Volume 27, Issue 4 (7-2023)                   IBJ 2023, 27(4): 205-213 | Back to browse issues page


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Pourmollaei S, Farshbaf-Khalili A, Barzegari A, Bastani S, Babaie S, Fattahi* A et al . Anticancer Effect of Enterococcus faecium, Isolated from Vaginal Fluid, on Ovarian Cancer Cells. IBJ 2023; 27 (4) :205-213
URL: http://ibj.pasteur.ac.ir/article-1-3846-en.html
1- Department of Midwifery, Faculty of Nursing and Midwifery, Tabriz University of Medical Sciences, Tabriz, Iran, Department of Midwifery, Faculty of Nursing and Midwifery, Tabriz University of Medical Sciences, Tabriz, Iran
2- Aging Research Institute, Physical Medicine, and Rehabilitation Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran, Aging Research Institute, Physical Medicine, and Rehabilitation Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran
3- Research Center of Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran, Research Center of Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran
4- Womenʼs Reproductive Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran, Womenʼs Reproductive Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
5- Department of Midwifery, Faculty of Nursing and Midwifery, Tabriz University of Medical Sciences, Tabriz, Iran
Abstract:  
Background: Given the association between cervicovaginal microbiota and OVC, we investigated the effect of Enterococcus faecium conditioned medium (CM) on OVC (Caov-4) cells.
Methods: CM was obtained from the bacterium E. faecium isolated from the vagina of healthy women. The Caov-4 cells were treated with varying concentrations of CM that comprised co-cultured bacteria with 0.2, 0.5, 1, 1.5, and 2 OD for 12, 24, and 48 h. The apoptosis and growth of cancer cells were evaluated by 4′,6-diamidino-2-phenylindole (DAPI) staining, flow cytometry, and DNA laddering assay. Moreover, the expression of PTEN, BAX, BCL2, and AKT1 genes were analyzed using real-time PCR. 
Results: The CM at a concentration of 0.5 OD from the cultured bacteria and incubation time of 48 h showed the highest negative effect on the viability of cancer cells. The CM treatment increased DNA fragmentation and also induced apoptosis in Caov-4 cells. Interestingly, CM could decrease the expression of proapoptotic genes were less, while antiapoptotic genes were more than fluorouracil in the presence of CM.
Conclusion: CM of human-derived E. faecium could have an anticancer effect on OVC cells in a concentration- and time-dependent manner. This study demonstrated that E. faecium secretes anticancer substances into the CM, which could directly affect the viability and apoptosis of cancer cells.
* Corresponding Author Address: Department of Midwifery, Faculty of Nursing and Midwifery, Tabriz University of Medical Sciences, Tabriz, Iran

