Int J Curr Pharm Res, Vol 10, Issue 2, 81-85Original Article

ANTI CANCER STUDIES OF SELECTIVE MANNICH BASES BY IN SILICO METHOD

L. MURUGANANDAMa*, MAHESWARI R.a

aDepartment of Chemistry, Saranathan College of Engineering, Tiruchirappalli, India
Email: muruganandam-che@saranathan.ac.in

Received: 25 Dec 2017, Revised and Accepted: 05 Feb 2018


ABSTRACT

Objective: To evaluate the anticancer activities of selective Mannich bases by in silico methods.

Methods: X-ray crystallographic structure of Estrogen receptor protein (PDB ID 2YAT) was downloaded from the protein data bank (PDB) and is docked with the target Mannich bases using Accelyrs Discovery Studio client version 2.5 software.

Results: Based on the in silico analysis results of the target compounds with standard drug tamoxifen, the best-docked compound is identified and its anticancer activity is confirmed by using in vitro MTS analysis using Raju and Jurkat cell lines.

Conclusion: The mannich base compound N-[(Diphenylamino) methyl] acetamide showed fourfold higher activity than standard drug tamoxifen, may be used to overcome the drug resistance of Estrogen receptor protein.

Keywords: Mannich bases, Docking, Estrogen, Anticancer


INTRODUCTION

Docking, a computational tool often provides comprehensive insight into molecular mechanisms of biological processes [1]. The main objective of docking is to determine the best possible conformation of protein-ligand, protein-protein and/or another type of interactions with minimal energy [2]. Such studies give a path to explore novel products rapidly and economically that could be very specific for a particular target [3]. The relationship between chemical structure and biological activity is the basis for designing and synthesis of new drugs [4]. A huge number of papers related to Mannich bases are published in various pharmaceutical journals is the direct evidence of the application of these compounds [5]. They are beta amino ketones prepared by condensation of a compound with active hydrogen(s) with an amine (primary or secondary) and formaldehyde (any aldehyde) [6]. These bioactive leads are used for the synthesis of various clinically useful compounds containing aminoalkyl chain like cocaine, fluoxetine, atropine etc [7]. Mannich bases are known to possess potent activities like anti-microbial, antimalarial, anti-HIV, anti-cancer, anticonvulsant activities and so forth [8]. Mannich bases have remarkable biological potential which is remaining unexplored. However, our work would expectantly shed light on anticancer activities of specific Mannich bases.

Estrogens, natural hormones are important in sexual development and other body functions. Before menopause, they are produced mainly in the ovaries. After menopause, they are produced mainly in fat tissue. Women who begin menstruating early, or who start menopause late, produce more estrogen over their lifetimes and have a higher risk of breast cancer. A high level of estrogen is linked with increased risk of breast cancer which mediates its biological effects such as genesis, malignant progression, cell apoptosis and other important roles by binding to the Estrogen Receptor present in the breast cancer cells [9]. The Estrogen Receptor mainly exists in two forms: Estrogen Receptor alpha and Estrogen Receptor Beta. The major causes of breast cancer are identified by abnormal expression of Estrogen Receptor α-positive affecting about 70% of the primary breast cancer patients [10]. The Estrogen Receptor alpha plays a pivotal role in controlling transcription of nuclear DNA necessary for mammary gland development [11] and it is also an essential factor for breast cancer signalling network [12]. It also regulates cell proliferation and differentiation through a paracrine mechanism [13] hence, the inhibition of Estrogen Receptor has become a major approach for preventing and treating breast cancer [14]. The drugs which are currently used, for the treatments of breast cancer interferes with either estrogen production or estrogen action which causes so many side effects such as blood clots, strokes, uterine cancer, or cataracts[15] The side effects of the currently used drug made us to explore an alternative approach to finding out new drug compound which are having anti-breast cancer So, we proposed to examine the anticancer activity of the synthesized Mannich bases against Estrogen receptor protein (PDB ID 2YAT) by molecular docking studies.

