A431

AcronymDefinition
A431human epidermoid carcinoma cells
References in periodicals archive ?
Katiyar, "Berberine inhibits growth, induces G1 arrest and apoptosis in human epidermoid carcinoma A431 cells by regulating Cdki-Cdk-cyclin cascade, disruption of mitochondrial membrane potential and cleavage of caspase 3 and PARP," Carcinogenesis, vol.
Axworthy et al., "Radioimmunotherapy of A431 xenografted mice with pretargeted B3 antibodystreptavidin and90Y-labeled 1, 4, 7, 10-tetraazacyclododecaneN, N/, N/, N"'-tetraacetic acid (DOTA)-biotin," Cancer Research, vol.
Sengupta et al., "Regulation of Bcl-2 expression by HuR in HL60 leukemia cells and A431 carcinoma cells," Molecular Cancer Research, vol.
EGCG has been shown to have various anticancer effects in A431 epidermoid carcinoma cell line by blocking and inhibiting the tyrosine kinase activity of ErbB1 [83].
Thus, for example, diosgenin has antiproliferativeactivity, namely, inprostatecancer(PC-3 and DU-145 cells) [23], colon carcinoma (HCT-116 and HT-29 cells) [24], erythroleukemia (HEL cells) [27], squamous carcinoma (A431, Hep2, and RPMI2650 cells) [28], hepatocellular carcinoma (HepG2 and HCC cells) [6,25,29], gastric cancer (BGC-823 cells) [30], lung cancer (A549 cells) [31], breast cancer (MCF-7) [6,32-34], and human chronic myeloid leukemia (CML) (K562 cells) [1].
Petukhova, "Functional compartmentalisation of NF-[kappa]B-associated proteins in A431 cells," Cell Biology International, vol.
Shukla, "[6]-Gingerol induced reactive oxygen species regulated mitochondrial cell death pathway in human epidermoid carcinoma A431 cells," Chemico-Biological Interactions, vol.
reported that sanguinarine had preferential, concentration dependent tumour cytotoxicity when tested against the A431 epidermoid carcinoma cell line and normal human epidermal keratinocytes derived from foreskin.
There are also some other similar reports about the role of STAT3 in the radioresistance of A431 squamous cell carcinoma, glioma, and head and neck carcinoma [27-29].
canadensis and the [H.sub.2]O extracts prepared from the residual plant materials were investigated for their cytotoxic properties on HeLa, MCF-7 and A431 cell lines using the MTT assay.
These findings contrast from earlier reports, in which ZnO NPs have shown to cause statistically significant DNA damage at concentrations of 5 [micro]g/mL and 0.8 [micro]g/mL after an exposure period of 6 hours in human epidermal cells (A431).
http://www.ivis.org/advances/rc es/ A431 2.0708.ES.pdf?LA=2