2015-04-20

Screening of Novel CXC Chemokine Receptor 4 Inhibitors From Ethyl Acetate Extract of Alpinia purpurata Using GC-MS Analysis and its Molecular Docking Studies

Anusooriya, P., Arul Raj, C., Chella Perumal, P., Sowmya, S., Vidya,B., Pratibha, P., Gopalakrishnan, V.K.*

Cancer Biology and Medicinal Chemistry Unit, Department of Biochemistry and Bioinformatics, Karpagam University, Coimbatore,Tamil Nadu, India 641 021

Available Online: 20th April, 2015

ABSTRACT

CXCR4 is the receptor for a chemokine, CXCL12 (stromal cell-derived factor-1, SDF-1), it has been proven to be involved in several problematic diseases, including AIDS, cancer cell metastasis, leukemia cell progression and rheumatoid arthritis. Hence it’s thought to be an important therapeutic target to overcome of these diseases. Alpinia purpurata belongs to the family of Zingiberaceae and it possesses many biological activities. Therefore, the aim of present study is to identify the novel CXCR4 inhibitors from the bioactive compounds present in ethyl acetate extract of Alpinia purpurata using GC-MS analysis and its molecular docking studies. Results, GC-MS analysis shown that, ethyl acetate extract of Alpinia purpurata contain 32 bioactive compounds. Molecular docking studies of theses bioactive compounds (Glide 5.5 from Schrödinger suite) revealed that, out of 32 bioactive compounds, 1,2,3-trimethyl-5-propan-2-ylbenzene, Isocamphane, 1,10-Dimethyl-2-methylene-trans-decalin,1-Bromoeicosane,2-(2-Isopropenyl-5- ethylcyclopentylmethoxy) tetrahydropyran, Dihexadecylphosphate, Naphthalene, 1,1′-(1,2-ethanediyl)bis[decahydro- shows the better glide score compared with Cyclophophamide (FDA approved drug). ADME properties (Qikprop 2.3 from Schrödinger suite) of these bioactive compounds were under the acceptable range. Based on the result it can be concluded that, these bioactive compounds may act as novel inhibitors for CXCR4. In future it may focus on current discoveries in CXCR4 inhibition.

Keywords:  CXCR4, A. purpurata, GC-MS, Docking analysis, ADME properties.

INTRODUCTION

The chemokine receptor CXCR4 belongs to the large super family of G protein-coupled receptors and has been identified to play a crucial role in a number of biological processes, including the trafficking and homeostasis of immune cells such as T lymphocytes1.CXCR4 has also been found to be a prognostic marker in various types of cancer, including leukemia and breast cancer, and recent evidence has highlighted the role of CXCR4 in prostate cancer2. Several independent studies have shown that cancer cells have higher levels of CXCR4 expression compared to normal cells3.

In recent years the use of plants in the management and treatment of diseases has gained considerable importance. Plants and fruits are considered one of the main sources of biologically active compounds an estimate of the world health organization (WHO) states that around 85-90% of the world’s population consumes traditional herbal medicines4.Bioactive compounds from medicinal plants with anticancer and anti-inflammatory effects have become key resources in drug discovery fields for the treatment of various malignancies and immunological disorders 5. A huge reservoir of bioactive compounds exists in many species of plants of Earth, only a small percentage of which have been examined and continued to be an important source of anticancer agents. Worldwide effects are ongoing to identify new anticancer compounds from plants. With the current decline in the number of new molecular entities from the pharmaceutical industry, novel anticancer agents are being sought from traditional medicines6.

Alpinia is the largest genus of the family with more than 200 species7. Many Alpinia species are well-known medicinal herbs that have been shown by several previous studies to have various effects, namely, anti-inflammatory8, antioxidant, antimicrobial9.Rhizome has sharp odour, improves appetite, taste and voice. It is also used for headache, rheumatism, sore throat and renal disease10.

