Tayyaba Afsar

Growth inhibition and apoptosis in cancer cells induced by polyphenolic compounds of Acacia hydaspica : Involvement of multiple signal transduction pathways

Acacia hydaspica R. Parker is known for its medicinal uses in multiple ailments. In this study, we performed bioassay-guided fractionation of cytotoxic compounds from A. hydaspica and investigated their effects on growth and signaling activity in prostate and breast cancer cell lines. Four active polyphenolic compounds were identified as 7-O-galloyl catechin (GC), catechin (C), methyl gallate (MG), and catechin-3-O-gallate (CG). The four compounds inhibited prostate cancer PC-3 cell growth in a dose-dependent manner, whereas CG and MG inhibited breast cancer MDA-MB-231 cell growth. All tested compounds inhibited cell survival and colony growth in both cell lines, and there was evidence of chromatin condensation, cell shrinkage and apoptotic bodies. Further, acridine orange, ethidium bromide, propidium iodide and DAPI staining demonstrated that cell death occurred partly via apoptosis in both PC-3 and MDA-MB-231 cells. In PC-3 cells treatment repressed the expression of anti-apoptotic molecules Bcl-2, Bcl-xL and survivin, coupled with down-regulation of signaling pathways AKT, NFκB, ERK1/2 and JAK/STAT. In MDA-MB-231 cells, treatment induced reduction of CK2α, Bcl-xL, survivin and xIAP protein expression along with suppression of NFκB, JAK/STAT and PI3K pathways. Our findings suggest that certain polyphenolic compounds derived from A. hydaspica may be promising chemopreventive/therapeutic candidates against cancer.

Protective effect of Launaea procumbens against KBrO 3 induced nephrotoxicity in rats

Launaea procumbens is traditionally used in the treatment of renal dysfunction. In the present study, protective effects of L. procumbens against KBrO3-induced nephrotoxicity in rat were determined. In this study, 24 male albino rats (195 to 200 g) were equally divided into 4 groups. Group I was given saline (1 ml/kg b.w., 0.85% NaCl) and DMSO (1 ml/kg b.w.); Group II was treated with KBrO3 (30 mg/kg b.w., i.p.); Groups III and IV administered with KBrO3 and after 48 h with L. procumbens (100; 200 mg/kg b.w.). All the treatments were given twice a week for 6 weeks. The results revealed that KBrO3 induced oxidative stress as evidenced by the significant depletion (P < 0.01) of antioxidant enzymes (catalase CAT, superoxide dismutase, SOD, glutathione-S-transferase, GST, glutathione reductase; GSR, glutathione peroxidase GSH-px and quinone reductas, QR) and glutathione contents while enhanced markedly (P < 0.01) tissue nitrite, lipid peroxidation and hydrogen peroxide level in kidney. Coadministration revealed that L. procumbens methanol extract significantly (P < 0.01) protect the liver against KBrO3 mediated oxidative damage by restoring activity of antioxidant enzyme and lipid peroxidation which might be due to the presence plant bioactive constituents.