Cancer is a different disease in each patient, and improved treatment demands knowing more about the personal characteristics of each tumor. A CNIO team has discovered a new alteration in lung cancer, and thus a new therapeutic target to develop specific drugs. The finding is therefore a step towards customizing the treatment of lung cancer.

The work, published today in the journal Scientific Reports, has been possible thanks to the collaboration of the CNIO with Lilly.

The reported alteration affects a protein called NSD2. The research team, led by Maria Jose Barrero, has found that alterations in NSD2 act together with the already known RAS oncogene to promote the proliferation of lung cancer cells. It is actually a combination of two alterations, in NSD2 and the RAS oncogene, that promotes tumor growth.

In this way, the researchers have further subdivided the “RAS mutant” subtype of lung cancer.

A "NEW MOLECULAR DEFINITION” FOR LUNG CANCER

"We have identified a new molecular subtype of lung tumors," says Barrero. "Among tumors with mutations in RAS we have defined a subgroup in which NSD2 is overexpressed; that is to say, it is in excess amounts in the tumor."

The new “molecular definition” is important, because this variant of lung cancer cannot be fought only with drugs against oncogene RAS: "It is necessary to act against RAS and possibly also counteract the overexpression of NSD2," Barrero said.

At present, there are still no drugs targeting NSD2, but this protein has already been of interest for the pharmaceutical industry since it is known to be mutated in certain hematologic malignancies and overexpressed in several solid tumors. However, as the researchers explain in their paper, "Its contribution to the biology of solid tumors is still not well understood and will require additional research." For all these reasons, the CNIO group focused from the beginning in trying to understand the role of NSD2 in lung cancer. The work has been performed using cell lines of this type of cancer only, but researchers believe that overexpression of NSD2 could drive other tumors, acting in conjunction with RAS or other oncogenes. One of the next steps of the research is to "identify tumors and cell lines dependent on NSD2", as explained in Scientific Reports.

This is the first result of an Epigenetics collaboration between Lilly and the CNIO, a unique initiative in the Spanish biomedical research landscape that began three years ago. The CNIO-Lilly Epigenetics Laboratory, integrated by two researchers and two technicians, makes public the highlights of their research.

Reference article:

NSD2 contributes to oncogenic RAS-driven transcription in lung cancer cells through long-range epigenetic activation. Verónica García-Carpizo, Jacinto Sarmentero, Bomie Han, Osvaldo Graña, Sergio Ruiz-Llorente, David G. Pisano, Manuel Serrano, Harold B. Brooks , Robert M. Campbell & Maria J. Barrero. Scientific reports (2016). DOI: 10.1038/srep32952

Subscribe to Directory
Write an Article

Recent News

Exposure to Heat and Cold During Pregnan...

The research team observed changes in head circumf...

Using mobile RNAs to improve Nitrogen a...

AtCDF3 gene induced greater production of sugars a...

El diagnóstico genético neonatal mejor...

Un estudio con datos de los últimos 35 años, ind...

Highlight

Eosinófilos. ¿Qué significa tener val...

by Labo'Life

​En nuestro post hablamos sobre este interesante tipo de célula del...

Un ensayo de microscopía dinámica del ...

by CSIC - Centro Superior de Investigaciones Científicas

La revista ‘Nature Protocols’ selecciona esta técnica como “pro...

Photos Stream