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Cited by 294

The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.

Cellular Disposal of miR23b by RAB27-Dependent Exosome Release Is Linked to Acquisition of Metastatic Properties

Open access
Ostenfeld, Marie Stampe, Jeppesen, Dennis K., Laurberg, Jens R., Boysen, Anders T., Bramsen, Jesper B., Primdal-Bengtson, Bjarke, Hendrix, An, Lamy, Philippe, Dagnaes-Hansen, Frederik, Rasmussen, Mads H., Bui, Khan H., Fristrup, Niels, Christensen, Erik I., Nordentoft, Iver, Morth, Jens P., Jensen, Jørgen B., Pedersen, Jakob S., Beck, Martin, Theodorescu, Dan, Borre, Michael, Howard, Kenneth A., Dyrskjøt, Lars, Ørntoft, Torben Falck·2014·Cancer Research

Abstract

Exosomes are small secreted vesicles that can transfer their content to recipient cells. In cancer, exosome secretion has been implicated in tumor growth and metastatic spread. In this study, we explored the possibility that exosomal pathways might discard tumor-suppressor miRNA that restricts metastatic progression. Secreted miRNA characterized from isogenic bladder carcinoma cell lines with differing metastatic potential were uncoupled from binding to target transcripts or the AGO2–miRISC complex. In metastatic cells, we observed a relative increase in secretion of miRNA with tumor-suppressor functions, including miR23b, miR224, and miR921. Ectopic expression of miR23b inhibited invasion, anoikis, angiogenesis, and pulmonary metastasis. Silencing of the exocytotic RAB family members RAB27A or RAB27B halted miR23b and miR921 secretion and reduced cellular invasion. Clinically, elevated levels of RAB27B expression were linked to poor prognosis in two independent cohorts of patients with bladder cancer. Moreover, highly exocytosed miRNA from metastatic cells, such as miR23b, were reduced in lymph node metastases compared with patient-matched primary tumors and were correlated with increments in miRNA-targeted RNA. Taken together, our results suggested that exosome-mediated secretion of tumor-suppressor miRNA is selected during tumor progression as a mechanism to coordinate activation of a metastatic cascade. Cancer Res; 74(20); 5758–71. ©2014 AACR.

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Metadata

Authors
Ostenfeld, M. S., Jeppesen, D. K., Laurberg, J. R., Boysen, A. T., Bramsen, J. B., Primdal-Bengtson, B., Hendrix, A., Lamy, P., Dagnaes-Hansen, F., Rasmussen, M. H., Bui, K. H., Fristrup, N., Christensen, E. I., Nordentoft, I., Morth, J. P., Jensen, J. B., Pedersen, J. S., Beck, M., Theodorescu, D., Borre, M., Howard, K. A., Dyrskjøt, L., & Ørntoft, T. F.
Venue
Cancer Research
Published
2014-10-14
Volume
74
Issue
20
Pages
5758-5771
ISSN
  • 0008-5472 (ISSN-L)
  • 1538-7445
OpenAlex
W2152503181
Cited by
294
References
46
FWCI
10.22
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Cellular Disposal of miR23b by RAB27-Dependent Exosome Release Is Linked to Acquisition of Metastatic Properties. https://app.cochat.ai/papers/10.1158/0008-5472.can-13-3512
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Ostenfeld, M. S., Jeppesen, D. K., Laurberg, J. R., Boysen, A. T., Bramsen, J. B., Primdal-Bengtson, B., Hendrix, A., Lamy, P., Dagnaes-Hansen, F., Rasmussen, M. H., Bui, K. H., Fristrup, N., Christensen, E. I., Nordentoft, I., Morth, J. P., Jensen, J. B., Pedersen, J. S., Beck, M., Theodorescu, D., . . . Ørntoft, T. F. (2014). Cellular Disposal of miR23b by RAB27-Dependent Exosome Release Is Linked to Acquisition of Metastatic Properties. Cancer Research. https://doi.org/10.1158/0008-5472.can-13-3512

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.