Duus, Fritz

Le, Hoang Giau

Ngo, Duong Thuy Thi

Nguyen, Kim Phi Phung

Nguyen, Nha To

Pham, Tuyen Kim Nguyen

Ton, Quang That

English

Roskilde Universitet

RoskildeUniversityBiological test against breast adenocarcinoma cells (MCF-7) of acylated products of 3-methyl-4-thiorhodanineLe, Hoang Giau; Nguyen, Nha To; Ngo, Duong Thuy Thi ; Ton, Quang That; Nguyen, Kim PhiPhung; Pham, Tuyen Kim Nguyen; Duus, FritzPublished in:Journal of Science & Technology DevelopmentPublication date:2015Document VersionPublisher's PDF, also known as Version of recordCitation for published version (APA):Le, H. G., Nguyen, N. T., Ngo, D. T. T., Ton, Q. T., Nguyen, K. P. P., Pham, T. K. N., & Duus, F. (2015).Biological test against breast adenocarcinoma cells (MCF-7) of acylated products of 3-methyl-4-thiorhodanine.Journal of Science & Technology Development, 18(T1), 63-69.General rightsCopyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright ownersand it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights.            • Users may download and print one copy of any publication from the public portal for the purpose of private study or research.            • You may not further distribute the material or use it for any profit-making activity or commercial gain.            • You may freely distribute the URL identifying the publication in the public portal.Take down policyIf you believe that this document breaches copyright please contact rucforsk@ruc.dk providing details, and we will remove access to thework immediately and investigate your claim.Download date: 02. Dec. 2021TAÏP CHÍ PHAÙT TRIEÅN KH&CN, TAÄP 18, SOÁ T1 - 2015 Trang 63 Biological test against breast adenocarcinoma cells (MCF-7) of acylated products of 3-methyl-4 thiorhodanine    Lê Hoàng Giàu  Nguyễn Tô Nhã  Ngô Thị Thùy Dương  Tôn Thất Quang  Nguyễn Kim Phi Phụng University of Science, VNU-HCM  Phạm Nguyễn Kim Tuyến Sai Gon University   Fritz Duus  Roskilde University, Denmark      (Received on January 5 th 2015, accepted on June 22  th 2015) ABSTRACT Rhodanine and its derivatives are not only valued for their interesting chemical properties but also present a wide range of bioactivities and their chemical and pharmacological applications have been investigated. From 3-methyl-4-thiorhodanine we synthesized S-acylated and C-acylated products using (some) carboxylic acid chlorides and the obtained products were studied the anti-proliferative activity by a SRB (sulforhodamine B) assay against a human breast cancer cell line. The results showed that C-acylated products are better inhibitors than S-acylated products.  Key words: 3-methyl-4-thiorhodanine, 2-thioxo-1,3-thiazolane-4-one, C-acylated, S-acylated, breast cancer cell line (MCF-7).  INTRODUCTION Rhodanine derivatives have been proven to be attractive compounds due to their outstanding biological activities and have undergone rapid development as anticonvulsant, antibacterial, antiviral, and antidiabetic agents. At the same time, these have also been reported as Hepatitis C virus (HCV) protease inhibitors and used as inhibitors of uridine diphospho-N-acetylmuramate/L-alanine ligase. Recently, substituted rhodanines were investigated for the aggregation inhibitor properties. Rhodanines are classified as nonmutagenic and a long-term study on the clinical effects of the rhodanine-based Epalrestat as an anti-diabetic, demonstrated that it is well tolerated. Additionally, rhodanines have been designed as inhibitors of various enzymes such as bacterial  -lactamase and Mur ligases. Rhodanine derivatives were found to have marked mildew-proofing activity. It is interesting to note that the new mildew-proofing agents contain the structureN C SO present in many plant fungicides (tetramethylthiuram disulfide and the salts of dithiocarbamic acid). Due to various possibilities of chemical Science & Technology Development, Vol 18, No.T1- 2015 Trang 64 derivatization of the rhodanine ring, rhodanine-based compounds will probably remain a privileged scaffold in drug discovery. Therefore, the synthesis of these compounds is of considerable interest. Recent studies have revealed that 5-benzylidene-3-ethyl rhodanine induced cytotoxicity in a time- and concentration-dependent manner on leukemic cell line, CEM. [1, 