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Large noncoding RNA HOTAIR enhances aggressive biological behavior and is associated with short disease-free survival in human non-small cell lung cancer
•The expression of HOTAIR is associated with short disease-free survival of non-small cell lung cancer patients.•HOTAIR expression is significantly higher in brain metastatic lesions than in primary lesions.•Forced expression of HOTAIR enhances lung cancer cell migration and anchorage-independent ce...
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Published in: | Biochemical and biophysical research communications 2013-06, Vol.436 (2), p.319-324 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •The expression of HOTAIR is associated with short disease-free survival of non-small cell lung cancer patients.•HOTAIR expression is significantly higher in brain metastatic lesions than in primary lesions.•Forced expression of HOTAIR enhances lung cancer cell migration and anchorage-independent cell growth.
HOTAIR is one of long non-coding RNAs and its expression correlates with the prognosis and metastasis in various cancers. We showed that HOTAIR expression has an important role in the development of non-small cell lung cancer (NSCLC). In this study, we examined the expression of HOTAIR in 77 NSCLCs, their corresponding normal lung tissues and 6 brain metastases by quantitative real-time RT-PCR. High expression of HOTAIR (tumor/normal ratio ⩾2) was detected in 17 patients (22.1%) and was frequently found in patients with advanced stage, lymph node metastasis or lymph-vascular invasion and short disease free interval. Furthermore, brain metastases show significantly higher HOTAIR expression compared to primary cancer tissues. HOTAIR-expressing A549 cells showed induced cell migration and anchorage-independent cell growth in vitro. These results indicate the expression of HOTAIR enhanced the aggressive behavior of NSCLC cells. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/j.bbrc.2013.05.101 |