Printer Friendly

Short Communication - In-vitro Anticancer Activity of Copper (II) and Zinc (II) Complexes with Derived Schiff Base Ligands.

Byline: Qaisar Jamal, Salman Ahmad, Nazma Habib Khan, Sobia Wahid, Muhammad Ikram, Sadia Rehman, Syed Basit Rasheed and Akram Shah

Abstract

Derivatives of Schiff bases have been considerably screened for their anticancer potential. We aimed to investigate in-vitro anticancer activity of two transition metal compounds of derived Schiff bases; NM-3 (Tetrakis (2-{(E)-[(2- {[(Z)-(2-hydroxynapthyl) methylidene]amino} phenyl)imino] methyl}phenol) Copper(II) and NM-4 (Tetrakis (2-{(E)-[(2- {[(Z)-(2-hydroxynapthyl) methylidene] amino}phenyl)imino]methyl} phenol) zinc(II)), against human THP-1 leukemia cell line in-relation to miltefosine (standard chemotherapy). Mean % inhibition for NM-3 against THP-1 was higher than NM-4, although both were less effective than miltefosine. IC50 for miltefosine, NM-3 and NM-4 against THP-1was 0.000347uM, 44.9uM and 119uM; whereas, their cytotoxicity was 72.26uM, 255uM and 293.8uM, respectively against peripheral blood lymphocytes. Based on the findings of present study the compounds can be put in to list of candidacy for anticancer activity.

Key words

Schiff base ligands, Anti-cancer activity, THP1 cells.

Cancer treatment typically consists of surgery, radiations, chemotherapy or a combination of these. Chemotherapy remains the mainstay means for treatment of malignancies either by cytotoxicity or cytostasis. DNA damage and subsequent induction of apoptosis is the primary mechanism of cytotoxic drugs like antimetabolites and alkylating agents (Rixe and Fojo, 2007). Most of these chemotherapeutic agents suffer from poor therapeutic index. Genotoxic effects of anticancer drugs to normal cells are considered one of the most serious issues of chemotherapy, possibly due to risk of inducing secondary malignancies. Their side effects may vary with the formulation used, its dosage, duration of treatment and immune status of patient (Partridge et al., 2001). Although active cancer research has led to a number of novel and targeted solutions, many have clear limitations and there is still a dire need for discovering potent, safe and selective anticancer agents (Shashidhara et al., 2010).

Pyrimidinyl Schiff bases are indicated for their in-vitro antitumor activity (Osowole et al., 2010). In this study we aimed to assess the anti-cancer activity and associated cytotoxicity by two novel synthetic derivatives of Schiff bases namely NM-3 (Tetrakis(2-{(E)-[(2-{[(Z)-(2-hydroxynapthyl)methylidene]amino}phenyl)imino] methyl}phenol)Copper(II) and NM-4 (Tetrakis(2-{(E)-[(2-{[(Z)-(2-hydroxynapthyl)methylidene]amino}phenyl) imino]methyl}phenol)zinc(II)) (Fig. 1) in-comparison to the standard drug miltefosine (Zentaris, Frankfurt, Germany) on THP-1 leukemia cell line. Cytotoxic effects of these drugs were assessed using peripheral blood lymphocytes (PBLs) as a control cell line.

Materials and Methods

PBLs were isolated from fresh blood of a healthy volunteer using density gradient centrifugation. Four serially diluted concentrations of each compound (100uM, 75uM, 50uM, and 25uM) were tested for their in-vitro activity against THP-1 cells. The study methods were approved by Ethics Committee University of Peshawar. About 6 x 104 THP-1 cells/ml were re-suspended in RPMI-1640 (Sigma Aldrich, UK) growth medium and counting was done via haemocytometer after 24, 48 and 72 h. Viability of cells was determined using trypan blue exclusion technique. THP-1 cells, with 96 percent viability, were plated at 5x104cells/200 uL medium/well in 96 well flat-bottom micro titer plate. Each drug was applied in 4 concentrations in triplicate. Cells were incubated in humidified carbon dioxide incubator with 5% CO2 at 37AdegC. The test formulations were then applied on peripheral blood lymphocytes (PBLs) under the same conditions as described for THP1 cells.

