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Colorectal cancer cell-derived microvesicles are enriched in cell cycle-related mRNAs that promote proliferation of endothelial cells

BMC Genomics · 2009 · Vol. 10(1) · pp. 556–556
Bok Sil HongJi‐Hoon ChoHyun‐Jung KimEun-Jeong ChoiSangchul RhoJongmin KimJi Hyun KimDongsic ChoiYoon‐Keun KimDaehee HwangYong Song Gho

Abstract

Our study demonstrates that CRC cell-derived microvesicles are enriched in cell cycle-related mRNAs that promote proliferation of endothelial cells, suggesting that microvesicles of cancer cells can be involved in tumor growth and metastasis by facilitating angiogenesis-related processes. This information will help elucidate the pathophysiological functions of tumor-derived microvesicles, and aid in the development of cancer diagnostics, including colorectal cancer.

Extracellular vesicles in diseaseCancer-related molecular mechanisms researchMicroRNA in disease regulationMicrovesiclesBiologyMicrovesicleAngiogenesisCell cycleCell biologyCancer cellCarcinogenesisColorectal cancermicroRNA

MeSH terms

Cell CycleHumansModels, BiologicalRNA, MessengerColorectal NeoplasmsGene Expression ProfilingEndothelial CellsCell Line, TumorCell ProliferationExosomes

Funding

  • Korea Science and Engineering Foundation
Citations
439
FWCI
6.59
field-weighted impact
References
38
Percentile
98%
vs. same field & year
Citations per year
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