Having two mutated copies of the TP53 gene - as opposed to a single mutated copy - is associated with worse outcomes in myelodysplastic syndrome and acute myeloid leukemia.
YARDVILLE, New Jersey, Aug. 25, 2020 /PRNewswire/ --The MDS Foundation announces that a large international study led by researchers at Memorial Sloan Kettering finds that having two mutated copies of theTP53gene, as opposed to a single mutated copy, is associated with worse outcomes in myelodysplastic syndrome and acute myeloid leukemia. The findings have immediate clinical relevance for risk assessment and treatment of people with myelodysplastic syndrome.
Considered the "guardian of the genome,"TP53is the most commonly mutated gene in cancer.TP53's normal function is to detect DNA damage and prevent cells from passing this damage on to daughter cells. WhenTP53is mutated, the protein made from this gene (called p53) can no longer perform this protective function, which can result in cancer. Across many cancer types, mutations inTP53are associated with much worse outcomes, like disease recurrence and shorter survival.
As with all genes, there are two copies ofTP53in our cells. One copy we get from our mothers, the other we get from our fathers. Until now, it was unclear whether a mutation in one copy of TP53 TP53was enough to cause worse outcomes, or if mutations in both copies were necessary. A new study led by researchers at Memorial Sloan Kettering definitively answers this question for a blood cancer calledmyelodysplastic syndrome (MDS), a precursor toacute myeloid leukemia.
"Our study is the first to assess the impact of having one versus two dysfunctional copies ofTP53on cancer outcomes," says molecular geneticist Dr.Elli Papaemmanuil, a member of the Epidemiology and Biostatistics Department at MSK and the lead scientist on the study, whose results were published August 3 in the journalNature Medicine. "From our results, it's clear that you need to lose function of both copies to see evidence of genome instability and a high-risk clinical phenotype in MDS."
"The consequences for cancer diagnosis and treatment are immediate and profound," she says.
A LARGE, MULTICENTER STUDY
The study analyzed genetic and clinical data from 4,444 patients with MDS who were being treated at hospitals all over the world. Researchers from 25 centers in 12 countries were involved in the study, which was conducted under the aegis in collaboration with investigators in the International Working Group for Prognosis in MDS(IWG-PM)whose goal is to develop new international guidelines for the treatment of this disease. Findings were independently validated using data from the Japanese MDS working group led by Dr.SeishiOgawa'sgroup at Kyoto University.
"Currently, the existing guidelines do not consider genomic data, likeTP53and other acquired mutations, when assessing a person's prognosis or determining appropriate treatment for this disease," says Dr.Peter Greenberg, Director of Stanford University's MDS Center, Chair of the National Comprehensive Cancer Network Practice Guidelines Panel for MDS, and a participant in the study. "Studies are ongoing reflecting this need for change."
Tracey Iraca, MDS Foundation Executive Director stated, "This study is important in updating the IPSS-R to include molecule information in light of the more personalized treatments now being explored for MDS patients."
Using new computational methods and the database and collaborative input of the IWG-PM, the investigators found that about one-third of MDS patients had only one mutated copy ofTP53.These patients had similar outcomes as patients who did not have aTP53mutation that is, good response to treatment, low rates of disease progression, and better survival. Two-thirds of patients, on the other hand, had two mutated copies of TP53. These patients had much worse outcomes including treatment-resistant disease, rapid disease progression, and low overall survival. In fact, the researchers found thatTP53mutation status either 0/1 or 2 mutated copies of the gene was the most important variable when predicting outcomes.
"Our findings are of immediate clinical relevance to MDS patients," Dr. Papaemmanuil says. "Going forward, all MDS patients should have theirTP53status assessed at diagnosis."
As for why it takes two "hits" toTP53to see an effect on cancer outcomes, Dr.Elsa Bernard, a postdoctoral scientist in the Papaemmanuil lab and the study's first author, speculates that having one normal copy is enough to provide adequate protection against DNA damage. This would explain why having only one mutated copy was not associated with genome instability or any worse survival over having two normal copies.
Given the frequency ofTP53mutations in cancer, these results argue for examining the impact of one versus two mutations in other cancers as well. They also reveal the need for clinical trials designed specifically with these molecular differences in mind.
"With the increasing adoption of molecular profiling at the time of cancer diagnosis, we need large evidence-based studies to inform how to translate these molecular findings into optimal treatment strategies," Dr. Papaemmanuil says.
PARTICIPATING MDS FOUNDATION CENTERS OF EXCELLENCE:Karolinska Institute (Sweden), University of Pavia (Italy), La Fe University Hospital (Spain), Radboudumc Medical Center Nijmegen (The Netherlands), Amsterdam UMC (The Netherlands), Cochin Hospital (France), Chang Gung Memorial Hospital (Taiwan), Medical University of Vienna (Austria), Hannover Medical School (Germany), University Hospital Dresden (Germany), Federal University of Ceara (Brazil), University of Oxford (United Kingdom), Institute of Hematology and Blood Transfusion (Czech Republic), University Medicine Gttingen (Germany), Saint-Louis Hospital (France), Saint James's University Hospital (United Kingdom), Chulalongkorn University (Thailand), Nagasaki University (Japan), Kyoto University (Japan), Chugoku Central Hospital (Japan), Tokyo Medical University (Japan), Massachusetts General Hospital, Vanderbilt-Ingram Cancer Center,University of Rochester Medical Center, Dana-Farber Cancer Institute, UC San Diego Moores Cancer Center, Stanford University Cancer Institute,Memorial Sloan Kettering Cancer Center(United States).
ADDITIONAL PARTICIPATING CENTERS:Dsseldorf MDS Registry (Germany), Gruppo Romano Laziale MDS (Italy), University of Bologna (Italy), Institut Josep Carreras (Spain), Aou Careggi Hospital (Italy), Democritus University of Thrace (Greece), Hospital Israelita Albert Einstein (Brazil), Rete Ematologica Lombarda (Italy), Japanese Data Center for Hematopoietic Cell Transplantation (Japan), Tsukuba University (Japan), Gifu Municipal Hospital (Japan), Kobe City Medical Center General Hospital (Japan), Gifu University (Japan), NTT Medical Center Tokyo (Japan), Osaka Red Cross Hospital (Japan), Kurashiki Central Hospital (Japan), Sasebo City General Hospital (Japan)
FUNDING: This study was supported in part by the Celgene Corporation, the MDS Foundation, Inc., Bloodwise, Austrian Science Fund, Italian MIUR-PRIN grants, Associazione Italiana per la Ricerca sul Cancro, 51000 project, the Francois Wallace Monahan Fellowship, the Josie Robertson Foundation, the European Hematology Association, American Society of Hematology, Gabrielle's Angels Foundation, V Foundation, Damon Runyon-Rachleff, the Geoffrey Beene Foundation, the Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, and the Japanese Ministry of Education, Culture, Sports, Science and Technology. Dr. Papaemmanuil is a Josie Robertson-funded investigator at MSK. Drs. Papaemmanuil and Bernard have received research funding from Celgene.
The MDS Foundation, Inc.is an international non-profit advocacy organization whose mission is to support and educate patients and healthcare providers with innovative research into the fields of MDS, Acute Myeloid Leukemia (AML) and related myeloid neoplasms in order to accelerate progress leading to the diagnosis, control and cure of these diseases.
Media Contact:TraceyIraca, Executive Director, MDS Foundation, Inc.Phone: (609)298-1600 x 211Mobile: (609)647-2080Email: [emailprotected]
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