Isolated Flavonoids against Mammary Tumour Cells LM2

Author:

Carli Camila B. de A.1,Matos Djamile C. de1,Lopes Flávia C. M.1,Maia Danielle C. G.1,Dias Maristela B.1,Sannomiya Miriam2,Rodrigues Clenilson M.2,Andreo Marcio A.2,Vilegas Wagner2,Colombo Lucas L.3,Carlos Iracilda Z.1

Affiliation:

1. UNESP – São Paulo State University, Faculdade de Ciências Farmacêuticas, C. Postal 502, 14801 – 902, Araraquara, SP, Brazil

2. UNESP – São Paulo State University, Instituto de Química de Araraquara, C. Postal 355, 14801 – 970, Araraquara, SP, Brazil

3. Buenos Aires University, Instituto de Oncologia, UBA, Buenos Aires, Argentina

Abstract

1 The purpose of the present study was to investigate antitumour and anti-inflammatory activities of flavonoids isolated from Byrsonima crassa, Davilla elliptica and Mouriri pusa. The antitumour activity was measured by the MTT assay in murine mammary tumour cells (LM2) and the IC50 values of the fl avonoids tested ranged from (31.5 ± 2.97) to (203.1 ± 5.9) μg/ml. The fl avonoids (myricetin-3-O-α-L-rhamnopyranoside) and 3 (quercetin-3-Ogalactopyranoside) from D. elliptica were the most active ones against the tumour cells. The same samples were tested to determine the inhibition of the release of nitric oxide (NO) and of the tumour necrosis factor-alpha (TNF-α) in murine macrophages by the Griess and ELISA sandwich assay, respectively. Almost all the samples showed inhibitory activity to the release of NO but not of TNF-α. Of all substances tested, flavonoids 2 (quercetin) and 6 (myricetin) may show promising activity in the treatment of murine breast cancer by immunomodulatory and antiproliferative activities.

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

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