Pyrite bio-leachate, mine wastewater can sterilize the rice (Oryza sativa L.) seeds and promote the germination.

We developed the way to use pyrite bio-leachate (PBL), the wastewater of bioleaching of refractory gold ore in agriculture. PBL contains high amount of iron and at certain concentration, iron has toxicity on microorganisms. Therefore PBL can be used for rice seed sterilization. Method 1 is soaking rice seeds in 100%, 10%, and 2% PBL for 1, 2, 3, and 4 days (25℃) and drying them. Method 2 is soaking rice seeds in 100%, 10%, and 2% PBL for 30 min, 60 min, and 120 min (25℃), wetting for 2 days under the shade and drying for 5 days. Method 1 with 100%, 10%, and 2% PBL did not sterilize rice seeds completely. Method 2 with 100% and 10% PBL showed the complete sterilization effect and enhanced the germination of rice seeds in any soaking time. Similar results were achieved in seedbed experiments. PBL which has serious potential to pollute the environment can be used for rice seed sterilization. Soaking rice seeds in 100% and 10% PBL for 30 min, 60 min, and 120 min (25℃), wetting for 2 days under the shade and drying them for 5 days, can sterilize the rice seeds completely and enhance the germination.

NF-kappaB inhibition increases chemosensitivity to trichostatin A-induced cell death of Ki-Ras-transformed human prostate epithelial cells.

Chemoresistance has been one of the major problems in anticancer therapy. In our effort to find a potential molecular target for overcoming the chemoresistance in prostate cancer, a promising anticancer drug trichostatin A (TSA) induced cell death was found to be compromised by enhanced NF-kappaB activation in 267B1/K-ras human prostate epithelial cancer cells. However, both the NF-kappaB activation and chemoresistance were reduced by pretreatment with proteasome inhibitor-I (ProI), accompanied by accumulations of both IkappaBalpha and p65/RelA (but not p50/NF-kappaB1) in the cytoplasm. Clonogenic cell survival and soft agar assays further confirmed the increased TSA chemosensitivity of 267B1/K-ras cells by ProI treatment. Moreover, dominant negative mutant of IKKbeta, IkappaBalpha and p65 enhanced the chemosensitization, too. Unexpectedly, using LY294002 and PD98059, phosphatidylinositol-3-kinase and mitogen-activated protein kinase were also implied in TSA chemoresistance through NF-kappaB activation, while these compounds had showed no effect on radiosensitization in the cells. On the other hand, together with TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling) assay, activations of caspase-8 and caspase-3 by TSA and ProI were noticed, suggesting the involvement of apoptotic process in chemosensitization of 267B1/K-ras cells. Altogether, these results suggest that blocking the NF-kappaB activation pathway could be an efficient target for improving the TSA chemosensitization and applying to the development of anticancer therapeutics in Ki-Ras-overexpressing tumorigenic cells, including prostate cancer.