Alpinia purpurata is the medicinal plant belongs to the family of Zingiberaceae, it constituents promote antimicrobial activity against certain microorganisms11.In addition to the purported anti-inflammatory activity, its phytomedicinal potential to treat tuberculosis is also described12. Antidermatophytic13, antinociceptive14, hepatoprotective15, immunostimulatory 16, and anticancer17, activities. Alpinia purpurata may serve as potential antioxidant and anticancer agents against ovarian cancer cell lines18. Phytochemical studies on Alpinia purpurata revealed that it possess flavonoids, rutin, kaempferol-3-rutinoside and kaempferol-3-oliucronide19. Rutin had the highest concentration in both extracts. This flavonoid is widely distributed in the Plant Kingdom and, despite its hydrophilic character; it presents several therapeutic applications such as antioxidant activity, besides reducing arteriosclerosis risks and increasing vein tone, which improves the blood flow20. Therefore, objective of the study is to analyze the presence of bioactive compounds from ethyl acetate extract of Alpinia purpurata using GC-MS analysis and to screen the novel inhibitors for CXCR4 from the identified bioactive compounds by molecular docking studies.

MATERIALS AND METHODS

Plant collection

Alpinia purpurata was collected from Kanyakumari, Tamil Nadu, India. The plant specimen was authenticated by Dr. G.V.S. Murthy, Botanical Survey of India, Coimbatore, TNAU campus, India. A voucher specimen has been deposited in the laboratory for future reference (BSI/SC/5/23/10-11/Tech) 18.

Preparation of extract

The leaf of Alpinia purpurata were washed thoroughly in tap water, shade dried and powdered. The powder (100 g) was exhaustively extracted with ethyl acetate in the ratio of 1:5 for 24 h by using soxhlet apparatus. The extract was completely evaporated to dryness using rotary flash evaporator (Buchi type). The ethyl acetate extract of the plant was used for GC-MS analysis.

GC-MS analysis

GC-MS analysis of the whole plant extract of Alpinia purpurata was performed using the equipment Agilent technologies 7890 A. The equipment has a DB 35 – MS Capillary Standard non-polar column with dimensions of 30 mm×0.25 mm ID×0.25 μm film. The carrier gas used was Helium with at low of 1.0 ml/min. The injector was operated at 250 °C and the oven temperature was programmed as follows: 60 °C for 15 min, then gradually increased to 280 °C at 3 min. The identification of components was based on Willey and NIST libraries as well as comparison of their retention indices. The constituents were identified after comparison with those available in the computer library (NIST and Willey) attached to the GC-MS instrument and the results obtained have been tabulated.

In Silico Analysis

Preparation of protein structure

The 3D structure of CXCR4 was retrieved from the Protein Data Bank (PDB ID: 3OE6) and it was prepared by protein preparation wizards (standard methods) that are available in grid-based ligand docking with energetics21. Protein was optimized using sample water orientation and minimized by using RMSD 0.30 Å and OPLS (2005) force field.

Active site prediction

The active site (binding pockets) and functional residues of CXCR4 was identified and characterized by Site- Map module from Schrodinger package.  Site Map calculation begins with an initial search step that identifies or characterizes- through the use of grid points- one or more regions on the protein surface that may be suitable for binding ligands to the receptor. Contour maps were then generated, produced hydrophobic, hydrophilic maps hydrogen binding possibilities which may guide the protein- ligand docking analysis 22.

Ligand preparation

Totally 32 bioactive compounds (from GC-MS analysis) were used in molecular docking studies. These ligands were prepared using the LigPrep 2.4. The structure of each ligands were optimized by means of the OPLS 2005 force field using a default setting 23.

Molecular docking analysis

All docking analysis were performed by using the standard precision (SP) which is Standard mode of Glide 5.6 (Grid-based Ligand Docking with Energetic) module from Schrodinger 2012. All bioactive compounds were docked in to the binding site CXCR4 receptor using Glide 5.6. The scaling Vander Waals radii were 1.0 in the receptor grid generation. Grid was prepared with the bounding box set on 20Aº. The co-ordinates of this enclosing box with the help of the active site residues to be set default. The force field is using for the docking protocol is OPLS_2005. The lowest-energy docked complexes were found in the majority of similar docking conformations24.

ADME properties prediction

The CXCR4 inhibitors were checked for their ADME properties using QikProp 2.3 module. QikProp helps in analyzing the pharmacokinetics and pharmacodynamics of the ligand by accessing the drug like properties. Predicted significant ADME properties such as Molecular weight (MW), H-Bond donor, H-Bond acceptor and log P (O/W)25.

