PMID- 22811904 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20120823 LR - 20211021 IS - 2090-2115 (Electronic) IS - 2090-2107 (Print) IS - 2090-2107 (Linking) VI - 2012 DP - 2012 TI - Extracellular matrix proteins modulate antimigratory and apoptotic effects of Doxorubicin. PG - 268681 LID - 10.1155/2012/268681 [doi] LID - 268681 AB - Anticancer drug resistance is a multifactorial process that includes acquired and de novo drug resistances. Acquired resistance develops during treatment, while de novo resistance is the primary way for tumor cells to escape chemotherapy. Tumor microenvironment has been recently shown to be one of the important factors contributing to de novo resistance and called environment-mediated drug resistance (EMDR). Two forms of EMDR have been described: soluble factor-mediated drug resistance (SFM-DR) and cell adhesion-mediated drug resistance (CAM-DR). Anthracyclines, among the most potent chemotherapeutic agents, are widely used in clinics against hematopoietic and solid tumors. Their main mechanism of action relies on the inhibition of topoisomerase I and/or II and the induction of apoptosis. Beyond this well-known antitumor activity, it has been recently demonstrated that anthracyclines may display potent anti-invasive effects when used at subtoxic concentrations. In this paper, we will describe two particular modes of EMDR by which microenvironment may influence tumor-cell response to one of these anthracyclines, doxorubicin. The first one considers the influence of type I collagen on the antimigratory effect of doxorubicin (CAM-DR). The second considers the protection of tumor cells by thrombospondin-I against doxorubicin-induced apoptosis (SFM-DR). FAU - Said, Georges AU - Said G AD - UFR Pharmacie, FRE CNRS/URCA no. 3481, Universite de Reims Champagne-Ardenne, 51096 Reims, Cedex, France. FAU - Guilbert, Marie AU - Guilbert M FAU - Morjani, Hamid AU - Morjani H FAU - Garnotel, Roselyne AU - Garnotel R FAU - Jeannesson, Pierre AU - Jeannesson P FAU - El Btaouri, Hassan AU - El Btaouri H LA - eng PT - Journal Article DEP - 20120701 PL - Egypt TA - Chemother Res Pract JT - Chemotherapy research and practice JID - 101566606 PMC - PMC3395309 EDAT- 2012/07/20 06:00 MHDA- 2012/07/20 06:01 PMCR- 2012/07/01 CRDT- 2012/07/20 06:00 PHST- 2012/02/03 00:00 [received] PHST- 2012/04/30 00:00 [accepted] PHST- 2012/07/20 06:00 [entrez] PHST- 2012/07/20 06:00 [pubmed] PHST- 2012/07/20 06:01 [medline] PHST- 2012/07/01 00:00 [pmc-release] AID - 10.1155/2012/268681 [doi] PST - ppublish SO - Chemother Res Pract. 2012;2012:268681. doi: 10.1155/2012/268681. Epub 2012 Jul 1.