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Cited by 357

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Proteome profiling of exosomes derived from human primary and metastatic colorectal cancer cells reveal differential expression of key metastatic factors and signal transduction components

Open access
Ji, Hong, Greening, David W., Barnes, Thomas W., Lim, Justin W., Tauro, Bow J., Rai, Alin, Xu, Rong, Adda, Christopher, Mathivanan, Suresh, Zhao, Wei, Xue, Yanhong, Xu, Tao, Zhu, Hong‐Jian, Simpson, Richard J.·2013·PROTEOMICS

Abstract

Exosomes are small extracellular 40–100 nm diameter membrane vesicles of late endosomal origin that can mediate intercellular transfer of RNA s and proteins to assist premetastatic niche formation. Using primary (SW 480) and metastatic (SW 620) human isogenic colorectal cancer cell lines we compared exosome protein profiles to yield valuable insights into metastatic factors and signaling molecules fundamental to tumor progression. Exosomes purified using O pti P rep™ density gradient fractionation were 40–100 nm in diameter, were of a buoyant density ∼1.09 g/mL, and displayed stereotypic exosomal markers TSG 101, A lix, and CD 63. A major finding was the selective enrichment of metastatic factors (MET, S 100 A 8, S 100 A 9, TNC), signal transduction molecules (EFNB 2, JAG 1, SRC, TNIK), and lipid raft and lipid raft‐associated components (CAV 1, FLOT 1, FLOT 2, PROM 1) in exosomes derived from metastatic SW 620 cells. Additionally, using cryo‐electron microscopy, ultrastructural components in exosomes were identified. A key finding of this study was the detection and colocalization of protein complexes EPCAM‐CLDN 7 and TNIK‐RAP 2 A in colorectal cancer cell exosomes. The selective enrichment of metastatic factors and signaling pathway components in metastatic colon cancer cell‐derived exosomes contributes to our understanding of the cross‐talk between tumor and stromal cells in the tumor microenvironment.

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Metadata

Authors
Ji, H., Greening, D. W., Barnes, T. W., Lim, J. W., Tauro, B. J., Rai, A., Xu, R., Adda, C., Mathivanan, S., Zhao, W., Xue, Y., Xu, T., Zhu, H., & Simpson, R. J.
Venue
PROTEOMICS
Publisher
Wiley
Published
2013-05
Volume
13
Issue
10-11
Pages
1672-1686
ISSN
  • 1615-9853 (ISSN-L)
  • 1615-9861
OpenAlex
W1968542304
Cited by
357
References
7
FWCI
15.87
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Proteome profiling of exosomes derived from human primary and metastatic colorectal cancer cells reveal differential expression of key metastatic factors and signal transduction components. https://app.cochat.ai/papers/10.1002/pmic.201200562
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Ji, H., Greening, D. W., Barnes, T. W., Lim, J. W., Tauro, B. J., Rai, A., Xu, R., Adda, C., Mathivanan, S., Zhao, W., Xue, Y., Xu, T., Zhu, H., & Simpson, R. J. (2013). Proteome profiling of exosomes derived from human primary and metastatic colorectal cancer cells reveal differential expression of key metastatic factors and signal transduction components. PROTEOMICS. https://doi.org/10.1002/pmic.201200562

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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.