The discovery of p73 as a family member of p53 has instigated a number of s
tudies in search of its function, regulation, and involvement in tumorigene
sis. p73 has been identified as a transcription factor that can regulate p5
3-dependent transcriptional targets. Similarly to p53, p73 can induce apopt
osis in response to various stimuli, including certain types of DNA damage.
This evidence suggests that p73 may act as a tumor suppressor with overlap
ping functions of p53. While mutations of p73 appear rare in human tumors,
some leukemias have shown silencing of the gene by hypermethylation. Thus,
introduction of p73 into tumor cells possessing inactive p53 may provide a
valuable therapeutic approach. (C) 2001 Elsevier Science Ltd. All rights re
served.