P73 engages A2B receptor signalling to prime cancer cells to chemotherapy-induced death.

ABSTRACT: Tumour cells often acquire the ability to escape cell death, a key event leading to the development of cancer. In almost half of all human cancers, the capability to induce cell death is reduced by the mutation and inactivation of p53, a tumour suppressor protein that is a central regulator of apoptosis. As a result, there is a crucial need to identify different cell death pathways that could be targeted in malignancies lacking p53. p73, the closely related p53 family member, can regulate many p53 target genes and therefore some of the same cellular responses as p53. Unlike p53, however, p73 is seldom mutated in cancer, making it an attractive, alternative death effector to target. We report here the ability of p73 to upregulate the expression of the A2B receptor, a recently characterized

SUBMITTER: Long JS 

PROVIDER: S-EPMC4761646 | biostudies-literature | 2015 Oct

REPOSITORIES: biostudies-literature