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Pigeon Pea ( Cajanus cajan (L.) Millsp.) is a common food crop used in many parts of the world for nutritional purposes. One of its chemical constituents is cajanin stilbene acid (CSA), which exerts anticancer activity in vitro and in vivo. In an effort to identify molecular targets of CSA, we performed a kinome-wide approach based on the measurement of the enzymatic activities of 252 human kinases. The serine-threonine kinase WNK3 (also known as protein kinase lysine-deficient 3) was identified as the most promising target of CSA with the strongest enzymatic activity inhibition in vitro and the highest binding affinity in molecular docking in silico. The lowest binding affinity and the predicted binding constant pKi of CSA (-9.65 kcal/mol and 0.084 µM) were comparable or even better than those of the known WNK3 inhibitor PP-121 (-9.42 kcal/mol and 0.123 µM). The statistically significant association between WNK3 mRNA expression and cellular responsiveness to several clinically established anticancer drugs in a panel of 60 tumor cell lines and the prognostic value of WNK3 mRNA expression in sarcoma biopsies for the survival time of 230 patients can be taken as clues that CSA-based inhibition of WNK3 may improve treatment outcomes of cancer patients and that CSA may serve as a valuable supplement to the currently used combination therapy protocols in oncology.

Background: The low abundant cajanin stilbene acid (CSA) from Pigeon Pea (Cajanus cajan) has been shown to kill estrogen receptor α positive cancer cells in vitro and in vivo. Downstream effects such as cell cycle and apoptosis-related mechanisms have not been analyzed yet., Material and Methods: We analyzed the activity of CSA by means of flow cytometry (cell cycle distribution, mitochondrial membrane potential, MMP), confocal laser scanning microscopy (MMP), DNA fragmentation assay (apoptosis), Western blotting (Bax and Bcl-2 expression, caspase-3 activation) as well as mRNA microarray hybridization and Ingenuity pathway analysis., Results: CSA induced G2/M arrest and apoptosis in a concentration-dependent manner from 8.88 to 14.79 µM. The MMP broke down, Bax was upregulated, Bcl-2 downregulated and caspase-3 activated. Microarray profiling revealed that CSA affected BRCA-related DNA damage response and cell cycle-regulated chromosomal replication pathways., Conclusion: CSA inhibited breast cancer cells by DNA damage and cell cycle-related signaling pathways leading to cell cycle arrest and apoptosis., (Copyright © 2015 Elsevier GmbH. All rights reserved.)

Resveratrol, a natural polyphenolic compound, is abundantly found in plant foods and has been extensively studied for its anti-cancer properties. Given the important role of CSCs (Cancer Stem Cells) in breast tumorigenesis and progression, it is worth investigating the effects of resveratrol on CSCs. The article is an attempt to investigate the effects of resveratrol on breast CSCs. Resveratrol significantly inhibits the proliferation of BCSCs (breast cancer stem-like cells) isolated from MCF-7 and SUM159, and decreased the percentage of BCSCs population, consequently reduced the size and number of mammospheres in non-adherent spherical clusters. Accordingly, the injection of resveratrol (100 mg/kg/d) in NOD/SCID (nonobese diabetic/severe combined immunodeficient) mice effectively inhibited the growth of xenograft tumors and reduced BCSC population in tumor cells. After the reimplantation of primary tumor cells into the secondary mice for 30 d, all 6 control inoculations produced tumors, while tumor cells derived from resveratrol-treated mice only caused 1 tumor of 6 inoculations. Further studies by TEM (Transmission electron microscopy) analysis, GFP-LC3-II puncta formation assay and western blot for LC3-II, Beclin1 and Atg 7, showed that resveratrol induces autophagy in BCSCs. Moreover, resveratrol suppresses Wnt/β-catenin signaling pathway in BCSCs; over-expression of β-catenin by transfecting the plasmid markedly reduced resveratrol-induced cytotoxicity and autophagy in BCSCs. Our findings indicated that resveratrol inhibits BCSCs and induces autophagy via suppressing Wnt/β-catenin signaling pathway.

Abstract: In this study, resin adsorption as a means to enrich rare stilbenes cajaninstilbene acid (CSA) and longistyline C (LLC), and coumarin cajanuslactone (CL) from pigeon pea leaves was investigated. Among widely used twenty macroporous adsorption resins, NKA-9 resin presented higher adsorption capacity and desorption ratio in static tests. The adsorption kinetic model fitted better depended on types of compounds and pH values. The experimental adsorption data were better fitted to Langmuir isotherm (R 2 0.921–0.991) than Freundlich isotherm (R 2 0.753–0.988). In order to optimize the operating parameters for separating CSA, LLC and CL, dynamic adsorption and desorption tests were carried out. After one run treatment with NKA-9 resin, the contents of CSA, LLC and CL in the product were 10.82-, 9.07- and 108.90-fold increased with recovery yields of 81.31%, 89.76% and 96.77%, respectively. Moreover, NKA-9 resin exhibited excellent reusability within at least five cycles of adsorption/desorption. The developed methodology is a promising basis for large-scale preparation of CSA, LLC and CL from pigeon pea leaves. [Copyright &y& Elsevier]

A novel approach for synchronous extraction and enrichment of hydrophilic component and hydrophobic component with CO 2 -based switchable-solvent (SHS) from pigeon pea leaves was developed in the present study. After screening of SHS, N, N-dimethyl-cyclohexylamine (DMCHA)/water system was selected as the properest SHS for the extraction and enrichment process. To optimize this process, we conducted single factor experiments with the Box-Behnken design. The optimal parameters were as follows: solid-liquid ratio R (S/L) 40:1 (mg/mL), ultrasound time 15 min and bubbling CO 2 time 79 min (0.5 mL/s). Under the circumstances, the extraction yields of representative flavonoid vitexin and stilbene cajaninstilbenes acid (CSA) reached 1.80 ± 0.12 mg/g and 9.32 ± 0.08 mg/g, respectively, which were 1.06 and 1.49 folds to those by the traditional methods. And the contents of target compounds vitexin and CSA in the enriched extracts were 2.3% and 12.1%, which increased above 6.76 and 4.58 folds to that in extracts using 65% ethanol-UAE. And the results suggested that the N, N-dimethyl-cyclohexylamine (DMCHA)/water system can be guaranteed for at least 5 cycles with relatively stable extraction yields of vitexin and CSA. Furthermore, a theoretical study using density functional theory was put into effect to explore the properties of SHS and their relationship with the vitexin and CSA. The mechanism study showed that SHS had higher biocompatibility with target compounds due to the H-bonds. The present method was an eco-friendly, promising, and sustainable alternative to extract and enrich simultaneously hydrophilic and hydrophobic phytochemicals from plant materials. Image 1 • This paper developed a novel approach for efficient and recyclable extraction and enrichment of phytochemicals from the disused pigeon pea leaves in one solvent system. • The mechanism study showed that SHS had higher biocompatibility with target compounds due to the H-bonds using the density functional theory. • The switchable solvents have usually been used in the extraction of oil. Moreover, the exploit of SHS considering bioactive compounds from plants material has hardly been reported yet. [ABSTRACT FROM AUTHOR]