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Verfasst von:Yue, Shijing [VerfasserIn]   i
 Mu, Wei [VerfasserIn]   i
 Zöller, Margot [VerfasserIn]   i
Titel:Tspan8 and CD151 promote metastasis by distinct mechanisms
Verf.angabe:Shijing Yue, Wei Mu, Margot Zöller
E-Jahr:2013
Jahr:14 May 2013
Umfang:15 S.
Teil:volume:49
 year:2013
 number:13
 pages:2934-2948
 extent:15
Fussnoten:Gesehen am 26.07.2021
Titel Quelle:Enthalten in: European journal of cancer
Ort Quelle:Amsterdam [u.a.] : Elsevier, 1965
Jahr Quelle:2013
Band/Heft Quelle:49(2013), 13, Seite 2934-2948
ISSN Quelle:1879-0852
Abstract:Aim - CD151 and Tspan8 are metastasis-promoting tetraspanins. To define whether Tspan8 and CD151 fulfil redundant or additive activities, Tspan8 and CD151 were stably knocked-down in highly metastatic rat pancreatic adenocarcinoma BSp73ASML cells (ASMLwt, ASML-Tspan8kd, ASML-CD151kd). - Results - ASML-CD151kd and ASML-Tspan8kd cells metastasise via the lymphatics to the lung with delay and a 2-3-fold increased survival time compared to ASMLwt cells. Yet, CD151 and Tspan8 distinctly contribute to metastasis. Pronounced adhesion of ASML-Tspan8kd cells is due to CD151 associating with the alpha3 integrin chain, whereas strikingly increased ASML-CD151kd cell motility is efficiently inhibited by anti-beta4. These opposing Tspan8 and CD151 activities are due to distinct beta4 recruitment into Tspan8 complexes, accompanied by beta4 phosporylation, src recruitment, focal adhesion kinase (FAK) and Ras activation. On the other hand, CD151 associates more readily with proteases, particularly matrix metalloproteinase (MMP)13 and MMP9, than Tspan8. The stronger CD151-MMP association is accompanied by pronounced collagen I and IV and laminin111 degradation, also seen in metastatic tissue, and strengthens invasiveness. - Conclusion - CD151 and Tspan8 coordinately promote metastasis, where Tspan8 overrides the adhesive features of CD151 by recruiting integrins out of adhesion into motility promoting complexes. CD151 more efficiently than Tspan8 recruiting and activating MMP9 and MMP13 creates a path for migrating tumour cells.
DOI:doi:10.1016/j.ejca.2013.03.032
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.ejca.2013.03.032
 Volltext: https://www.sciencedirect.com/science/article/pii/S095980491300302X
 DOI: https://doi.org/10.1016/j.ejca.2013.03.032
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:LN332 binding integrins
 Metastasis
 MMPs
 Pancreatic adenocarcinoma
 Rat
 Tetraspanins
K10plus-PPN:1764372506
Verknüpfungen:→ Zeitschrift

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