Antipsychotic Drug Fluphenazine against Human Cancer Cells

被引:13
作者
Duarte, Diana [1 ,2 ,3 ]
Vale, Nuno [1 ,3 ,4 ]
机构
[1] Ctr Hlth Technol & Serv Res CINTESIS, OncoPharma Res Grp, Rua Doutor Placido da Costa S-N, P-4200450 Porto, Portugal
[2] Univ Porto, Fac Pharm, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[3] Univ Porto, Fac Med, CINTESIS RISE, Alameda Prof Hernani Monteiro, P-4200319 Porto, Portugal
[4] Univ Porto, Fac Med, Dept Community Med Hlth Informat & Decis MEDCIDS, Rua Doutor Placido da Costa S-N, P-4200450 Porto, Portugal
关键词
anticancer activity; fluphenazine; antipsychotic drugs; human cancer cell lines; RESISTANT KBV20C CELLS; INDUCED APOPTOSIS; PHENOTHIAZINES; NEUROBLASTOMA; INHIBITION; CALMODULIN; PROLIFERATION; CYTOTOXICITY; ANTICANCER; AUTOPHAGY;
D O I
10.3390/biom12101360
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drug repurposing is a strategy that can speed up and find novel clinical uses for already-approved drugs for several diseases, such as cancer. This process is accelerated compared to the development of new drugs because these compounds have already been tested in clinical trials and data related to their pharmacokinetics is already described, reducing the costs and time associated with the development of new anticancer therapeutics. Several studies suggest that the repurposing of fluphenazine for cancer therapy may be a promising approach, as this drug proved to reduce the viability of diverse cancer cell lines. In this review, intensive research of the literature was performed related to the anticancer potential of fluphenazine in different human cancer cells. We have found several research articles on the cytotoxic effect of fluphenazine in lung, breast, colon, liver, brain, leukemia, oral, ovarian, and skin cancer and have summarized the main findings in this review. Taken together, these findings suggest that fluphenazine may regulate the cell cycle, reduce cell proliferation, and cause apoptosis in several types of cancer cells, besides being an established calmodulin inhibitor. It was also found that this drug is able to target cancer-related proteins, such as ABCB1 and P-glycoprotein as well as to regulate the Akt and Wnt signaling pathways. Some studies also refer this drug causes DNA alterations and interferes with cell invasion and migration ability as well as with ROS generation. Collectively, these results imply that fluphenazine may be a favorable compound for further research in oncologic therapy.
引用
收藏
页数:17
相关论文
共 64 条
[1]   Prospects for repurposing CNS drugs for cancer treatment [J].
Abdelaleem, Mohamed ;
Ezzat, Hossam ;
Osama, Muhammed ;
Megahed, Adel ;
Alaa, Waleed ;
Gaber, Ahmed ;
Shafei, Ayman ;
Refaat, Alaa .
ONCOLOGY REVIEWS, 2019, 13 (01) :37-42
[2]  
[Anonymous], STUDY FLUPHENAZINE R
[3]  
[Anonymous], FLUPHENAZINE USES IN
[4]  
[Anonymous], FLUPHENAZINE TREATIN
[5]  
[Anonymous], 2009, Model List of Essential Medicines-16th List
[6]   Old wine in new bottles: Drug repurposing in oncology [J].
Antoszczak, Michal ;
Markowska, Anna ;
Markowska, Janina ;
Huczynski, Adam .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2020, 866
[7]   The many faces of calmodulin in cell proliferation, programmed cell death, autophagy, and cancer [J].
Berchtold, Martin W. ;
Villalobo, Antonio .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2014, 1843 (02) :398-435
[8]   Drug repurposing for ligand-induced rearrangement of Sirt2 active site-based inhibitors via molecular modeling and quantum mechanics calculations [J].
Bharadwaj, Shiv ;
Dubey, Amit ;
Kamboj, Nitin Kumar ;
Sahoo, Amaresh Kumar ;
Kang, Sang Gu ;
Yadava, Umesh .
SCIENTIFIC REPORTS, 2021, 11 (01)
[9]   Identification of thioridazine, an antipsychotic drug, as an antiglioblastoma and anticancer stem cell agent using public gene expression data [J].
Cheng, H-W ;
Liang, Y-H ;
Kuo, Y-L ;
Chuu, C-P ;
Lin, C-Y ;
Lee, M-H ;
Wu, A. T. H. ;
Yeh, C-T ;
Chen, E. I-T ;
Whang-Peng, J. ;
Su, C-L ;
Huang, C-Y F. .
CELL DEATH & DISEASE, 2015, 6 :e1753-e1753
[10]   Effects of the antianginal drug fendiline on Ca2+ movement in hepatoma cells [J].
Cheng, JS ;
Wang, JL ;
Lo, YK ;
Chou, KJ ;
Lee, KC ;
Liu, CP ;
Chang, HT ;
Jan, CR .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2001, 20 (07) :359-364