Selective upregulated expression of the α2-macroglobulin signaling receptor in highly metastatic 1-LN prostate carcinoma cells

被引:25
作者
Asplin, IR [1 ]
Misra, UK [1 ]
Gawdi, G [1 ]
Gonzalez-Gronow, M [1 ]
Pizzo, SV [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
关键词
alpha(2)-macroglobulin; prostate carcinoma; tumor progression; insulin;
D O I
10.1006/abbi.2000.2052
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular binding of receptor-recognized forms of alpha (2)-macroglobulin (alpha M-2*) is mediated by the low-density lipoprotein receptor related protein (LRP) and the alpha M-2 signaling receptor (alpha 2MSR). In nonmalignant cells, ligation of alpha 2MSR promotes DNA synthesis and cellular proliferation. Here, we report that insulin treatment of highly metastatic I-LN human prostate carcinoma selectively increases alpha 2MSR expression and binding of alpha M-2* to 1-LN cells, alpha M-2* induces transient increases in intracellular calcium and inositol 1,4,5-trisphosphate in insulin-treated I-LN cells, consistent with activation of alpha 2MSR. Inhibition of signaling cascades activated by insulin blocks upregulation of alpha 2MSR. By contrast, alpha M-2* does not bind to nor induce intracellular signaling in PC-3 cells, even though 1-LN cells were subcloned from PC-3 cells. We suggest that alpha M-2* behaves like a growth factor in these highly malignant cells. The 1-LN metastatic phenotype may result, in part, from aberrant expression of alpha 2MSR, indicating the possible involvement of alpha M-2* in tumor progression. (C) 2000 Academic Press.
引用
收藏
页码:135 / 141
页数:7
相关论文
共 53 条
[1]   PD-098059 IS A SPECIFIC INHIBITOR OF THE ACTIVATION OF MITOGEN-ACTIVATED PROTEIN-KINASE KINASE IN-VITRO AND IN-VIVO [J].
ALESSI, DR ;
CUENDA, A ;
COHEN, P ;
DUDLEY, DT ;
SALTIEL, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27489-27494
[2]   Insulin signal transduction through protein kinase cascades [J].
Avruch, J .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 182 (1-2) :31-48
[3]   Molecular mechanisms of tumor metastasis and angiogenesis [J].
Böhle, AS ;
Kalthoff, H .
LANGENBECKS ARCHIVES OF SURGERY, 1999, 384 (02) :133-140
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   PHOSPHATIDYLINOSITOL 3-KINASE ACTIVATION IS REQUIRED FOR INSULIN STIMULATION OF PP70 S6 KINASE, DNA-SYNTHESIS, AND GLUCOSE-TRANSPORTER TRANSLOCATION [J].
CHEATHAM, B ;
VLAHOS, CJ ;
CHEATHAM, L ;
WANG, L ;
BLENIS, J ;
KAHN, CR .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) :4902-4911
[6]   INSULIN ACTION AND THE INSULIN SIGNALING NETWORK [J].
CHEATHAM, B ;
KAHN, CR .
ENDOCRINE REVIEWS, 1995, 16 (02) :117-142
[7]   The host-tumor immune conflict: from immunosuppression to resistance and destruction [J].
Chouaib, S ;
AsselinPaturel, C ;
MamiChouaib, F ;
Caignard, A ;
Blay, JY .
IMMUNOLOGY TODAY, 1997, 18 (10) :493-497
[8]  
CHU CT, 1994, LAB INVEST, V71, P792
[9]  
Colombo MP, 1996, CANCER RES, V56, P2531
[10]   Activation of stress-activated protein kinase-3 (SAPK3) by cytokines and cellular stresses is mediated via SAPKK3 (MKK6); Comparison of the specificities of SAPK3 and SAPK2 (RK/p38) [J].
Cuenda, A ;
Cohen, P ;
BueeScherrer, V ;
Goedert, M .
EMBO JOURNAL, 1997, 16 (02) :295-305