Skip to main content
< Back to news
Proliferative and invasive capacity of tumour cells (centre) compared to normal cells (left) and effect of Trametinib treatment, which reduces the invasive capacity and tumoural load (right). Image: Marco Milán, IRB Barcelona.

Researchers at IRB Barcelona manage to selectively eliminate cells that express the RAS oncogene

A team, led by ICREA researcher Marco Milán from the Institute for Research in Biomedicine (IRB Barcelona) at PCB, have managed to inhibit the capacity of RAS to block cell death, thus eliminating malignant tumours without affecting the development of organs.The results of the study pave the way to combining irradiation treatments with the administration of RAS pathway inhibitors to eliminate tumour cells.


The RAS oncogene is activated in 30% of human cancers and it results in the proliferation and transformation of tumour cells. No effective inhibitor has been found for this protein to date.

ICREA researcher Marco Milán, head of the Development and Growth Control Laboratory at the Institute for Research in Biomedicine (IRB Barcelona), has led a study published in Cell Reports that identifies the weak point of RAS-expressing cells. 

Milán´s lab has used the fruit fly, Drosophila melanogaster, to demonstrate that the DNA damage caused by the high levels of cellular proliferation induced by RAS can be exploited therapeutically, thus paving the way to devising strategies to specifically eliminate tumour cells that activate this oncogene. 

Milán says, “RAS-expressing cells duplicate their DNA very quickly. As a result, errors and DNA damage occur. We have shown that RAS blocks the repair of this damage. In normal cells, this would cause cell death through the activation of the p53 tumour suppressor protein. But RAS blocks the ability of this protein to cause cell death, and this is precisely the aspect that we have exploited with both gene therapy and chemistry.”

In the study, the scientists used TRAMETINIB, a drug prescribed for human melanoma, to inhibit the ability of RAS to block cell death. This approach led to the elimination of malignant tumours—selectively and by cell death—without affecting the development of organs or the flies themselves. 

In the words of Lada Murcia and Marta Clemente, first authors of this study, “we have also shown that radiotherapy, which causes DNA damage, increases the sensitivity of RAS-expressing cells to gene therapy.” 

► Reference article: Lada Murcia, Marta Clemente-Ruiz, Priscillia Pierre-Elies, Anne Royou, and Marco Milán. “Selective killing of RAS-malignant tissues by exploiting oncogene-induced DNA damage“. Cell Reports (2019) DOI: 10.1016/j.celrep.2019.06.004

► For further information: IRB Barcelona website [+]