Biological characteristics of a cell subpopulation in tongue squamous cell carcinoma

Oral Dis. 2012 Mar;18(2):169-77. doi: 10.1111/j.1601-0825.2011.01860.x. Epub 2011 Oct 24.

Abstract

Objectives: To isolate the CD133+CD44+ cells from human tongue squamous cell carcinoma (TSCC) Tca8113 cell line and investigate biological characteristics of them.

Materials and methods: Immunomagnetic microbeads were applied to sort the CD133+CD44+ cells. Flow cytometry was used to detect isolation purity. The proliferation, clone-formation efficiencies, invasion and migration, gene expressions, and tumor-formation abilities were analyzed among CD133+CD44+, CD133-CD44-, and total population of cells.

Results: The average purities of CD133+ and CD44+ cells reached 97.3% and 98.7%, respectively. The proliferation of CD133+CD44+ cells was significantly higher than the other two groups. The clone-forming efficiency of three groups was 70%, 8%, and 14%, respectively. The average invaded and migrated cell numbers of CD133+CD44+ and total population cells were 132 and 36.2, 311.6, and 156.2, respectively. The expressions of Bcl-2 and Sox2 in CD133+CD44+ cells were significantly higher than those in total population cells. A total of 10(4) CD133+CD44+ cells could form secondary tumors in nude mice, while the total population group needed 10(6) cells.

Conclusions: The CD133+CD44+ subpopulation cells possess stem-like characteristics. They appear to be the potential targets for future biology therapy of human TSCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen
  • Animals
  • Antigens, CD / immunology*
  • Antigens, CD / isolation & purification
  • Antigens, Neoplasm / biosynthesis
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / isolation & purification*
  • Carcinoma, Squamous Cell / immunology
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / pathology*
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Separation
  • Clone Cells
  • Flow Cytometry
  • Glycoproteins / immunology*
  • Glycoproteins / isolation & purification
  • Humans
  • Hyaluronan Receptors / immunology*
  • Hyaluronan Receptors / isolation & purification
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplastic Stem Cells / cytology*
  • Neoplastic Stem Cells / immunology
  • Peptides / immunology*
  • Peptides / isolation & purification
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / isolation & purification
  • SOXB1 Transcription Factors / biosynthesis
  • SOXB1 Transcription Factors / genetics
  • SOXB1 Transcription Factors / isolation & purification
  • Tongue Neoplasms / immunology
  • Tongue Neoplasms / metabolism
  • Tongue Neoplasms / pathology*

Substances

  • AC133 Antigen
  • Antigens, CD
  • Antigens, Neoplasm
  • CD44 protein, human
  • Glycoproteins
  • Hyaluronan Receptors
  • PROM1 protein, human
  • Peptides
  • Prom1 protein, mouse
  • Proto-Oncogene Proteins c-bcl-2
  • SOX2 protein, human
  • SOXB1 Transcription Factors