Receptor for Hyaluronic Acid-Mediated Motility is Associated with Poor Survival in Pancreatic Ductal Adenocarcinoma

被引:37
作者
Cheng, Xiao-Bo [1 ,2 ]
Sato, Norihiro [1 ]
Kohi, Shiro [1 ]
Koga, Atsuhiro [1 ]
Hirata, Keiji [1 ]
机构
[1] Univ Occupat & Environm Hlth, Sch Med, Dept Surg 1, Kitakyushu, Fukuoka 8078555, Japan
[2] China Med Univ, Affiliated Hosp 4, Dept Breast Surg, Shenyang, Liaoning, Peoples R China
关键词
Receptor for hyaluronic acid-mediated motility; pancreatic ductal adenocarcinoma; prognostic factor; poor survival; ACUTE MYELOID-LEUKEMIA; RHAMM-R3 PEPTIDE VACCINATION; BINDING-PROTEIN; MYELODYSPLASTIC SYNDROME; RHO-KINASE; CELL-CYCLE; EXPRESSION; CD44; CARCINOMAS; CD168;
D O I
10.7150/jca.12990
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Receptor for hyaluronic acid (HA)-mediated motility (RHAMM) is a nonintegral cell surface receptor involved in the aggressive phenotype in a wide spectrum of human malignancies, but the significance of RHAMM in pancreatic ductal adenocarcinoma (PDAC) remains unknown. In this study, we investigated the expression of RHAMM and its clinical relevance in PDAC. RHAMM mRNA expression was examined in 8 PDAC cell lines and in primary pancreatic cancer and adjacent non-tumor tissues from 14 patients using real-time RT-PCR. Western blotting was carried out to analyze the expression of RHAMM protein in PDAC cell lines. We also investigated the expression patterns of RHAMM protein in tissue samples from 70 PDAC patients using immunohistochemistry. The RHAMM mRNA expression was increased in some PDAC cell lines as compared to a non-tumorous pancreatic epithelial cell line HPDE. The RHAMM mRNA expression was significantly higher in PDAC tissues as compared to corresponding non-tumorous pancreatic tissues (P < 0.0001). The RHAMM protein expression was higher in the vast majority of PDAC cell lines relative to the expression in HPDE. The immunohistochemical analysis revealed strong expression of RHAMM in 52 (74%) PDAC tissues. Strong expression of RHAMM was significantly associated with a shorter survival time (P = 0.038). In multivariate analysis, tumor stage (P = 0.039), residual tumor (P = 0.015), and strong RHAMM expression (P = 0.034) were independent factors predicting poor survival. Strong expression of RHAMM may predict poor survival in PDAC patients and may provide prognostic and, possibly, therapeutic value.
引用
收藏
页码:1093 / 1098
页数:6
相关论文
共 45 条
[1]   Hyaluronate receptors mediating glioma cell migration and proliferation [J].
Akiyama, Y ;
Jung, S ;
Salhia, B ;
Lee, SP ;
Hubbard, S ;
Taylor, M ;
Mainprize, T ;
Akaishi, K ;
van Furth, W ;
Rutka, JT .
JOURNAL OF NEURO-ONCOLOGY, 2001, 53 (02) :115-127
[2]   CD44 IS THE PRINCIPAL CELL-SURFACE RECEPTOR FOR HYALURONATE [J].
ARUFFO, A ;
STAMENKOVIC, I ;
MELNICK, M ;
UNDERHILL, CB ;
SEED, B .
CELL, 1990, 61 (07) :1303-1313
[3]  
Assmann V, 1999, J CELL SCI, V112, P3943
[4]   The pattern of expression of the microtubule-binding protein RHAMM/IHABP in mammary carcinoma suggests a role in the invasive behaviour of tumour cells [J].
Assmann, V ;
Gillett, CE ;
Poulsom, R ;
Ryder, K ;
Hart, IR ;
Hanby, AM .
JOURNAL OF PATHOLOGY, 2001, 195 (02) :191-196
[5]  
Assmann V, 1996, CLIN CANCER RES, V2, P1607
[6]   INTERACTION BETWEEN CD44 AND HYALURONATE IS DIRECTLY IMPLICATED IN THE REGULATION OF TUMOR-DEVELOPMENT [J].
BARTOLAZZI, A ;
PEACH, R ;
ARUFFO, A ;
STAMENKOVIC, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :53-66
[7]   Hyaluronan-mediated CD44 interaction with RhoGEF and Rho kinase promotes Grb2-associated binder-1 phosphorylation and phosphatidylinositol 3-kinase signaling leading to cytokine (Macrophage-Colony stimulating factor) production and breast tumor progression [J].
Bourguignon, LYW ;
Singleton, PA ;
Zhu, HB ;
Diedrich, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29420-29434
[8]  
Cheng XB, 2013, PLoS One, V8, DOI DOI 10.1371/JOURNAL.PONE.0080765
[9]   Filling the mosaic of p53 actions p53 represses RHAMM expression [J].
Godar, Samuel ;
Weinberg, Robert A. .
CELL CYCLE, 2008, 7 (22) :3479-3479
[10]   mRNA expression of leukemia-associated antigens in patients with acute myeloid leukemia for the development of specific immunotherapies [J].
Greiner, J ;
Ringhoffer, M ;
Taniguchi, M ;
Li, LI ;
Schmitt, A ;
Shiku, H ;
Döhner, H ;
Schmitt, M .
INTERNATIONAL JOURNAL OF CANCER, 2004, 108 (05) :704-711