2] Cancer is one of the difficult diseases to be cured, and very few effective drugs are available. The development of novel, efficient, and less toxic anticancer agents remains an important and challenging goal in medicinal chemistry. For specific types of cancer occurring only in women, breast cancer is the second most frequent type of cancer in the world (1.05 million cases) and is by far the most common malignant disease in women (22 % of all new cancer cases) [3]. The MCF-7 human breast cancer cell line has been used as an excellent experimental model to improve the efficacy of different therapies before their use in patients [4]. The SRB (sulforhodamine B) method, as originally developed by Skehan et al. [5] is simple, accurate and yields reproducible results. The cells are briefly washed, fixed and stained with this dye (SRB). The incorporated dye is then liberated from the cells in a Tris base solution. An increase or decrease in the number of cells (total biomass) results in a concomitant change in the amount of dye incorporated by the cells in the culture. This indicates the degree of cytotoxicity caused by the test material. In this paper we report the chemical structures of novel derivatives of 3-methyl-4-thiorhodanine which are different in substituents and structures of carbon side chain. Furthermore, in vitro anticancer activity as well as the structure - activity relationships are described. The drastic influence of different substituents and side chains on the inhibition is shown in detail and could contribute to a deeper understanding of the anticancer properties of these interesting classes of compounds. EXPERIMENTAL Chemistry The acylation of 3-methyl-4-thiorhodanine (3-methyl-1,3-thiazolane-2,4-dithione) with ten aromatic acid chlorides were performed at two different positions: carbon in position 5 and sulfur in position 4, respectively, to afford two different isomers [6]. By using pyridine as base, pure S-acylated products were exclusively obtained for all substituents, on the contrary, with sodium hydroxide as base, the obtained products were pure C-acylated ones for all subsituents (see Figure 1). S-acylated products of 5 aliphatic acid chlorides (XCOCl where X is methyl, ethyl, iso-propyl, tert-butyl and benzyl) with 3-methyl-4-thiorhodanine were also synthesized by the same method. The structures of these compounds were confirmed by their 1H and 13C-NMR spectra.  SNCH3HHS SXOCl12345SNCH3S S12345OHXX= NO2, CF3, Br,       Cl, F, H, CH3,       C(CH3)3, OCH3,       N(CH3)2+SNCH3S S12345HOXSodium hydroxidePyridineC-acylatedS-acylated3-Methyl-4-thiorhodanineDioxane, 80oCCH2Cl2, 0-4oC Figure 1. Chemical structures of the C- and S- acylated products of  3-methyl-4-thiorhodanine by ten aromatic carboxylic acid chlorides TAÏP CHÍ PHAÙT TRIEÅN KH&CN, TAÄP 18, SOÁ T1 - 2015 Trang 65 Cytotoxicity The cytotoxic activity of the products was screened by using the sulforhodamine B colorimetric assay method in the MCF-7 cell line. All the assays were done in Molecular Biological Laboratory- Genetic Department-University of Science- VNU-HCMC.  Cell culture MCF-7 cells were cultured in E’MEM (Eagle's minimal essential medium) media which was supplemented with 10 % fetal bovine serum and the cells were maintained at 37 oC in a 5 % CO2 atmosphere with 95 % humidity [7]. Protocol All adherent cell lines were detached from the culture flasks by addition of 1mL of 0.05 % trypsin-EDTA to make single cell suspensions and viable cells were counted by trypan blue exclusion in a hemacytometer and diluted with medium to give the final concentration. Since the investigated compounds were insoluble in water, they were initially dissolved in DMSO and further diluted with culture medium for analysis. The concentration of DMSO was less than 0.5 % which was found to be non-toxic to the cells. Cells were inoculated at densities 10.000 cells per well and were preincubated for 24hrs  at 37 °C to allow stabilization prior to addition of complexes. Subsequently, the different complexes were incubated for 48 h in an atmosphere of 5 % CO2 and 95 % relative humidity. The end point of the procedure was determined by the sulforhodamine B (SRB) method, as described below.  