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Acyl-CoA thioesterase 8 is a specific protein related to nodal metastasis and prognosis of lung adenocarcinoma

Authors
Jung, Woon YongKim, Young HyeRyu, Young JoonKim, Baek-HuiShin, Bong KyungKim, AereeKim, Han Kyeom
Issue Date
May-2013
Publisher
Elsevier
Keywords
Lung; Adenocarcinoma; Neoplasm metastasis; Prognosis; Proteomics
Citation
Pathology Research and Practice, v.209, no.5, pp.276 - 283
Indexed
SCIE
SCOPUS
Journal Title
Pathology Research and Practice
Volume
209
Number
5
Start Page
276
End Page
283
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/162777
DOI
10.1016/j.prp.2013.02.008
ISSN
03440338
Abstract
Metastasis is a major cause of cancer recurrence or death. This study attempted to quantitatively identify different proteins in metastatic lung adenocarcinoma. The NIT quotient [number of metastatic lymph nodes (n)/tumor diameter (cm)] was used to select samples with an extreme metastatic phenotype. Among the six fresh frozen lung adenocarcinoma specimens, the three showing the highest NIT quotient represented the metastatic group, and others with the greatest tumor diameters without metastasis represented the non-metastatic group. After 2-dimensional electrophoresis, the significantly different protein spots were selected by image analysis and analyzed with MALDI-TOF mass spectrometry. Acyl-CoA thioesterase 8 isoform c (ACOT8) was one of most overexpressed proteins in the metastatic group, and it was validated by Western blot and immunohistochemical staining on 108 paraffin-embedded tumor samples. High ACOT8 expression was correlated with lymph node metastasis (p = 0.002), recurrence (p = 0.034), predominant histologic subtypes (p = 0.007), and higher stage (p = 0.005). In multivariate analysis, high ACOT8 expression was significantly associated with increased risks of lymph node metastasis (p = 0.009) and cancer-related death (p = 0.030), independent of clinical factors. ACOT8 may be a candidate prognostic biomarker and therapeutic target of lung adenocarcinoma.
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