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Up-regulation of lysophosphatidylcholine acyltransferase 1 (LPCAT1) is linked to poor prognosis in breast cancer

Dysregulation of lipid metabolism is common in cancer. Lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been implicated with various cancer types. Here we analyzed by immunohistochemistry its expression in 2,197 breast cancers. LPCAT1 staining was found in 97.8% of 1,774 interpretable tumors,...

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Detalles Bibliográficos
Autores principales: Lebok, Patrick, von Hassel, Aurelia, Meiners, Jan, Hube-Magg, Claudia, Simon, Ronald, Höflmayer, Doris, Hinsch, Andrea, Dum, David, Fraune, Christoph, Göbel, Cosima, Möller, Katharina, Sauter, Guido, Jacobsen, Frank, Büscheck, Franziska, Prien, Kristina, Krech, Till, Krech, Rainer Horst, von der Assen, Albert, Wölber, Linn, Witzel, Isabell, Schmalfeldt, Barbara, Geist, Stefan, Paluchoswski, Peter, Wilke, Christian, Heilenkötter, Uwe, Terracciano, Luigi, Müller, Volkmar, Wilczak, Waldemar, Burandt, Eike Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781992/
https://www.ncbi.nlm.nih.gov/pubmed/31533087
http://dx.doi.org/10.18632/aging.102287
Descripción
Sumario:Dysregulation of lipid metabolism is common in cancer. Lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been implicated with various cancer types. Here we analyzed by immunohistochemistry its expression in 2,197 breast cancers. LPCAT1 staining was found in 97.8% of 1,774 interpretable tumors, including 48.1% with weak, 28.7% with moderate, and 14.4% with strong expression. The frequency of LPCAT1 positivity depended on the histological tumor type. Moderate or strong LPCAT1 positivity was more common in cancers of no special type (NST) (46.2%) than in lobular carcinomas (25.9%; p<0.0001). Strong LPCAT1 was associated with BRE grade, tumor cell proliferation and overall survival in all cancers and in the subgroup of NST cancers (p<0.0001, each). In the subset of NST cancers the prognostic effect of LPCAT1 expression was independent of pT, and BRE grade (p<0.0001 each). A comparison with molecular features showed that LPCAT1 was strongly associated with estrogen receptor negativity (p<0.0001), progesterone receptor negativity (p<0,0001), amplification of HER2 (p<0.0001) and MYC (p=0.0066), as well as deletions of PTEN (p<0.0001) and CDKNA2 (p=0.0151). It is concluded that LPCAT1 overexpression is linked to adverse tumor features and poor prognosis in breast cancer. These data also highlight the important role of lipid metabolism in breast cancer biology.