天美传媒

Staphylococcus; Naphthoquinone; Anthraquinones; Tumour promotion; Cell cycle; Carcinoma cells

Introduction

Compound 1 has been isolated from the roots of Cratoxylum formosum, the leaves of Symphonia globulifera, and the seeds of Vismia laurentii. The only reported natural source of compound 2 is Newbouldia laevis in which it can be isolated from the roots. Compound 3 is a key active ingredient of the ethanol extract from roots of Chinese rhubarb that has been commercialised in China for controlling powdery mildews. Compound 3 was purified from several plants including Rumex japonicus, Radix Boehmeriae, Discocleidion rufescens, Senna septemtrionalis, etc. Compounds 4 and 5 are mostly found in plants of the genus Vismia, whilst compound 6 was reported in Vimia laurentii and Psorospermum species. Compounds previously showed antimicrobial activities against a panel of bacteria and fungi compound exhibited antibacterial activities against Chlorella fusa and Bacillus megaterium, respectively and compound 1 showed antileishmanial and cytotoxic activities against HeLa, HT-29 and KB cell lines [1]. Compound 1 also exhibited significant antibacterial activities on Pseudomonas aeruginosa, Bacillus cereus, Staphylococcus aureus, Streptococcus faecalis and Salmonella typhi with minimal inhibitory concentration below 10μg/ml. In the present work, we examined at first, the cytotoxicity of compounds 1–6 against MiaPaCa-2, CCRF-CEM, and CEM/ADR5000 cell lines, then we selected compounds 1 and 2 which were tested on a panel of cancer cells. Their possible modes of action were also investigated and reported herein [2]. The six naturally occuring compounds tested included one xanthone named xanthone V1 and five quinones amongst which were three anthraquinones known as physcion ; vismiaquinone and 1,8-dihydroxy-3-geranyloxy-6- methylanthraquinone, one naphthoquinone known as 2-acetylfuro-1,4- naphthoquinone and one binaphthoquinone named bisvismiaquinone. The four studied naphtoquinones have compound 3 as the basic moiety. The preliminary cytotoxicity of the six studied compounds on CCRF-CEM, CEM/ADR5000 and MiaPaca-2 is summarized in [3]. Only xanthone V1 and 2-acetylfuro-1, 4-naphthoquinone as well as doxorubicin were able to reduce the proliferation of the three cell lines by up to 50%, when tested at 20 μg/ml. Physcion was previously found to have no cytotoxic activity on some cancer cell lines such as K562, HeLa, Calu-1, Wish and Raji and was not significantly active as observed in the present work. However, the low activity of 8-dihydroxy- 3-geranyloxy-6-methylanthraquinone, as well as bisvismiaquinone and vismiaquinone also bearing physcion moiety clearly highlights the low cytotoxicity of the studied anthraquinones [4]. It can be deduced that the best cytotoxic activity of the studied compounds were obtained with the tested xanthone and naphthoquinone. Xanthone V1 and 2-acetylfuro-1,4-naphthoquinone were therefore selected and tested on several cancer cells. The IC50 values obtained are reported in and values below 20 μg/ml were recorded on 12 of the 14 tested cancer cell lines for xanthone V1 and 14/14 for 2-acetylfuro-1,4-naphthoquinone.

Methodology

Considering the cut-off points of 4 μg/ml or 10 μM for good cytotoxic compounds, values around or below this set point were obtained by xanthone V1 on 9/14 tested cancer cell lines and 11/14 for 2-acetylfuro-1,4-naphthoquinone [5]. The most sensitive cell lines were breast MCF-7 and cervix HeLa and Caski, leukemia PF- 382 and melanoma colo-38. The liver is the main organ involved in drug metabolism. Therefore AML12 hepatocyte was chosen in the present work to evaluate the cytotoxicity of the compounds on non- cancer cells. Interestingly, the two compounds were generally less toxic on AML12 cells, the IC50 being above 20 μg/ml [6]. In addition, the two compounds showed respectively, 65.8% and 59.6% inhibition of the growth of blood capillaries on the chorioallantoic membrane of quail eggs in the anti-angiogenic assay, suggesting that negative effect on tumour promotion in vivo could be expected. To the best of our knowledge, the anticancer activity of 2-acetylfuro-1, 4-naphthoquinone is being reported herein for the first time meanwhile the cytotoxicity of xanthone V1 was reported on HeLa, HT-29 and KB cell lines as shown in (Figure 1).

Figure 1: Cell lines.

