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antitumor compounds from marine actinomycetes抗肿瘤化合物从海洋放线菌
Mar. Drugs 2009, 7, 210-248; doi:10.3390/md7020210
OPEN ACCESS
Marine Drugs
ISSN 1660-3397
/journal/marinedrugs
Review
Antitumor Compounds from Marine Actinomycetes
Carlos Olano, Carmen Méndez and José A. Salas *
Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias
(I.U.O.P.A), Universidad de Oviedo, 33006 Oviedo, Spain; E-Mails: olanocarlos@uniovi.es (C.O.);
cmendezf@uniovi.es (C.M.)
* Author to whom correspondence should be addressed; E-Mail: jasalas@uniovi.es; Tel.: +34-985-
103652; Fax: +34-985-103652
Received: 25 May 2009; in revised form: 8 June 2009 / Accepted: 11 June 2009 /
Published: 11 June 2009
Abstract: Chemotherapy is one of the main treatments used to combat cancer. A great
number of antitumor compounds are natural products or their derivatives, mainly produced
by microorganisms. In particular, actinomycetes are the producers of a large number of
natural products with different biological activities, including antitumor properties. These
antitumor compounds belong to several structural classes such as anthracyclines,
enediynes, indolocarbazoles, isoprenoides, macrolides, non-ribosomal peptides and others,
and they exert antitumor activity by inducing apoptosis through DNA cleavage mediated
by topoisomerase I or II inhibition, mitochondria permeabilization, inhibition of key
enzymes involved in signal transduction like proteases, or cellular metabolism and in some
cases by inhibiting
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