Selection for TRAIL resistance results in melanoma cells with high proliferative potential.

Abstract:

:To better understand the outcome of the interaction between TNF-related apoptosis-inducing factor (TRAIL) and tumor cells, we studied TRAIL-resistant melanoma cells resulting from prolonged exposure to TRAIL and found that they had higher proliferative activity than the parental cells both in vitro and in vivo. This was associated with reduced p53 and p21 expression and increased activation of Erk1/2 and Akt. Accelerated proliferation was not due to TRAIL-mediated signaling but appeared to be the result of selection of previously existing, characteristically distinct cells. Moreover, responses of p53 to stimulation in the TRAIL-resistant cells appeared to be impaired.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Wu JJ,Zhang XD,Gillespie S,Hersey P

doi

10.1016/j.febslet.2005.02.041

keywords:

subject

Has Abstract

pub_date

2005-03-28 00:00:00

pages

1940-4

issue

9

eissn

0014-5793

issn

1873-3468

pii

S0014-5793(05)00250-4

journal_volume

579

pub_type

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