This study thus confirms the cytotoxic potency of xanthone V1 on a large number of cancer cell lines [7]. The effects on xanthone V1 and 2-acetylfuro-1, 4-naphthoquinone on the cell cycle distribution, apoptosis induction and caspase 3/7 activity were investigated in CCRF-CEM cell line. Xanthone V1 was able to induce cell cycle arrest at higher concentration. At 2×IC50, the cell number in S-phase gradually increased with time upon treatment with xanthone V1, and the highest amount was observed after 72 h, suggesting a cycle arrest at this phase [8]. Up to 8.51% and 10.53% apoptotic cells were observed after 72 h upon treatemnt of CCRF-CEM cells with xanthone V1 at IC50 and 2×IC50, respectively. This result is in accordance with the activation of caspases 3/7, though the effect at 2×IC50 was less than that obtained at a concentration corresponding to IC50 value [9]. This is obviously due to the fact that, despite the activation of caspase induced by this compound, the ratio of cell number-activity might still be better at IC50 than at 2×IC50. 2-acetylfuro-1,4-naphthoquinone induced cell cycle arrest in S-phase when tested at 2×IC50 and IC50 values in a time- dependant manner. This compound induced apoptosis, eventhough without caspase 3/7 activation. This suggests that the activation of caspase might not be the main pathway for apoptosis induction by 2-acetylfuro-1,4-naphthoquinone.The overall results of the present work highlight the anticancer potency of xanthone V1 and 2-acetylfuro- 1,4-naphthoquinone, and clearly justify the fact that all compounds with any pharmacological activity should also be evaluated for its cytotoxicity. The most sensitive cancer cell lines to xanthone V1 and 2-acetylfuro-1, 4-naphthoquinone was Colo-38, HeLa and Caski with IC50 values being closer or lower those obtained with doxorubicin. In addition, MCF-7 and PF-382 also showed high sensitivity to xanthone V1 and 2-acetylfuro-1, 4-naphthoquinone respectively [10]. The cytotoxicity of acetylfuro-1,4-naphthoquinone is being reported for the first time. Regarding the medical impact of these cancers, the activities of these two molecules could be considered as very important. In fact, breast cancer is the most frequently diagnosed cancer and the leading cause of cancer death among females worldwide, accounting for 23% of the total cancer cases and 14% of the cancer deaths, meanwhile cervix and colon cancers are also amongst the most common cancer in economically developing and developed world respectively. Cell lines were obtained from different sources; Prof. Axel Sauerbrey, University of Jena, Jena, Germany: CCRF-CEM, CEM/ADR5000, HL- 60; German Collection for Microorganisms and Cell Culture (DSMZ), Braunschweig, Germany: PF-382; Dr. Jörg Hoheisel, DKFZ, Heidelberg, Germany: MiaPaCa-2, Capan-1 pancreatic adenocarninoma, MCF-7 breast adenocarcinoma, SW-680 colon carcinoma cells; Tumor Bank, German Cancer Research Center, Heidelberg, Germany: 786-0 renal carcinoma cells, U87MG glioblastoma-astrocytoma cells, A549 lung adenocarcinoma, Caski and HeLa cervical carcinoma cells, Colo-38 skin melanoma cells; ATCC, USA: AML12 hepatocytes [11].

Discussion

A panel of fourteen cancer cell lines including human CCRF- CEM leukemia cells and their multidrug-resistant subline, CEM/ ADR5000, PF-382 leukemia T-cells, and HL-60 promyelocytic leukemia, MiaPaCa-2 and Capan-1pancreatic adenocarninoma, MCF- 7 breast adenocarcinoma, SW-680 colon carcinoma cells, 786-0 renal carcinoma cells, U87MG glioblastoma-astrocytoma cells, A549 lung adenocarcinoma, Caski and HeLa cervical carcinoma cells, Colo- 38 skin melanoma cells, as well as AML12 hepatocytes, were used. CCRF-CEM, CEM/ADR5000 and MiaPaCa-2 cells were used for the preliminary assay and the most actives compounds were tested on other cell lines. Leukemia cells were maintained in RPMI 1640 containing 100 units/ml penicillin and 100 μg/ml streptomycin and supplemented with heat-inactivated 10% fetal bovine serum. All cultured cells were maintained in a humidified environment at 37°C with 5% CO2. Doxorubicin was used as a positive control [12]. The concentration of DMSO was not greater than 0.1% in all experiments. Alamar Blue or Resazurin reduction assay was used to assess the cytotoxicity of the studied samples. The assay tests cellular viability and mitochondrial function. Briefly, adherent cells were grown in tissue culture flasks, and then harvested by treating the flasks with 0.025% trypsin and 0.25 mM EDTA for 5 min. Once detached, cells were washed, counted and an aliquot was placed in each well of a 96-well cell culture plate in a total volume of 100 μl. Cells were allowed to attach overnight and then treated with samples. The final concentration of samples ranged from 20-0.16 μg/ml. After 48 h, 20 μl resazurin 0.01% w/v solution was added to each well and the plates were incubated at 37°C for 1–2 h. Fluorescence was measured on an automated 96-well Infinite M2000 Pro™ plate reader using an excitation wavelength of 544 nm and an emission wavelength of 590 nm. For leukemia cells, aliquot of 5×104 cells/ml were seeded in 96-well plates, and extracts were added immediately. After 24 h incubation, plates were treated with resazurin solution as above mentioned. Doxorubicin was used as positive control [13]. Each assay was done at least three times, with two replicates each. The viability was compared based on a comparison with untreated cells as shown in (Figure 2).

