Title : The impact of arsenic trioxide and all-trans retinoic acid on p53 R273H-codon mutant glioblastoma.

Pub. Date : 2014 May

PMID : 24399651






9 Functional Relationships(s)
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1 The impact of arsenic trioxide and all-trans retinoic acid on p53 R273H-codon mutant glioblastoma. Arsenic Trioxide tumor protein p53 Homo sapiens
2 The results showed that U87-p53(R273H) cells generated more rapid neurosphere growth than U87-p53(wt) but inhibition of neurosphere proliferation was seen with both ATO and ATRA. Arsenic Trioxide tumor protein p53 Homo sapiens
3 U87-p53(R273H) neurospheres showed resistance to differentiation into glial cells and neuronal cells with ATO and ATRA exposure. Arsenic Trioxide tumor protein p53 Homo sapiens
4 ATO was able to generate apoptosis at high doses and proliferation of U87-p53(wt) and U87-p53(R273H) cells was reduced with ATO and ATRA in a dose-dependent manner. Arsenic Trioxide tumor protein p53 Homo sapiens
5 ATO was able to generate apoptosis at high doses and proliferation of U87-p53(wt) and U87-p53(R273H) cells was reduced with ATO and ATRA in a dose-dependent manner. Arsenic Trioxide tumor protein p53 Homo sapiens
6 ATO was able to generate apoptosis at high doses and proliferation of U87-p53(wt) and U87-p53(R273H) cells was reduced with ATO and ATRA in a dose-dependent manner. Arsenic Trioxide tumor protein p53 Homo sapiens
7 ATO was able to generate apoptosis at high doses and proliferation of U87-p53(wt) and U87-p53(R273H) cells was reduced with ATO and ATRA in a dose-dependent manner. Arsenic Trioxide tumor protein p53 Homo sapiens
8 Elevated pERK1/2 and p53 expression was seen in U87-p53(R273H) neurospheres, which could be reduced with ATO and ATRA treatment. Arsenic Trioxide tumor protein p53 Homo sapiens
9 Elevated pERK1/2 and p53 expression was seen in U87-p53(R273H) neurospheres, which could be reduced with ATO and ATRA treatment. Arsenic Trioxide tumor protein p53 Homo sapiens