Literature DB >> 31186739

In vitro effect of curcumin in combination with chemotherapy drugs in Ph+ acute lymphoblastic leukemia cells.

Uriel Francisco Santana-Bejarano1,2, Lucina Bobadilla-Morales1,2,3, Lucero Mendoza-Maldonado1,2, Elizabeth Torres-Anguiano1,2, Sinhue Alejandro Brukman-Jiménez1,2, Cesar Cenobio Barba-Barba3, Jorge Román Corona-Rivera1,2, Alfredo Corona-Rivera1,2,3.   

Abstract

Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL), is characterized by the t(9;22)(q34q11) that generates the BCR-ABL protein with uncontrolled tyrosine kinase activity. Recently, a connection between BCR-ABL signaling with NF-κB activation mediated by CK2 has been hypothesized. Approximately 95% of patients with Ph+ ALL have the BCR-ABLp190 isoform, which causes aggressive leukemia with a high rate of chemotherapy resistance. Therefore, the use of compounds that could improve the efficacy of chemotherapy drugs is of particular interest. Curcumin is an active chemical in turmeric with antineoplastic potential; it regulates protein-kinases by modulating downstream molecular pathways. The present study evaluated the effect of curcumin in combination with the chemotherapeutic drugs vincristine, imatinib and daunorubicin in the human OP-1 cell line. Several doses of the chemotherapy drugs were examined, and the effects were evaluated following 12, 24 and 48 h of exposure. The interaction between the chemotherapy drugs and curcumin was determined by the dose-effect curve, which generated a combination index (CI); these data were represented in isobolograms. In addition, the individual effect of each drug was compared with its effect in combination with curcumin on cell viability, apoptosis degree, NF-κB activation and gene expression changes. The present study observed that curcumin potentiates the efficacy of vincristine and imatinib, generating an additive/synergistic effect in a dose- and time-dependent manner. These combinations significantly increased the apoptosis degree, decreased the activation of NF-κB and the expression of its regulated genes. Conversely treatment with daunorubicin + curcumin combination produced an antagonistic/additive effect in a dose-dependent manner, and this combination significantly increased the apoptosis degree. However, this effect seems not to be associated with NF-κB activity, as no significant changes were observed in its activation or in the expression of the genes that it regulates. The results of the present study demonstrate that curcumin may be used as an adjuvant agent for chemotherapy in patients with Ph+ ALL.

Entities:  

Keywords:  BCR-ABL; NF-κB; curcumin; daunorubicin; imatinib; vincristine

Year:  2019        PMID: 31186739      PMCID: PMC6507345          DOI: 10.3892/ol.2019.10204

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  28 in total

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Authors:  K J Livak; T D Schmittgen
Journal:  Methods       Date:  2001-12       Impact factor: 3.608

Review 2.  Circuitry of nuclear factor kappaB signaling.

Authors:  Alexander Hoffmann; David Baltimore
Journal:  Immunol Rev       Date:  2006-04       Impact factor: 12.988

Review 3.  Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies.

Authors:  Ting-Chao Chou
Journal:  Pharmacol Rev       Date:  2006-09       Impact factor: 25.468

4.  Treatment of P190 Bcr/Abl lymphoblastic leukemia cells with inhibitors of the serine/threonine kinase CK2.

Authors:  S Mishra; V Pertz; B Zhang; P Kaur; H Shimada; J Groffen; Z Kazimierczuk; L A Pinna; N Heisterkamp
Journal:  Leukemia       Date:  2006-11-02       Impact factor: 11.528

5.  Resistance of bcr-abl-positive acute lymphoblastic leukemia to daunorubicin is not mediated by mdr1 gene expression.

Authors:  Mamta Gupta; Anil Kumar; Sunil Dabadghao
Journal:  Am J Hematol       Date:  2002-11       Impact factor: 10.047

6.  Phase I clinical trial of curcumin, a chemopreventive agent, in patients with high-risk or pre-malignant lesions.

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Journal:  Anticancer Res       Date:  2001 Jul-Aug       Impact factor: 2.480

7.  Imatinib.

Authors:  K Lyseng-Williamson; B Jarvis
Journal:  Drugs       Date:  2001       Impact factor: 9.546

8.  Phase II study of sphingosomal vincristine in patients with recurrent or refractory adult acute lymphocytic leukemia.

Authors:  Deborah A Thomas; Andreas H Sarris; Jorge Cortes; Stefan Faderl; Susan O'Brien; Francis J Giles; Guillermo Garcia-Manero; Maria A Rodriguez; Fernando Cabanillas; Hagop Kantarjian
Journal:  Cancer       Date:  2006-01-01       Impact factor: 6.860

9.  Resistance to imatinib of bcr/abl p190 lymphoblastic leukemia cells.

Authors:  Suparna Mishra; Bin Zhang; Jess M Cunnick; Nora Heisterkamp; John Groffen
Journal:  Cancer Res       Date:  2006-05-15       Impact factor: 12.701

10.  Activity of vincristine, L-ASP, and dexamethasone against acute lymphoblastic leukemia is enhanced by the BH3-mimetic ABT-737 in vitro and in vivo.

Authors:  Min H Kang; Yun Hee Kang; Barbara Szymanska; Urszula Wilczynska-Kalak; Michael A Sheard; Theresa M Harned; Richard B Lock; C Patrick Reynolds
Journal:  Blood       Date:  2007-05-29       Impact factor: 22.113

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