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Pregled bibliografske jedinice broj: 61950

The carcinostatic and proapoptotic potential of the lipid peroxidation product 4-hydroxynonenal is associated with its conjugation to proteins in human cervical carcinoma cells (HeLa) in vitro


Sović, Andrea; Žarković, Neven; Borović, Suzana; Lončarić, Iva; Kreuzer, Thomas; Žarković, Kamelija; Kališnik, Tea; Wäg, Georg; Hrašćan, Reno; Wintersteiger, Reinhold; Schaur, Rudolf Jörg
The carcinostatic and proapoptotic potential of the lipid peroxidation product 4-hydroxynonenal is associated with its conjugation to proteins in human cervical carcinoma cells (HeLa) in vitro // Workshop: Pathobiochemistry of 4-hydroxynonenal
Graz, 2000. (pozvano predavanje, međunarodna recenzija, sažetak, znanstveni)


Naslov
The carcinostatic and proapoptotic potential of the lipid peroxidation product 4-hydroxynonenal is associated with its conjugation to proteins in human cervical carcinoma cells (HeLa) in vitro

Autori
Sović, Andrea ; Žarković, Neven ; Borović, Suzana ; Lončarić, Iva ; Kreuzer, Thomas ; Žarković, Kamelija ; Kališnik, Tea ; Wäg, Georg ; Hrašćan, Reno ; Wintersteiger, Reinhold ; Schaur, Rudolf Jörg

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

Izvornik
Workshop: Pathobiochemistry of 4-hydroxynonenal / - Graz, 2000

Skup
PATHOBIOCHEMISTRY OF 4-HYDROXYNONENAL

Mjesto i datum
Graz, Austrija,, 27.-28. 09. 2000

Vrsta sudjelovanja
Pozvano predavanje

Vrsta recenzije
Međunarodna recenzija

Sažetak
Previous studies have shown that the lipid peroxidation product 4-hydroxynonenal (HNE) acts as a cell growth modulator if used at low, physiological concentrations, being strongly cytotoxic at higher concentrations for a number of cells. These effects of HNE also appeared to be mutually dependent on the effects of serum growth factors. The aim of this investigation was to study the concentration-dependent response of human cervical carcinoma (HeLa) cells in vitro with respect to the intracellular uptake of exogenous HNE, the cellular proliferative and replicative activity, energy metabolism, overall gene expression and susceptibility to apoptosis. Cell counting was used to determine the proliferation rate and the replicative activity was quantified by the 3H-thymidine incorporation assay. The MTT assay was applied as an index of energy metabolism. The occurrence and intracellular distribution was studied with monoclonal antibodies directed against HNE-protein conjugates. Binding of HNE to serum proteins was determined with the same antibodies by Western blotting. Differential gene expression was studied by differential display RT-PCR and novel photometric assay denoted Titer-TACS was used for in situ detection and quantitation of apoptosis in monolayer cultures. A physiological concentration of HNE (1?M) had hardly any effect on the parameters of the replicative activity and the energy metabolism. No morphological changes were observed and the number of HNE-positive cells was not significantly different compared to the untreated control cells whilemost of the aldehyde appeared to be bound to serum proteins (albumin fraction). A tenfold higher concentration (10 ?M) was found to be cytostatic. Spindle shaped cells with a picnotic nucleus were observed occasionally, as well as mambrane blebs, which were HNE-positive. The number of HNE-positive cells was significantly increased compared with both to the control cells and cells treated with 1?M HNE, but in the presence of serum the effects of 10 ?M HNE were abolished due to its binding to the serum proteins. Finally, 100 ?M HNE was cytotoxic for the HeLa cells. Most of the cells were picnotic, together with a few spindle shaped or oval cells. The staining for HNE was diffuse and strong (90% of the cells were HNE-positive) while even binding of the aldehyde to serum proteins did not prevent its cytotoxic effects. This concentration of HNE caused acute stress response of the cells resulting in decreased expression of several yet unidentified genes. The altered pattern of gene expression was manifested in programmed cell death, i.e. an increased number of apoptotic cells afer treatment with low (1 and 10 ?M) concetrations of HNE. A rebound effect was observed, i.e. a decrease of apoptotic cells after 24 hrs followed by an overshooting increase after 48 hrs. For HeLa carcinoma cells there appears to be a concentration range of HNE where it does not cause necrosis but preferentially apoptosis. In this concentration range HNE is cytochemically detectable within the cells as protein conjugate. It is proposed that a possible differential sensitivity of cancer cells and teir normal counterparts to the cytostatic activity of HNE should be explored.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove
Institut "Ruđer Bošković", Zagreb,
Medicinski fakultet, Zagreb