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RAB38 is a potential prognostic factor for tumor recurrence in non-small cell lung cancer
Ras-related protein Rab-38 (RAB38) is a member of the Ras small G protein family that regulates intracellular vesicular trafficking. Although the expression of is reportedly deregulated in several types of cancer, its role in tumor biology remains to be elucidated. In the present study, the expressi...
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Published in: | Experimental and therapeutic medicine 2019-09, Vol.18 (3), p.2598-2604 |
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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: | Ras-related protein Rab-38 (RAB38) is a member of the Ras small G protein family that regulates intracellular vesicular trafficking. Although the expression of
is reportedly deregulated in several types of cancer, its role in tumor biology remains to be elucidated. In the present study, the expression of
was analyzed in tumor specimens from patients with non-small cell lung cancer (NSCLC) with tumor recurrence within 4 years (Group R), and those remaining disease-free following initial surgery (Group NR), by reverse transcription-semi-quantitative PCR and subsequent semi-quantification using ImageJ v4.0 software. The results revealed that the expression of
in Group R and NR specimens was positively associated with tumor recurrence; a high expression level was also associated with poor survival rate in these patients. Using NSCLC cell lines, it was demonstrated that tumor cells with mutations in the active epidermal growth factor receptor (EGFR) gene expressed higher levels of RAB38 compared with those with the wild-type gene by reverse transcription-PCR and western blot analysis. Furthermore, following specific RAB38 gene knockdown by short hairpin RNA transfection,
mutants exhibited markedly reduced invasiveness when compared with cells transfected with empty vector controls by Matrigel Transwell assays. These results suggest that
is an important prognostic factor in NSCLC, and may serve a critical role in NSCLC-associated tumor metastasis. |
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ISSN: | 1792-1074 1792-0981 1792-1082 |
DOI: | 10.3892/ol.2019.10547 |