RESULTS AND DISCUSSION

CXCR4 is the predominant chemokine receptor in ovarian cancer and has also been implicated in many other cancers including prostate, colon and ovary. Recent studies have suggested that malignant cells use chemokine receptor/ligand interactions to home in on common metastatic sites like bone marrow and the lungs. In some cancers, over-expression of CXCR4 has been observed to lead to metastasis26. This particular interaction is vital in early embryonic development as it is required for the correct formation of vascular, nervous, hematopoietic and cardiac systems27.Faults in the CXCR4/CXCL12 interaction during the embryonic stage can lead to several defects including cardiac dysfunction and bone marrow defects.

Herbal treatment proves its efficacy in medicinal field without any side effects as synthetic medicines have; hence it’s preferred to be more beneficial. Plant extracts as well as plant-derived compounds are found to be excellent medicinal agents for several cancers.

GC-MS analysis shows that, ethyl acetate extract of Alpinia purpurata has 32 bioactive compounds. A peak level in the chromatogram graph indicates the maximum amount of Naphthalene, 1, 1’-(1, 2-ethanediyl) bis [decahydro- (22.94 %) present in the extract was showed in figure 1 and table1.

These bioactive compounds posses many biological activities such as antioxidant, anticancer, anti-inflammatory, hypocholesterolemic, antiarthritic, antimicrobial, antidiabetic activity etc., Octadecadienoic acid (Z, Z) have the property of anti inflammatory, hypocholesterolemic and antiarthritic activity which was reported by the earlier workers 28, 29. Naphthalene also having good antimicrobial activity30.Geranylgeranyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway used by organisms in the biosynthesis of terpenes and terpenoids. In plants it is also the precursor to carotenoids, gibberellins, tocopherols, and chlorophylls. Geranylgeraniol had a broader protective effect against the cytotoxicity of statins than exogenous ubiquinone. Therefore, geranylgeraniol may be a more useful and practical means of limiting the toxicities of Statins, without reducing their efficacy as cholesterol lowering agents31. Phytol is one part of the cholorophyll and important in plant biosynthesis. When human as well as rodents are fed free phytol a high proportion is absorbed and converted into phytonic acid. The phytol conversion of phytonic acid is a natural rexinoid it shows antidiabetic activity in type II Diabetic patients32. Hexadeconoic acid has the property of antioxidant and antimicrobial activities33. All cholorophyll derivatives are having antioxidant properties34. N-hexadecane has also been used as a Substrate for the bacterial production of biosurfactants35. N-Hexadecane has been utilized in model studies of the transmembrane domain (TMD) of G protein, as related to the kinetics of poly (ethylene glycol) (PEG)-mediated fusion of small unilamellar vesicles36.

The CXCR4 protein was retrieved (from PDB ID: 3OE6) and prepared for further studies. On the other hand, the bioactive compounds (from Alpinia purpurata) were prepared. The best active site (binding pocket/site) was preferred based on the site score and hydrophobic/hydrophilic areas, which holds better binding cavity. The binding site residues of PPARγ were predicted and it may involve in the binding of substrate and small molecule. Thus, all these residues were confirmed as CXCR4 active site residues and picked to generate grid in the centroid of these residues for molecular docking approach.

The molecular docking is frequently used to predict the binding orientation of small molecule drug candidate to their protein targets in order to predict the affinity and activity of the small molecule. The docking results revealed that,32 bioactive compounds were complexes with CXCR4 protein shown in table 2.Among these bioactive compounds,1,2,3-trimethyl-5-propan-2-ylbenzene,Isocamphane,1,10-Dimethyl-2-methylene-trans-decalin,1-Bromoeicosane,2-(2-Isopropenyl-5-methylcyclopentylmethoxy)tetrahydropyran,Dihexadecylphosphate,Naphthalene, 1,1′-(1,2-ethanediyl)bis[decahydro- shows the better glide score of -6.137,-5.180,-5.701,5.603,-5.357,-6.414,-5.107 respectively when compared with FDA approved drug of cyclophosphamide glide score -5.040. These bioactive compounds complexes with CXCR4 were shown in figure 2 to 9. The highest negative value of glide score has been indicated that, these complexes may have good affinity and it may have the inhibitory activity against CXCR4. The ADME properties prediction results (shown in table 3) of these bioactive compounds were under acceptable range.

