Telomere biology: Cancer firewall or aging clock?

被引:15
|
作者
Mitteldorf, J. J. [1 ]
机构
[1] MIT, Dept EAPS, Cambridge, MA 02138 USA
关键词
telomere; telomerase; cancer; programmed aging; adaptive aging; evolution; SENESCENT CELLS; EXPRESSION; LENGTH; AGE; MORTALITY; DYNAMICS; BLOOD; SPAN; DNA;
D O I
10.1134/S0006297913090125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been a decade since the first surprising discovery that longer telomeres in humans are statistically associated with longer life expectancies. Since then, it has been firmly established that telomere shortening imposes an individual fitness cost in a number of mammalian species, including humans. But telomere shortening is easily avoided by application of telomerase, an enzyme which is coded into nearly every eukaryotic genome, but whose expression is suppressed most of the time. This raises the question how the sequestration of telomerase might have evolved. The predominant assumption is that in higher organisms, shortening telomeres provide a firewall against tumor growth. A more straightforward interpretation is that telomere attrition provides an aging clock, reliably programming lifespans. The latter hypothesis is routinely rejected by most biologists because the benefit of programmed lifespan applies only to the community, and in fact the individual pays a substantial fitness cost. There is a long-standing skepticism that the concept of fitness can be applied on a communal level, and of group selection in general. But the cancer hypothesis is problematic as well. Animal studies indicate that there is a net fitness cost in sequestration of telomerase, even when cancer risk is lowered. The hypothesis of protection against cancer has never been tested in animals that actually limit telomerase expression, but only in mice, whose lifespans are not telomerase-limited. And human medical evidence suggests a net aggravation of cancer risk from the sequestration of telomerase, because cells with short telomeres are at high risk of neoplastic transformation, and they also secrete cytokines that exacerbate inflammation globally. The aging clock hypothesis fits well with what is known about ancestral origins of telomerase sequestration, and the prejudices concerning group selection are without merit. If telomeres are an aging clock, then telomerase makes an attractive target for medical technologies that seek to expand the human life- and health-spans.
引用
收藏
页码:1054 / 1060
页数:7
相关论文
共 50 条
  • [1] Telomere biology: Cancer firewall or aging clock?
    J. J. Mitteldorf
    Biochemistry (Moscow), 2013, 78 : 1054 - 1060
  • [2] Telomere biology in aging and cancer
    Wright, WE
    Shay, JW
    JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2005, 53 (09) : S292 - S294
  • [3] Telomere biology in aging and cancer: early history and perspectives
    Hayashi, Makoto T.
    GENES & GENETIC SYSTEMS, 2017, 92 (03) : 107 - 118
  • [4] Telomere biology in human aging and aging syndromes
    Klapper, W
    Parwaresch, R
    Krupp, G
    MECHANISMS OF AGEING AND DEVELOPMENT, 2001, 122 (07) : 695 - 712
  • [5] Telomere biology in healthy aging and disease
    Oeseburg, Hisko
    de Boer, Rudolf A.
    van Gilst, Wiek H.
    van der Harst, Pim
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2010, 459 (02): : 259 - 268
  • [6] Telomere biology in healthy aging and disease
    Hisko Oeseburg
    Rudolf A. de Boer
    Wiek H. van Gilst
    Pim van der Harst
    Pflügers Archiv - European Journal of Physiology, 2010, 459 : 259 - 268
  • [7] Healthy aging and disease: role for telomere biology?
    Zhu, Haidong
    Belcher, Matthew
    van der Harst, Pim
    CLINICAL SCIENCE, 2011, 120 (9-10) : 427 - 440
  • [8] Telomere biology of the chicken: A model for aging research
    Swanberg, Susan E.
    O'Hare, Thomas H.
    Robb, Elizabeth A.
    Robinson, Charmaine M.
    Chang, Hong
    Delany, Mary E.
    EXPERIMENTAL GERONTOLOGY, 2010, 45 (09) : 647 - 654
  • [9] The Role of Telomere Biology in Cancer
    Xu, Lifeng
    Li, Shang
    Stohr, Bradley A.
    ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 8, 2013, 8 : 49 - 78
  • [10] Telomere biology of pediatric cancer
    Tabori, Uri
    Dome, Jeffrey S.
    CANCER INVESTIGATION, 2007, 25 (03) : 197 - 208