Skip to main content
Erschienen in: Pediatric Surgery International 12/2010

01.12.2010 | Original Article

Expression patterns of microRNAs are altered in hypoxic human neuroblastoma cells

verfasst von: Tetsuya Yamagata, Jyoji Yoshizawa, Shinsuke Ohashi, Katsuhiko Yanaga, Takao Ohki

Erschienen in: Pediatric Surgery International | Ausgabe 12/2010

Einloggen, um Zugang zu erhalten

Abstract

Background/Purpose

There was a report that microRNA (miRNA) controls multiple genes. In addition, there are some reports that the presence of neoplastic cells that are hypoxic because of rapid tumor development is related to prognosis. As a step toward identifying the role of miRNA in hypoxic tumor cells, the present study was designed to determine which miRNAs have increased expression and which have decreased expression in hypoxic neuroblastoma cells.

Methods

For this study, we used seven neuroblastoma cell lines. In four with MYCN was amplified; in the other three MYCN was non-amplified. Neuroblastoma cells were cultured under hypoxic conditions. The expression levels of 662 kinds of miRNA in the hypoxic cells were quantified by gene array.

Results

We found that the expression of 85 kinds of miRNA was increased. Expression of six of these mRNAs was increased in two or more cell lines. Hsa-miR-143, -145, and -210 were each expressed in four of the seven cell lines. In addition, expression of 48 kinds of miRNA was decreased. Expression of five was decreased in two cell lines. There was no relation between the expression of miRNA and the amplification of MYCN.

