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Human MOB1 expression in non-small-cell lung cancer
Hidefumi Sasaki1, Osamu Kawano, Katsuhiko Endo
1Department of Surgery II, Nagoya City University Medical School, Japan. hisasaki@med.nagoya-cu.ac.jp
Clinical Lung Cancer
|February 22, 2007
Summary
Decreased human MOB1 (hMOB1) mRNA expression is observed in non-small-cell lung cancer (NSCLC). This finding suggests hMOB1 may be involved in early tumor invasion and the development of lung cancer.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Human MOB1 (hMOB1) is a homologue of a key cell cycle regulator.
- Loss of mitotic checkpoint control in mammalian cells leads to genomic instability and tumor progression.
- Genomic instability is a hallmark of cancer, including non-small-cell lung cancer (NSCLC).
Purpose of the Study:
- To investigate the expression of hMOB1 in NSCLC.
- To determine the correlation between hMOB1 expression and clinicopathologic features in NSCLC patients.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) was used to quantify hMOB1 mRNA levels.
- hMOB1 mRNA expression was compared between 60 NSCLC tissues and adjacent normal lung tissues.
- Expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA.
Main Results:
- hMOB1 mRNA expression was significantly decreased in NSCLC tissues compared to normal lung tissues (P = 0.0437).
- Decreased hMOB1 expression was particularly noted in early-stage (pT1) NSCLC compared to advanced-stage (pT4) tumors (P = 0.0362).
- No significant correlation was found between hMOB1 expression and patient age, sex, or pathological N stage.
Conclusions:
- Reduced hMOB1 mRNA expression may indicate an early stage of tumor invasion in NSCLC.
- The loss of mitotic checkpoint control mediated by hMOB1 could play a role in lung cancer development.
- hMOB1 warrants further investigation as a potential biomarker or therapeutic target in NSCLC.