Camptothecin hl-60
WebHL-60 cells exposed to okadaic acid and camptothecin underwent morphological and biochemical changes typical of apoptosis, including internucleosomal DNA fragmentation and PAI-2 cleavage.
Camptothecin hl-60
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WebWe investigated expression of cyclin A in HL-60 cells after induction of apoptosis with doxorubicin and etoposide. Following apoptotic trigger, both cells arrested in G2/M phase of the cell cycle... WebOct 1, 2001 · The study identifies and delineates signaling factors involved in BN80915-induced apoptosis in HL-60 cells. Cell cycle analysis of HL-60 cells treated with graded …
WebJun 1, 2000 · Camptothecin (50 mM), a cytotoxic quinoline alkaloid which inhibits the DNA enzyme topoisomerase I, was used as a positive control (King et al., 2000). ... Internalization of Bacillus intermedius... WebThis potent antioxidant is a cytoprotectant in several experimental models. However, its neuroprotective activities are scarcely available, especially in the hippocampal region associated with...
WebApr 27, 2010 · Polysaccharopeptide (PSP) from Coriolus versicolor (Yunzhi) is used as a supplementary cancer treatment in Asia. The present study aims to investigate whether PSP pre-treatment can increase the response of the human leukemia HL-60 cells to apoptosis induction by Camptothecin (CPT). We used bivariate bromodeoxyuridine/propidium … WebOct 1, 2003 · (A) HL-60 cells were treated with various doses of camptothecin, a DNA topoisomerase I inhibitor, for 20 hours. (B) H-7 cells were deprived of IL-3 for the indicated times. (Upper panels) Proteins were extracted and subjected to SDS-PAGE and Western blotting with anti-Bax antibody.
WebResearch Polysaccharopeptides derived from Coriolus versicolor potentiate the S-phase specific cytotoxicity of Camptothecin (CPT) on human leukemia HL-60 cells Jennifer Man-Fan. article as: Wan et al., Polysaccharopeptides derived from. properly cited. Research Polysaccharopeptides derived from Coriolus versicolor potentiate the S-phase ...
WebCamptothecin [47, 48]. binds non-covalently with topoisomerase-I and suppresses their catalytic activity, thus show- Vinblastine and its derivatives have been used ing anti-cancer properties. ... (HL-60, MCF-7) with IC50 value Due to the large diversity of endophytic fungi, (5.8, 20.15 μM) [92]. Incarxanthone B, a novel various novel cytotoxic ... csidentity experianWebNov 5, 2015 · The effect of vincristine, cisplatin or 10-hydroxy camptothecin on inducing apoptosis of HL-60 cells co-cultured with the MS-5 cell layer within 48 h was tested with/without E5. eagle country local newsWebJul 26, 2024 · CP6 displayed potent and comparable cytotoxicity. Interestingly, CP6 exhibited weak cytotoxicity against the normal cell line HUVEC and HL-7702 with a higher IC 50 (22.5 μM) and (18.5 μM). CP6 show minimal cytotoxicity against the human cervix adenocarcinoma cancer cell line HeLa with an IC 50 of 5.5 μM. csidc land allotment chhattisgarhWebJun 1, 1992 · Camptothecin or teniposide induced apoptosis selectively in S phase of HL-60 cells; apoptotic cells from camptothecin-treated cultures, however, despite the marked nucleolysis, still expressed p120. csidd regulationsWebJan 15, 2024 · In summary, 12 novel biotinylated camptothecin derivatives were designed, synthesized, and evaluated for anticancer activities against a panel of five human cancer … eagle country 99.3 wschWeb14808-60-7 Wt. % 60 - 100 1 - 5 This product is a hazardous chemical as defined by the OSHA Hazard Communication Standard, 29 CFR 1910.1200. Gypsum (calcium sulfate) … eagle country eagle cam facebookWebCamptothecin is a naturally occurring alkaloid derived from the plant Camptotheca acuminata that was identified in an anticancer drug discovery screen in the 1960s.67 … eagle country online local news