scholarly journals Epigenetic Modifications, and Alterations in Cell Cycle and Apoptosis Pathway in A549 Lung Carcinoma Cell Line upon Exposure to Perfluoroalkyl Substances

Toxics ◽  
2020 ◽  
Vol 8 (4) ◽  
pp. 112
Author(s):  
Musarrat Jabeen ◽  
Muhammad Fayyaz ◽  
Joseph Irudayaraj

Per- and polyfluoroalkyl substances (PFAS) are a group of human-made compounds with strong C-F bonds, and have been used in various manufacturing industries for decades. PFAS have been reported to deleterious effect on human health, which has led to studies identifying the possible toxicity and toxicity routes of these compounds. We report that these compounds have the potential to cause epigenetic modifications, and to induce dysregulation in the cell proliferation cycle as well as apoptosis in A549 lung cancer cells when exposed to 10-, 200- and 400 μM concentrations of each compound. Our studies show that exposure to perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) may cause hypomethylation in the epigenome, but changes in the epigenetic makeup are not evident upon exposure to GenX. We establish that exposure to lower doses of these compounds causes the cells’ balance to shift to cell proliferation, whereas exposure to higher concentrations shifts the balance more towards apoptosis. Furthermore, the apoptosis pathway upon exposure to GenX, PFOA, and PFOS has also been identified. Our findings suggest that exposure to any of these compounds may have profound effects in patients with pre-existing lung conditions or could trigger lung cancinogenesis.

2001 ◽  
Vol 34 (2) ◽  
pp. 193-202 ◽  
Author(s):  
Masafumi Tomita ◽  
Toshiko Okuyama ◽  
Tetsuya Ishikawa ◽  
Kazuo Hidaka ◽  
Tsutomu Nohno

2022 ◽  
Vol 34 (2) ◽  
pp. 289-296
Author(s):  
Ahmed A. Emara ◽  
Ahmed M. Darwesh ◽  
Mohamed A. Mostafa ◽  
Ahmed A. Ahmed ◽  
Khaled W. Rashad ◽  
...  

Cucurbitacins are a class of highly oxidized tetracyclic triterpenoids. It’s hydrophobic properties and poor solubility in water, polymeric micellar systems exhibited improved antitumor efficacy because of a better solubilization and targeting after local and/or systemic administration. The aim of the present work was to evaluate the anticancer activity of CEG-AgNPs against benzo[a]pyren (BaP)-induced lung carcinoma. CEG-AgNPs was prepared, characterized and evaluated for its cytotoxic activity against A549 lung carcinoma cell line. Also, the anticancer activity of CEG-AgNPs (70.25 mg/kg) against BaP-induced lung carcinoma was evaluated in vivo, using 30 adult mice for 43 days. IC50 of CEG-AgNPs against A549 lung carcinoma cell line were approximately 94.47 μg/mL. Administration of BaP (50 mg/kg b.w.) to mice induced lung carcinoma with a significant increase in lung MMP-2, MMP-9, MMP-12, MDA, IL-6 and NF-κB as well as significant decreased in lung CAT, GPx and GSH level. Also, treatment with BaP produced significant increase in lung VEGF-C, COX-2 and Bcl-2 gene expression as compared to control group. Daily oral administration of CEG-AgNPs to mice treated with BaP showed a significant protection against-induced increase in lung MMP-2, MMP-9, MMP-12, MDA, IL-6 and NF-κB levels. The treatment also resulted in a significant increase in lung CAT, GPx and GSH level. In addition, the CEG-AgNPs could inhibit lung VEGF-C, COX-2 and Bcl-2 gene expression as compared to BaP treated mice. The histological and MRI examination showed that a significant normalization has been observed through in CEG-AgNPs treated mice. The biochemical, histological and MRI results showed that CEG-AgNPs have potent anticancer activity against BaP-induced lung carcinoma through modulating multiple cellular behaviours and signaling pathways leading to the suppression of adaptive immune responses.


2017 ◽  
Vol 42 (5) ◽  
Author(s):  
Leyla Yurttaş ◽  
Betül Kaya Çavuşoğlu ◽  
Arda Sever ◽  
Gülşen Akalin Çiftçi

AbstractObjective(s):In this study, it was aimed to synthesize new chemotherapeutic agents based on known antiproliferative properties of benzothiazol-2-amine moiety. The antitumor activity of the newly synthesized compounds was determined against A549 lung cancer cell lines.Methods:Eighteen compounds were obtained by two steps synthetic route. The anticancer potency of the compounds were detected using MTT assay and flow cytometric analysis on A549 cell line. Some physicochemical properties of the compounds were calculated, virtually.Results:Compounds 15 and 18 showed the highest cytotoxic activity even than cisplatin. Also, it was determined that compound 18 caused 19.1% (early and late) apoptosis whereas cisplatin caused 21.6% (early and late).Conclusion:Considering the calculated virtual data, eighteen new compounds were found within the boundaries of Lipinski rule of five to be an oral drug. Besides, the most potent compounds 15 and 18 were detected that both have 1-methylbenzimidazole structure, and also methoxy and ethoxy substituents on benzothiazole ring.


Author(s):  
Ehsan Soleymaninejadian

: Hydroxyl CoA Dehydrogenase (HADH) is one of the key enzymes in fatty acid β-oxidation. Recently, Hydroxyl CoA Dehydrogenase gene mutation and knockdown were found to be correlated with hyperinsulinemia and central nervous system diseases. As the HADH is one of the critical enzymes in the β-oxidation pathway, the interconnection between HADH and tumorigenicity still is unclear. So, we used Short hairpin RNA (ShRNA) to knock down short-chain hydroxyl CoA dehydrogenase (HADHSC) in human non-small lung carcinoma cell line, H1299, followed by checking cell proliferation, DNA replication, and mRNA level of some the most essential enzymes in glycolysis cycle and Krebs. Cell proliferation was checked by comparing the cell numbers in knockdown and control cells. DNA replication in the H1299 cell line was studied after applying 5-ethynyl 2’-deoxyuridine (EDU) and 4’-6 diamidino-2-phenylindol (DAPI) DNA synthesis Assay. The data revealed a significant decrease in cell proliferation and DNA replication in the cells that the HADHSC was knocked down compared to the control cells. Besides, mRNA levels of the enzymes that needed adenosine triphosphate (ATP) for their activity were decreased abruptly. Furthermore, lactate dehydrogenase (LDHA) mRNA level decreased, and glucose uptake assay showed a tremendous decrease in glucose consumption by H1299 cells with HADHSC knockdown.


2017 ◽  
Vol 46 (40) ◽  
pp. 13745-13755 ◽  
Author(s):  
Daniel Salvador-Gil ◽  
Lourdes Ortego ◽  
Raquel P. Herrera ◽  
Isabel Marzo ◽  
M. Concepción Gimeno

Unprecedented α-hydrazidophosphonate group 11 metal complexes have been prepared, with various coordination modes of ligands to metal atoms. They present an excellent cytotoxic activity in HeLa (cervical carcinoma) and A549 (lung carcinoma) cell lines, with IC50values among the lowest found in silver or copper complexes.


RSC Advances ◽  
2016 ◽  
Vol 6 (33) ◽  
pp. 27775-27787 ◽  
Author(s):  
Shiny P. J. ◽  
Amitava Mukherjee ◽  
Natarajan Chandrasekaran

Therapeutic potential of the biosynthesised silver and platinum nanoparticles against lung carcinoma cell line. Cellular death was induced by oxidative stress followed by apoptosis.


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