Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2014 | 1 | 1 |

Article title

N-cadherin in cancer dormancy

Content

Title variants

Languages of publication

EN

Abstracts

EN
N-cadherin is an adhesion protein, which is
important for intercellular interaction. It is involved in cell
migration and motility during embryonic development,
neuronal synapsis and cancer metastasis. There are several
signaling cascades affected by N-cadherin including TGF-β,
Rho family. N-cadherin is associated at the cytoplasmic
domain with catenins (α, β, γ and p120) to facilitate
metastasis. An increase in N-cadherin with down regulation
of E-cadherin occurs during epithelial mesenchymal
transition. Overexpression of N-cadherin is associated with
cell cycle arrest, which correlates with a similar property
of cancer stem cells (CSC). Connexin expression, which is
important in CSC dormancy, is regulated by N-cadherin.
This review discusses the potential of N-cadherin to be
involved in maintaining CSCs, and to investigate pathways
in N-cadherin expression. A better understanding of the
role of N-Cadherin in CSC biology may identify new targets
for the treatment of cancer.

Publisher

Year

Volume

1

Issue

1

Physical description

Dates

online
10 - 8 - 2015
accepted
15 - 6 - 2015
received
24 - 4 - 2015

Contributors

author
  • Dept. of Medicine, Hematology/Oncology, New Jersey
    Medicine School, Rutgers University, Newark, NJ, USA
  • Graduate School of Biomedical
    Science, Rutgers University, Newark, NJ, USA
  • Dept. of Medicine, Hematology/Oncology, New Jersey
    Medicine School, Rutgers University, Newark, NJ, USA
  • Graduate School of Biomedical
    Science, Rutgers University, Newark, NJ, USA

