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Erschienen in: Journal of Cancer Research and Clinical Oncology 8/2009

01.08.2009 | Original Paper

Mitochondrial DNA content in paired normal and cancerous breast tissue samples from patients with breast cancer

verfasst von: Alex Xiu-Cheng Fan, Ramin Radpour, Mahdi Montazer Haghighi, Corina Kohler, Peng Xia, Sinuhe Hahn, Wolfgang Holzgreve, Xiao Yan Zhong

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 8/2009

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Abstract

Introduction

We develop a multiplex quantitative real-time PCR for synchronized analysis of mitochondrial DNA (mtDNA) and nuclear DNA (nDNA) to investigate relative mtDNA abundance in paired normal and cancerous breast tissues.

Materials and methods

The amounts of nDNA and mtDNA in 102 tissue samples were quantified for both glyceraldehype-3-phosphodehydrogenase (GAPDH) gene and mtDNA encoded ATPase (MTATP) 8 gene. The average threshold cycle (Ct) number values of the nDNA and mtDNA were used to calculate relative mtDNA content in breast tissues.

Results

The median delta Ct (ΔCt) and the median mtDNA content for normal and cancerous breast tissues were 6.73 and 2.54, as well as 106.50 and 5.80 (P = 0.000, respectively). The mtDNA content was decreased in 82% of cancerous breast tissues compared with the normal ones. The changes were associated with hormone receptor status.