MATERIALS AND METHODS

In silico anticancer screening

The docking study was performed using Accelyrs Discovery Studio client version 2.5software. The X-ray crystallographic structure of Estrogen receptor protein (PDB ID 2YAT) was downloaded from the protein data bank (PDB). A grid-based molecular docking method, C-DOCKER algorithm was used to dock the synthesized molecules into the protein active site. The designed structures were submitted to CHARMm (Chemistry at ARvard Macromolecular Mechanics) force field for structure refinement. All water molecules, bound inhibitor and other heteroatoms were removed from the macromolecule and polar hydrogen atoms were added. Energy minimization was carried out for all compounds using CHARMm force field to make stable conformation of the protein. A final minimization of the ligand in the rigid receptor using non-softened potential was performed. For each final pose, the CHARMm energy (interaction energy plus ligand strain) and the interaction energy alone were calculated. The poses were sorted by CHARMm energy and the top scoring (most negative, thus favorable to binding) poses.

In vitro anticancer screening

With the help of docking results obtained, the compound showing best anticancer activity was identified. In order to confirm the same, in vitro MTTS assay method was performed for the best-docked compound.

Cell lines

Two cell lines manely Raji and Jukart were chosen. The number of cells is massively expanded in a minimal number of passages, and the cells are cryo-preserved to provide a consistent, long-term frozen stock for future use. Cells are grown and passaged in antibiotic-free growth medium to ensure the absence of microbial contaminants [16].

Preparation and inoculation of cells

Cells are separated into single cell suspensions by a gentle pipetting action, then counted using tryphan-blue exclusion on a Hemocytometer or by a counter [17]. After counting, dilutions are done to give the appropriate cell densities for inoculation onto the microtiter plates. Cells were inoculated in a volume of 100 µl per well at densities between 5000 and 4000 cells per well. A 100 µl aliquot of complete medium is added to cell-free wells. Prior to the inclusion of cell lines in the screening panel, their growth and compatibility were determined.

Sample preparation

All the samples were initially solubilized in phosphate buffer saline at 1:1 ratio and were filtered using membrane filter to avoid microbial contamination.

MTT assay

The assay was performed in a 96 well tissue culture plate (Greiner, U. S. A), using various negative controls and positive controls. After the addition of cell, media and solutions of complexes, the cultures were incubated in an incubator (TC2323, Shel lab, U. S. A) with 95% air, 5% CO2 and humidified atmosphere at 37˚C for 72 h. The assay was monitored after 72 h based on spectrophotometer method by using an ELISA reader. After reading the plates, the 10 µl tetrazolium compound MTT was added to the wells and incubated. After the incubation period, the MTT was reduced by mitochondrial dehydrogenase as a result of which the colour changed. Detergent SDS was added to the wells to solubilize the formazan crystals. The absorbance was read by making use of an ELISA reader at 570 nm. The rate of tetrazolium reduction is directly proportional to the rate of cell proliferation [18].

RESULTS AND DISCUSSION

The docking results of Mannich bases and tamoxifen with Estrogen receptor protein (PDB ID 2YAT) were depicted in table 1 and their interactions with the active site of a target protein are given in fig. 1-7.

Table 1: CDOCKER energy results of docked compounds

S. No. Compound name CDOCKER energy
1 N-[(Diphenylamino)methyl]acetamide -29.2172
2 N-[(Diphenylamino)methyl]acrylamide -27.1711
3 N-[Morpholino(phenyl)methyl]acetamide -24.4197
4 [Morpholino(phenyl)methyl]benzamide -23.1426
5 N-[Phenyl(pyrrolidin-1-yl)methyl]acetamide -16.5583
6 N-[Phenyl(pyrrolidin-1-yl)methyl]benzamide -12.7149
7 Tamoxifen -7.62965

