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Expression of lysophosphatidic acid acyltransferase beta (LPAAT-β) in ovarian carcinoma: correlation with tumour grading and prognosis
Lysophosphatidic acid acyltransferase beta (LPAAT-β) is an enzyme involved in lipid biosynthesis whose role in tumour progression has been of emerging interest in the last few years. We investigated the expression of LPAAT-β by reverse transcriptase–polymerase chain reaction and immunohistochemistry...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362024/ https://www.ncbi.nlm.nih.gov/pubmed/15841084 http://dx.doi.org/10.1038/sj.bjc.6602528 |
Sumario: | Lysophosphatidic acid acyltransferase beta (LPAAT-β) is an enzyme involved in lipid biosynthesis whose role in tumour progression has been of emerging interest in the last few years. We investigated the expression of LPAAT-β by reverse transcriptase–polymerase chain reaction and immunohistochemistry in 10 ovarian cell lines as well as in a cohort of 106 ovarian tumours and normal ovaries. Lysophosphatidic acid acyltransferase beta mRNA was found in all cell lines and ovarian tumours examined. Expression of LPAAT-β protein was significantly increased in ovarian carcinomas compared to benign ovarian tissue (χ(2) test P-value=0.001, Kruskal–Wallis test P-value <0.0001). Furthermore, LPAAT-β expression was positively associated with higher tumour grade (P=0.044), higher mitotic index (P<0.0001) and tumour stage (P=0.032). Expression of LPAAT-β was significantly linked to reduced overall survival time (P=0.024) as well as to shorter progression-free survival time (P=0.012) in patients younger than 60 years. Our study shows that LPAAT-β is upregulated in ovarian cancer and is more prevalent in poorly differentiated tumours. In addition, LPAAT-β expression is a predictor of a worse prognosis in patients younger than 60 years. Further studies are needed to investigate if LPAAT-β may serve as a therapeutic target for certain subgroups of patients. |
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