Effects of Albumin-Chlorogenic Acid Nanoparticles on Apoptosis and PI3K/Akt/mTOR Pathway Inhibitory Activity in MDA-MB-435s Cells

被引:5
作者
Alzahrani, Badr [1 ]
Elderdery, Abozer Y. [1 ]
Alsrhani, Abdullah [1 ]
Alzerwi, Nasser A. N. [2 ]
Althobiti, Maryam Musleh [3 ]
Rayzah, Musaed [2 ]
Idrees, Bandar [4 ]
Elkhalifa, Ahmed M. E. [5 ,6 ]
Subbiah, Suresh K. [7 ]
Mok, Pooi Ling [8 ]
机构
[1] Jouf Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Sakaka 72388, Saudi Arabia
[2] Majmaah Univ, Coll Med, Dept Surg, POB 66, Al Majmaah 11952, Saudi Arabia
[3] Shaqra Univ, Coll Appl Med Sci, Dept Clin Lab Sci, Shaqra 11961, Saudi Arabia
[4] Prince Sultan Mil Med City Riyadh, Dept Surg, Makkah Al Mukarramah Rd, As Sulimaniyah 12233, Saudi Arabia
[5] Saudi Elect Univ, Coll Hlth Sci, Dept Publ Hlth, Riyadh 11673, Saudi Arabia
[6] Univ El Imam El Mahdi, Fac Med Lab Sci, Dept Haematol, Kosti 1158, Sudan
[7] Bharath Inst Higher Educ & Res, Ctr Mat Engn & Regenerat Med, Chennai 600073, India
[8] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Biomed Sci, Serdang 43400, Malaysia
关键词
MDA-MB435s cells; albumin; chlorogenic acid; biogenic nanoparticles; apoptosis; anti-cancer; SILVER NANOPARTICLES; CANCER; RESISTANCE; RELEASE;
D O I
10.3390/nano13091438
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we synthesized, characterized, and explored the anti-microbial and anti-cancer effects of albumin-chlorogenic acid nanoparticles (NPs). Characterization studies with a UV-vis spectrophotometer, FTIR, PL spectrum, TEM, FESEM, XRD, and DLA analysis showed patterns confirming the physio-chemical nature of biogenic nanocomposites. Further, anti-microbial studies using bacterial strains Staphylococcus aureus, Streptococcus pneumonia, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, Vibrio cholera, and fungal strain Candida albicans showed significant (p < 0.05) anti-bacterial and anti-fungal activities. Next, we used MDA-MB-435s, a human cell line, to evaluate the anti-cancer effects of albumin-chlorogenic acid NPs. Cytotoxic studies revealed its IC50 concentration at 24 mu g/mL after a 24 h treatment of MDA-MB-435s cells. We chose this IC50 dose to analyze albumin-chlorogenic acid NPs anti-cancer effects in vitro. MDA-MB-435s cells exposed to our NPs were studied via AO/EtBr staining, cell cycle analyses via PI staining, the status of whole genomic damage via comet assay, levels of apoptotic cells via annexin V/PI staining, ROS generation via DCFH-DA staining, an assay of antioxidant enzymes catalase, superoxide dismutase, and antioxidant GSH, via ELISA analyses of apoptotic markers caspase-3, 8, 9, Bax, Bcl-2, CytC, and p53, PI3/AKT/mTOR pathway. Our results collectively showed albumin-chlorogenic acid NPs induced apoptosis via p53-dependent and PI3/AKT/mTOR inhibition in MDA-MB-435s cells. Our results denote albumin-chlorogenic acid NPs can be used as an effective candidate for anti-microbial and anti-cancer applications; however, further in vivo confirmatory studies are warranted.
引用
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页数:17
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