Fig. 1: Interaction details of N-[(diphenylamino)methyl]acetamide with active site amino acids of 2YAT receptor

Fig. 2: Iinteraction details of N-[(diphenylamino)methyl]acrylamide with active site amino acids of 2YAT receptor

Fig. 3: Interaction details of N-[morpholino(phenyl)methyl]acetamide with active site amino acids of 2YAT receptor

Fig. 4: Interaction details of [morpholino(phenyl)methyl]benzamide(MBB) with active site amino acids of 2YAT receptor

Fig. 5: Interaction details of N-[phenyl(pyrrolidin-1-yl)methyl]acetamide with active site amino acids of 2yat receptor

Fig. 6: Interaction details of N-[phenyl(pyrrolidin-1-yl)methyl]benzamide (PBB) with active site amino acids of 2YAT receptor

Fig. 7: Interaction details of tamoxifen with active site amino acids of 2YAT receptor

In this study, tamoxifen used as a standard ligand for comparison of docked compounds results. Tamoxifen is a nonsteroidal triphenylethylene derivative that binds to the estrogen receptor. It has both estrogenic and antiestrogenic actions, depending on the target tissue. It is strongly antiestrogenic on the mammary epithelium, hence its use in both the prevention and treatment of breast cancer; it is proestrogenic on the uterine epithelium, hence the current controversy regarding its safety in cancer prevention especially since an increased incidence of endometrial carcinoma has been found in women treated chronically with tamoxifen. Tamoxifen shown CDOCKER energy of-7.62965 kcal/mole-1. It means the tamoxifen shown lower binding affinity with 2YAT protein compared with our compounds. There is no hydrogen bond involved between tamoxifen and receptor. Only one Pi-Pi interaction was involved in between phenyl ring of the tamoxifen and His524. Additionally, several electrostatic and Van der waal’s interaction are involved to make binding affinity of tamoxifen. The docking results of compounds with active site amino acids of 2YAT receptor were showed better binding interaction. In particular, the binding affinity of the N-[(Diphenylamino) methyl] acetamide was found four-fold higher than standard. The ketone group of N-[(Diphenylamino) methyl] acetamide molecule formed by one strong hydrogen bond (distance 1.98A °) with Arg 394 residue. To confirm the higher anticancer activity of N-[(Diphenylamino) methyl] acetamide MTT assay was performed by in vitro methods and the results were given in table 2.

Table 2: Anticancer activity against raji and jukart cell lines

Concentration Raji cell line (a) Jurkat cell line (b)
25 0.19 0.23
50 0.19 0.23
100 0.19 0.22
200 0.18 0.22
400 0.18 0.21

(a)Cell Control (CC) = 0.19ng; (b) Cell Control = 0.23ng, Higher absorbance values of the target compound at various concentrations indicate an increase in cells viability of the target compound.

CONCLUSION

The mannich base compound N-[(Diphenylamino) methyl] acetamide showed fourfold higher activity than standard drug tamoxifen, may be used to overcome the drug resistance of Estrogen receptor protein.

AUTHORS CONTRIBUTIONS

All the author have contributed equally

CONFLICT OF INTERESTS

Declared none

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About this article

Title

ANTI CANCER STUDIES OF SELECTIVE MANNICH BASES BY IN SILICO METHOD

Keywords

Mannich bases, Docking, Estrogen, Anticancer

DOI

10.22159/ijcpr.2018v10i2.25877

Date

15-03-2018

Additional Links

Manuscript Submission

Journal

International Journal of Current Pharmaceutical Research
Vol 10, Issue 2 (Mar-Apr), 2018 Page: 81-85

Online ISSN

0975-7066

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Authors & Affiliations

L. Muruganandam
Department of Chemistry, Saranathan College of Engineering, Tiruchirappalli, India

Maheswari R.
Department of Chemistry, Saranathan College of Engineering, Tiruchirappalli, India


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