idw - Informationsdienst
Wissenschaft
Aging is characterized by a decrease in regenerative capacity and organ maintenance as well as an increasing risk of cancer which coincide with mutations in stem and progenitor cells. In a working paper, researchers of Leibniz Institute for Age Research – Fritz Lipmann Institute (FLI), Jena/Germany, University of Glasgow, UK, and Buck Institute for Research on Aging, USA, summarize and contrast international research results on the various cell-intrinsic mechanisms that lead to a clonal dominance of mutant stem and progenitor cells in aging tissues. The review will be published in the journal Cell Stem Cell on June 4th.
The incidence of tissue dysfunction, diseases and many types of cancer exponentially increases above the age of 45, showing a growing number of mutant stem or progenitor clones in the hematopoietic system, and the intestinal epithelium. New research results indicate that an increasing number of mutations in tissue stem cells are the main reason for carcinogenesis in age, starting years before the disease occurs. However, the mechanisms that initiate stem cell mutations and lead to their clonal dominance are poorly understood. Researchers from renowned age and cancer research institutes in Jena/Germany (Fritz Lipmann Institute (FLI)), Glasgow/UK (Beatson Institute for Cancer Research) and Novato/USA (Buck Institute for Research on Aging) now compiled and presented existing research results in order to show new approaches for the explanation of this dominance.
In general, the review shows that an increase of clonal dominance of mutant stem cells depends on the kind of tissue, the organism type as well as on which mutations occur and which pathways are affected. For example, the effects of replication stress and telomere shortening in the human hematopoietic system are stronger than in the intestinal epithelium. In mice, there is no dependency between the clonal dominance of mural mutant intestine stem cells and the mice’s growing age. Further, the clonal dominance of mutant stem cells can be context dependent, e.g. occurs in the context of intestinal inflammation but not in the non-inflamed intestine. It’s a challenge for prospective research to find tissue-specific antecedents and consequences of cell mutations, especially with regard to the increasing dominance of mutations during aging.
Furthermore, the research experts highlight the loss of stem cell quiescence, replication-associated DNA damage, telomere shortening, epigenetic alterations, and metabolic challenges as determinants of stem cell mutations and clonal dominance in aging.
“There’s a wide variety of reasons for the clonal dominance of mutant stem cells, and research is still in the beginning”, Prof. Dr. K. Lenhard Rudolph, Scientific Director of FLI, resumes. “But we have to attach a high importance to this new research field regarding the development of therapies that aim to improve health in age. If we succeed to identify the antecedents of mutant stem cells’ dominance in age, these processes can be targeted and diminished, thus leading to a lower risk of cancer and disease in our later years.”
Publication.
Adams PD, Jasper H, Rudolph KL. Aging Induced Stem Cell Mutations as Drivers for Disease and Cancer. Cell Stem Cell 2015, doi: http://dx.doi.org/10.1016/j.stem.2015.05.002.
Embargo.
+++ June 4th, 12:00 noon EST +++
Contact.
Dr. Evelyn Kästner
Leibniz Institute for Age Research – Fritz Lipmann Institute (FLI)
Beutenbergstr. 11, D-07745 Jena
Tel.: +49 3641-656373, Fax: +49 3641-656351, E-Mail: presse@fli-leibniz.de
------------------------
Background Information
The Leibniz Institute for Age Research – Fritz Lipmann Institute (FLI) is the first German research organization dedicated to biomedical aging research since 2004. More than 330 members from over 30 nations explore the molecular mechanisms underlying aging processes and age-associated diseases. For more information, please visit http://www.fli-leibniz.de.
The Leibniz Association connects 89 independent research institutions that range in focus from the natural, engineering and environmental sciences via economics, spatial and social sciences to the humanities. Leibniz Institutes address issues of social, economic and ecological relevance. They conduct knowledge-driven and applied basic research, maintain scientific infrastructure and provide research-based services. The Leibniz Association identifies focus areas for knowledge transfer to policy-makers, academia, business and the public. Leibniz Institutes collaborate intensively with universities – in the form of “WissenschaftsCampi” (thematic partnerships between university and non-university research institutes), for example – as well as with industry and other partners at home and abroad. They are subject to an independent evaluation procedure that is unparalleled in its transparency. Due to the institutes’ importance for the country as a whole, they are funded jointly by the Federation and the Länder, employing some 18,100 individuals, including 9,200 researchers. The entire budget of all the institutes is approximately 1.64 billion EUR. See http://www.leibniz-association.eu for more information.
http://www.fli-leibniz.de - Website Leibniz Institute for Age Research – Fritz Lipmann Institute (FLI)
Criteria of this press release:
Journalists, Scientists and scholars, all interested persons
Biology, Chemistry, Medicine, Nutrition / healthcare / nursing
transregional, national
Research results, Scientific Publications
English
You can combine search terms with and, or and/or not, e.g. Philo not logy.
You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).
Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.
You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).
If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).