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Published in: Strahlentherapie und Onkologie 1/2013

01-01-2013 | Original article

Influence of osteopontin silencing on survival and migration of lung cancer cells

Authors: B. Polat, MD, G. Wohlleben, A. Katzer, C.S. Djuzenova, A. Technau, M. Flentje

Published in: Strahlentherapie und Onkologie | Issue 1/2013

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Abstract

Background and purpose

Osteopontin (OPN) is a multifunctional protein overexpressed in many cancers and is involved in tumor progression and metastasis. In lung cancer, elevated OPN expression is associated with an unfavorable prognosis. Therefore, inhibition of OPN is an attractive approach for improving survival.

Materials and methods

We used siRNA to specifically downregulate OPN expression in A549 lung cancer cells. OPN silencing was evaluated with quantitative reverse transcriptase polymerase chain reaction (RT-PCR) for mRNA levels and with Western blotting for protein levels. Effects on cell proliferation were measured by cell counting. The influence on tumor cell migration was detected using a modified Boyden chamber. Changes in cell cycle distribution were assessed by flow cytometry. Using the colony formation assay, we determined changes in radiosensitivity.

Results

A specific and effective downregulation of OPN expression was detected in both RNA and protein levels. Cell proliferation and cell migration were significantly reduced by OPN silencing after 24 h and the effects were further increased by the addition of irradiation. The cell cycle distribution showed a reduction in S phase and an increase in cells arrested in both G0/G1 and G2/M phases. Specific enhancement of radiosensitivity was clearly shown after OPN knockdown.

Conclusion

The combination of OPN silencing and irradiation showed a synergistic effect leading to reduced cell survival.
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Metadata
Title
Influence of osteopontin silencing on survival and migration of lung cancer cells
Authors
B. Polat, MD
G. Wohlleben
A. Katzer
C.S. Djuzenova
A. Technau
M. Flentje
Publication date
01-01-2013
Publisher
Springer-Verlag
Published in
Strahlentherapie und Onkologie / Issue 1/2013
Print ISSN: 0179-7158
Electronic ISSN: 1439-099X
DOI
https://doi.org/10.1007/s00066-012-0238-5

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