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Pregled bibliografske jedinice broj: 910435

Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting


Kirchofer, Juraj; Jukić, Marijana; Glavaš-Obrovac, Ljubica
Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting // 3th international Cholnoky symposium
Pečuh, Mađarska, 2017. str. 1-1 (poster, međunarodna recenzija, sažetak, ostalo)


CROSBI ID: 910435 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting

Autori
Kirchofer, Juraj ; Jukić, Marijana ; Glavaš-Obrovac, Ljubica

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo

Skup
3th international Cholnoky symposium

Mjesto i datum
Pečuh, Mađarska, 11.05.2017. - 12.05.2017

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
purine nucleoside derivatives, Akt expression, CaCo-2, NCI-H358

Sažetak
Most of anticancer drugs are not target-specific, affecting normal cells also. Newly synthesized N-9-sulfonylpurine derivatives belong to the group of antimetabolites that achieve specific effects through interaction with natural metabolites. The aim of this study is to determine possible changes in the expression of the Akt protein, a central effector in the PI3K signalling pathway, in adenocarcinoma (CaCo-2) and bronchioalveolar carcinoma (NCI-H358) cells after treatment with two N-9-sufonylpurine derivatives. After 24 hrs of treatment cells were lysed and cellular proteins were isolated. Protein concentration was determined by the BCA protein assay with bovine serum albumin as a standard. Presence of Akt protein in total isolated cellular proteins was determined by the Western blot method using Akt antibody. Relative quantification of the Akt protein obtained on the membrane was made with the ImageJ program. Results of Western blot analysis showed no significant change in expression level of Akt protein after treatment of CaCo-2 cells with SPD1 and SDP12 derivatives compared to untreated cells. Applied SPD1 on NCI-H358 caused moderately increased Akt protein expression in relation to the control cells. Obtained results suggest that Akt signaling pathway is not affected by tested compounds.

Izvorni jezik
Engleski



POVEZANOST RADA



Citiraj ovu publikaciju:

Kirchofer, Juraj; Jukić, Marijana; Glavaš-Obrovac, Ljubica
Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting // 3th international Cholnoky symposium
Pečuh, Mađarska, 2017. str. 1-1 (poster, međunarodna recenzija, sažetak, ostalo)
Kirchofer, J., Jukić, M. & Glavaš-Obrovac, L. (2017) Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting. U: 3th international Cholnoky symposium.
@article{article, author = {Kirchofer, Juraj and Juki\'{c}, Marijana and Glava\v{s}-Obrovac, Ljubica}, year = {2017}, pages = {1-1}, keywords = {purine nucleoside derivatives, Akt expression, CaCo-2, NCI-H358}, title = {Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting}, keyword = {purine nucleoside derivatives, Akt expression, CaCo-2, NCI-H358}, publisherplace = {Pe\v{c}uh, Ma\djarska} }
@article{article, author = {Kirchofer, Juraj and Juki\'{c}, Marijana and Glava\v{s}-Obrovac, Ljubica}, year = {2017}, pages = {1-1}, keywords = {purine nucleoside derivatives, Akt expression, CaCo-2, NCI-H358}, title = {Analysis of Akt protein expression in CaCo2 and NCI-H358 cells treated with N-sulfonylpurine derivatives by Western blotting}, keyword = {purine nucleoside derivatives, Akt expression, CaCo-2, NCI-H358}, publisherplace = {Pe\v{c}uh, Ma\djarska} }




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