Title of article :
Programmed cell death (PCD) associated with the stilbene motif of arotinoids: discovery of novel apoptosis inducer agents possessing activity on multidrug resistant tumor cells
Author/Authors :
Daniele Simoni، نويسنده , , Marinella Roberti، نويسنده , , Francesco Paolo Invidiata، نويسنده , , Riccardo Rondanin، نويسنده , , Riccardo Baruchello، نويسنده , , Cinzia Malagutti، نويسنده , , Angelica Mazzali، نويسنده , , Marcello Rossi and Sabrina Selvi ، نويسنده , , Stefania Grimaudo، نويسنده , , Luisa Dusonchet، نويسنده , , Maria Meli، نويسنده , , Maria Valeria Raimondi، نويسنده , , Natale DʹAlessandro، نويسنده , , Manlio Tolomeo، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
5
From page :
2669
To page :
2673
Abstract :
Considering that the stereochemistry of the C9–C10 alkenyl portion of natural 9-cis-RA, as the one of the olefinic moiety of the previously described isoxazole retinoid 4, seems of particular importance for their apoptotic activity, we prepared a novel class of TTNPB analogues bearing both the cis or trans configuration of the alkenyl portion. The compounds were evaluated in vitro for their cytotoxic and apoptotic activities. We discovered that the cis-TTNPB 9c possesses apoptotic activity comparable with that of the retinoid 4. Moreover, the amino arotinoid 16c showed potent apoptotic activity in HL60 promyelocytic leukemia cells. Interestingly, 16c proved to be a particularly potent apoptosis-inducing agent active in multidrug resistant (MDR) cell lines. Therefore, to the best of our knowledge, 16c may represent the first known aminoarotinoid endowed with potent apoptotic activity in MDR cells. Taken together, these results seem to point out that the cis-stilbene motif of arotinoids may be at least an important feature in conferring cytotoxic and apoptotic activity to this class of compounds.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2000
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
791178
Link To Document :
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