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izvor podataka: crosbi

Running for time: circadian rhythms and melanoma (CROSBI ID 206671)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Markova-Car, Elitza Petkova ; Jurišić, Davor ; Ilić, Nataša ; Kraljević Pavelić, Sandra Running for time: circadian rhythms and melanoma // Tumor biology, 35 (2014), 9; 8359-8368. doi: 10.1007/s13277-014-1904-2

Podaci o odgovornosti

Markova-Car, Elitza Petkova ; Jurišić, Davor ; Ilić, Nataša ; Kraljević Pavelić, Sandra

engleski

Running for time: circadian rhythms and melanoma

Circadian timing system includes an input pathway transmitting environmental signals to a core oscillator that generates circadian signals responsible for the peripheral physiological or behavioural events. Circadian 24-hours rhythms regulate diverse physiologic processes. Deregulation of these rhythms is associated with a number of pathogenic conditions including depression, diabetes, metabolic syndrome and cancer. Melanoma is a less common type of skin cancer yet more aggressive often with a lethal ending. However, little is known about circadian control in melanoma and exact functional associations between core clock genes and development of melanoma skin cancer. This paper therefore, comprehensively analyses current literature data on the involvement of circadian clock components in melanoma development. In particular, the role of circadian rhythms deregulation is discussed in the context of DNA repair mechanisms and influence of UV radiation and artificial light exposure on cancer development. The role of Arylalkylamine N-acetyltransferase (AANAT) enzyme and impact of melatonin, as a major output factor of circadian rhythm, and its protective role in melanoma are discussed in details. We hypothesize that further understanding of clock genes involvement and circadian regulation might foster discoveries in the field of melanoma diagnostics and treatment.

clock genes; circadian rhythm; melatonin; cancer; melanoma

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Podaci o izdanju

35 (9)

2014.

8359-8368

objavljeno

1010-4283

10.1007/s13277-014-1904-2

Povezanost rada

nije evidentirano

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