Conclusion

Our finding suggests that decreased mtDNA content in breast cancer may have diagnostic and prognostic value for the disease.
Literatur
Zurück zum Zitat Ellinger J, Muller SC, Wernert N, von Ruecker A, Bastian PJ (2008) Mitochondrial DNA in serum of patients with prostate cancer: a predictor of biochemical recurrence after prostatectomy. BJU Int 102(5):628–632PubMedCrossRef Ellinger J, Muller SC, Wernert N, von Ruecker A, Bastian PJ (2008) Mitochondrial DNA in serum of patients with prostate cancer: a predictor of biochemical recurrence after prostatectomy. BJU Int 102(5):628–632PubMedCrossRef
Zurück zum Zitat Jain KK (2007) Cancer biomarkers: current issues and future directions. Curr Opin Mol Ther 9:563–571PubMed Jain KK (2007) Cancer biomarkers: current issues and future directions. Curr Opin Mol Ther 9:563–571PubMed
Zurück zum Zitat Kim MM, Clinger JD, Masayesva BG, Ha PK, Zahurak ML, Westra WH et al (2004) Mitochondrial DNA quantity increases with histopathologic grade in premalignant and malignant head and neck lesions. Clin Cancer Res 10:8512–8515. doi:10.1158/1078-0432.CCR-04-0734 PubMedCrossRef Kim MM, Clinger JD, Masayesva BG, Ha PK, Zahurak ML, Westra WH et al (2004) Mitochondrial DNA quantity increases with histopathologic grade in premalignant and malignant head and neck lesions. Clin Cancer Res 10:8512–8515. doi:10.​1158/​1078-0432.​CCR-04-0734 PubMedCrossRef
Zurück zum Zitat Lebrecht D, Kokkori A, Ketelsen UP, Setzer B, Walker UA (2005) Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin. J Pathol 207:436–444. doi:10.1002/path.1863 PubMedCrossRef Lebrecht D, Kokkori A, Ketelsen UP, Setzer B, Walker UA (2005) Tissue-specific mtDNA lesions and radical-associated mitochondrial dysfunction in human hearts exposed to doxorubicin. J Pathol 207:436–444. doi:10.​1002/​path.​1863 PubMedCrossRef
Zurück zum Zitat Masuyama M, Iida R, Takatsuka H, Yasuda T, Matsuki T (2005) Quantitative change in mitochondrial DNA content in various mouse tissues during aging. Biochim Biophys Acta 1723:302–308PubMed Masuyama M, Iida R, Takatsuka H, Yasuda T, Matsuki T (2005) Quantitative change in mitochondrial DNA content in various mouse tissues during aging. Biochim Biophys Acta 1723:302–308PubMed
Zurück zum Zitat Meierhofer D, Mayr JA, Foetschl U, Berger A, Fink K, Schmeller N et al (2004) Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis 25:1005–1010. doi:10.1093/carcin/bgh104 PubMedCrossRef Meierhofer D, Mayr JA, Foetschl U, Berger A, Fink K, Schmeller N et al (2004) Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis 25:1005–1010. doi:10.​1093/​carcin/​bgh104 PubMedCrossRef
Zurück zum Zitat Mizumachi T, Suzuki S, Naito A, Carcel-Trullols J, Evans TT, Spring PM et al (2008a) Increased mitochondrial DNA induces acquired docetaxel resistance in head and neck cancer cells. Oncogene 27:831–838. doi:10.1038/sj.onc.1210681 PubMedCrossRef Mizumachi T, Suzuki S, Naito A, Carcel-Trullols J, Evans TT, Spring PM et al (2008a) Increased mitochondrial DNA induces acquired docetaxel resistance in head and neck cancer cells. Oncogene 27:831–838. doi:10.​1038/​sj.​onc.​1210681 PubMedCrossRef
Zurück zum Zitat Mizumachi T, Naito MLA, Furusawa J, Fan CY, Siegel ER et al (2008b) Increased distributional variance of mitochondrial DNA content associated with prostate cancer cells as compared with normal prostate cells. Prostate 68:408–417. doi:10.1002/pros.20697 PubMedCrossRef Mizumachi T, Naito MLA, Furusawa J, Fan CY, Siegel ER et al (2008b) Increased distributional variance of mitochondrial DNA content associated with prostate cancer cells as compared with normal prostate cells. Prostate 68:408–417. doi:10.​1002/​pros.​20697 PubMedCrossRef
Zurück zum Zitat Simonnet H, Alazard N, Pfeiffer K, Gallou C, Beroud C, Demont J et al (2002) Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma. Carcinogenesis 23:759–768. doi:10.1093/carcin/23.5.759 PubMedCrossRef Simonnet H, Alazard N, Pfeiffer K, Gallou C, Beroud C, Demont J et al (2002) Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma. Carcinogenesis 23:759–768. doi:10.​1093/​carcin/​23.​5.​759 PubMedCrossRef
Zurück zum Zitat Tseng LM, Yin PH, Chi CW, Hsu CY, Wu CW, Lee LM et al (2006) Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer. Genes Chromosomes Cancer 45:629–638. doi:10.1002/gcc.20326 PubMedCrossRef Tseng LM, Yin PH, Chi CW, Hsu CY, Wu CW, Lee LM et al (2006) Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer. Genes Chromosomes Cancer 45:629–638. doi:10.​1002/​gcc.​20326 PubMedCrossRef
Zurück zum Zitat Wang Y, Liu VW, Xue WC, Tsang PC, Cheung AN, Ngan HY (2005) The increase of mitochondrial DNA content in endometrial adenocarcinoma cells: a quantitative study using laser-captured microdissected tissues. Gynecol Oncol 98:104–110. doi:10.1016/j.ygyno.2005.04.015 PubMedCrossRef Wang Y, Liu VW, Xue WC, Tsang PC, Cheung AN, Ngan HY (2005) The increase of mitochondrial DNA content in endometrial adenocarcinoma cells: a quantitative study using laser-captured microdissected tissues. Gynecol Oncol 98:104–110. doi:10.​1016/​j.​ygyno.​2005.​04.​015 PubMedCrossRef
Zurück zum Zitat Webb P (1986) 24-hour energy expenditure and the menstrual cycle. Am J Clin Nutr 44:614–619PubMed Webb P (1986) 24-hour energy expenditure and the menstrual cycle. Am J Clin Nutr 44:614–619PubMed
Zurück zum Zitat Ye C, Shu XO, Wen W, Pierce L, Courtney R, Gao YT et al (2008) Quantitative analysis of mitochondrial DNA 4977-bp deletion in sporadic breast cancer and benign breast diseases. Breast Cancer Res Treat 108:427–434. doi:10.1007/s10549-007-9613-9 PubMedCrossRef Ye C, Shu XO, Wen W, Pierce L, Courtney R, Gao YT et al (2008) Quantitative analysis of mitochondrial DNA 4977-bp deletion in sporadic breast cancer and benign breast diseases. Breast Cancer Res Treat 108:427–434. doi:10.​1007/​s10549-007-9613-9 PubMedCrossRef
Zurück zum Zitat Yin PH, Lee HC, Chau GY, Wu YT, Li SH, Lui WY et al (2004) Alteration of the copy number and deletion of mitochondrial DNA in human hepatocellular carcinoma. Br J Cancer 90:2390–2396PubMed Yin PH, Lee HC, Chau GY, Wu YT, Li SH, Lui WY et al (2004) Alteration of the copy number and deletion of mitochondrial DNA in human hepatocellular carcinoma. Br J Cancer 90:2390–2396PubMed
Metadaten
Titel
Mitochondrial DNA content in paired normal and cancerous breast tissue samples from patients with breast cancer
verfasst von
Alex Xiu-Cheng Fan
Ramin Radpour
Mahdi Montazer Haghighi
Corina Kohler
Peng Xia
Sinuhe Hahn
Wolfgang Holzgreve
Xiao Yan Zhong
Publikationsdatum
01.08.2009
Verlag
Springer-Verlag
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 8/2009
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-008-0533-9

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