Briefly, adherent cell cultures were fixed in situ by adding 50 µL of cold 50 % (w/v) trichloroacetic acid (TCA) and incubated during for 60 minutes at 4 °C. The supernatant was then discarded, and the plates were washed five times with deionized water and dried. 100 µL of SRB solution (0.4 % w/v in 1 % acetic acid) was added to each well and incubated for 10 min at room temperature. The plates were air-dried and the bound stain was solubilized with Tris buffer and the optical densities were read on an automated spectrophotometric plate reader at 492 nm and 620 nm. All of the experiments were carried out at least three times [8]. Plate design The components in each well of the control is the same as in each well of sample but positive control is camptothecin 0.01 µg/mL replaced for sample, negative control is complete medium, solvent control has no sample, blank control has no cell.  The growth inhibition was determined by using the following equation       where OD’ = OD492 ‒ OD620  OD  = OD’cell ‒ OD’blank  ODc: OD of 0.25% DMSO ODs: OD of sample  % I =  (1-csODOD) x 100 Science & Technology Development, Vol 18, No.T1- 2015 Trang 66 RESULT AND DISCUSSION  Table 1. In vitro cytotoxicity of obtained products (100 µg/mL) against MCF-7 cells Structure of samples Substituents (X) Code of sample Cell growth inhibition (I %) Mean   SD SNCH3S S12345OHX Aromatic C-acylated products NO2 C1 69.18 3.099 CF3 C2 67.14 4.923 Br C3 68.22 4.205 Cl C4 72.94 2.407 F C5 85.31 2.784 H C6 77.78 1.700 CH3 C7 71.88 3.237 C(CH3)3 C8 70.61 1.444 OCH3 C9 83.26 2.138 N(CH3)2 C10 28.90 4.075 SNCH3S S12345HOX  Aromatic S-acylated products NO2 S1 19.41 5.068 CF3 S2 Not determined * Br S3 27.83 5.589 Cl S4 13.82 3.082 F S5 8.91 3.025 H S6 5.67 4.201 CH3 S7 6.10 5.795 C(CH3)3 S8 12.98 4.754 OCH3 S9 59.73 2.647 N(CH3)2 S10 18.38 2.255 SNCH3S S12345HOX Aliphatic S-acylated products CH3 S11 6.37 11.298 C2H5 S12 -3.85 4.713 CH(CH3)2 S13 0.43 4.849 C(CH3)3 S14 -2.82 7.435 CH2C6H5 S15 7.70 5.479 Camptothecin (Positive control) 38.60  2.551 (*): lack of sample  The cytotoxic activity of the products against the MCF-7 cell line, screened by the SBR assay, expressed as a percentage of cell growth inhibition (I %), are presented in Table 1. In general, tested compounds with a percentage of inhibition higher than 50% may be potential agents for cancer chemoprevention. In Table 1, most of the C-acylated aromatic products (except the substituent N(CH3)2) at 100 µg/ml possess  inhibitive percentages higher than 50 % (67-85 %) indicating a high cytotoxic activity against breast cancer cells. On the contrary, almost all S-acylated aromatic products (except the substituent OCH3) did not show any significant cytotoxicity against MCF-7, and especially, the S-acylated aliphatic products performed a very weak inhibitive TAÏP CHÍ PHAÙT TRIEÅN KH&CN, TAÄP 18, SOÁ T1 - 2015 Trang 67 ability. The observation showed that the disappearance of benzene ring resulted in a reduction of cytotoxicity.  Among the S-acylated products, the one with substituent OCH3 is the most active (59 %). Besides, the C-acylated derivative with substituent OCH3 was also one of the products performing high cytotoxicity (83 %). The presence of a methoxy group on the benzene ring seems to be necessary to produce high cytotoxicity. That result is also in agreement with the comments in some papers [9].  The presence of the dimethylamino group in both C- and S-acylated products induced loss of cytotoxicity (%I was 28.90 % and 18.38 %, respectively). In summary, C-acylated products were always more active than S-acylated products. This result is in agreement with the observation by Matsumoto [10] and some other authors [9] that the presence of  a methoxyl group in the molecule has an important role in the cytotoxic ability.  