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il\VOLVEMENT OF RETII\OIC ACID II{ - MSpace at the University of ...

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deriv<strong>at</strong>ives <strong>of</strong> adriamycin which have less toxic effects and higher antitumor potential<br />

(Muggia and Green 1991) as well as understanding <strong>the</strong> basis <strong>of</strong> adriamycin-induced<br />

cardiomyop<strong>at</strong>hy and congestive heart failure. The l<strong>at</strong>ter has been <strong>the</strong> focus <strong>of</strong> <strong>the</strong> research<br />

in Dr. Singal's labor<strong>at</strong>ory and particularly <strong>of</strong> my <strong>the</strong>sis research.<br />

I.a.2.Chemical structure: Adriamycin ) as a member <strong>of</strong> <strong>the</strong> anthracycline family, is a<br />

tetracyclic aglycone with a glycosidic bond <strong>at</strong>tached amino sugar (Fig.l). Adriamycin<br />

(1984) can also be syn<strong>the</strong>sized from daunomycin using <strong>the</strong> method first described by<br />

Arcamone (Quigley et al. 1980).<br />

Figure 1: Chemical structure <strong>of</strong> adriamycin<br />

I.b. Mechanisms <strong>of</strong> action<br />

Several processes are thought to be involved in <strong>the</strong> antineoplastic activity <strong>of</strong><br />

adriamycin such as;<br />

Intercal<strong>at</strong>ion with DNA causing intemrption<br />

<strong>of</strong> transcription and protein<br />

syn<strong>the</strong>sis<br />

Free radical gener<strong>at</strong>ion causing <strong>the</strong> form<strong>at</strong>ion <strong>of</strong><br />

lipid peroxides and irreversible<br />

cell damage

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