Enhanced cellular functions through induction of LPA2 by cisplatin in fibrosarcoma HT1080 cells

• Published in: Molecular and cellular biochemistry 2017-07, Vol.431 (1-2), p.29-35
• Main Authors: Takahashi, Kaede, Fukushima, Kaori, Fukushima, Nobuyuki, Honoki, Kanya, Tsujiuchi, Toshifumi
• Format: Article
• Language: English
• Subjects: Biochemistry; Biomedical and Life Sciences; Cardiology; Life Sciences; Medical Biochemistry; Oncology
• ISSN: 0300-8177; 1573-4919
• DOI: 10.1007/s11010-017-2971-7

Lysophosphatidic acid (LPA) is a simple biophysical lipid which interacts with at least six subtypes of G protein-coupled LPA receptors (LPA 1 –LPA 6 ). In cancer cells, LPA signaling via LPA receptors is involved in the regulation of malignant properties, such as cell growth, motility, and invasion. The aim of this study was to assess whether LPA receptors regulate cellular functions of fibrosarcoma cells treated with anticancer drug. HT1080 cells were maintained by the stepwise treatment of cisplatin (CDDP) at a range of 0.01 to 1.0 µM for approximately 6 months. The cell motile and invasive activities of long-term CDDP-treated (HT-CDDP) cells were significantly stimulated by LPA treatment, while HT-CDDP cells in the static state showed the low cell motile and invasive activities in comparison with HT1080 cells. Since the expression level of LPAR2 gene was markedly elevated in HT-CDDP cells, LPA 2 knockdown cells were generated from HT-CDDP cells. The cell motile and invasive activities of HT-CDDP cells were reduced by LPA 2 knockdown. In colony assay, large-sized colonies formed by long-term CDDP treatment were suppressed by LPA 2 knockdown. In addition, LPA 2 knockdown cells reduced LPA production by autotaxin (ATX), correlating with ATX expression level. These results suggest that LPA signaling via LPA 2 may play an important role in the regulation of cellular functions in HT1080 cells treated with CDDP.