CONCLUSION

The medicinal plant of Alpinia purpurata (ethyl acetate extract) posses 32 bioactive compounds were identified by GC-MS analysis. These bioactive compounds have been reported to have much biological activity against variety of human diseases. The molecular docking studies exposed that, out of these bioactive compounds1,2,3-trimethyl-5-propan-2-ylbenzene, Isocamphane, 1,10-Dimethyl-2-methylene-trans-decalin, 1-Bromoeicosane, 2-(2-Isopropenyl-5-methylcyclopentylmethoxy) tetrahydropyran, Dihexadecyl phosphate, Naphthalene, 1,1′-(1,2-ethanediyl)bis[decahydro- shows the better glide score compared with Cyclophophamide (FDA approved drug). ADME properties of these bioactive compounds were under the acceptable range. Therefore it can be concluded that, these bioactive compounds may act as novel inhibitors for CXCR4. In future, these compounds may lead to identify their potential biological activities by in vitro and in vivo studies.

CONFLICT OF INTEREST

The authors declare that there is no conflict of interests regarding the publication of this paper.

ACKNOWLEDGEMENT

The authors are thankful to our Chancellor, Chief Executive Officer, Vice-Chancellor and Registrar of Karpagam University for providing facilities and encouragement. We extend our deepest thanks to R.Vasanth, Senior executive, Indian Products Limited, QAQC laboratory for GC-MS analysis & Dr. R. Raghu, Executive Director, Schrodinger for providing us an opportunity to use Schrodinger Suite (in silico analysis).

REFERENCES

Tian J, Xuehua X and Dale H. Chemotaxis, chemokine receptors and human disease, Cytokine 2008; 44, 1–8.

Furusato B, Mohamed A, Uhlen M, J.S.Rhim.CXCR4 and cancer, Pathology International, 2010; 60, 497-505.

Kang H, Watkins G, Douglas-Jones A, Mansel RE, W.G.Jiang. The elevated level of CXCR4 is correlated with nodal metastasis of human breast cancer, Breast2005; 14, 360-7, 2005.

WHO Report.World Health Organization, Geneva, WHO/EDM/TRM/2002; 21, 19.

Perumal PC, Sophia D, Raj CA, Ragavendran P, Starlin T, Gopalakrishnan VK. In vitro antioxidant activities and HPTLC analysis of ethanolic extract of Cayratia trifolia (L.), Asian Pacific Journal of Tropical Disease 2012; 2, S952-S956.

Dhanamani M, Lakshmi Devi S and Kannan S. Ethno medicinal plants for cancer therapy, Journal of Drug and Medicine 2011; 3, 1-10.

Albuquerque ESB, Neves LJ. Anatomia foliar de Alpinia zerumbet (Pers.) Burtt & Smith (Zingiberaceae), Acta Botonica Brasilica 2004; 18,109–121.

Israf DA, Khaizurin TA, Syahida A, Lajis NH, Khozirah S. Cardamonin inhibits COX and iNOS expression via inhibition of p65NF-kappaB nuclear translocation and Ikappa-B phosphorylation in RAW 264.7 macrophage cells. Immunology 2007; 44, 673– 679.

Chen IN, Chang CC, Ng CC, Wang CY, Shyu YT, Chang TL. Antioxidant and antimicrobial activity of Zingiberaceae plants in Taiwan. Plant foods for human Nutrition 2008; 63, 15–20.

Prajapathi ND, Purohit SS, Arun KS, Kumar T. A Handbook of medicinal plants. A complete source Book.India: Agrobios Edn 1, vol. 35, 2003.

Kochuthressia KP, John BS, Joelri ML, Jaseentha MO, Senthilkumar SR. Efficient regeneration of Alpinia purpurata (Vieill.) K.Schum. plantlets from rhizome bud explants. International research journal of plant science 2010; 1, 43-47.

Oliver BV, Allan P, Macabeo G, Dietamer G, Karsten K, Scott GF, Alicia MA. Phytoconstituents from Alpinia purpurata and their in vitro inhibitory activity against Mycobacterium tuberculosis, Pharmacognosy magazine 2010; 6,339-344

Trakranrungsie N, Chatchawanchonteera A, Khunkitti W. Ethnoveterinary study for antidermatophytic activity of Piper betle, Alpinia galanga and Allium ascalonicum extracts in vitro, Research Vetnery Science 2008; 84,80–84.

Arambewela LSR, Arawwawala LDAM, Ratnasooriya WD. Antinociceptive activities of aqueous and ethanolic extracts of Alpinia calcaratarhizomes in rats, Journal of Ethnopharmacology 2004; 95,311– 316.

