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Antiproliferative effects of salinomycin and TRAIL on GBM cell lines We have evaluated the effect of salinomycin on the proliferation of three human glioblastoma cell lines, U87MG, U251 and T98G. salinomycin in the feed additive, premixtures and feedingstuffs. For the quantification of salinomycin in chicken tissues the Applicant submitted a single laboratory validated and further verified method based on reverse phase HPLC coupled to a triple quadrupole mass spectrometer in electrospray ionisation mode using matrix Sacox® microGranulates, containing salinomycin sodium (SAL-Na), for chickens for fattening and chickens reared for laying have been recently re-evaluated by Panel on Additives and Products or Substances used in Animal Feed. Following an urgent request from the European Commission, the safety and efficacy of the product when fed to rabbits for fattening was assessed based on the available data Salinomycin sodium (SAL-Na) is active against certain Gram-positive bacteria, while Gram-negative species are resistant. SAL-Na at the proposed concentration is unlikely to increase shedding of Salmonella, Escherichia coli and Campylobacter and or induce resistance and cross-resistance to antimicrobials important in human and animal therapy. SAL-Na is safe for chickens for fattening at 70 mg Promising results from a few clinical pilot studies reveal that salinomycin is able to effectively eliminate cancer stem cells and to induce partial clinical regression of heavily pretreated and therapy-resistant cancers.

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Although the study was focused on breast cancer, Salinomycin will do the same in most epithelial cancers. Salinomycin was administered to chickens intravenously, in the left wing vein, at a dose of 0.25 mg /kg and orally at a dose of 2.5 mg /kg. Residue studies were carried out with supplemented feed at the rate of 100 mg /kg of feed for monensin in turkeys and 70 mg /kg for salinomycin in chickens, respectively. Promising results from preclinical trials in human xenograft mice and a few clinical pilote studies reveal that salinomycin is able to effectively eliminate CSCs and to induce partial clinical regression of heavily pretreated and therapy-resistant cancers. Based on these findings, salinomycin was therapeutically applicated "first-in-man" in 2010, in the context of a pilot clinical trial with a small cohort of patients with metastatic breast, ovarian, and head and neck cancers. Salinomycin (Sal), which is a polyether ionophore antibiotic from Streptomyces albus, has been proven to be able to kill different types of human cancer cells, most likely via interfering with ABC drug transporters, the Wnt/β-catenin signaling pathway, or other pathways. In vitro: Several hepatocellular carcinoma (HCC) cell lines were treated with Sal. Five experiments were conducted to test the anticoccidial efficacy of salinomycin (AHR-3096C, A. H. Robins) at 66 ppm and its compatibility with roxarsone (50 ppm) under floor pen conditions Monensin (100, 121 ppm), lasalocid (75, 125 ppm), and shuttle programs of salinomycin-monensin (66/100 ppm) or monensin-salinomycin (100/66 ppm) were included for comparison.

Together we will beat cancer About cancer Cancer types Cancers in general Causes of cancer Coping with Clinical trials offered by the Johns Hopkins Sidney Kimmel Comprehensive Cancer Center. We are experiencing extremely high call volume related to COVID-19 vaccine interest.

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av I Ekberg · 1980 — Shall we restrict ourselves to the results of provenance research or shall we proceed further? [Scots pine, Pinus sylvestris, Norway spruce, Picea abies, Sweden]  Clinical trials of three such HA formulations (termed hyaluronic acid The HA-PTX [199], HA-DOX [200], and HA-salinomycin [201] micelles exhibited more  hos antracykliner hos patienter med diffus stor B-cell; Clinical Research News The Molecular Basis for Inhibition of Stemlike Cancer Cells by Salinomycin  Clinical Research News.

Shall we restrict ourselves to the results of provenance

Salinomycin is able to effectively eliminate CSCs and to induce partial clinical regression of heavily pretreated and therapy-resistant cancers. It has also been demonstrated as a positive ionotropic and chronotropic agent that increased cardiac output, left ventricular systolic pressure, heart rate, mean arterial pressure, coronary artery vasodilatation and blood flow, and plasma Clinical Trial Klinisk prövning [Publikationstyp] Svensk definition. En i förväg planerad klinisk studie av säkerhet, effektivitet eller optimalt doseringsschema för ett eller flera diagnostiska, terapeutiska eller profylaktiska läkemedel, apparater eller tekniker, utförd på människor som valts ut enligt fördefinierade urvalskriterier och observeras för förutbestämda indikationer In Denmark, clinical trials must also be notified to a research ethics committee, which performs an overall assessment of the trial's ethical aspects. Before a clinical trial can be started, approvals must be obtained from both a research ethics committee and the Danish Medicines Agency. Clinical trials can also be sponsored by two or more persons or organisations. This is referred to as joint or co-sponsorship.

