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Link discovered between rare form of anemia, cancer

Date:
October 16, 2015
Source:
Centro Nacional de Investigaciones Oncologicas (CNIO)
Summary:
More than 20 percent of people affected by Diamond-Blackfan anemia, a rare disease, develop various types of tumors throughout their lives. Now researchers have created the first animal model with this type of anemia that also recapitulates the predisposition to cancer. The finding could potentially improve current treatments for this type of anemia, which, to date, are only effective in resolving the hematological disorders.
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FULL STORY

Researchers from the Tumour Suppression Group at the Spanish National Cancer Research Centre (CNIO), headed by Manuel Serrano, have discovered the molecular mechanisms that determine cancer predisposition in patients with Diamond-Blackfan anemia (DBA). To achieve this, they have created the first animal model that recapitulates key characteristics of this type of anemia in humans, including high cancer susceptibility. The finding, published in the journal Cell Reports, could potentially improve current treatments for this disease, which are effective in resolving the haematological disorders but not in preventing the greater predisposition to cancer.

DBA is a rare type of anemia that affects 5 people per million. It is characterised by blood disorders, short stature and malformations in the heart, palate and hands. Previous observational studies had reported that around 20% of these patients develop various types of cancer during their first 46 years of life; in particular, lymphomas -- tumours of the blood -- but also solid tumours such as colon cancer, osteosarcoma and gynaecological cancers. Other studies had developed animal models that recapitulate the characteristics of this type of anemia, but not the predisposition to cancer.

Now, CNIO researchers have achieved this by working on the RPL11 protein. They have discovered that mice with partial deficiency of RPL11 (i.e. one of the two copies of the gene is faulty) not only suffer from the incorrect generation and maturation of red blood cells (causing anemia), but are also predisposed to lymphomagenesis -- the development of lymphomas.

INFLUENCE ON THE 'GUARDIAN OF THE GENOME'

DBA patients display alterations in ribosomal proteins, those that belong to the ribosomes, the organelles within cells that are responsible for synthesising proteins. However, when other research groups generated animal models with mutations in some of these proteins, those animal models experienced haematological disorders that are typical of anemia -- red blood cells are not produced or do not mature properly -- but cancer predisposition was not reported. CNIO researchers decided to work specifically on the ribosomal protein RPL11 to try to recapitulate this feature in their animal model, and they were successful.

Manuel Serrano, who has led the study, explains why they chose to focus on this protein: "Cells need the ribosomes to function properly in order to proliferate and grow; we knew that when something goes wrong in these organelles, RPL11 operates as a switch that activates the p53 gene to stop the cells from proliferating and forming tumours; this mechanism is called ribosomal stress. P53 is one of the main tumour suppressor genes identified to date, to the extent that its relevance in preventing cancer has led to it being named the guardian of the genome. This important function made us think that the protein could play a crucial role in the cancer predisposition observed in patients with DBA: if RPL11 is mutated, it loses the ability to activate p53 to prevent tumours caused by cellular damage."

In addition to impairing the normal function of the p53 tumour suppressor gene, mutations in RPL11 also increase the levels of the MYC oncogene, a protein that, when produced at abnormally high levels, can promote the development of tumours. "We believe that in DBA both factors combined contribute to induce the development of cancer," says Lucía Morgado-Palacín, researcher and lead author of this paper. "One of the next steps in the research would be to confirm that this p53 malfunction and the high levels of MYC are also present in human patients suffering from this type of anemia."

IMPROVING DBA THERAPIES

If the results of the research are confirmed in humans, it could represent a qualitative leap in the treatment of Diamond-Blackfan anemia. "Today, they are administered corticosteroids and given blood transfusions -- which only relieve the symptoms of the anemia by increasing the levels of red blood cells -- or they undergo a bone marrow transplant, the definitive treatment. However, none of these therapies addresses the observed cancer predisposition in these patients. Our animal model will be very useful to study if any of the existing cancer therapies might be effective against this characteristic of DBA," says Gianluca Varetti, CNIO researcher who has also participated in the study.


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Materials provided by Centro Nacional de Investigaciones Oncologicas (CNIO). Note: Content may be edited for style and length.


Journal Reference:

  1. Lucia Morgado-Palacin, Gianluca Varetti, Susana Llanos, Gonzalo Gomez-Lopez, Dolores Martinez, Manuel Serrano. Partial loss of Rpl11 in adult mice recapitulates Diamond-Blackfan anemia and promotes lymphomagenesis. Cell Reports, October 2015 DOI: 10.1016/j.celrep.2015.09.038

Cite This Page:

Centro Nacional de Investigaciones Oncologicas (CNIO). "Link discovered between rare form of anemia, cancer." ScienceDaily. ScienceDaily, 16 October 2015. <www.sciencedaily.com/releases/2015/10/151016115446.htm>.
Centro Nacional de Investigaciones Oncologicas (CNIO). (2015, October 16). Link discovered between rare form of anemia, cancer. ScienceDaily. Retrieved May 23, 2017 from www.sciencedaily.com/releases/2015/10/151016115446.htm
Centro Nacional de Investigaciones Oncologicas (CNIO). "Link discovered between rare form of anemia, cancer." ScienceDaily. www.sciencedaily.com/releases/2015/10/151016115446.htm (accessed May 23, 2017).

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