Kadota S, Tezuka Y, Prasain JK, Ali MS, Banskota AH. Novel diarylheptanoids of Alpinia blepharocalyx, Current Topics Medicinal Chemistry 2003; 3,203–225.

Bendjeddou D, Lalaoui K and Satta D. Immunostimulating activity of the hot water-soluble polysaccharide extracts of Anacyclus pyrethrum, Alpinia galanga and Citrullus colocynthis. Journal of Ethnopharmacology 2003; 88,155–160.

An N, Zou ZM, Tian Z, Luo XZ, Yang SL, Xu LZ. Diarylheptanoids from the rhizomes of Alpinia officinarum and their anticancer activity. Fitoterapia 2008, 79, 27–31.

Arulraj C, Ragavendran P, Sophia D, Rathi MA, Gopalakrishnan VK. Evaluation of in vitro antioxidant and anticancer activity of Alpinia purpurata, Chinese Journal of Natural Medicine 2012, 10, 0263-0268.

Victorio CP, Kuster RM, Lage CLS. Detection of flavonoids in Alpinia purpurata (Vieill.) K. Schum. Leaves using high performance liquid chromatography, Revista Brasileira de Plantas Medicinais Botucatu 2009; 11,147-153.

Kreft I, Fabjan N, Yasumoto K. Rutin content in buckwheat(Fagopyrum esculentum Moench.) food materials and products. Food Chemistry 2006; 98, 508-12.

version 5.5. (2012) Schrodinger, LLC, NewYork.

Protein Preparation Wizard Maestro. (2012) Schrödinger LLC, New York.

LigPrep version 2.4. (2012) Schrödinger, LLC, New York.

Glide version 5.6. (2012) Schrödinger, LLC, New York.

QikProp, Version 3.2. (2012) Schrodinger, LLC, New York.

Muller A, Homey B, Soto H, Ge N, Catron D, Buchanan ME, McClanahan T, Murphy E, Yuan W, Wagner SN, Barrera JL, Mohar A, Verastegui, E Zlotnik A. Involvement of chemokine receptors in breast cancer metastasis, Nature 2001, 410:50-6

Nagasawa T, Hirota S, Tachibana K, Takakura N, Nishikawa S, Kitamura Y, Yoshida N, Kikutani H and Kishimoto T. Defects of B-cell lymphopoiesis and bone-marrow myelopoiesis in mice lacking the CXC chemokine PBSF/SDF-1, Nature 1996; 382,635-8

Rani LS, Mohan VR, Regini GS, Kalidass C. GC-MS analysis of ethanolic extract of Pothos scandens leaf, Journal of Herbal Medicinal Toxicology 2009; 3,159–160

Ponnamma SU, Manjunath K. GC-MS Analysis of phytocomponents in the methanolic extract of Justicia wynaadensis (nees) T. anders, International Journal of pharma and bio sciences 2012, 3,570–576

Uma B, Prabhakar K, Rajendran S, Sarayu LY. Studies on GC/MS spectroscopic analysis of some bioactive antimicrobial compounds from Cinnamomum zeylanicum. Journal of Medicinal Plants 2009; 8:125–131

Liao JK. Clinical implications for statins pleiotropy. Current Opinion Lipidology 2005; 16,624–629

Steinberg D, Avigan J, mize CE, Baxter JH, Cammermeyer J, Fales HM. Effects of dietary phytol and phytanic acid in animals. Journal of lipid Research 1966; 7,684-691

Bodoprost J , Rosemeyer H. Analysis of phenacylester derivatives fatty acids from human skin surface sebum by reversed-phase HPTLC: chromatographic mobility as a function of physicochemical properties, International Journal of Molecular Sciences 2007; 8,1111-1124.

Nagavamsikrishna A, Ramgopal M, Venkarataman B Balaji M. Anti diabetic efficancy of ethanolic extract of Phragmites vallatoria on STZ induced diabetic rats, International Journal of pharmacy and pharmaceutical sciences 2012; 4,118-12.

Noordman WH, Janssen DB. Rhamnolipid stimulates uptake of hydrophobic compounds by Pseudomonas aeruginosa, Applied environmental microbiology 2002; 68, 4502-4508.

Dennison SM, Greenfield N, Lenard J, Lentz BR. VSV transmembrane domain (TMD) peptide promotes PEG-mediated fusion of liposomes in a conformationally sensitive fashion, Biochemistry 2002; 41, 14925-14934.

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