Title : p53-independent apoptosis induced by paclitaxel through an indirect mechanism.

Pub. Date : 1997 Sep 2

PMID : 9275183






6 Functional Relationships(s)
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1 p53-independent apoptosis induced by paclitaxel through an indirect mechanism. Paclitaxel transformation related protein 53, pseudogene Mus musculus
2 We tested the requirement for wild-type p53 in the response of tumor cells to treatment with paclitaxel (trade name Taxol), an antineoplastic agent that stabilizes cellular microtubules. Paclitaxel transformation related protein 53, pseudogene Mus musculus
3 Although paclitaxel is broadly effective against human tumor xenografts in mice, including some known to carry p53 mutations, we found that p53-containing mouse tumor cells were significantly more sensitive to direct treatment with this drug than were p53-deficient tumor cells. Paclitaxel transformation related protein 53, pseudogene Mus musculus
4 Although paclitaxel is broadly effective against human tumor xenografts in mice, including some known to carry p53 mutations, we found that p53-containing mouse tumor cells were significantly more sensitive to direct treatment with this drug than were p53-deficient tumor cells. Paclitaxel transformation related protein 53, pseudogene Mus musculus
5 Although paclitaxel is broadly effective against human tumor xenografts in mice, including some known to carry p53 mutations, we found that p53-containing mouse tumor cells were significantly more sensitive to direct treatment with this drug than were p53-deficient tumor cells. Paclitaxel transformation related protein 53, pseudogene Mus musculus
6 Conditioned medium from paclitaxel-treated macrophages was capable of inducing p53-independent apoptosis when applied to transformed mouse embryonic fibroblasts and was inhibitable by antibodies against TNF-alpha. Paclitaxel transformation related protein 53, pseudogene Mus musculus