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Oxidized collagen and 4-hydroxynonenal suppress growth of human breast cancer stem cells (CROSBI ID 604347)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa

Mrakovcic, Lidija ; Cipak, Ana ; Ciz, Milan ; Lojek, Antonin ; Mihaylova, Boryana ; Goshev, Ivan ; Jaganjac, Morana ; Cindric, Marina ; Balic, Marija ; Zarkovic, Neven. Oxidized collagen and 4-hydroxynonenal suppress growth of human breast cancer stem cells. 2010

Podaci o odgovornosti

Mrakovcic, Lidija ; Cipak, Ana ; Ciz, Milan ; Lojek, Antonin ; Mihaylova, Boryana ; Goshev, Ivan ; Jaganjac, Morana ; Cindric, Marina ; Balic, Marija ; Zarkovic, Neven.

engleski

Oxidized collagen and 4-hydroxynonenal suppress growth of human breast cancer stem cells

Breast cancer is a leading cause of mortality and morbidity in women, mostly due to high metastatic capacity of mammary carcinoma cells. It has been revealed recently that metastases of breast cancer comprise a fraction of specific stem-like cells, denoted as cancer stem cells (CSCs). Breast CSCs, expressing specific surface markers CD44+CD24–/lowESA+ usually disseminate in the bone marrow, being able to spread further and cause late metastases. The fundamental factor influencing the growth of CSCs is the microenvironment, especially the interaction of CSCs with extracellular matrix (ECM). The structure and function of ECM proteins, such as the dominating ECM protein collagen is influenced not only by cancer cells but also by various cancer treatments. Since surgery, radio and chemotherapy are associated with oxidative stress we analyzed the growth of breast cancer CD44+CD24–/lowESA+ cell line SUM159 cultured on collagen matrix in vitro, using either native collagen or the one modified by hydroxyl radical. While native collagen supported the growth of CSCs, oxidatively modified one was not supportive. The SUM159 cell cultures were further exposed to a supraphysiological (35 μM) dose of the major bioactive lipid peroxidation product 4-hydroxynonenal (HNE), a well known as “second messenger of free radicals”, which has a strong affinity to bind to proteins and acts as a cytotoxic or as growth regulating signaling molecule. Native collagen, but not oxidised, abolished cytotoxicity of HNE, while oxidized collagen did not reduce cytotoxicity of HNE at all. These preliminary findings indicate that beside direct cytotoxic effects of anticancer therapies consequential oxidative stress and lipid peroxidation modify the microenvironment of CSCs influencing oxidative homeostasis that could additionally act against cancer.

Oxidized collagen; 4-hydroxynonenal; growth suppression; breast cancer stem cells

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Podaci o prilogu

2010.

objavljeno

Podaci o matičnoj publikaciji

Podaci o skupu

HDIR-1, From bench to clinics is a first meeting of Croatian associtaion for cancer research (HDIR-1, Hrvatsko društvo za istraživanje raka)

poster

11.11.2010-11.11.2010

Zagreb, Hrvatska

Povezanost rada

nije evidentirano