@article {85, title = {Evaluation of Phytochemical Content of White Tea Clone 100 and Changes the Expression of Tumor Suppressor Genes on Colorectal Cancer Cell Line HCT116}, journal = {Pharmacognosy Research}, volume = {11}, year = {2019}, month = {August 2019}, pages = {224-229}, type = {Original Article}, chapter = {224}, abstract = {

Aim/Background: Colorectal carcinoma cancer is one of the main types of cancer with high death rate of patients, according to their non-healthy lifestyle. In this research, we evaluated inhibitory of white tea clone 100 extract on colorectal cancer cell line HCT-116, and its effectiveness in expression level of three tumor suppressor genes. Materials and Methods: Total polyphenolic content in all samples were measured using the Folin{\textendash}Ciocalteu method, and free radical adsorption investigated by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay. 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used to evaluate the white tea extract inhibitory effect on HCT-116 cells. Results: Among different extraction methods, the white tea aqueous extracts produced the highest amount of polyphenols and DPPH radical scavenging activity (36.67 {\textpm} 0.54 mg gallic acid equivalent/g dry weight and 71.74\% {\textpm} 0.42\%, respectively). Cell survival analysis in the MTT assay indicated that aqueous white tea extract could reduce the viability of HCT-116 cells in 8, 16, and 24 h considerably, related to the concentration-dependent manner. The real-time polymerase chain reaction results indicated the significantly increased expression level (P \< 0.05) of tumor suppressor genes DCC, TGFBR2, and P53 in the concentration of 1000 μg/ml at 24 h. Conclusion: White tea aqueous extract because of having hydroxyl group in its structure at optimal concentration in all three times of experimental, could lead to a positive changes effect on gene expression in the tumor suppressor family.

}, keywords = {3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay, HCT-116 cell line, Radical scavenging activity, Tumor suppressor genes, White tea}, doi = {10.4103/pr.pr_39_19}, author = {Fereydoon Bondarian and Asa Ebrahimi and Frouzandeh Mahjoubi and Eslam Majidi Hervan and Reza Azadi Gonbad} } @article {396, title = {Isolation and Characterization of Chemopreventive Agent from Sphaeranthus amaranthoides Burm F}, journal = {Pharmacognosy Research}, volume = {8}, year = {2016}, month = {December 2015}, pages = {61-65}, type = {Original Article}, chapter = {61}, abstract = {

Objective: To investigate the in vitro cytotoxic effect and to isolate and characterize a chemopreventive secondary metabolite from Sphaeranthus amaranthoides Burm F (sivakaranthai). Materials and Methods: In vitro cytotoxic effect was carried out by 3 (4,5-dimethylthiazol-2-yl) 2,5-diphenyltetrazolium bromide assay. Different concentrations of the extracts were tested on three different cell lines namely A549, HT29, and MCF7. The chloroform extract was subjected to column chromatography, and the isolated compound was characterized by various spectral methods and by single crystal X-ray crystallography. Results: The concentration that cause 50\% growth inhibition value of chloroform extract was found to be 0.9 and 19 μg/mL against MCF7 and A549 cell lines, respectively. Chloroform extract was subjected to column chromatography for the isolation of phytoconstituent. The structure of the isolated compound was identified by spectroscopic techniques such as infrared, nuclear magnetic resonance, XRD, and mass spectroscopy. On comparison of complete spectral detail of the compound, the proposed structure was identified as chrysosplenol D (a flavonoid). Chrysosplenol D was isolated for the first time from this plant. Conclusion: The chloroform extract had higher cytotoxic effect, and the isolated chrysosplenol D may be responsible for the anti-proliferative effect of the plant.

}, keywords = {3 (4, 5-dimethylthiazol-2-yl) 2, 5-diphenyltetrazolium bromide assay, Characterization, Chemopreventive agent, Chrysosplenol D, Isolation, Sphaeranthus amaranthoides}, doi = {10.4103/0974-8490.171101}, author = {S. Gayatri and R. Suresh and C. Uma Maheswara Reddy and K. Chitra} } @article {395, title = {Chemical Constituents and Bioactivities of Glinus Oppositifolius}, journal = {Pharmacognosy Research}, volume = {7}, year = {2015}, month = {June 2015}, pages = {138-147}, type = {Original Article }, chapter = {138}, abstract = {

Objectives: To isolate the secondary metabolites from the dichloromethane (DCM) extracts of Glinus oppositifolius; to test for the cytotoxicity of a new triterpene, oppositifolone (1); and to test for the hypoglycemic, analgesic, and antimicrobial potentials of 1, DCM and aqueous leaf extracts of G. oppositifolius. Methods: The compounds were isolated by silica gel chromatography and identified by nuclear magnetic resonance spectroscopy. The cytotoxicity potential of 1 was tested using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Triterpene 1, DCM, and aqueous leaf extracts were tested for hypoglycemic potential using the oral glucose tolerance test; analgesic potential using the tail-flick assay, and antimicrobial potential using the disc diffusion method. Results: The DCM extracts of G. oppositifolius afforded 1, squalene, spinasterol, oleanolic acid, phytol, and lutein from the leaves; squalene and spergulagenin A from the stems; and spinasterol from the roots. Triterpene 1 was cytotoxic against human colon carcinoma 116 with an IC50 value of 28.7 but did not exhibit cytotoxicity against A549. The aqueous leaf extract at 200 mg/kg body weight (BW) exhibited hypoglycemic activity with a pronounced \% blood glucose reduction of 70.76\% {\textpm}17.4\% within 0.5 h after introduction. The DCM leaf extract showed a lower \% blood glucose reduction of 18.52\% {\textpm}13.5\% at 200 mg/kg BW within 1.5 h after introduction, while 1 did not exhibit hypoglycemic activity. The samples did not exhibit analgesic property and were inactive against multiple drug resistant bacterial pathogens. Conclusion: The compounds responsible for the hypoglycemic activity of G. oppositifolius which are fast acting (0.5 h) are found in the aqueous leaf extract.

}, keywords = {3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay, Analgesic, Antimicrobial, Cytotoxic, Glinus oppositifolius Linn, Hypoglycemic, Molluginaceae, Oppositifolone}, doi = {10.4103/0974-8490.150520}, author = {Consolacion Y. Ragasa and Esperanza C. Cabrera and Oscar B. Torres and Adiel Inah Buluran and Dinah L. Espineli and Dennis D. Raga and Chien-Chang Shen} }