Your browser doesn't support javascript.
loading
AMACR overexpression acts as a negative prognostic factor in oral squamous cell carcinoma.
He, Hong-Lin; Lee, Ying-En; Chang, Min-Te; Shiue, Yow-Ling; Chang, Shih-Lun; Chen, Tzu-Ju; Chiu, Chang-Ta.
Affiliation
  • He HL; Department of Pathology, Chi Mei Medical Center, Tainan, Taiwan.
  • Lee YE; Department of Pathology, E-DA Hospital, I-Shou University, Kaohsiung, Taiwan.
  • Chang MT; Department of Anesthesiology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Shiue YL; Institute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan.
  • Chang SL; Department of Oral and Maxillofacial Surgery, Chi Mei Medical Center, Tainan, Taiwan.
  • Chen TJ; Institute of Biomedical Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan.
  • Chiu CT; Department of Otolaryngology, Chi Mei Medical Center, Yongkang District, Tainan City, Taiwan.
Int J Med Sci ; 15(6): 638-644, 2018.
Article in En | MEDLINE | ID: mdl-29725255
ABSTRACT

Background:

Alpha-methylacyl-CoA racemase (AMACR) is a key enzyme responsible for the metabolism of branched-chain fatty acids. It has been found to be an important prognostic factor in numerous types of cancers. This study was aimed to investigate the expression of AMACR and its prognostic significance in patients with oral squamous cell carcinoma (SCC).

Methods:

Analysis of publicly available microarray data of oral SCC revealed that AMACR was significantly upregulated in tumor tissue compared with normal mucosa. We further assessed the protein expression of AMACR in 164 patients with oral SCC by immunohistochemistry. The prognostic impact of AMACR expression and its association with various clinicopathological parameters were statistically analyzed.

Results:

AMACR overexpression was significantly associated with advanced tumor status (P=0.001), advanced nodal status (P=0.036), increased vascular invasion (P=0.026) and increased perineural invasion (P=0.004). Patients with high expression level of AMACR had significantly worse disease-specific survival (DSS), distant metastasis-free survival (DMFS) and local recurrence-free survival (LRFS) (all P<0.0001). In multivariate analysis, AMACR overexpression was also an independent negative prognostic factor for DSS (hazard ratio [HR] 4.410, 95% confidence interval [CI] 2.285-8.511, P<0.001), DMFS (HR 5.157, 95% CI 2.756-9.651, P<0.001) and LRFS (HR 4.462, 95% CI 2.429-8.198, P<0.001).

Conclusions:

High expression of AMACR was not only a key adverse prognostic factor but also a potential therapeutic target in oral SCC.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prognosis / Mouth Neoplasms / Carcinoma, Squamous Cell / Racemases and Epimerases Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Int J Med Sci Journal subject: MEDICINA Year: 2018 Document type: Article Affiliation country: Taiwan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prognosis / Mouth Neoplasms / Carcinoma, Squamous Cell / Racemases and Epimerases Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Int J Med Sci Journal subject: MEDICINA Year: 2018 Document type: Article Affiliation country: Taiwan