In 2009, a groundbreaking result was published in the scientific journal Cell , showing that Salinomycin can be effective in killing the cancer stem cells (CSC), the cancer cell population that is responsible for chemo resistance and metastasis. Although the study was focused on breast cancer, Salinomycin will do the same in most epithelial cancers. Salinomycin was administered to chickens intravenously, in the left wing vein, at a dose of 0.25 mg /kg and orally at a dose of 2.5 mg /kg. Residue studies were carried out with supplemented feed at the rate of 100 mg /kg of feed for monensin in turkeys and 70 mg /kg for salinomycin in chickens, respectively. Promising results from preclinical trials in human xenograft mice and a few clinical pilote studies reveal that salinomycin is able to effectively eliminate CSCs and to induce partial clinical regression of heavily pretreated and therapy-resistant cancers. Based on these findings, salinomycin was therapeutically applicated "first-in-man" in 2010, in the context of a pilot clinical trial with a small cohort of patients with metastatic breast, ovarian, and head and neck cancers. Salinomycin (Sal), which is a polyether ionophore antibiotic from Streptomyces albus, has been proven to be able to kill different types of human cancer cells, most likely via interfering with ABC drug transporters, the Wnt/β-catenin signaling pathway, or other pathways.
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Salinomycin, traditionally used as an anti-coccidial drug, has recently been shown to possess anti-cancer and anti-cancer stem cell (CSC) effects, as well as activities to overcome multi-drug resistance based on studies using human cancer cell lines, xenograft mice, and in case reports involving cancer patients in pilot clinical trials. Therefore, salinomycin may be considered as a promising novel anti-cancer agent despite its largely unknown mechanism of action. Surprisingly, a small scale of clinical trial has demonstrated that salinomycin only exerted minimal side effects at antineoplastic dosages (200–250 μg·kg − 1, i.v., every second day for 3 weeks) in human . Analogously, our data also showed that the cytotoxicity of salinomycin on the UM cells is about 11~21-fold as high as that of the normal retinal pigmented epithelium cells, which implied the safety of salinomycin used in treatment of UM. Five experiments were conducted to test the anticoccidial efficacy of salinomycin (AHR-3096C, A. H. Robins) at 66 ppm and its compatibility with roxarsone (50 ppm) under floor pen conditions Monensin (100, 121 ppm), lasalocid (75, 125 ppm), and shuttle programs of salinomycin-monensin (66/100 ppm) or monensin-salinomycin (100/66 ppm) were included for comparison. Thus, here we aimed to investigate the activity of salinomycin against tumor initiating cells isolated from patients with colorectal cancer. Methods: Primary tumor-initiating cells (TIC) isolated from human patients with colorectal liver metastases or from human primary colon carcinoma were exposed to salinomycin and compared to treatment with 5-FU and oxaliplatin.

Breast cancer stem cell selectivity of synthetic nanomolar- active salinomycin analogs. Research output: Contribution to journal › Article. 14 Jun 2018 Naujokat, C.; Steinhart, R. Salinomycin as a drug for targeting human cancer stem cells. J. Biomed. Biotechnol. 2012, 2012, 604076, DOI:  Close.
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J. Biomed. Biotechnol. 2012, 2012, 604076, DOI:  Close. Research Article to understand the molecular mechanisms involved in cancer drug resistance and to study the activity of new drugs, e.g. salinomycin. Salinomycin.

Salinomycin sodium salt (Salinomycin sodium) acts on the Wnt/Fzd/LRP complex, blocks Wnt-induced LRP6 phosphorylation, and causes degradation of the LRP6 protein.
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Clinical trial: N/A. Reference: [1] Wang F,He L,Dai WQ,Xu YP,Wu D,Lin CL,Wu SM,Cheng P,Zhang Y,Shen M,Wang CF,Lu J,Zhou YQ,Xu XF,Xu L,Guo CY. Salinomycin inhibits proliferation and induces apoptosis of human hepatocellular carcinoma cells in vitro and in vivo. PLoS One.2012;7(12):e50638. RESEARCH ARTICLE Salinomycin: Anti-tumor activity in a pre-clinical colorectal cancer model Johannes Klose ID 1*, Stefan Trefz1, Tobias Wagner1, Luca Steffen1, Arsalie Preißendo¨ rfer Charrier1, Praveen Radhakrishnan1, Claudia Volz1, Thomas Schmidt ID 1, Alexis Ulrich1, Sebastian M. Dieter2, Claudia Ball3, Hanno Glimm2,3,4,5, Martin Schneider1 1 Department of General, Visceral and The ionophore salinomycin has been shown to kill cancer stem cells and is therefore a promising future salinomycin's mechanism of action is of great importance to understanding salinomycin's safety and potential for clinical application. 4. Salinomycin's effect on CSC National Cancer Institute of Canada Clinical Trials Group: Salinomycin is a polyether antibiotic with properties of an ionophore, which is commonly used as cocciodiostatic drug and has been shown to be highly effective in the elimination of cancer stem Salinomycin sodium salt (Salinomycin sodium), an antibiotic potassium ionophore, is a potent inhibitor of Wnt/β-catenin signaling. Salinomycin sodium salt (Salinomycin sodium) acts on the Wnt/Fzd/LRP complex, blocks Wnt-induced LRP6 phosphorylation, and causes degradation of the LRP6 protein.