Published October 24, 2015 | Version v1
Journal article

Tumorigenic hybrids between mesenchymal stem cells and gastric cancer cells enhanced cancer proliferation, migration and stemness

  • 1. Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu (China)
  • 2. The Affiliated Hospital, Jiangsu University, Zhenjiang, Jiangsu 212000 P. R. (China)

Description

Emerging evidence indicates that inappropriate cell-cell fusion might contribute to cancer progression. Similarly, mesenchymal stem cells (MSCs) can also fuse with other cells spontaneously and capable of adopting the phenotype of other cells. The aim of our study was to investigate the role of MSCs participated cell fusion in the tumorigenesis of gastric cancer. We fused human umbilical cord mesenchymal stem cells (hucMSCs) with gastric cancer cells in vitro by polyethylene glycol (PEG), the hybrid cells were sorted by flow cytometer. The growth and migration of hybrids were assessed by cell counting, cell colony formation and transwell assays. The proteins and genes related to epithelial-mesenchymal transition and stemness were tested by western blot, immunocytochemistry and real-time RT-PCR. The expression of CD44 and CD133 was examined by immunocytochemistry and flow cytometry. The xenograft assay was used to evaluation the tumorigenesis of the hybrids. The obtained hybrids exhibited epithelial- mesenchymal transition (EMT) change with down-regulation of E-cadherin and up-regulation of Vimentin, N-cadherin, α-smooth muscle actin (α-SMA), and fibroblast activation protein (FAP). The hybrids also increased expression of stemness factors Oct4, Nanog, Sox2 and Lin28. The expression of CD44 and CD133 on hybrid cells was stronger than parental gastric cancer cells. Moreover, the migration and proliferation of heterotypic hybrids were enhanced. In addition, the heterotypic hybrids promoted the growth abilities of gastric xenograft tumor in vivo. Taken together, our results suggest that cell fusion between hucMSCs and gastric cancer cells could contribute to tumorigenic hybrids with EMT and stem cell-like properties, which may provide a flexible tool for investigating the roles of MSCs in gastric cancer. The online version of this article (doi:10.1186/s12885-015-1780-1) contains supplementary material, which is available to authorized users

Availability note (English)

Available from http://dx.doi.org/10.1186/s12885-015-1780-1; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620013

Additional details

Publishing Information

Journal Title
BMC cancer (Online)
Journal Volume
15
Journal Page Range
vp.
ISSN
1471-2407

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47084335
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CELL PROLIFERATION; HYBRIDIZATION; IN VITRO; IN VIVO; MIGRATION; NEOPLASMS; POLYETHYLENE GLYCOLS; STEM CELLS
Descriptors DEC
ALCOHOLS; ANIMAL CELLS; DISEASES; GLYCOLS; HYDROXY COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC POLYMERS; POLYMERS; SOMATIC CELLS

Optional Information

Copyright
Copyright (c) Xue et al. 2015
Notes
PMCID: PMC4620013; PMID: 26498753; PUBLISHER-ID: 1780; OAI: oai:pubmedcentral.nih.gov:4620013