Contributo in atti di convegno, 2016, ENG

Antiproliferative activity of Pyrrolo[3,2-c]quinoline derivatives against breast cancer cells

F. Mingoia 1), C. Di Sano 2), M. Fazzari 3), A. Martorana 4), A. Lauria 4), V. Bravatà 5) G. I. Forte 5), L. Minafra 5)

1)ISMN-CNR Palermo 2) IBIM-CNR Palermo 3) RIMED Palermo 4) STEBICEF, Università di Palermo 5) IBFM-CNR Cefalù

Thanks to a new synthetic approach recently developed by us1, a new series of pyrrolo[3,2-c]quinoline (PQ) derivatives, has been synthesized permitting us to introduce suitable functional groups in different positions of the scaffold. The latter known for possessing a wide range of biological activities, including anticancer2. The one dose screening (10 ?M) performed by the National Cancer Institute (NCI, USA) against 60 types of tumor cell lines including several panel such as leukemia, lung, renal, CNS, prostate, breast, melanoma, ovarian and colon cancers, allowed us to identify a clear profile of selectivity and potency. Thus, for the most promising derivatives, we undertaken in dept biological investigations. In detail, the 4-substituted piperonil one, which exhibited a preliminary 58% and 18% of growth inhibition in the NCI testing against MCF-7 and MDA-MB-231, respectively, are here submitted to further investigations in order to get new insights on the mode of action. Therefore, a dose response profile at 24, 48 and 72 h was undertaken. More details will be shown at the poster session

Tecnologie, Ricerca di base, interdisciplinare traslazionale in ambito biomedico. Simposio IBIM-CNR/STEBICEF, Palermo IV meeting IBIM-CNR/STEBICEF, pp. 70–70, Palermo, 15/12/2016, 16/12/2016

Keywords

Antiproliferative, Pyrrolo[3, 2-c]quinoline derivatives, breast cancer

CNR authors

Minafra Luigi, Mingoia Francesco Michele, Di Sano Caterina

CNR institutes

ISMN – Istituto per lo studio dei materiali nanostrutturati

ID: 391957

Year: 2016

Type: Contributo in atti di convegno

Creation: 2018-09-27 17:36:18.000

Last update: 2020-09-30 14:42:30.000

External links

OAI-PMH: Dublin Core

OAI-PMH: Mods

OAI-PMH: RDF

External IDs

CNR OAI-PMH: oai:it.cnr:prodotti:391957