New epigenetic drug against Mantle Cell Lymphoma
A new study by doctor Manel Esteller, Director of the Epigenetics and Cancer Biology Program (PEBC) of the Bellvitge Biomedical ResearchInstitute (IDIBELL), ICREA Researcher and Professor of Genetics at the University of Barcelona, presents an epigenetic drug capable of slowing down cell growth in Mantle Cell Lymphoma (MCL), a type of cancer characterized by its aggressive behavior, its delayed diagnosis with affectation of different organs and its origin from the lymphocytes B. The research results, published in Haematologica, the European Hematology Society (EHA) scientific journal, may be an answer to current medical need for new treatments that increase long-term survival in this disease.
IMAGE: THESE ARE CELLS OF A PATIENT WITH MANTLE LYMPHOMA BEFORE (LEFT IMAGE) AND AFTER (RIGHT IMAGE) OF TREATMENT WITH THE DRUG. INHIBITION OF CELL GROWTH IS OBSERVED.
“Our laboratory is interested in finding new compounds with epigenetic activity and anti-tumor effects. Working together with organic chemists and the Quimatryx company we obtained a molecule that inhibits the HDAC6 gene, a protein that chemically modifies another protein by acetylation”, says Manel Esteller, main author of the study. The research has also been carried out with the clinical collaboration of the Hematology Services of the Catalan Institute of Oncology (ICO) in Hospitalet and Badalona, as well as the Josep Carreras Institute (IJC).
“After testing it on several types of cancer, we realized that the efficacy of the new molecule was at its peak in this type of lymphoma. This beneficial effect was observed in cultured cells, murine studies and cells extracted from patients. In addition, the substance is very specific when it comes to reaching its target, with apparent little toxicity to healthy cells of the same patient, such as T lymphocytes”, adds the IDIBELL researcher about the study in Haematologica.
12% of all cancers worldwide are linked to blood cells, be it leukemia, lymphoma or myeloma, diagnosing a new patient every two minutes. Although some types of these hematological oncological diseases are curable, for others there are not sufficiently effective treatments. “What makes us especially happy in this case is that the possible use of the drug in clinical trials for next year begins to be considered”, concludes Esteller.
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