99
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      High molecular weight hyaluronan mediates the cancer resistance of the naked mole-rat

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The naked mole-rat displays exceptional longevity, with a maximum lifespan exceeding 30 years 13 . This is the longest reported lifespan for a rodent species and is especially striking considering the small body mass of the naked mole-rat. In comparison, a similarly sized house mouse has a maximum lifespan of 4 years 4, 5 . In addition to their longevity, naked mole-rats show an unusual resistance to cancer. Multi-year observations of large naked mole-rat colonies did not detect a single incidence of cancer 2, 6 . Here we identify a mechanism responsible for the naked mole-rat’s cancer resistance. We found that naked mole-rat fibroblasts secrete extremely high molecular weight hyaluronan (HA), which is over five times larger than human or mouse HA. This high molecular weight HA accumulates abundantly in naked mole rat tissues due to the decreased activity of HA-degrading enzymes and a unique sequence of hyaluronan synthase 2 ( HAS2). Furthermore, the naked mole-rat cells are more sensitive to HA signaling, as the naked mole rat cells have a higher affinity to HA than the mouse or human cells. Perturbation of the signaling pathways sufficient for malignant transformation of mouse fibroblasts fails to transform naked mole-rat cells. However, once high molecular weight HA is removed by either knocking down HAS2 or overexpressing the HA-degrading enzyme, Hyal2, naked mole-rat cells become susceptible to malignant transformation and readily form tumors in mice. We speculate that naked mole-rats have evolved a higher concentration of HA in the skin to provide skin elasticity needed for life in underground tunnels. This trait may have then been co-opted to provide cancer resistance and longevity to this species.

          Related collections

          Most cited references18

          • Record: found
          • Abstract: found
          • Article: not found

          CD44: from adhesion molecules to signalling regulators.

          Cell-adhesion molecules, once believed to function primarily in tethering cells to extracellular ligands, are now recognized as having broader functions in cellular signalling cascades. The CD44 transmembrane glycoprotein family adds new aspects to these roles by participating in signal-transduction processes--not only by establishing specific transmembrane complexes, but also by organizing signalling cascades through association with the actin cytoskeleton. CD44 and its associated partner proteins monitor changes in the extracellular matrix that influence cell growth, survival and differentiation.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Hyaluronidases: their genomics, structures, and mechanisms of action.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Hyaluronan in tissue injury and repair.

              A hallmark of tissue injury and repair is the turnover of extracellular matrix components. This review focuses on the role of the glycosaminoglycan hyaluronan in tissue injury and repair. Both the synthesis and degradation of extracellular matrix are critical contributors to tissue repair and remodeling. Fragmented hyaluronan accumulates during tissue injury and functions in ways distinct from the native polymer. There is accumulating evidence that hyaluronan degradation products can stimulate the expression of inflammatory genes by a variety of immune cells at the injury site. CD44 is the major cell-surface hyaluronan receptor and is required to clear hyaluronan degradation products produced during lung injury; impaired clearance of hyaluronan results in persistent inflammation. However, hyaluronan fragment stimulation of inflammatory gene expression is not dependent on CD44 in inflammatory macrophages. Instead, hyaluronan fragments utilize both Toll-like receptor (TLR) 4 and TLR2 to stimulate inflammatory genes in macrophages. Hyaluronan also is present on the cell surface of lung alveolar epithelial cells and provides protection against tissue damage by interacting with TLR2 and TLR4 on these parenchymal cells. The simple repeating structure of hyaluronan appears to be involved in a number of important aspects of noninfectious tissue injury and repair that are dependent on the size and location of the polymer as well as the interacting cells. Thus, the interactions between the endogenous matrix component hyaluronan and its signaling receptors initiate inflammatory responses, maintain structural cell integrity, and promote recovery from tissue injury.
                Bookmark

                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                31 May 2013
                19 June 2013
                18 July 2013
                18 January 2014
                : 499
                : 7458
                : 346-349
                Affiliations
                [1 ]Department of Biology, University of Rochester, Rochester NY 14627
                [3 ]School of Life Science and Technology, Tongji University, 1239 Siping Rd., Shanghai, China, 200092
                [4 ]Institute of Evolution, University of Haifa, Haifa 31905, Israel
                Author notes
                [* ]Correspondence and requests for materials should be addressed to Vera Gorbunova, University of Rochester, 434 Hutchison Hall, River Campus, Rochester NY 14627-0211, Phone: 585-275-7740, Fax: 585-275-2070, vera.gorbunova@ 123456rochester.edu . Andrei Seluanov, University of Rochester, 432 Hutchison Hall, River Campus, Rochester NY 14627-0211, Phone: 585-275-6636, Fax: 585-275-2070, andrei.seluanov@ 123456rochester.edu
                [2]

                Present address: Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115

                [#]

                These authors contributed equally.

                Article
                NIHMS474645
                10.1038/nature12234
                3720720
                23783513
                0b27ae88-e69c-4b13-ac05-623b06ccf342

                Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                History
                Funding
                Funded by: National Institute on Aging : NIA
                Award ID: R01 AG031227 || AG
                Funded by: National Institute on Aging : NIA
                Award ID: R01 AG027237 || AG
                Categories
                Article

                Uncategorized
                Uncategorized

                Comments

                Comment on this article