Cells (THP-1 and PBLs) were counted after 48 h after trypan blue exclusion. Percentage inhibition was interpreted by viable cell count (Lavanya et al., 2010) using:

% Inhibition = Treated - Control / Control x 100

IC50 values for each concentration of NM-3, NM-4 and miltefosine were estimated in GraphPad Prism (V.4) by non-linear sigmoidal curve-fitting of cell-line's %inhibition versus log-transformed drug concentration values (Miller, 2003). Therapeutic index (TI) was also calculated. TI is a simple ratio of 50% toxic concentration to macrophages to 50% efficacy concentration against cells and is a better parameter for such comparisons (Grogl et al., 2013).

Results and discussion

Both the test compounds in our study showed a concentration dependent inhibition of the THP1 cells.

Table I.- Percent inhibition and IC50 values of compounds onTHP1 and PBLs.

Formulation###IC50 (uM)###IC50 (uM)###Therapeutic

###THP1###PBLs###index

###(95%CI*)###(95%CI)###(TI)

NM-3###44.91###255###5.67

###(0.06-3.27x104) (0.87-7.48x104)

NM-4###119.7###293.8###2.45

###(0.14-1.05 x104) (0.15-5.95x104)

Miltefosine###0.000347###72.26###2.07x105

NM-3 demonstrated an effective growth inhibition of 79.3%, 88.9%, 92.3% and 97.3% at 100uM, 75uM, 50uM, and 25uM, respectively (Fig. 2). In-vitro anti-cancer effect of NM3 and NM4 on THP1 and toxicity in PBLs control cell line was evaluated in terms of IC50s (Table I). NM3 proved to be a more potent formulation (IC50=44.99uM) compared to NM4 (IC50=119.7uM), although with an efficacy less than miltefosine (IC50=0.000347uM). Metal complexes of Schiff base ligands have been demonstrated to exhibit improved biopotency than the free ligands (Kumar-Naik et al., 2014). Many have been tested for their bioactivity as antioxidants, antimicrobials (Singh, et al., 2007) and anticancer activity against certain types of leukemia (Aliyu and Ado, 2011; Srivastva et al., 2014).

Cu (II) and Pd (II) complexes of these bases are demonstrated to be effective against MCF-7 (human breast adenocarcinoma) and HT-29 (colon carcinoma) cell lines (Osowole and Akpan, 2012). Fluorescence and electronic spectra studies indicate that complexes of copper (I), nickel (I) and zinc (I) operate by intercalating DNA. Complexes of copper (I), nickel (I) and zinc (I) have reported cancer inhibition rates of 53.3%, 51.7% and 32.2%, respectively to EAC (Ehrlich ascites carcinoma) in-vivo (Chunhua et al., 1993).

Miltefosine was the most cytotoxic drug with an IC50 of 72.26 in PBLs and a consistently higher % inhibition through all the four studied concentrations. NM4 had the least cytotoxic effect followed by NM3. However, in terms of percent inhibition, at higher concentrations NM4 showed higher cytotoxicity than miltefosine (Table I; Fig. 2). Though the MN3 and MN4 show much higher IC50 values than the standard drug, their cytotoxicity is much less than the standard drug. Considering the lower cytotoxicity, the compounds get at least to the list of candidacy at this stage of experimentation. The standard being with higher toxicity is still used as a drug. Other studies like Dorlo et al. (2012) have also reported Miltefosine to be causing testicular atrophy and teratogenic effects. Complexes containing zinc and copper ligands are known to show marked cytotoxicity to human promyolicytic leukemia (HL60) cell line (Khoo et al., 2014).

Studies have reported a comparatively higher cytotoxicity of Cu (II) containing complexes to cancer cells (Osowole et al., 2010; Osowole and Akpan, 2012).

As discussed above, derived Schiff base complexes have effectual anticancer activity against leukemia. In this study, copper-containing complex (NM-3) (TI=5.67) apparently showed better performance than the containing zinc (II) (NM-4) (TI=2.45) (Table I). Drug development for cancer, in general, is an area of active research for scientists and pharmaceutical innovationists. Our findings not only present the compounds as potential candidates for anticancer activity, but also prove them less cytotoxic to the normal cells.

