Oklahoma IDeA Network of Biomedical Research Excellence (OK-INBRE; P20GM103447; DRW)

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Oklahoma IDeA Network of Biomedical Research Excellence (OK-INBRE; P20GM103447; DRW)

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Publications

Toxicity of Organic and Inorganic Nickel in Pancreatic Cell Cultures: Comparison to Cadmium

Wallace, David R.; Buha-Đorđević, Aleksandra; Benton, Alexander

(Pharmaceutical Association of Serbia, 2020)

TY  - JOUR
AU  - Wallace, David R.
AU  - Buha-Đorđević, Aleksandra
AU  - Benton, Alexander
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3770
AB  - Nickel compounds are Group 1 carcinogens and possibly cancer-causing in the pancreas. We examined the toxicity of nickel in both 2-D and 3-D pancreatic cell cultures, to determine the LD50 for organic and  inorganic nickel  in normal and cancerous  cells. Assays with cadmium chloride  were performed to be  a comparison  to potential nickel-induced  toxicity.  Cells were exposed to twelve concentrations of NiCl2 or Ni-(Ac)2 for 48h (2-D), or six concentrations for 48 hours (3-D). There was a significant (P=0.0016) difference between HPNE and AsPC-1 LD50values after cadmium exposure, at 69.9 μM and 29.2 μM, respectively. Neither form of nickel exhibited toxicity in 2-D or 3-D cultures, but after 48h, changes in spheroid morphology were observed. The inability of Ni to reduce viable cell numbers suggests a toxic mechanism that differs from cadmium, also a Group 1 carcinogen. The cell microenvironment was not a factor in nickel toxicity with no changes in viable cells in either 2-D or 3-D cultures. These studies only examined cytotoxicity, and not genotoxicity, a potential mechanism of nickel carcinogenicity. Alterations in DNA function or the expression of apoptotic proteins/processes would take longer to manifest. Current work focuses on cellular changes following extended nickel exposure.
AB  - Uloga nikla, toksičnog metala, u nastanku karcinoma pankreasa još uvek nije u potpunosti ispitana. Cilj rada je da ispita toksičnost nikla (Ni) u 2-D i 3-D kulturi ćelija pankreasa, kako bi se utvrdila LD50 vrednost za organski i neorganski nikl u normalnim i tumorskim ćelijama. Ispitivanja su izvršena i sa kadmijumom (Cd), metalom čija je uloga u nastanku karcinoma pankreasa potvrđena u prethodnim istraživanjima, a u svrhu poređenja sa potencijalnom toksičnošću izazvanom Ni. Ćelije su bile tretirane sa 12 različitih koncentracija NiCl2 ili Ni-(Ac)2 tokom 48h (2-D), odnosno sa šest različitih koncentracija tokom 48 sati (3-D). Nijedan oblik Ni nije ispoljio toksičnost u 2-D ili 3-D kulturama, ali nakon 48h primećene su promene u sferoidnoj morfologiji. Nemogućnost Ni da smanji broj vijabilnih ćelija sugeriše mehanizam karcinogeneze različit od mehanizma koji ispoljava Cd. Ipak, da bi se uočile izmene u funkciji DNK ili izražavanju apoptotičkih proteina/procesa potrebno je duže vremena, pa su dalja istraživanja upravo fokusirana na ćelijske promene nakon produžene izloženosti nikla.
PB  - Pharmaceutical Association of Serbia
T2  - Arhiv za farmaciju
T1  - Toxicity of Organic and Inorganic Nickel in Pancreatic Cell Cultures: Comparison to Cadmium
T1  - Toksičnost organskog i neogranskog nikla u ćelijskim kulturama pankreasa: poređenje sa kadmijumom
VL  - 70
IS  - 6
SP  - 344
EP  - 359
DO  - 10.5937/arhfarm70-29277
ER  - 
@article{
author = "Wallace, David R. and Buha-Đorđević, Aleksandra and Benton, Alexander",
year = "2020",
