Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9890040 | The International Journal of Biochemistry & Cell Biology | 2005 | 18 Pages |
Abstract
The prominent expression of tenascin-C in the stroma of most solid tumors, first observed in the mid 1980s, implicates tenascin-C in tumorigenesis. This is also supported by in vitro experiments that demonstrate the capacity of tenascin-C to stimulate tumor growth by various mechanisms including promotion of proliferation, escaping immuno-surveillance and positively influencing angiogenesis. However, tumorigenesis in tenascin-C knock-out mice is not significantly different from that observed in control animals. Perhaps this is not unexpected if one considers that tenascin-C may act as an oncogene. The potential role of tenascin-C in tumorigenesis through its oncogenic action on cellular signaling will be discussed in this review, including how tenascin-C mediated tumor cell detachment might affect genome stability.
Keywords
frizzledSRFWntLPAId2SREDKK1H2AXSOX4EGFRMCMPDGFRαEDNRACKIhistone 2AxTropomyosin-1TM1FAKCDKMMPLRPMEFMAPKROSTCF/LEFtenascin-CALKlysophosphatidic acidOncogeneTrkRho kinaseTumor suppressionStem cellsSignalingDickkopf 1chromatin assembly factor 1Serum response elementmouse embryo fibroblastFibronectinAnaplastic lymphoma kinaseMetalloproteaseMEKCDK inhibitorMolecular weightgenomic stabilityLDL receptor-related proteinmitogen activated protein kinaseFrzCell cycleCASKfocal adhesion kinasecyclin dependent kinaseReactive oxygen speciesendothelin receptor type AEpidermal growth factor receptortyrosine receptor kinaseRock
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Authors
Gertraud Orend,