Correlation of P-ACC and COX-2 expression in non-small cell lung cancer tissues
10.3969/j.issn.1000-8179.20131266
- VernacularTitle:非小细胞肺癌组织中P-ACC及COX-2的相关性研究
- Author:
Shaojin LI
;
Xiangmin ZHANG
;
Rong LI
;
Lianbin LIU
;
Yongqiang YE
;
Dongmei WANG
;
Zhongbing LUO
- Publication Type:Journal Article
- Keywords:
non-small cell lung cancer;
P-ACC;
COX-2;
immunohistochemistry
- From:
Chinese Journal of Clinical Oncology
2014;(1):68-72
- CountryChina
- Language:Chinese
-
Abstract:
Objective:A study was conducted to determine the expression of acetyl-coa carboxylase product of phosphorylation (P-ACC) and an enzyme called cyclooxygenase 2 (COX-2) in non-small cell lung cancer (NSCLC) tissue, as well as the relationship and correlations between tumor size, lymph node metastasis, clinical stage, and pathological type. Methods: Sixty-two patients with NSCLC lung cancer tissues were included in the patient group, whereas 20 patients who underwent lobectomy for other reasons and had normal lung tissues were included in the control group. Immunohistochemical streptavidin peroxidase method was used to detect the expression of P-ACC and COX-2 in lung cancer and normal lung tissues. Results:The positive expressions of P-ACC and COX-2 in NSCLC lung cancer and normal lung tissues were significantly different (P<0.05). In NSCLC tissues, the positive expression of P-ACC was significantly associated with tumor size (P<0.05), but was not significantly associated with lymph node metastasis, clinical stage, and pathological type. We found no correlation between the positive expression of COX-2 and tumor size, lymph node metasta-sis, clinical stage and pathological type. Further analysis revealed that the positive expression of P-ACC and COX-2 in NSCLC was sig-nificantly and negatively correlated (r=-2.37, P=0.032). Conclusion:The positive expression of COX-2 in NSCLC greatly increased compared with that of P-ACC, and a significantly negative correlation was observed between them. We propose that the positive expres-sion of P-ACC reduction may activate the positive expression of COX-2 and promote the occurrence, development, invasion, and metas-tasis of NSCLC.