abstract = "Nickel compounds are Group 1 carcinogens and possibly cancer-causing in the pancreas. We examined the toxicity of nickel in both 2-D and 3-D pancreatic cell cultures, to determine the LD50 for organic and  inorganic nickel  in normal and cancerous  cells. Assays with cadmium chloride  were performed to be  a comparison  to potential nickel-induced  toxicity.  Cells were exposed to twelve concentrations of NiCl2 or Ni-(Ac)2 for 48h (2-D), or six concentrations for 48 hours (3-D). There was a significant (P=0.0016) difference between HPNE and AsPC-1 LD50values after cadmium exposure, at 69.9 μM and 29.2 μM, respectively. Neither form of nickel exhibited toxicity in 2-D or 3-D cultures, but after 48h, changes in spheroid morphology were observed. The inability of Ni to reduce viable cell numbers suggests a toxic mechanism that differs from cadmium, also a Group 1 carcinogen. The cell microenvironment was not a factor in nickel toxicity with no changes in viable cells in either 2-D or 3-D cultures. These studies only examined cytotoxicity, and not genotoxicity, a potential mechanism of nickel carcinogenicity. Alterations in DNA function or the expression of apoptotic proteins/processes would take longer to manifest. Current work focuses on cellular changes following extended nickel exposure., Uloga nikla, toksičnog metala, u nastanku karcinoma pankreasa još uvek nije u potpunosti ispitana. Cilj rada je da ispita toksičnost nikla (Ni) u 2-D i 3-D kulturi ćelija pankreasa, kako bi se utvrdila LD50 vrednost za organski i neorganski nikl u normalnim i tumorskim ćelijama. Ispitivanja su izvršena i sa kadmijumom (Cd), metalom čija je uloga u nastanku karcinoma pankreasa potvrđena u prethodnim istraživanjima, a u svrhu poređenja sa potencijalnom toksičnošću izazvanom Ni. Ćelije su bile tretirane sa 12 različitih koncentracija NiCl2 ili Ni-(Ac)2 tokom 48h (2-D), odnosno sa šest različitih koncentracija tokom 48 sati (3-D). Nijedan oblik Ni nije ispoljio toksičnost u 2-D ili 3-D kulturama, ali nakon 48h primećene su promene u sferoidnoj morfologiji. Nemogućnost Ni da smanji broj vijabilnih ćelija sugeriše mehanizam karcinogeneze različit od mehanizma koji ispoljava Cd. Ipak, da bi se uočile izmene u funkciji DNK ili izražavanju apoptotičkih proteina/procesa potrebno je duže vremena, pa su dalja istraživanja upravo fokusirana na ćelijske promene nakon produžene izloženosti nikla.",
publisher = "Pharmaceutical Association of Serbia",
journal = "Arhiv za farmaciju",
title = "Toxicity of Organic and Inorganic Nickel in Pancreatic Cell Cultures: Comparison to Cadmium, Toksičnost organskog i neogranskog nikla u ćelijskim kulturama pankreasa: poređenje sa kadmijumom",
volume = "70",
number = "6",
pages = "344-359",
doi = "10.5937/arhfarm70-29277"
}
Wallace, D. R., Buha-Đorđević, A.,& Benton, A.. (2020). Toxicity of Organic and Inorganic Nickel in Pancreatic Cell Cultures: Comparison to Cadmium. in Arhiv za farmaciju
Pharmaceutical Association of Serbia., 70(6), 344-359.
https://doi.org/10.5937/arhfarm70-29277
Wallace DR, Buha-Đorđević A, Benton A. Toxicity of Organic and Inorganic Nickel in Pancreatic Cell Cultures: Comparison to Cadmium. in Arhiv za farmaciju. 2020;70(6):344-359.
doi:10.5937/arhfarm70-29277 .
Wallace, David R., Buha-Đorđević, Aleksandra, Benton, Alexander, "Toxicity of Organic and Inorganic Nickel in Pancreatic Cell Cultures: Comparison to Cadmium" in Arhiv za farmaciju, 70, no. 6 (2020):344-359,
https://doi.org/10.5937/arhfarm70-29277 . .
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