4.5 Article

The expression level of lysophosphatidylcholine acyltransferase 1 (LPCAT1) correlates to the progression of prostate cancer

Journal

EXPERIMENTAL AND MOLECULAR PATHOLOGY
Volume 92, Issue 1, Pages 105-110

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.yexmp.2011.11.001

Keywords

Lysophosphatidylcholine acyltransferase 1 (LPCAT1); Prostate cancer; Biomarkers; Tissue microarray (TMA); Immunohistochemistry (IHC)

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Funding

  1. Department of Pathology at the University of Mississippi Medical Center
  2. NIH [P20RR016476 MS/INBRE/NCRR/NIH]
  3. Division Of Human Resource Development
  4. Direct For Education and Human Resources [0811638] Funding Source: National Science Foundation

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Background: Lysophosphatidylcholine acyltransferase 1 (LPCAT1), the enzyme catalyzing the reaction in remodeling of phosphatidylcholine (PC) has been reported to express in prostate. However, its diagnostic and prognostic values remain unclear. Methods: Immunohistochemistry (IHC) for LPCAT1 was performed on the tissue microarray (TMA) slides containing 251 samples from 148 patients with various prostatic disorders. The association of expression level of LPCAT1 with the progression of prostate cancer was analyzed. Results: LPCAT1 IHC mean score was the highest in metastatic prostate cancer (8.00 +/- 1.28), which was significantly higher than that in primary prostate cancer (4.63 +/- 3.00, p = 9.73E-07), in high grade prostatic intraepithelial neoplasia (HGP1N, 2.72 +/- 2.47, p = 1.02E-12), and in benign prostate (2.68, p = 6.17E-12). The mean score in primary prostate cancer was significantly higher than that in HGPIN (p = 4.09E-04) and in benign prostate (p = 2.74E-04). There was no significant difference in the mean score between HGPIN and benign prostate (p = 0.951). LPCAT1 IHC score also correlated to the tumor grade and stage of prostate cancer. Patients who underwent prostatectomy for prostate cancer and developed biochemical recurrence or clinical metastasis had higher LPCAT1 IHC score than those who underwent prostatectomy for prostate cancer and did not develop biochemical recurrence and clinical metastasis. The association of LPCAT1 with the progression of prostate cancer was independent of patient race and age. PSA level and positivity of surgical resection margins. Conclusions: LPCAT1 correlates with the progression of prostate cancer and could be a new biomarker in diagnosis, prognosis and studying the pathogenesis of prostate cancer. Published by Elsevier Inc.

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