Enhanced Antitumoral Activity of Extracts Derived from Cultured Udotea flabellum (Chlorophyta).

Evid Based Complement Alternat Med

Department of Marine Resources, Cinvestav, Km 6 Carretera Antigua a Progreso, Cordemex, A.P. 73, 97310 Mérida, YUC, Mexico.

Published: November 2011


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Very few studies have been performed to evaluate the effect of culture conditions on the production or activity of active metabolites in algae. Previous studies suggest that the synthesis of bioactive compounds is strongly influenced by irradiance level. To investigate whether the antiproliferative activity of Udotea flabellum extracts is modified after cultivation, this green alga was cultured under four photon flux densities (PFD) for 30 days. After 10, 20, and 30 days, algae were extracted with dichloromethane: methanol and screened for antiproliferative activity against four human cancer cell lines (laryngeal-Hep-2, cervix-HeLa, cervix squamous-SiHa and nasopharynx-KB) by SRB assay. Lipid and phenol content were evaluated by standardized methods on algae organic extracts. After 10 days of cultivation, organic U. flabellum extracts showed a significant increase in antiproliferative activity on Hela and SiHa cells when compared to noncultured algae extracts. Extracts obtained after 10 and 20 days of culture were active on KB and Hep-2 cells. Total phenol and polyunsaturated fatty acid content in organic extracts changed with cultivation time but not by irradiance treatment. Extracts from U. flabellum obtained after 10 and 20 days of culture have been selected for fractionation and isolation of active compounds.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142931PMC
http://dx.doi.org/10.1155/2011/969275DOI Listing

Publication Analysis

Top Keywords

antiproliferative activity
12
extracts
8
udotea flabellum
8
flabellum extracts
8
organic extracts
8
extracts days
8
days culture
8
activity
5
days
5
enhanced antitumoral
4

Similar Publications

Introduction: Chemotherapy remains essential despite advances in immunotherapy, radiotherapy, and biological therapy. However, the wide range of chemical drugs is limited by a narrow therapeutic index, low selectivity, and the development of resistance. In this regard, new high-efficiency drugs are in extremely high demand.

View Article and Find Full Text PDF

PARP inhibitors play a crucial role in cancer therapy, with PARP7 emerging as a promising target for immunotherapy by modulating the cGAS-STING pathway. In this study, the piperazine ring of Olaparib was replaced with a bicyclo[1.1.

View Article and Find Full Text PDF

Lithobates palmipes is a frog species whose skin secretions contain peptides belonging to the ranatuerin, brevinin, and temporin families. In this study, the peptide ranatuerin-2PMe was isolated and evaluated for its antimicrobial, hemolytic, antiproliferative, and chemotactic activities. Ranatuerin-2PMe (2933.

View Article and Find Full Text PDF

Alantolactone prevents testosterone-induced benign prostatic hyperplasia in rats via modulation of PTEN/PI3K/AKT axis.

Biochem Biophys Res Commun

September 2025

Department of Pharmacology and Toxicology, Faculty of Pharmacy, King Abdulaziz University, Jeddah, 21589, Saudi Arabia. Electronic address:

Current treatment options for benign prostatic hyperplasia (BPH) suffer intolerable adverse effects. The goal of this investigation was to evaluate the possible protective effects of alantolactone (ALA) in testosterone (TEST)-induced BPH in rats. Wistar rats were grouped into 5 batches namely; Control, ALA (10 mg/kg), TEST, TEST + ALA (5 mg/kg) and TEST + ALA (10 mg/kg).

View Article and Find Full Text PDF

Two series of triazolo[1,5-a]pyrimidines were designed and synthesized as antiproliferative agents targeting multi kinase inhibition aiming to increase potency and combat drug resistance. The synthesized compounds were tested for their antiproliferative activity. The triazolopyrimidine derivatives 9b, 9c, 12b and 12c showed promising anticancer activities, in particular, compounds 12b and 12c displayed broad spectrum antiproliferative potential against NCI cancer cell lines with GI mean value of 10.

View Article and Find Full Text PDF