., & Lunec, J. (2003). Oxidative injury due to its antioxidant, anti-inflammatory and anti-apoptotic
DNA damage: mechanisms, mutation, and disease. The FASEB Journal, effects. Experimental and Toxicologic Pathology, 67(7-8), 427-433.
17(10), 1195-1214. https://doi.org/10.1096/fj.02-0752rev https://doi.org/10.1016/j.etp.2015.04.008
Cooke, M.S., Evans, M.D., Herbert, K.E., & Lunec, J. (2000). Urinary 8-oxo- Meng, H.Z., Ni, X.F., Yu, H.N., Wang, S.S., & Shen, S.R. (2017). Effects of
2′-deoxyguanosine—source, significance and supplements. Free radical astaxanthin on oxidative stress induced by Cu 2+ in prostate cells.
research, 32(5), 381-397.7. https://doi.org/10.1080/10715760000300391 Journal of Zhejiang University-SCIENCE B, 18(2), 161-171.
Deveci Ozkan, A., Kaleli, S., Onen, H.I., Sarihan, M., Guney Eskiler, G., https://doi.org/10.1631/jzus.B1500296
Kalayci Yigin, A., & Akdogan, M. (2020). Anti-inflammatory effects of Morley, K.L., Ferguson, P.J., & Koropatnick, J. (2007). Tangeretin and
nobiletin on TLR4/TRIF/IRF3 and TLR9/IRF7 signaling pathways in nobiletin induce G1 cell cycle arrest but not apoptosis in human breast
prostate cancer cells. Immunopharmacology and immunotoxicology, 42(2), and colon cancer cells. Cancer letters, 251(1), 168-178.
93-100. https://doi.org/10.1080/08923973.2020.1725040 https://doi.org/10.1016/j.canlet.2006.11.016
DeWeese, T.L., Hruszkewycz, A.M., & Marnett, L.J. (2001). Oxidative stress Myara, I., Charpentier, C., & Lemonnier, A. (1982). Optimal conditions for
in chemoprevention trials. Urology, 57(4), 137-140. prolidase assay by proline colorimetric determination: application to
https://doi.org/10.1016/S0090-4295(00)00959-6 iminodipeptiduria. Clinica Chimica Acta, 125(2), 193-205.
Dusabimana, T., Kim, S.R., Kim, H.J., Park, S.W., & Kim, H. (2019). https://doi.org/10.1016/0009-8981(82)90196-6
Nobiletin ameliorates hepatic ischemia and reperfusion injury through Ohkawa, H., Ohishi, N., & Yagi, K. (1979). Assay for lipid peroxides in
the activation of SIRT-1/FOXO3a-mediated autophagy and animal tissues by thiobarbituric acid reaction. Analytical biochemistry,
mitochondrial biogenesis. Experimental & molecular medicine, 51(4), 1-16. 95(2), 351-358. https://doi.org/10.1016/0003-2697(79)90738-3
https://doi.org/10.1038/s12276-019-0245-z Park, M. H., & Hong, J. T. (2016). Roles of NF-κB in cancer and
Gates, M.A., Vitonis, A.F., Tworoger, S.S., Rosner, B., Titus‐Ernstoff, L., & inflammatory diseases and their therapeutic approaches. Cells, 5(2), 15.
Hankinson, S.E. (2009). Flavonoid intake and ovarian cancer risk in a https://doi.org/10.3390/cells5020015
population‐based case‐control study. International journal of cancer, Phang, J.M., & Liu, W. (2012). Proline metabolism and cancer. Frontiers in
124(8), 1918-1925. https://doi.org/10.1002/ijc.24151 bioscience (Landmark edition), 17, 1835-1845.
Goh, J. X. H., Tan, L. T. H., Goh, J. K., Chan, K. G., Pusparajah, P., Lee, L. https://dx.doi.org/10.2741/4022
H., & Goh, B. H. (2019). Nobiletin and derivatives: Functional Phang, J.M., Liu, W., Hancock, C.N., & Fischer, J.W. (2015). Proline
compounds from citrus fruit peel for colon cancer chemoprevention. metabolism and cancer: emerging links to glutamine and collagen.
Cancers, 11(6), 867. https://doi.org/10.3390/cancers11060867 Current opinion in clinical nutrition and metabolic care, 18(1), 71-77.
