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| Content Provider | PubMed Central |
|---|---|
| Author | Liu, Yan Johnson, Soren M. Fedoriw, Yuri Rogers, Arlin B. Yuan, Hong Krishnamurthy, Janakiraman Sharpless, Norman E. |
| Abstract | Previous authors have suggested that tumor suppressor expression promotes aging while preventing cancer, but direct experimental support for this cancer-aging hypothesis has been elusive. Here, by using somatic, tissue-specific inactivation of the p16INK4a tumor suppressor in murine T- or B-lymphoid progenitors, we report that ablation of p16INK4a can either rescue aging or promote cancer in a lineage-specific manner. Deletion of p16INK4a in the T lineage ameliorated several aging phenotypes, including thymic involution, decreased production of naive T cells, reduction in homeostatic T-cell proliferation, and attenuation of antigen-specific immune responses. Increased T-cell neoplasia was not observed with somatic p16INK4a inactivation in T cells. In contrast, B lineage–specific ablation of p16INK4a was associated with a markedly increased incidence of systemic, high-grade B-cell neoplasms, which limited studies of the effects of somatic p16INK4a ablation on B-cell aging. Together, these data show that expression of p16INK4a can promote aging and prevent cancer in related lymphoid progeny of a common stem cell. |
| Related Links | http://dx.doi.org/10.1182/blood-2010-09-304402 |
| Starting Page | 3257 |
| File Format | |
| ISSN | 15280020 |
| e-ISSN | 15280020 |
| Journal | Blood |
| Issue Number | 12 |
| Volume Number | 117 |
| Language | English |
| Publisher | American Society of Hematology |
| Publisher Date | 2011-03-24 |
| Access Restriction | Open |
| Rights Holder | American Society of Hematology |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Hematology Biochemistry Immunology |
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