Conclusion

Our results thus suggest a possible causal relation between these three miRNAs and the malignancy of neuroblastoma in hypoxic conditions.
Literatur
1.
Zurück zum Zitat Cohn SL, Pearson AD, London WB et al (2009) The international neuroblastoma risk group (INRG) classification system: An INRG task force report. J Clin Oncol 27:289–297CrossRefPubMed Cohn SL, Pearson AD, London WB et al (2009) The international neuroblastoma risk group (INRG) classification system: An INRG task force report. J Clin Oncol 27:289–297CrossRefPubMed
3.
Zurück zum Zitat Yoshizawa J, Mizuno R, Yoshida T et al (2000) Inhibitory effect of TNP-470 on hepatic metastasis of mouse neuroblastoma. J Surg Res 93:82–87CrossRefPubMed Yoshizawa J, Mizuno R, Yoshida T et al (2000) Inhibitory effect of TNP-470 on hepatic metastasis of mouse neuroblastoma. J Surg Res 93:82–87CrossRefPubMed
4.
Zurück zum Zitat Tammela T, Zarkada G, Wallgard E et al (2008) Blocking VEGFR-3 suppresses angiogenic sprouting and vascular network formation. Nature 31(454):656–660CrossRef Tammela T, Zarkada G, Wallgard E et al (2008) Blocking VEGFR-3 suppresses angiogenic sprouting and vascular network formation. Nature 31(454):656–660CrossRef
5.
Zurück zum Zitat Hua Z, Lv Q, Ye W et al (2006) MiRNA-directed regulation of VEGF and other angiogenic factors under hypoxia. PLoS ONE 1:e116CrossRefPubMed Hua Z, Lv Q, Ye W et al (2006) MiRNA-directed regulation of VEGF and other angiogenic factors under hypoxia. PLoS ONE 1:e116CrossRefPubMed
6.
Zurück zum Zitat Chen Y, Stallings RL (2007) Differential patterns of microRNA expression in neuroblastoma are correlated with prognosis, differentiation, and apoptosis. Cancer Res 67:976–983CrossRefPubMed Chen Y, Stallings RL (2007) Differential patterns of microRNA expression in neuroblastoma are correlated with prognosis, differentiation, and apoptosis. Cancer Res 67:976–983CrossRefPubMed
7.
Zurück zum Zitat Schulte JH, Horn S, Otto T et al (2008) MYCN regulates oncogenic Micro RNAs in neuroblastoma. Int J Cancer 122:699–704CrossRefPubMed Schulte JH, Horn S, Otto T et al (2008) MYCN regulates oncogenic Micro RNAs in neuroblastoma. Int J Cancer 122:699–704CrossRefPubMed
8.
Zurück zum Zitat Takagi T, Iio A, Nakagawa Y et al (2009) Decreased expression of microRNA-143 and -145 in human gastric cancers. Oncology 77:12–21CrossRefPubMed Takagi T, Iio A, Nakagawa Y et al (2009) Decreased expression of microRNA-143 and -145 in human gastric cancers. Oncology 77:12–21CrossRefPubMed
9.
Zurück zum Zitat Slaby O, Svoboda M, Fabian P et al (2007) Altered expression of miR-21, miR-31, miR-143, and miR-145 is related to clinicopathologic features of colorectal cancer. Oncology 72:397–402CrossRefPubMed Slaby O, Svoboda M, Fabian P et al (2007) Altered expression of miR-21, miR-31, miR-143, and miR-145 is related to clinicopathologic features of colorectal cancer. Oncology 72:397–402CrossRefPubMed
10.
Zurück zum Zitat Calin GA, Croce CM (2006) MicroRNA—cancer connection: the beginning of a new tale. Cancer Res 66:7390–7394CrossRefPubMed Calin GA, Croce CM (2006) MicroRNA—cancer connection: the beginning of a new tale. Cancer Res 66:7390–7394CrossRefPubMed
11.
Zurück zum Zitat Camps C, Buffa FM, Colella S et al (2008) hsa-miR-210 is induced by hypoxia and is an independent prognostic factor in breast cancer. Clin Cancer Res 12:1340–1348CrossRef Camps C, Buffa FM, Colella S et al (2008) hsa-miR-210 is induced by hypoxia and is an independent prognostic factor in breast cancer. Clin Cancer Res 12:1340–1348CrossRef
12.
Zurück zum Zitat Elia L, Quintavalle M, Zhang J et al (2009) The knockout of miR-143 and -145 alters smooth muscle cell maintenance and vascular homeostasis in mice: correlates with human disease. Cell Death Differ 16:1590–1598CrossRefPubMed Elia L, Quintavalle M, Zhang J et al (2009) The knockout of miR-143 and -145 alters smooth muscle cell maintenance and vascular homeostasis in mice: correlates with human disease. Cell Death Differ 16:1590–1598CrossRefPubMed
13.
Zurück zum Zitat Kulshreshtha R, Ferracin M, Wojcik SE et al (2007) A microRNA signature of hypoxia. Mol Cell Biol 27:1859–1867CrossRefPubMed Kulshreshtha R, Ferracin M, Wojcik SE et al (2007) A microRNA signature of hypoxia. Mol Cell Biol 27:1859–1867CrossRefPubMed
14.
15.
Zurück zum Zitat Harris AL (2002) Hypoxia—a key regulatory factor in tumour growth. Nat Rev Cancer 2:38–47CrossRefPubMed Harris AL (2002) Hypoxia—a key regulatory factor in tumour growth. Nat Rev Cancer 2:38–47CrossRefPubMed
16.
Zurück zum Zitat Welch C, Chen Y, Stallings RL (2007) MicroRNA-34a functions as a potential tumor suppressor by inducing apoptosis in neuroblastoma cells. Oncogene 26:5017–5022CrossRefPubMed Welch C, Chen Y, Stallings RL (2007) MicroRNA-34a functions as a potential tumor suppressor by inducing apoptosis in neuroblastoma cells. Oncogene 26:5017–5022CrossRefPubMed
17.
Zurück zum Zitat Cole KA, Attiyeh EF, Mosse YP et al (2008) A functional screen identifies miR-34a as candidate neuroblastoma tumor suppressor gene. Mol Cancer Res 6:735–742CrossRefPubMed Cole KA, Attiyeh EF, Mosse YP et al (2008) A functional screen identifies miR-34a as candidate neuroblastoma tumor suppressor gene. Mol Cancer Res 6:735–742CrossRefPubMed
18.
Zurück zum Zitat Nikiforova MN, Tseng GC, Steward D et al (2008) MicroRNA expression profiling of thyroid tumors: biological significance and diagnostic utility. J Clin Endocrinol Metab 93:1600–1608CrossRefPubMed Nikiforova MN, Tseng GC, Steward D et al (2008) MicroRNA expression profiling of thyroid tumors: biological significance and diagnostic utility. J Clin Endocrinol Metab 93:1600–1608CrossRefPubMed
19.
Zurück zum Zitat Liao R, Sun J, Zhang L et al (2008) MicroRNAs play a role in the development of human hematopoietic stem cells. J Cell Biochem 104:805–817CrossRefPubMed Liao R, Sun J, Zhang L et al (2008) MicroRNAs play a role in the development of human hematopoietic stem cells. J Cell Biochem 104:805–817CrossRefPubMed
Metadaten
Titel
Expression patterns of microRNAs are altered in hypoxic human neuroblastoma cells
verfasst von
Tetsuya Yamagata
Jyoji Yoshizawa
Shinsuke Ohashi
Katsuhiko Yanaga
Takao Ohki
Publikationsdatum
01.12.2010
Verlag
Springer-Verlag
Erschienen in
Pediatric Surgery International / Ausgabe 12/2010
Print ISSN: 0179-0358
Elektronische ISSN: 1437-9813
DOI
https://doi.org/10.1007/s00383-010-2700-8

Weitere Artikel der Ausgabe 12/2010

Pediatric Surgery International 12/2010 Zur Ausgabe

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.