MELLO, JOYCE C. deMORAES, VIVIAN W.R.WATASHI, CAROLINA M.SILVA, DEYSE C. daCAVALCANTI, LEIDE P.FRANCO, MARGARETH K.K.D.YOKAICHIYA, FABIANOARAUJO, DANIELE R. deRODRIGUES, TIAGO2016-08-152016-08-152016MELLO, JOYCE C. de; MORAES, VIVIAN W.R.; WATASHI, CAROLINA M.; SILVA, DEYSE C. da; CAVALCANTI, LEIDE P.; FRANCO, MARGARETH K.K.D.; YOKAICHIYA, FABIANO; ARAUJO, DANIELE R. de; RODRIGUES, TIAGO. Enhancement of chlorpromazine antitumor activity by pluronics F127/L81 nanostructured system against human multidrug resistant leukemia. <b>Pharmacological Research</b>, v. 111, p. 102-112, 2016. DOI: <a href="https://dx.doi.org/10.1016/j.phrs.2016.05.032">10.1016/j.phrs.2016.05.032</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/26585.1043-6618http://repositorio.ipen.br/handle/123456789/26585The development of specific tyrosine kinase inhibitors (TKIs) revolutionized the treatment of chronic myeloid leukemia (CML). However, chemoresistance of tumor cells to TKIs has already been described, and several mechanisms account for the multidrug resistance (MDR) phenotypes, including the overexpression of P-glycoprotein (P-gp). This decreases the rate of healing and complete tumor remission. Nanotechnological tools have been studied to allow advances in this field. Poloxamers (Pluronics®) have been proposed as drug carriers to improve therapeutic efficacy and decrease side effects, even in cancer therapy, due to their ability to inhibit P-gp. Antipsychotic phenothiazines have been described as potent cytotoxic drugs against several types of tumor cells in vitro. Here, we show that nanostructured micellar systems containing the phenothiazine derivative chlorpromazine (CPZ) potentiated the cytotoxicity of free CPZ and increased the selectivity against CML tumor cells, demonstrating the pharmacological potential of these poloxamer-based nanostructured systems containing CPZ in cancer therapy.102-112openAccesstumor cellsneoplasmstherapyleukemiananostructuresdrugsphenothiazineschlorpromazineantineoplastic drugsmicellar systemssmall angle scatteringin vitrocell culturestoxicityArtigo de periódico11110.1016/j.phrs.2016.05.03288.13