Güney Eskiler, G., Özkan, A.D., & Kaleli, S. (2018). Metastatik prostat https://dx.doi.org/10.1097%2FMCO.0000000000000121
kanserinde nobiletinin sitotoksik ve apoptotik etkisinin belirlenmesi. Phang, J.M. (2019). Proline metabolism in cell regulation and cancer
Sakarya Tıp Dergisi, 8(4), 766-774. https://doi.org/10.31832/smj.485666 biology: recent advances and hypotheses. Antioxidants & redox signaling,
He, W. T., Wan, H., Hu, L., Chen, P., Wang, X., Huang, Z., & Han, J. (2015). 30(4), 635-649. https://doi.org/10.1089/ars.2017.7350
Gasdermin D is an executor of pyroptosis and required for interleukin- Shen, M.M., & Abate-Shen, C. (2010). Molecular genetics of prostate cancer:
1β secretion. Cell research, 25(12), 1285-1298. new prospects for old challenges. Genes & development, 24(18), 1967-
https://doi.org/10.1038/cr.2015.139 2000. https://doi.org/10.1101/gad.1965810
Huang, H., Li, L., Shi, W., Liu, H., Yang, J., Yuan, X., & Wu, L. (2016). The Surichan, S., Arroo, R.R., Ruparelia, K., Tsatsakis, A.M., &
multifunctional effects of nobiletin and its metabolites in vivo and in Androutsopoulos, V.P. (2018). Nobiletin bioactivation in MDA-MB-468
vitro. Evidence-Based Complementary and Alternative Medicine, 2016. breast cancer cells by cytochrome P450 CYP1 enzymes. Food and
https://doi.org/10.1155/2016/2918796 Chemical Toxicology, 113, 228-235.
Huynh, T.Y.L., Zareba, I., Baszanowska, W., Lewoniewska, S., & Palka, J. https://doi.org/10.1016/j.fct.2018.01.047
(2020). Understanding the role of key amino acids in regulation of Wagner, B.A., Evig, C.B., Reszka, K.J., Buettner, G.R., & Burns, C.P. (2005).
proline dehydrogenase/proline oxidase (prodh/pox)-dependent Doxorubicin increases intracellular hydrogen peroxide in PC3 prostate
apoptosis/autophagy as an approach to targeted cancer therapy. cancer cells. Archives of biochemistry and biophysics, 440(2), 181-190.
Molecular and cellular biochemistry, 466(1), 35-44. https://doi.org/10.1016/j.abb.2005.06.015
https://doi.org/10.1007/s11010-020-03685-y
Xiao, J., Capanoglu, E., Jassbi, A.R., & Miron, A. (2016). Advance on the
Jana, S., & Choudhuri, M.A. (1981). Glycolate metabolism of three flavonoid C-glycosides and health benefits. Critical Reviews in Food
submersed aquatic angiosperms: effect of heavy metals. Aquatic Botany, Science and Nutrition, 56(sup1), S29-S45.
11, 67-77. https://doi.org/10.1016/0304-3770(81)90047-4 https://doi.org/10.1080/10408398.2015.1067595
Kawabata, K., Murakami, A., & Ohigashi, H. (2005). Nobiletin, a citrus Xiong, Y., Chen, D., Yu, C., Lv, B., Peng, J., Wang, J., & Lin, Y. (2015). Citrus
flavonoid, down-regulates matrix metalloproteinase-7 (matrilysin) nobiletin ameliorates experimental colitis by reducing inflammation
expression in HT-29 human colorectal cancer cells. Bioscience, and restoring impaired intestinal barrier function. Molecular nutrition &
biotechnology, and biochemistry, 69(2), 307-314. food research, 59(5), 829-842. https://doi.org/10.1002/mnfr.201400614
https://doi.org/10.1271/bbb.69.307
Zhang, R., Chen, J., Mao, L., Guo, Y., Hao, Y., Deng, Y., & Yuan, M. (2020).
Kunimasa, K., Ikekita, M., Sato, M., Ohta, T., Yamori, Y., Ikeda, M., & Nobiletin triggers reactive oxygen species-mediated pyroptosis
Oikawa, T. (2010). Nobiletin, a citrus polymethoxyflavonoid, through regulating autophagy in ovarian cancer cells. Journal of
suppresses multiple angiogenesis‐related endothelial cell functions and agricultural and food chemistry, 68(5), 1326-1336.
angiogenesis in vivo. Cancer science, 101(11), 2462-2469. https://doi.org/10.1021/acs.jafc.9b07908
https://doi.org/10.1111/j.1349-7006.2010.01668.x
Zheng, G.D., Hu, P.J., Chao, Y.X., Zhou, Y., Yang, X.J., Chen, B.Z., & Cai, Y.
Lee, Y.S., Cha, B.Y., Choi, S.S., Choi, B.K., Yonezawa, T., Teruya, T., & Woo, (2019). Nobiletin induces growth inhibition and apoptosis in human
J.T. (2013). Nobiletin improves obesity and insulin resistance in high-fat nasopharyngeal carcinoma C666‐1 cells through regulating PARP‐
diet-induced obese mice. The Journal of nutritional biochemistry, 24(1), 2/SIRT 1/AMPK signaling pathway. Food science & nutrition, 7(3), 1104-
156-162. https://doi.org/10.1016/j.jnutbio.2012.03.014 1112. https://doi.org/10.1002/fsn3.953
Liu, F., Zhang, H., Li, Y., & Lu, X. (2019). Nobiletin suppresses oxidative
stress and apoptosis in H9c2 cardiomyocytes following
88
Yüksel & Deveci Özkan (2021) Comm. J. Biol. 5(1), 84–89.
Zhou, J.F., Xiao, W.Q., Zheng, Y.C., Dong, J., & Zhang, S.M. (2006).
Increased oxidative stress and oxidative damage associated with
chronic bacterial prostatitis. Asian journal of andrology, 8(3), 317-323.
https://doi.org/10.1111/j.1745-7262.2006.00144.x
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