CONCLUSION In the acylation reaction of 3-methyl-4-thiorhodanine, C- or S-acylated products can be obtained depending on the reaction conditions. We found out the best way to obtain either fully S-acylated or fully C-acylated products. C-acylated products showed strong inhibitory ability and may be potent inhibitors of MCF-7 cell proliferation used for cancer chemoprevention. Therefore the relevance of these results needs to be investigated further. Khảo sát hoạt tính gây độc tế bào ung thư vú (MCF-7) của các dẫn xuất acyl hóa của 3-methyl-4-thiorhodanine   Lê Hoàng Giàu  Nguyễn Tô Nhã  Ngô Thị Thùy Dương  Tôn Thất Quang  Nguyễn Kim Phi Phụng Trường Đại học Khoa học Tự nhiên, ĐHQG-HCM  Phạm Nguyễn Kim Tuyến  Đại Học Sài Gòn  Fritz Duus Trường Đại học Roskilde, Đan Mạch. TÓM TẮT Phản ứng acyl hóa 3-methyl-4-thiorhodanin (2-thioxo-1,3-thiazolan-4-on) bởi các clorur acid có thể xảy ra ở 2 vị trí: C số 5 hay S ở vị trí số 4 để tạo ra sản phẩm là dẫn xuất C-acyl hóa,  S-acyl hóa tùy thuộc vào việc sử dụng loại xúc tác base nào. Trong báo cáo này chúng tôi thử hoạt tính gây độc đối với tế bào ung thư vú (MCF-7) áp dụng trên các dẫn xuất S-acyl hóa và C-acyl hóa đã tổng hợp được và kết quả cho thấy các dẫn xuất C-acyl hóa có hoạt tính Science & Technology Development, Vol 18, No.T1- 2015 Trang 68 gây độc tế bào cao hơn các dẫn xuất S-acyl hóa.  Từ khóa: 3-Methyl-4-thiorhodanin, 2-thioxo-1,3-thiazolan-4-on, S-acyl hóa, C-acyl hóa, tế bào ung thư vú, MCF-7.  REFERENCES [1]. S. Ravi, K.K. Chiruvella, K. Rajesh, V. Prabhu, S.C. Raghavan, 5-Isopropylidene-3-ethyl rhodanine induce growth inhibition followed by apoptosis in leukemia cells, European Journal of Medicinal Chemistry, 45, 2748 (2010). [2]. B.T. Moorthy, S. Ravi, M. Srivastava, K.K. Chiruvella, H. Hemlal, O. Joy, S.C. Raghavan, Novel rhodanine derivatives induce growth inhibition followed by apoptosis, Bioorganic & Medicinal Chemistry Letters, 20, 6297 (2010). [3]. D.M. Parkin, Pathology and genetics of tumors of the breast and female genital organs, Lancet Oncol, 2, 533 (2001). [4]. S. Matsuo, S. Tanako, J. Yamashita, M. Ogawa, Growth inhibition, G1-arrest, and apoptosis in MCF-7 human breast cancer cells by novel highly lipophilic 5-fluorouracil derivatives, Anticancer Res, 12, 1575 (2000). [5]. P. Skehan, R. Storeng, D. Scudiero, A. Monks, J. McMohan, D. Vistica, J.T. Warren, H. Bokesch S. Kenney, M.R. Boyd, New colorimetric cytotoxic assay for anticancer-drug screening, J. Natl. Cancer Inst, 82, 1107 (1990). [6]. N.T. Nhã, Synthesis and biological assay against MCF-7 cell line of S-acylated and C-acylated 3-methyl-4-thiorhodanine, Luận văn Thạc sĩ, Bộ môn Hoá Hữu Cơ, Trường ĐH Khoa Học Tự Nhiên, ĐHQG-HCM (2011). [7]. K.T. Papazisis, G.D. Geromichalos, K.A. Dimitriadis, A.H. Kortsaris, Optimization of the sulforhodamine B colorimetric assay, Journal of Immunological Methods, 208, 151 (1997). [8]. R. Tammy, L. Bush, E.D. Cross Doersen, E.A. Cashman, S.P. Wright, J.H. Zwolshen, G.F. Davis, D.P. Matthews, D.M. Bender, A.J. Bitonti, Clomiphene analogs with activity in vitro and in vivo against human breast cancer cells, Biochemical Pharmacology, 55, 841 (1998). [9]. J.C. Le Bail, F. Varnat, J.C. Nicolasb, G. Habrioux, Estrogenic and antiproliferative activities on MCF-7 human breast cancer cells by flavonoids, Cancer Letters 130, 209 (1998). [10]. K. Matsumoto, Y. Akao,  K. Ohguchi, T. Ito, T. Tanaka, M. Iinumad, Y. Nozawaa, Xanthones induce cell-cycle arrest and apoptosis in human colon cancer DLD-1 cells, Bioorganic & Medicinal Chemistry, 13, 6064 (2005).      TAÏP CHÍ PHAÙT TRIEÅN KH&CN, TAÄP 18, SOÁ T1 - 2015 Trang 69 APPENDIX                                         DMSO 0.25%-Negative control (0.00%)                           Camptothecin - Positive control (38.60%) Appendix 1. Morphological observation of breast cancer cells (MCF-7) of negative and positive control after administration and the percentage of cell growth inhibition                     C5 (85.31 %)                                  C9 (83.26 %)                                        C10 (28.90 %) Appendix 2. Morphological observation of breast cancer cells (MCF-7) after administration of some C-acylated products and the percentages of cell growth inhibition             S6 (5.67 %)      S9 (59.73 %)   S12 (-3.85 %) Appendix 3. Morphological observation of breast cancer cells (MCF-7) after administration of some S-acylated products and the percentages of cell growth inhibition   

Biological test against breast adenocarcinoma cells (MCF-7) of acylated products of 3-methyl-4-thiorhodanine

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Biological test against breast adenocarcinoma cells (MCF-7) of acylated products of 3-methyl-4-thiorhodanine

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