References

  • [1] Grunwald GB, Geller RL, Lilien J. Enzymatic dissectionof embryonic cell adhesive mechanisms. J Cell Biol1980;85:766-76.
  • [2] Zuppinger C, Eppenberger-Eberhardt M, Eppenberger HM.N-Cadherin: structure, function and importance in theformation of new intercalated disc-like cell contacts in cardiomyocytes.Heart Failure Rev 2000;5:251-7.[Crossref]
  • [3] Wahl JK, 3rd, Kim YJ, Cullen JM, Johnson KR, Wheelock MJ.N-cadherin-catenin complexes form prior to cleavage of theproregion and transport to the plasma membrane. J Biol Chem2003;278:17269-76.
  • [4] Kim JB, Islam S, Kim YJ, Prudoff RS, Sass KM, Wheelock MJ,et al. N-Cadherin extracellular repeat 4 mediates epithelialto mesenchymal transition and increased motility. J Cell Biol2000;151:1193-206.
  • [5] Uemura K, Kitagawa N, Kohno R, Kuzuya A, Kageyama T,Chonabayashi K, et al. Presenilin 1 is involved in maturationand trafficking of N-cadherin to the plasma membrane. JNeurosci Res 2003;74:184-91.
  • [6] Tamura K, Shan WS, Hendrickson WA, Colman DR, ShapiroL. Structure-function analysis of cell adhesion by neural (N-)cadherin. Neuron 1998;20:1153-63.[Crossref]
  • [7] Jin X, Walker MA, Felsovalyi K, Vendome J, Bahna F, MannepalliS, et al. Crystal structures of Drosophila N-cadherin ectodomainregions reveal a widely used class of Ca(2)+-free interdomainlinkers. Proc Natl Acad Sci 2012;109:E127-34.[WoS]
  • [8] Garcia-Castro MI, Vielmetter E, Bronner-Fraser M. N-Cadherin, acell adhesion molecule involved in establishment of embryonicleft-right asymmetry. Science 2000;288:1047-51.
  • [9] Marrs GS, Theisen CS, Bruses JL. N-cadherin modulatesvoltage activated calcium influx via RhoA, p120-catenin, andmyosin-actin interaction. Mol Cell Neurosci 2009;40:390-400.[WoS]
  • [10] Kalluri R, Weinberg RA. The basics of epithelial-mesenchymaltransition. J Clin Invest 2009;119:1420-8.
  • [11] Harbeck N, Untch M, Pache L, Eiermann W. Tumour celldetection in the bone marrow of breast cancer patients atprimary therapy: results of a 3-year median follow-up. Br JCancer 1994;69:566-71.
  • [12] Patel SA, Ramkissoon SH, Bryan M, Pliner LF, Dontu G, Patel PS,et al. Delineation of breast cancer cell hierarchy identifies thesubset responsible for dormancy. Scientific Rep 2012;2:906.[WoS]
  • [13] Zeisberg M, Neilson EG. Biomarkers for epithelialmesenchymaltransitions. J Clin Inves 2009;119:1429-37.
  • [14] Dick JE. Stem cell concepts renew cancer research. Blood2008;112:4793-807.
  • [15] Paez D, Labonte MJ, Bohanes P, Zhang W, Benhanim L, Ning Y, etal. Cancer dormancy: a model of early dissemination and latecancer recurrence. Clin Cancer Res 2012;18:645-53.[Crossref]
  • [16] Samanta D, Gilkes DM, Chaturvedi P, Xiang L, Semenza GL.Hypoxia-inducible factors are required for chemotherapyresistance of breast cancer stem cells. Proc Natl Acad Sci2014;111:E5429-38.[WoS]
  • [17] Sadler NM, Harris BR, Metzger BA, Kirshner J. N-cadherinimpedes proliferation of the multiple myeloma cancer stemcells. Am J Blood Res 2013;3:271-85.
  • [18] Mu Y, Zang G, Engstrom U, Busch C, Landstrom M. TGFbetainducedphosphorylation of Par6 promotes migration andinvasion in prostate cancer cells. Br J Cancer 2015.[Crossref]
  • [19] Luwor RB, Hakmana D, Iaria J, Nheu TV, Simpson RJ, Zhu HJ.Single live cell TGF-beta signalling imaging: breast cancer cellmotility and migration is driven by sub-populations of cellswith dynamic TGF-beta-Smad3 activity. Mol Cancer 2015;14:50.[WoS][Crossref]
  • [20] Sato M, Kadota M, Tang B, Yang HH, Yang YA, Shan M, et al.An integrated genomic approach identifies persistent tumorsuppressive effects of transforming growth factor-beta inhuman breast cancer. Breast Cancer Res 2014;16:R57.[Crossref][WoS]
  • [21] de Caestecker MP, Piek E, Roberts AB. Role of transforminggrowth factor-beta signaling in cancer. J Natl Cancer Inst2000;92:1388-402.[Crossref]
  • [22] Miyazono K. Transforming growth factor-beta signaling inepithelial-mesenchymal transition and progression of cancer.Proc Japan Acad Series B, Phy Biol Sci 2009;85:314-23.[WoS]
  • [23] Yang H, Wang L, Zhao J, Chen Y, Lei Z, Liu X, et al. TGF-betaactivatedSMAD3/4 complex transcriptionally upregulatesN-cadherin expression in non-small cell lung cancer. LungCancer 2015;87:249-57.[WoS]
  • [24] Laplante I, Beliveau R, Paquin J. RhoA/ROCK and Cdc42regulate cell-cell contact and N-cadherin protein level duringneurodetermination of P19 embryonal stem cells. J Neurobiol2004;60:289-307.
  • [25] Suyama K, Shapiro I, Guttman M, Hazan RB. A signalingpathway leading to metastasis is controlled by N-cadherin andthe FGF receptor. Cancer Cell 2002;2:301-14.[Crossref]
  • [26] Derycke LD, Bracke ME. N-cadherin in the spotlight of cell-celladhesion, differentiation, embryogenesis, invasion andsignalling. Intl J Dev Biol 2004;48:463-76.
  • [27] Ono M, Kosaka N, Tominaga N, Yoshioka Y, Takeshita F,Takahashi RU, et al. Exosomes from bone marrow mesenchymalstem cells contain a microRNA that promotes dormancy inmetastatic breast cancer cells. Science Signaling 2014;7:ra63.[WoS][Crossref]
  • [28] Lim PK, Bliss SA, Patel SA, Taborga M, Dave MA, Gregory LA,et al. Gap junction-mediated import of microRNA from bonemarrow stromal cells can elicit cell cycle quiescence in breastcancer cells. Cancer Res 2011;71:1550-60.
  • [29] Frenzel EM, Johnson RG. Gap junction formation betweencultured embryonic lens cells is inhibited by antibody toN-cadherin. Dev Biol 1996;179:1-16.
  • [30] Arai F, Hosokawa K, Toyama H, Matsumoto Y, Suda T. Roleof N-cadherin in the regulation of hematopoietic stem cells inthe bone marrow niche. Ann New York Acad Sci 2012;1266:72-7.[WoS]
  • [31] Vandyke K, Chow AW, Williams SA, To LB, Zannettino AC.Circulating N-cadherin levels are a negative prognosticindicator in patients with multiple myeloma. Br J Haematol2013;161:499-507.[WoS]
  • [32] Willecke K, Eiberger J, Degen J, Eckardt D, Romualdi A,Guldenagel M, et al. Structural and functional diversity ofconnexin genes in the mouse and human genome. Biol Chem2002;383:725-37.
  • [33] Wei CJ, Francis R, Xu X, Lo CW. Connexin43 associated withan N-cadherin-containing multiprotein complex is requiredfor gap junction formation in NIH3T3 cells. J Biol Chem2005;280:19925-36.
  • [34] Kelland L. Drug evaluation: ADH-1, an N-cadherin antagonisttargeting cancer vascularization. Curr Opin Mol Therap2007;9:86-91.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_1515_cdth-2015-0002
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.