Researchers found that inhibiting protein BMI1 was able to impair tumour growth in lung cancer. The study was led by Professor Daniel Tenen, Director of CSI Singapore et al. Lung cancer is one of the deadliest cancers in the world, accounting for 30% of tumour-related deaths. Like many solid tumours, lung cancer is very heterogeneous (consisting of cancer cells which behave and respond differently) and hence there is currently no single efficient drug which is able to treat all patients.
Prof Tenen has worked on the differentiation factor C/ EBPa for several decades, demonstrating that it is an important tumour suppressor, first in acute myelogenous leukemia, and subsequently, in studies in collaboration with Dr Levantini, in lung cancer. In addition, loss of C/EBPa has also been found to have a role in the development of other cancer types such as hepatic, squamous cell, and prostate cancer. Despite this, the ways in which C/EBPa suppresses tumour formation still remains unknown.
In the past few years, Dr Levantini continued the investigation of C/EBPa in lung cancer. She confirmed one subtype of lung cancer ie non-small cell lung cancer (NSCLC) frequently expressed low levels of C/EBPa. Low or absent C/EBPa resulted in poorer survival when they corresponded with a reciprocally high expression of BMI1, a gene implicated in the development of tumours of colon, breast, and stomach, as well as some forms of leukemia. Dr Levantini then went on to conduct a pre-clinical study in which deleting C/EBPa resulted in NSCLC. Analysis of this study led to the discovery that C/EBPa suppressed lung tumour formation by inhibiting the expression of BMI1. Dr Levantini then demonstrated that reducing the levels of BMI1 by genetic means, or by using a drug reducing expression of BMI1, led to inhibition of tumour formation.
“This study has established an important link between C/EBPa and BMI1 for the first time. Furthermore, these findings suggest that assessment of expression levels of these proteins could be used as a way to predict which patients might benefit from drugs which inhibit BMI1, some of which are currently being evaluated in clinical trials,” said Prof Tenen. Knowing the substantial role that BMI1 plays in the formation and development of aggressive lung cancer types, the findings will contribute to the development of better therapies for cancer patients. http://stm.sciencemag.org/content/8/350/350ra104
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