Differential expression of lysophosphatidic acid receptor-2 in intestinal and diffuse type gastric cancer

被引:32
作者
Yamashita, H
Kitayama, J
Shida, D
Ishikawa, M
Hama, K
Aoki, J
Arai, H
Nagawa, H
机构
[1] Univ Tokyo, Dept Surg Oncol, Bunkyo Ku, Tokyo 1138655, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Surg Oncol, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Pharmaceut Sci, Tokyo, Japan
关键词
lysophosphatidic acid; LPA2; gastric cancer;
D O I
10.1002/jso.20397
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives: Lysophosphatidic acid (LPA), a natural phospholipid, can modulate diverse cellular responses through LPA receptor, LPA(1-4). Although LPA, is known to be widely expressed in human tissues, the distribution of other LPA receptors is not characterized in malignant tissues. Recently, it was reported that malignant transformation resulted in aberrant expression of LPA(2) in a various type of cancer, suggesting the positive role of LPA2 in tumor development. Methods: We investigated the expression of the LPA2 receptor immunohistochemically in 204 gastric cancers and analyzed the relationship between the expression of LPA2 and clinicopathological features. Results: LPA(2) was preferentially expressed (67%) in intestinal-type cancer that was significantly higher than that in diffuse-type cancer (32%, P < 0.0001). The expression of LPA2 showed correlation with a higher rate of lymphatic and venous invasion, lymphatic metastasis, and resultingly tumor stage in diffuse-type cancer, but not in intestinal-type cancer. Conclusions: Our results highlight the possibility that LPA2 expression is an important process in the carcinogenesis of gastric cancer, especially in intestinal-type cancer. Since LPA can transactivate HGF receptor (c-Met) as well as EGF-receptor, LPA may promote the progression of gastric cancer in diffuse-type with high expression of c-Met. The development of LPA(2)-specific antagonists might have future therapeutic relevance in the treatment as well as prevention of gastric cancer.
引用
收藏
页码:30 / 35
页数:6
相关论文
共 31 条
  • [1] Characterization of a novel subtype of human G protein-coupled receptor for lysophosphatidic acid
    An, SZ
    Bleu, T
    Hallmark, OG
    Goetzl, EJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (14) : 7906 - 7910
  • [2] Molecular cloning and characterization of a novel human G-protein-coupled receptor, EDG7, for lysophosphatidic acid
    Bandoh, K
    Aoki, J
    Hosono, H
    Kobayashi, S
    Kobayashi, T
    Murakami-Murofushi, K
    Tsujimoto, M
    Arai, H
    Inoue, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) : 27776 - 27785
  • [3] Helicobacter pylori CagA protein targets the c-Met receptor and enhances the motogenic response
    Churin, Y
    Al-Ghoul, L
    Kepp, O
    Meyer, TE
    Birchmeier, W
    Naumann, M
    [J]. JOURNAL OF CELL BIOLOGY, 2003, 161 (02) : 249 - 255
  • [4] Lysophosphatidic acid receptors
    Contos, JJA
    Ishii, I
    Chun, J
    [J]. MOLECULAR PHARMACOLOGY, 2000, 58 (06) : 1188 - 1196
  • [5] Requirement for the IpA1 lysophosphatidic acid receptor gene in normal suckling behavior
    Contos, JJA
    Fukushima, N
    Weiner, JA
    Kaushal, D
    Chun, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (24) : 13384 - 13389
  • [6] Characterization of lpa2 (Edg4) and lpa1/lpa2 (Edg2/Edg4) lysophosphatidic acid receptor knockout mice:: Signaling deficits without obvious phenotypic abnormality attributable to lpa2
    Contos, JJA
    Ishii, I
    Fukushima, N
    Kingsbury, MA
    Ye, XQ
    Kawamura, S
    Brown, JH
    Chun, J
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (19) : 6921 - 6929
  • [7] Genomic characterization of the lysophosphatidic acid receptor gene, IpA2/Edg4, and identification of a frameshift mutation in a previously characterized cDNA
    Contos, JJA
    Chun, J
    [J]. GENOMICS, 2000, 64 (02) : 155 - 169
  • [8] CORREA P, 1992, CANCER RES, V52, P6735
  • [9] Coyle WJ, 1999, AM J GASTROENTEROL, V94, P2885, DOI 10.1111/j.1572-0241.1999.01432.x
  • [10] Lysophosphatidic acid is a bioactive mediator in ovarian cancer
    Fang, XJ
    Schummer, M
    Mao, ML
    Yu, SX
    Tabassam, FH
    Swaby, R
    Hasegawa, Y
    Tanyi, JL
    LaPushin, R
    Eder, A
    Jaffe, R
    Erickson, J
    Mills, GB
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2002, 1582 (1-3): : 257 - 264