High mitochondrial DNA copy number and bioenergetic function are associated with tumor invasion of esophageal squamous cell carcinoma cell lines

Chen Sung Lin, Hui Ting Lee, Shu Yu Lee, Yao An Shen, Liang Shun Wang, Yann Jang Chen, Yau Huei Wei

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

We previously reported a gradual increase of relative mitochondrial DNA (mtDNA) copy number during the progression of esophageal squamous cell carcinoma (ESCC). Because mitochondria are the intracellular organelles responsible for ATP production, we investigated the associations among mtDNA copy number, mitochondrial bioenergetic function, tumor invasion and the expression levels of epithelial mesenchymal transition (EMT) markers in a series of seven ESCC cell lines, including 48T, 81T, 146T, TE1, TE2, TE6 and TE9. Among them, TE1 had the highest relative mtDNA copy number of 240.7%. The mRNA of mtDNA-encoded ND1 gene (2.80), succinate-supported oxygen consumption rate (11.21 nmol/min/106 cells), ATP content (10.7 fmol/cell), and the protein level of mitochondrial transcription factor A (TFAM) were the highest and the lactate concentration in the culture medium (3.34 mM) was the lowest in TE1. These findings indicate that TE1 exhibited the highest bioenergetic function of mitochondria. Furthermore, TE1 showed the highest trans-well migration activity of 223.0 cells/field, the highest vimentin but the lowest E-cadherin protein expression levels, which suggest that TE1 had the highest invasion capability. We then conducted a knockdown study using pLKO.1-based lentiviral particles to infect TE1 cells to suppress the expression of TFAM. Molecular analyses of the parental TE1, control TE1-NT and TFAM knockdown TE1-sh-TFAM(97) cells were performed. Interestingly, as compared to the control TE1-NT, TE1-sh-TFAM(97) exhibited lower levels of the relative mtDNA copy number (p = 0.001), mRNA of mtDNA-encoded ND1 gene (p = 0.050), succinate-supported oxygen consumption rate (p = 0.065), and ATP content (p = 0.007), but had a higher lactate concentration in the culture medium (p = 0.010) and higher protein level of lactate dehydrogenase. A decline in mitochondrial bioenergetic function was observed in TE1-sh-TFAM(97). Significantly, compared to the control TE1-NT, TE1-sh-TFAM(97) had a lower trans-well migration activity (p <0.001), a higher E-cadherin level but a lower vimentin protein level, which indicates a decrease of invasiveness. Taken together, we suggest that high relative mtDNA copy number and bioenergetic function of mitochondria may confer an advantage for tumor invasion of ESCC.

Original languageEnglish
Pages (from-to)11228-11246
Number of pages19
JournalInternational Journal of Molecular Sciences
Volume13
Issue number9
DOIs
Publication statusPublished - 2012

Fingerprint

Mitochondrial DNA
cultured cells
Energy Metabolism
Tumors
DNA
tumors
deoxyribonucleic acid
cancer
Cells
Cell Line
lactates
Mitochondria
mitochondria
adenosine triphosphate
Adenosinetriphosphate
Neoplasms
proteins
Proteins
oxygen consumption
cells

Keywords

  • Bioenergetic function
  • Epithelial mesenchymal transition (EMT)
  • Esophageal squamous cell carcinoma (ESCC)
  • Invasion
  • Mitochondrial DNA (mtDNA)

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Spectroscopy
  • Inorganic Chemistry
  • Catalysis
  • Molecular Biology
  • Computer Science Applications
  • Medicine(all)

Cite this

High mitochondrial DNA copy number and bioenergetic function are associated with tumor invasion of esophageal squamous cell carcinoma cell lines. / Lin, Chen Sung; Lee, Hui Ting; Lee, Shu Yu; Shen, Yao An; Wang, Liang Shun; Chen, Yann Jang; Wei, Yau Huei.

In: International Journal of Molecular Sciences, Vol. 13, No. 9, 2012, p. 11228-11246.

Research output: Contribution to journalArticle

Lin, Chen Sung ; Lee, Hui Ting ; Lee, Shu Yu ; Shen, Yao An ; Wang, Liang Shun ; Chen, Yann Jang ; Wei, Yau Huei. / High mitochondrial DNA copy number and bioenergetic function are associated with tumor invasion of esophageal squamous cell carcinoma cell lines. In: International Journal of Molecular Sciences. 2012 ; Vol. 13, No. 9. pp. 11228-11246.
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AU - Lee, Hui Ting

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AU - Wang, Liang Shun

AU - Chen, Yann Jang

AU - Wei, Yau Huei

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