Antitumor Activity of New Olivacine Derivatives

被引:10
作者
Piasny, Janusz [1 ]
Wiatrak, Benita [1 ]
Dobosz, Agnieszka [1 ]
Tylinska, Beata [2 ]
Gebarowski, Tomasz [1 ]
机构
[1] Wroclaw Med Univ, Dept Basic Med Sci, PL-50556 Wroclaw, Poland
[2] Wroclaw Med Univ, Dept Organ Chem, PL-50556 Wroclaw, Poland
关键词
pyridocarbazole; olivacine; P-glycoprotein; multiple drug resistance; MUTANT P53; MULTIDRUG-RESISTANCE; ANTICANCER ACTIVITY; P-GLYCOPROTEIN; DNA; ELLIPTICINE; S16020-2;
D O I
10.3390/molecules25112512
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
Olivacine is an alkaloid-containing pyridocarbazole structure. It is isolated from the bark of the evergreen timber tree, Aspidosperma olivaceum. Its well-documented anticancer activity led to the synthesis of new derivatives, which are semisynthetic and fully synthetic pyridocarbazoles. This study aimed to evaluate the potential antineoplastic activity of four newly synthesized olivacine derivatives. Multidrug resistance is a common phenomenon causing failure in the chemotherapy of many tumors. It is mainly related to increased function of P-glycoprotein, an efflux pump removing cytostatic out of the cells. The cell lines used in the study were colorectal carcinoma cell lines: LoVo (doxorubicin-sensitive) and LoVo/DX (doxorubicin-resistant). The NHDF cell line was used to assess cell viability. First, the cells were incubated with olivacine derivatives. In the next step, the following assays were performed: DCF-DA assay, MTT assay, rhodamine 123 assay, detection of apoptosis, proliferation inhibition-mitotic index. The tested compounds showed higher antineoplastic potential and lower toxicity than the reference compound ellipticine. The results indicate that the new olivacine derivatives are good candidates for future anticancer drugs.
引用
收藏
页数:12
相关论文
共 32 条
[1]   The Yin-Yang Regulation of Reactive Oxygen Species and MicroRNAs in Cancer [J].
Babu, Kamesh R. ;
Tay, Yvonne .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (21)
[2]   Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound [J].
Bykov, VJN ;
Issaeva, N ;
Shilov, A ;
Hultcrantz, M ;
Pugacheva, E ;
Chumakov, P ;
Bergman, J ;
Wiman, KG ;
Selivanova, G .
NATURE MEDICINE, 2002, 8 (03) :282-288
[3]   ELLIPTICINE INCREASES THE SUPERHELICAL DENSITY OF INTRACELLULAR SV40-DNA BY INTERCALATION [J].
CHU, Y ;
HSU, MT .
NUCLEIC ACIDS RESEARCH, 1992, 20 (15) :4033-4038
[4]   The role of p53 in chemosensitivity and radiosensitivity [J].
El-Deiry, WS .
ONCOGENE, 2003, 22 (47) :7486-7495
[5]  
FOSSE P, 1992, MOL PHARMACOL, V42, P590
[6]   TOPOISOMERASE-II BINDS TO ELLIPTICINE IN THE ABSENCE OR PRESENCE OF DNA - CHARACTERIZATION OF ENZYME DRUG-INTERACTIONS BY FLUORESCENCE SPECTROSCOPY [J].
FROELICHAMMON, SJ ;
PATCHAN, MW ;
OSHEROFF, N ;
THOMPSON, RB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (25) :14998-15004
[7]  
Gebarowska E, 1999, FOLIA HISTOCHEM CYTO, V37, P135
[8]   Effect of new olivacine derivatives on p53 protein level [J].
Gebarowski, Tomasz ;
Wiatrak, Benita ;
Gebczak, Katarzyna ;
Tylinska, Beata ;
Gasiorowski, Kazimierz .
PHARMACOLOGICAL REPORTS, 2020, 72 (01) :214-224
[9]   1,5-dimethyl-6H-pyridazino[4,5-b]carbazole, a 3-aza bioisoster of the antitumor alkaloid olivacine [J].
Haider, N ;
Sotelo, E .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2002, 50 (11) :1479-1483
[10]  
Jasztold-Howorko R, 2013, ACTA POL PHARM, V70, P823