Addiction of MYCN Amplified Tumours to B-MYB Underscores a Reciprocal Regulatory Loop

作者：Gualdrini Francesco; Corvetta Daisy; Cantilena Sandra; Chayka Olesya; Tanno Barbara; Raschella Giuseppe; Sala Arturo^*

来源：Oncotarget, 2010, 1(4): 278-288.

• neuroblastoma
• oncogene
• synthetic lethality
• transcription factor

MYCN is a member of the MYC family of oncoproteins frequently amplified or overexpressed in aggressive, paediatric tumours of the nervous system. In this study we have identified the gene B-MYB, encoding the transcription factor also known as MYBL2, as a downstream target of MYCN. Using multiple in silico databases we show that expression of B-MYB significantly correlates with that of MYCN in neuroblastoma patients. MYCN binds to and activates the B-MYB gene in vivo and in vitro. Blunting B-MYB expression by RNA interference causes reduced proliferation of MYCN amplified, but not MYCN-non amplified, neuroblastoma cell lines, indicating that tumour cells are addicted to B-MYB in a MYCN dependent manner. Notably, B-MYB binds in vivo to the MYCN amplicon and is required for its expression. We conclude that MYCN and B-MYB are engaged in a reciprocal regulatory loop whose pharmacological targeting could be beneficial to patients with the aggressive forms of cancer in which MYCN is amplified.

• 出版日期2010-8