Acknowledgments

We are thankful to volunteers and staff at Department of Zoology, University of Peshawar for their unprecedented support.

Statement of conflicts of interest

Authors bear no conflict of interest.

References

Aliyu, H.N. and Ado, I., 2011. Biokemistri, 23: 9-16.

Chunhua, C., Zishen, W. and Zhenhuan, Y., 1993. Synth. React. Inorg. Met. Org. Chem., 23: 1725-1733. https://doi.org/10.1080/15533179308016718

Dorlo, T.P.C., Balasegaram, M., Beijnen J.H. and de Vries P.L., 2012. J. Antimicrob. Chemother., 67: 2576-2597. https://doi.org/10.1093/jac/dks275

Eguzo, K. and Camazine, B., 2012. J. Cancer Sci. Ther., 4: 223-226. https://doi.org/10.4172/1948-5956.1000145

Grogl, M., Hickman, M., Ellis, W., Hudson, T., Lazo, J.S., Sharlow, E.R., Johnson J., Berman, J. and Sciotti, R.J., 2013. Am. J. trop. Med. Hyg., 88: 216-221. https://doi.org/10.4269/ajtmh.11-0812

Khoo, T., Break, M.K., Crouse, K.A., Ibrahim, M., Tahir, M.I.M., Ali, A.M., Cowley, A.R., Watkin, D.J. and Tarafder, M.T.H., 2014. Inorg. Chim. Acta, 413: 68-76. https://doi.org/10.1016/j.ica.2014.01.001

Kumar-Naik, K.H., Selvaraj, S. and Naik, N., 2014. Spectrochim. Acta A: Mol. Biomol. Spectrosc., 131: 599-605. https://doi.org/10.1016/j.saa.2014.03.038

Lavanya, R., Maheshwari, S.H., Harish, G., Raj, J.B., Kamali, S., Hemamalani, D., Varma, J.B. and Reddy, C.U., 2010. Linn. Res. J. Pharm. Biol. Chem. Sci., 1: 737-744.

Miller, J.R., 2003. GraphPad Prism Version 4.0. Step-by-step examples. GraphPad Software Inc., San Diego, CA.

Osowole, A.A. and Akpan, E.J., 2012. Eur. J. appl. Sci., 4; 14-20.

Osowole, A.A., Kempe, R., Schobert, R. and Balogun, S.A., 2010. Can. J. Pure appl. Sci., 4: 1169-1178.

Partridge, A.H., Burstein, H.J. and Winer, E.P., 2001. J. natl. Cancer Inst. Monogr., 30: 135-142. https://doi.org/10.1093/oxfordjournals.jncimonographs.a003451

Rixe, O. and Fojo, T., 2007. Clin. Cancer Res., 13: 7280-7287. https://doi.org/10.1158/1078-0432.CCR-07-2141

Shashidhara, K.V., Kumar, A., Kumar, M., Sarkar, J. and Sinha, S., 2010. Bioorg. Med. Chem. Lett., 20: 7205-7211. https://doi.org/10.1016/j.bmcl.2010.10.116

Singh, K., Barwa, M.S. and Tyagi, P., 2007. Eur. J. med. Chem., 42: 394-402. https://doi.org/10.1016/j.ejmech.2006.09.021

Srivastva, A.N., Singh, N.P. and Shriwastaw, C.K., 2014. J. Serb. Chem. Soc., 79: 421-433. https://doi.org/10.2298/JSC130123148S
COPYRIGHT 2018 Asianet-Pakistan
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Publication:Pakistan Journal of Zoology
Article Type:Report
Date:Dec 31, 2018
Words:1739
Previous Article:Short Communication - Detection and Characterization of Clostridium perfringens Serotype D from Small Ruminants of Balochistan.
Next Article:Short Communication - Storage of Bacteriophages at 4AdegC Leads to no Loss in Their Titer after One Year.
Topics:

Terms of use | Privacy policy | Copyright © 2020 Farlex, Inc. | Feedback | For webmasters