Flavonoids and Phenolcarboxylic Acids from Lamium album

2019 ◽  
Vol 55 (6) ◽  
pp. 1159-1160 ◽  
Author(s):  
E. Kh. Botirov
2020 ◽  
Vol 21 (2) ◽  
pp. 401 ◽  
Author(s):  
Teodora Costea ◽  
Oana Cezara Vlad ◽  
Luminita-Claudia Miclea ◽  
Constanta Ganea ◽  
János Szöllősi ◽  
...  

The aim of the manuscript is to discuss the influence of plant polyphenols in overcoming multidrug resistance in four types of solid cancers (breast, colorectal, lung and prostate cancer). Effective treatment requires the use of multiple toxic chemotherapeutic drugs with different properties and targets. However, a major cause of cancer treatment failure and metastasis is the development of multidrug resistance. Potential mechanisms of multidrug resistance include increase of drug efflux, drug inactivation, detoxification mechanisms, modification of drug target, inhibition of cell death, involvement of cancer stem cells, dysregulation of miRNAs activity, epigenetic variations, imbalance of DNA damage/repair processes, tumor heterogeneity, tumor microenvironment, epithelial to mesenchymal transition and modulation of reactive oxygen species. Taking into consideration that synthetic multidrug resistance agents have failed to demonstrate significant survival benefits in patients with different types of cancer, recent research have focused on beneficial effects of natural compounds. Several phenolic compounds (flavones, phenolcarboxylic acids, ellagitannins, stilbens, lignans, curcumin, etc.) act as chemopreventive agents due to their antioxidant capacity, inhibition of proliferation, survival, angiogenesis, and metastasis, modulation of immune and inflammatory responses or inactivation of pro-carcinogens. Moreover, preclinical and clinical studies revealed that these compounds prevent multidrug resistance in cancer by modulating different pathways. Additional research is needed regarding the role of phenolic compounds in the prevention of multidrug resistance in different types of cancer.


1991 ◽  
Vol 559 (1-2) ◽  
pp. 499-504 ◽  
Author(s):  
Ulrike Seitz ◽  
Günther Bonn ◽  
Peter Oefner ◽  
Michael Popp

Author(s):  
VA Chipeva ◽  
DC Petrova ◽  
ME Geneva ◽  
MA Dimitrova ◽  
PA Moncheva ◽  
...  

1984 ◽  
Vol 20 (4) ◽  
pp. 501-502
Author(s):  
R. K. Yasinov ◽  
N. V. Syrovezhko ◽  
G. P. Yakovlev

Molecules ◽  
2018 ◽  
Vol 23 (8) ◽  
pp. 2022 ◽  
Author(s):  
Marta Czarnecka ◽  
Marta Świtalska ◽  
Joanna Wietrzyk ◽  
Gabriela Maciejewska ◽  
Anna Gliszczyńska

Phenolic acids and its methoxy derivatives are known to induce caspase-mediated apoptosis activity and exhibit cytotoxic effect towards various cancer cell lines. However, their low stability and poor bioavailability in the human organism extensively restrict the utility of this group of compounds as anticancer and health-promoting agents. In this report, a series of eight novel phosphatidylcholines (3a-b, 5a-b, 7a-b, 8a-b) containing anisic or veratric acids (1a-b) at sn-1 and/or sn-2 positions were synthesized. The phenoylated phospholipids were obtained in good yields 28–66%. The structures of novel compounds were determined by their spectroscopic data. All synthesized compounds were evaluated for their antiproliferative activity towards six cancer cell lines and normal cell line Balb/3T3. Lipophilization of phenolcarboxylic acids significantly increased their anticancer properties. The asymmetrically substituted phenoylated phosphatidylcholines exhibited higher antiproliferative effect than free acids. Lysophosphatidylcholine (7b) effectively inhibited the proliferation of human leukaemia (MV4-11), breast (MCF-7), and colon (LoVo) cancer cell lines at concentrations of 9.5–20.7 µm and was from 19 to 38-fold more active than corresponding free veratric acid. The conjugation of anisic/veratric acids with the phosphatidylcholine have proved the anticancer potential of these phenolcarboxylic acids and showed that this type of lipophilization is an effective method for the production of active biomolecules.


2006 ◽  
Vol 34 (1) ◽  
pp. 88-91 ◽  
Author(s):  
Kalina I. Alipieva ◽  
Rilka M. Taskova ◽  
Soren R. Jensen ◽  
Nedjalka V. Handjieva

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