Over-expression of lysophosphatidic acid receptor-2 in human invasive ductal carcinoma

Joji Kitayama, Dai Shida, Akihiro Sako, Makoto Ishikawa, Kotaro Hama, Junken Aoki, Hiroyuki Arai, Hirokazu Nagawa

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89 Citations (Scopus)


Lysophosphatidic acid (LPA) is a bioactive phospholipid with diverse effects on various cells. It interacts with at least three G-protein-coupled transmembrane receptors, namely LPA1, LPA2 and LPA3, whose expression in various tumours has not been fully characterized. In the present study we characterized the expression profile of LPA receptors in human breast cancer tissue and assessed the possible roles of each receptor. Methods: The relative expression levels of each receptor's mRNA against β-actin mRNA was examined in surgically resected invasive ductal carcinomas and normal gland tissue using real-time RT-PCR. LPA2 expression was also examined immunohistochemically using a rat anti-LPA2 monoclonal antibody. Results: In 25 cases normal and cancer tissue contained LPA1 mRNA at similar levels, whereas the expression level of LPA2 mRNA was significantly increased in cancer tissue as compared with its normal counterpart (3479.0 ± 426.6 versus 1287.3 ± 466.8; P < 0.05). LPA3 was weakly expressed in both cancer and normal gland tissue. In 48 (57%) out of 84 cases, enhanced expression of LPA2 protein was confirmed in carcinoma cells as compared with normal mammary epithelium by immunohistochemistry. Over-expression of LPA2 was detected in 17 (45%) out of 38 premenopausal women, as compared with 31 (67%) out of 46 postmenopausal women, and the difference was statistically significant (P < 0.05). Conclusion: These findings suggest that upregulation of LPA2 may play a role in carcinogenesis, particularly in postmenopausal breast cancer.

Original languageEnglish
Article numberR640
JournalBreast Cancer Research
Issue number6
Publication statusPublished - 2004 Sep 22
Externally publishedYes


  • Carcinogenesis
  • Immunohistochemistry
  • Lysophosphatidic acid
  • RT-PCR

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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