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Pregled bibliografske jedinice broj: 75252

Antineoplastic Activity of Novel N-1-Sulfonypyrimidine Derivatives


Glavaš-Obrovac, Ljubica; Karner, Ivan; Žinić, Biserka; Pavelić, Krešimir
Antineoplastic Activity of Novel N-1-Sulfonypyrimidine Derivatives // Anticancer Research, 21 (2001), 1979-1986 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 75252 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Antineoplastic Activity of Novel N-1-Sulfonypyrimidine Derivatives
(Antineoplastic activity of aovel N-1-aulfonypyrimidine derivatives)

Autori
Glavaš-Obrovac, Ljubica ; Karner, Ivan ; Žinić, Biserka ; Pavelić, Krešimir

Izvornik
Anticancer Research (0250-7005) 21 (2001); 1979-1986

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
N-1-sulfonylpyrimidine derivatives; antitumor activity; human tumor cells; apoptosis

Sažetak
We evaluated the potential activity of novel N-1-sulfonyl derivatives of pyrimidine bases uracil and cytosine on pancreatic carcinoma cells (MIAPaCa2), colon carcinomas cells (HT-29, CaCo2), cervical carcinoma cells (HeLa) and poorly-differentiated cells from lymph node metastasis of colon carcinoma (SW-620). The cytotoxicity of N-1-sulfonylpyrimidine derivatives was analyzed with the MTT cell survival assay and their antiproliferative activity was measured via radioactive precursors incorporation assay. The N-1-sulfonylpyrimidine derivatives affected the growth of all examined cell lines at concentrations of 10-8-10-5 M, by 25-70%. Growth inhibition depended on the tumor cell line type and the concentration of investigated compounds. The compounds 2, 4, 7, 8 and 9 inhibited DNA, RNA and protein synthesis in CaCo2, MIAPaCa2 and HeLa cells. The exposure of tumor cells in vitro to compounds 2, 4, 7, 8, 9, 10 and 11, at the 10-6 M concentration, caused both morphological (condensation of chromatin, cell shrinkage), as well as biochemical changes (ladder pattern of DNA fragmentation and exposure of phosphatidylserine on outer lipid bilayer plasma membrane) characteristic of apoptosis. After 24 hours of the N-1-sulfonylpyrimidine derivative application, the p53 oncoprotein expression could not be detected by immunocytochemical analysis. On the basis of present results it can be concluded that novel N-1-sulfonylpyrimidine derivatives are promising antitumor agents with a strong antiproliferative activity and an ability to induce apoptosis in treated tumor cells.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove:
Institut "Ruđer Bošković", Zagreb,
Klinički bolnički centar Osijek


Citiraj ovu publikaciju:

Glavaš-Obrovac, Ljubica; Karner, Ivan; Žinić, Biserka; Pavelić, Krešimir
Antineoplastic Activity of Novel N-1-Sulfonypyrimidine Derivatives // Anticancer Research, 21 (2001), 1979-1986 (međunarodna recenzija, članak, znanstveni)
Glavaš-Obrovac, L., Karner, I., Žinić, B. & Pavelić, K. (2001) Antineoplastic Activity of Novel N-1-Sulfonypyrimidine Derivatives. Anticancer Research, 21, 1979-1986.
@article{article, author = {Glava\v{s}-Obrovac, Ljubica and Karner, Ivan and \v{Z}ini\'{c}, Biserka and Paveli\'{c}, Kre\v{s}imir}, year = {2001}, pages = {1979-1986}, keywords = {N-1-sulfonylpyrimidine derivatives, antitumor activity, human tumor cells, apoptosis}, journal = {Anticancer Research}, volume = {21}, issn = {0250-7005}, title = {Antineoplastic Activity of Novel N-1-Sulfonypyrimidine Derivatives}, keyword = {N-1-sulfonylpyrimidine derivatives, antitumor activity, human tumor cells, apoptosis} }
@article{article, author = {Glava\v{s}-Obrovac, Ljubica and Karner, Ivan and \v{Z}ini\'{c}, Biserka and Paveli\'{c}, Kre\v{s}imir}, year = {2001}, pages = {1979-1986}, keywords = {N-1-sulfonylpyrimidine derivatives, antitumor activity, human tumor cells, apoptosis}, journal = {Anticancer Research}, volume = {21}, issn = {0250-7005}, title = {Antineoplastic activity of aovel N-1-aulfonypyrimidine derivatives}, keyword = {N-1-sulfonylpyrimidine derivatives, antitumor activity, human tumor cells, apoptosis} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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