Citescore is produced by Scopus, and can be a little higher or different compared to the impact factor produced by Journal Citation Report.
administration, which was similar to that measured after i.v.
In addition, flow cytometrical analysis revealed that most of these cells were accumulated in the G2/M phase of the cell cycle, and a new peak located in the G2/M phase of tetraploid cells emerged. In adenocarcinoma the mean content was 66.5 +/- 14 fmoles/mg of protein. Lycorine is a member of the alkaloid group from the bulb of the amaryllidaceae.
JAMA - Journal of the American Medical Association, Q2. AII, ZCC, and DES had similar affinities for the EBSII in the three cell lines. These results indicate that thymidylate synthase inhibition increases when the intracellular folate is exogenously supplemented and maintained at an adequate concentration.
Ten consecutive crypts from the proximal and distal portion of each specimen were scored for nuclear aberrations and the karyorrhectic index (KI) was determined. On the other hand, the cells treated with 100 microM of the drug did not increase in volume and their progress in the cell cycle was almost completely blocked. The antitumor activity of MKT-077 was confirmed using human tumor xenografts in nude mice. . those of the individual authors and contributors and not of the publisher and the editor(s). Mitochondrial dysfunction has been associated with Dox-induced cardiotoxicity.
AAPS Journal. Doxorubicin (Dox) is a chemotherapeutic agent widely used for the treatment of numerous cancers.
For this purpose, we investigated the optimal duration of whole body hyperthermia (WBH) (41.5 degrees C) when administered simultaneously with carboplatin (CBDCA). Overcoming the blood–brain barrier (BBB) is a major challenge in the development of therapies for central nervous system (CNS) disorders. Dihydrofolate reductase inhibitors are an important class of drugs, as evidenced by their use as antibacterial, antimalarial, antifungal, and anticancer agents.
September, 2017 issue.
However, clinical usage in the treatment of cancers has been limited by its hypercalaemic effects. The rats were sacrificed 18 hours later and their colons were removed. Antitumoral macrophages (MAK) were obtained by the culture of human mononuclear cells in hydrophobic bags.
New vitamin D analogues may be promising drugs for the treatment of advanced ovarian carcinomas.
administration of human AGP (87:1 ratio). In a series employing ferric ammonium citrate (0.46% Fe), in addition to ferrous sulfate (0.11% Fe) and ferric ammonium sulfate (0.12% Fe), DMH injection was started on day 15 and the animals necropsied 22 weeks after the last of 23 doses.
The influence of physical activity in 1,2 dimethylhydrazine induced colon carcinogenesis in the rat.
In the present study, our aim was to investigate the expression of mRNA and protein for somatostatin receptor types-1, -2, -3, -4, -5 (SSTR-1–5) in human UM tissue samples and in OCM-1 and OCM-3 human UM cell lines by qRT-PCR, western blot and ligand competition assay.
In our opinion, antisense oligonucleotides, which can be used in the form of targeted ointments, provide real hope as a treatment that will eliminate cancer cells near the tumor focus both before and after surgery. In this study, the activity of eugenol was evaluated in a human cervical, Eugenol is a phytochemical present in different plant products, e.g., clove oil.
Adenocarcinomas occurred in the small intestine and were more prominent in the control and 15% guar gum dietary groups but fewer with the ferric ammonium sulfate supplement. Synergistic effects of danazol and mifepristone on the cytotoxicity of UCN-01 in hormone-responsive breast cancer cells. The effects of ZCC could be partially reversed by washing the drug out of cells. Anticancer Research Journal Impact (Facteur d'impact) 2019:
We have recently shown that AII and its major metabolite Z-alpha-chlorochalcone (ZCC) inhibit proliferation of both estrogen-responsive and -nonresponsive human breast cancer cells, suggesting its mechanism is not mediated by the type I estrogen receptor (ER).
adalah Q2.
Thirty-two quinoxaline-derivatives of 3-substituted-4-(quinoxalin-6-yl) pyrazoles, Uveal melanoma (UM) is the most common primary intraocular malignancy in adults, with an incidence of 4–5 cases per million. Abbreviation,
However, the clinical use of Dox is limited by its unwanted cardiotoxicity.
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