Figure 2: Cancer cells.

Natural products are well recognized as sources of drugs in several human ailments. In the present work, we carried out a preliminary screening of six natural compounds, xanthone V1; 2-acetylfuro- 1,4-naphthoquinone; physcion; bisvismiaquinone; vismiaquinone; 1,8-dihydroxy-3-geranyloxy-6-ethylanthraquinone against MiaPaCa-2 pancreatic and CCRF-CEM leukemia cells and their multidrug- resistant subline, CEM/ADR5000. Compounds 1 and 2 were then tested in several other cancer cells and their possible modes of action were investigated. The tested compounds were previously isolated from the Cameroonian medicinal plants Vismia laurentii and Newbouldia laevis. The preliminary cytotoxicity results allowed the selection of xanthone V1 and 2-acetylfuro-1,4-naphthoquinone, which were then tested on a panel of cancer cell lines [14]. The study was also extended to the analysis of cell cycle distribution, apoptosis induction, caspase 3/7 activation and the anti-angiogenic properties of xanthone V1 and 2-acetylfuro-1,4-naphthoquinone. IC50 values around or below 4 μg/ ml were obtained on 64.29% and 78.57% of the tested cancer cell lines for xanthone V1 and 2-acetylfuro-1, 4-naphthoquinone, respectively. The most sensitive cell lines were breast MCF-7, cervix HeLa and Caski, leukemia PF-382 and melanoma colo-38. The two compounds showed respectively, 65.8% and 59.6% inhibition of the growth of blood capillaries on the chorioallantoic membrane of quail eggs in the anti- angiogenic assay. Upon treatment with two fold IC50 and after 72 h, the two compounds induced cell cycle arrest in S-phase, and also significant apoptosis in CCRF-CEM leukemia cells. Imaging of the vascularized quail eggs was performed using a digital camera with 3×-magnification objective. For illumination, a mercury-arc-lamp was used which provided a high fraction of blue and UV-light to obtain good contrast values between yolk and vessels. The pictured image section had a size of 5×5 mm. Following image acquisition, quantitative analysis was performed using a software routine which was written in the Image J-macro language, and the total small vessels number was then determined by the system. The percentage inhibition of vascularization was calculated as previously described.

Conclusion

The overall results of the present study provided evidence for the cytotoxicity of compounds xanthone V₁ and 2-acetylfuro-1, 4-aphthoquinone, and bring supportive data for future investigations that will lead to their use in cancer therapy.

Acknowledgement

None

Conflict of Interest

None

1. Saarinen R (2006) . OSO UK : 29-257

,

2. Rovner MH (2005) . Health Expect US 8: 1-3.

, ,

3. Marc EL, Chris B, Arul C, David F, Adrian H, et al. (2005) . Breast Cancer Res Treat EU 90: 1-3.

Indexed at, ,

4. Casamayou MH (2001) . GUP US: 1-208.

  ,

5. Baralt L, Weitz TA (2012)  . WHI EU 22: 509-512.

       , ,

6. Kline KN (1999) , J Health Commun UK: 119-141.

 

     , ,

7. Keller C (1994) . J Fem Stud Relig USA 10: 53-72.

,

8. Hamashima C, Shibuya D, Yamazaki H, Inoue K, Fukao A, et al. (2008) . Jpn J Clin Oncol UK 38:259-267.

  , ,

9. Sabatino SA, White MC, Thompson TD (2015) . MMWR US 64:464-468.

  ,     

10. Brawley OW, Kramer BS (2005) . J Clin Oncol US 23:293-300.

  ,

11. Warner E (2011) .  N Engl J Med US 365: 1025-1032.

  ,

12.  Berwick DM (1998) . Ann Intern Med US 128: 651-656.

, ,

13. Connor BO (2000) Routledge UK: 1-279.

,

14. Lynch K (2019) . Society 56: 550-554.

  , ,