Downregulation of olfactomedin 4 expression contributes to tumorigenesis of non-small cell lung cancer

International Journal of Clinical and Experimental Physiology

  • Wenmei Su1Department of Oncology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, CHINA.
  • Liang Luo1Department of Oncology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, CHINA.
  • Fenping Wu2Department of Radiotherapy, The Tumor Hospital of Chengdu, The Seventh People‘s Hospital of Chendu, Sichuan, CHINA.
  • Zhennan Lai1Department of Oncology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, CHINA.
  • Xiaofang Li1Department of Oncology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, CHINA.
  • Zhong Xie1Department of Oncology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, CHINA.
  • Zhixiong Yang1Department of Oncology, Affiliated Hospital of Guangdong Medical College, Zhanjiang, Guangdong, CHINA.

Volume 1 Issue 2 Pages 125-130

DOI: 10.4103/2348-8093.137408

Abstract

Background and Aim: Olfactomedin 4 (OLFM4), a member of the ‘sense of smell’ mediated olfactomedin-related protein family, confers resistance to glycoprotein apoptosis. This study aims to examine the correlation between OLFM4 expression and clinicopathologic data in non-small cell lung cancer (NSCLC), including the prognosis of patients. Methods: Ninety-eight NSCLC patients from 2001 to 2013 were included in the study. OLFM4 expression was compared between lung cancer tissues and adjacent non-tumor tissues. In total, 98 and 27 specimens were used for immunohistochemistry (IHC) and quantitative real-time polymerase chain reaction (RT-PCR), respectively. The association of OLFM4 with clinicopathological parameters was evaluated using Pearson’s correlation. Overall survival (OS) was evaluated by Kaplan–Meier survival analysis. Results: IHC and RT-PCR analyses demonstrated low expression of OLFM4 in the cancer tissues (P < 0.05). High OLFM4 expression was positively correlated with peritumor intravascular cancer emboli (P = 0.013) but not associated with other clinical features, such as age, gender, tumor size, NSCLC subtype, or lymph node status (P > 0.05). Kaplan–Meier survival curves showed that the OS rate was not significantly associated with OLFM4 expression (P = 0.927). Conclusion: High OLFM4 expression could be a potential protective factor but not a prognostic factor for the tumorigenesis of NSCLC.

Keywords

  • Immunohistochemistry
  • non-small cell lung cancer
  • olfactomedin 4
  • quantitative real-time polymerase chain reaction
International Journal of Clinical and Experimental Physiology

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