References
1. Torre LA, Trabert B, DeSantis CE, Miller KD, Samimi G, Runowicz CD, Gaudet MM, Jemal A, Siegel RL. Ovarian cancer statistics, 2018. CA: a cancer journal for clinicians 2018; 68(4): 284-296 [DOI:10.3322/caac.21456]
2. Allemani C, Weir HK, Carreira H, Harewood R, Spika D, Wang XS, Bannon F, Ahn JV, Johnson CJ, Bonaventure A. Global surveillance of cancer survival 1995-2009: analysis of individual data for 25 676 887 patients from 279 population-based registries in 67 countries (CONCORD-2). The lancet 2015; 385(9972): 977-1010 [DOI:10.1016/S0140-6736(14)62038-9]
3. Glance A. Ovarian cancer: an overview. Am Fam Physician 2009; 80(6): 609-616
4. Poveda A, Ray-Coquard I, Romero I, Lopez-Guerrero JA, Colombo N. Emerging treatment strategies in recurrent platinum-sensitive ovarian cancer: focus on trabectedin. Cancer treatment reviews 2014; 40(3): 366-375 [DOI:10.1016/j.ctrv.2013.08.001]
5. Nené NR, Reisel D, Leimbach A, Franchi D, Jones A, Evans I, Knapp S, Ryan A, Ghazali S, Timms JF. Association between the cervicovaginal microbiome, BRCA1 mutation status, and risk of ovarian cancer: a case-control study. The lancet oncology 2019; 20(8): 1171-1182 [DOI:10.1016/S1470-2045(19)30340-7]
6. Smyth D, Keogh K. Ovarian cancer risk linked to missing bacteria. Cancer Nursing; 5: 11. doi: 10.7748/cnp.18.5.11.s9 [DOI:10.7748/cnp.18.5.11.s9]
7. Pourmollaei S, Barzegari A, Farshbaf-Khalili A, Nouri M, Fattahi A, Shahnazi M, Dittrich R. Anticancer effect of bacteria on cervical cancer: Molecular aspects and therapeutic implications. Life Sci 2020; 246: 117413. [DOI:10.1016/j.lfs.2020.117413]
8. Dasari S, Kathera C, Janardhan A, Praveen Kumar A, Viswanath B. Surfacing role of probiotics in cancer prophylaxis and therapy: A systematic review. Clin Nutr 2017; 36(6): 1465-1472. [DOI:10.1016/j.clnu.2016.11.017]
9. Javadi L, Ghavami M, Khoshbaten M, Safaiyan A, Barzegari A, Gargari BP. The effect of probiotic and/or prebiotic on liver function tests in patients with nonalcoholic fatty liver disease: a double blind randomized clinical trial. Iran Red Crescent med j 2017; 19(4): e46017. [DOI:10.5812/ircmj.46017]
10. Haghshenas B, Nami Y, Abdullah N, Radiah D, Rosli R, Barzegari A, Yari Khosroushahi A. Potentially probiotic acetic acid bacteria isolation and identification from traditional dairies microbiota. Int j food sci tech 2015; 50(4): 1056-1064. [DOI:10.1111/ijfs.12718]
11. Nowak A, Paliwoda A, Błasiak J. Anti-proliferative, pro-apoptotic and anti-oxidative activity of Lactobacillus and Bifidobacterium strains: A review of mechanisms and therapeutic perspectives. Crit rev food sci nutr 2019; 59(21): 3456-3467. [DOI:10.1080/10408398.2018.1494539]
12. Sharma P, Kaur S, Kaur R, Kaur M, Kaur S. Proteinaceous Secretory Metabolites of Probiotic Human Commensal Enterococcus hirae 20c, E. faecium 12a and L12b as Antiproliferative Agents Against Cancer Cell Lines. Front microbiol 2018; 9: 948. [DOI:10.3389/fmicb.2018.00948]
13. Kakelar HM, Barzegari A, Hanifian S, Barar J, Omidi Y. Isolation and molecular identification of Lactobacillus with probiotic potential from abomasums driven rennet. Food chem 2019; 272: 709-714 [DOI:10.1016/j.foodchem.2018.08.081]
14. Atashpaz S, Khani S, Barzegari A, Barar J, Vahed SZ, Azarbaijani R, Omidi Y. A robust universal method for extraction of genomic DNA from bacterial species. Microbiology 2010; 79(4): 538-542 [DOI:10.1134/S0026261710040168]
15. Thirabunyanon M, Hongwittayakorn P. Potential probiotic lactic acid bacteria of human origin induce antiproliferation of colon cancer cells via synergic actions in adhesion to cancer cells and short-chain fatty acid bioproduction. Appl biochem biotechnol 2013; 169(2): 511-525. [DOI:10.1007/s12010-012-9995-y]
16. Saadat YR, Saeidi N, Vahed SZ, Barzegari A, Barar J. An update to DNA ladder assay for apoptosis detection. BioImpacts 2015; 5(1): 25-28. [DOI:10.15171/bi.2015.01]
17. Chimchang J, Theparee T, Wongein S, Trivirot T, Tanasupawa S, Taweechotipatr M, Wongsatayanon B. Screening of Potential Probiotic Lactic Acid Bacteria with Anticancer Properties. J med assoc thai 2016; 99: S70-S78.
18. Salek F, Mirzaei H, Khandaghi J, Javadi A, Nami Y. Apoptosis induction in cancer cell lines and anti-inflammatory and anti-pathogenic properties of proteinaceous metabolites secreted from potential probiotic Enterococcus faecalis KUMS-T48. Sci rep 2023; 13(1): 7813. [DOI:10.1038/s41598-023-34894-2]
19. Rajoka MSR, Zhao H, Lu Y, Lian Z, Li N, Hussain N, Shao D, Jin M, Li Q, Shi J. Anticancer potential against cervix cancer (HeLa) cell line of probiotic Lactobacillus casei and Lactobacillus paracasei strains isolated from human breast milk. Food funct 2018; 9(5): 2705-2715. [DOI:10.1039/C8FO00547H]
20. Hwang CH, Lee NK, Paik HD. The anti-cancer potential of heat-killed Lactobacillus brevis KU15176 upon AGS cell lines through intrinsic apoptosis pathway. Int j mol sci 2022; 23(8): 4073. [DOI:10.3390/ijms23084073]
21. Li Y, Tong Z, Ling J. Effect of the three Enterococcus faecalis strains on apoptosis in MC 3T3 cells. Oral dis 2019; 25(1): 309-318. [DOI:10.1111/odi.12883]
22. Ding C, Han F, Xiang H, Wang Y, Li Y, Zheng J, Xue W, Ding X, Tian P. Probiotics ameliorate renal ischemia-reperfusion injury by modulating the phenotype of macrophages through the IL-10/GSK-3β/PTEN signaling pathway. Pflüg arch eur j physiol 2019; 471(4): 573-581. [DOI:10.1007/s00424-018-2213-1]
23. Sungur T, Aslim B, Karaaslan C, Aktas B. Impact of Exopolysaccharides (EPSs) of Lactobacillus gasseri strains isolated from human vagina on cervical tumor cells (HeLa). Anaerobe 2017; 47: 137-144. [DOI:10.1016/j.anaerobe.2017.05.013]
24. Rajoka MSR, Zhao H, Mehwish HM, Li N, Lu Y, Lian Z, Shao D, Jin M, Li Q, Zhao L. Anti-tumor potential of cell free culture supernatant of Lactobacillus rhamnosus strains isolated from human breast milk. Food res int 2019; 123: 286-297. [DOI:10.1016/j.foodres.2019.05.002]
25. Sethy C, Kundu CN. 5-Fluorouracil (5-FU) resistance and the new strategy to enhance the sensitivity against cancer: Implication of DNA repair inhibition. Biomed pharmacother 2021; 137: 111285. [DOI:10.1016/j.biopha.2021.111285]
26. De Leblanc ADM, Matar C, Thériault C, Perdigón G. Effects of milk fermented by Lactobacillus helveticus R389 on immune cells associated to mammary glands in normal and a breast cancer model. Immunobiology 2005; 210(5): 349-358. [DOI:10.1016/j.imbio.2005.05.024]
27. Lin D, Gao Y, Zhao L, Chen Y, An S, Peng Z. Enterococcus faecalis lipoteichoic acid regulates macrophages autophagy via PI3K/Akt/mTOR pathway. Biochem biophys res commun 2018; 498(4): 1028-1036. [DOI:10.1016/j.bbrc.2018.03.109]
28. Zhang Y, Cao L, Nguyen D, Lu H. TP53 mutations in epithelial ovarian cancer. Transl cancer res 2016; 5(6): 650. [DOI:10.21037/tcr.2016.08.40]

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