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Pancreatic cancer-initiating cell exosome message transfer into noncancer-initiating cells: the importance of CD44v6 in reprogramming

Wang, Zhe ; Sun, Hanxue ; Provaznik, Jan ; Hackert, Thilo ; Zöller, Margot

In: Journal of Experimental & Clinical Cancer Research, 38 (2019), Nr. 132. pp. 1-20. ISSN 1756-9966

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Download (5MB) | Lizenz: Creative Commons LizenzvertragPancreatic cancer-initiating cell exosome message transfer into noncancer-initiating cells: the importance of CD44v6 in reprogramming by Wang, Zhe ; Sun, Hanxue ; Provaznik, Jan ; Hackert, Thilo ; Zöller, Margot underlies the terms of Creative Commons Attribution 4.0

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Abstract

Background: Cancer-initiating cell (CIC) exosomes (CIC-TEX) are suggested reprogramming Non-CIC. Mode of message transfer and engagement of CIC-markers being disputed, we elaborated the impact of CD44v6 and Tspan8 on the response of Non-CIC.

Methods: Non-metastasizing CD44v6- and Tspan8-knockdown (kd) pancreatic cancer cells served as Non-CIC. CIC-TEX coculture-induced changes were evaluated by deep-sequencing and functional assays. Tumor progression was surveyed during in vivo CIC-TEX treatment.

Results: Deep-sequencing of CIC-TEX-cocultured CD44v6kd-Non-CIC revealed pronounced mRNA changes in signaling, transport, transcription and translation; altered miRNA affected metabolism, signaling and transcription. CIC-TEX coculture-induced changes in Tspan8kd-Non-CIC mostly relied on CIC-TEX-Tspan8 being required for targeting. CIC-TEX transfer supported apoptosis resistance and significantly promoted epithelial mesenchymal transition, migration, invasion and (lymph)angiogenesis of the kd Non-CIC in vitro and in vivo, deep-sequencing allowing individual mRNA and miRNA assignment to altered functions. Importantly, CIC-TEX act as a hub, initiated by CD44v6-dependent RTK, GPCR and integrin activation and involving CD44v6-assisted transcription and RNA processing. Accordingly, a kinase inhibitor hampered CIC-TEX-fostered tumor progression, which was backed by an anti-Tspan8 blockade of CIC-TEX binding.

Conclusions: This in depth report on the in vitro and in vivo impact of CIC-TEX on CD44v6kd and Tspan8kd Non-CIC unravels hub CIC-TEX activity, highlighting a prominent contribution of the CIC-markers CD44v6 to signaling cascade activation, transcription, translation and miRNA processing in Non-CIC and of Tspan8 to CIC-TEX targeting. Blocking CIC-TEX binding/uptake and uptake-initiated target cell activation significantly mitigated the deleterious CIC-TEX impact on CD44v6kd and Tspan8kd Non-CIC.

Document type: Article
Journal or Publication Title: Journal of Experimental & Clinical Cancer Research
Volume: 38
Number: 132
Publisher: BioMed Central ; Springer
Place of Publication: London ; Berlin, Heidelberg
Date Deposited: 22 May 2019 15:24
Date: 2019
ISSN: 1756-9966
Page Range: pp. 1-20
Faculties / Institutes: Service facilities > European Molecular Biology Laboratory (EMBL)
Medizinische Fakultät Heidelberg > Chirurgische Universitätsklinik
DDC-classification: 610 Medical sciences Medicine
Uncontrolled Keywords: CD44v6, Tspan8, Pancreatic cancer stem cells, Exosome biogenesis, Exosome message transfer, Noncancer stem cell reprogramming
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