L'histoire naturelle du cancer de prostate métastatique

25 novembre 2008

Auteurs : T. Lebret, A. Méjean
Référence : Prog Urol, 2008, 18, S327, suppl. S7
   
 
 

 

 
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Références

 

Tantivejkul K., Kalikin L.M., Pienta K.J. Dynamic process of prostate cancer metastasis to bone J Cell Biochem 2004 ;  91 : 706-717 [cross-ref]
 
Bill-Axelson A., Holmberg L., Filén F., et al. Radical prostatectomy versus watchful waiting in localized prostate cancer: the Scandinavian prostate cancer group-4 randomized trial J Natl Cancer Inst 2008 ;  100 (16) : 1144-1154 [cross-ref]
 
D’Amico A.V., Chen M.H., Roehl K.A., Catalona W.J. Preoperative PSA velocity and the risk of death from prostate cancer after radical prostatectomy N Engl J Med 2004 ;  351 (2) : 125-135
 
D’Amico A.V. Screening for prostate carcinoma: prostate-specific antigen--friend or foe? Cancer 2005 ;  103 (5) : 881-883
 
Nelson WG, Saad F, Debruyne FMJ, et al. Prostate Cancer. 6th International Consultation on new developments in Prostate Cancer and Prostate diseases. 2006 6th edition. 309-345.
 
Ward J.F., Blute M.L., Slezak J., Bergstralh E.J., Zincke H. The longterm clinical impact of biochemical recurrence of prostate cancer 5 or more years after radical prostatectomy J Urol 2003 ;  170 : 1872-1876 [cross-ref]
 
Okotie O.T., Aronson W.J., Wieder J.A., et al. Predictors of metastatic disease in men with biochemical failure following radical prostatectomy J Urol 2004 ;  171 (6pt1) : 2260-2264 [cross-ref]
 
D’Amico A.V., Moul J.W., Carroll P.R., Sun L., Lubeck D., Chen M.H. Surrogate end point for prostate cancer-specific mortality after radical prostatectomy or radiation therapy J Natl Cancer Inst 2003 ;  95 : 1376-1383
 
Freedland S.J., Humphreys E.B., Mangold L.A., Eisenberger M., Dorey F.J., Walsh P.C., Partin A.W. Risk of prostate cancer-specific mortality following biochemical recurrence after radical prostatectomy JAMA 2005 ;  294 (4) : 433-439 [inter-ref]
 
Albertsen P.C., Hanley J.A., Penson D.F., Barrows G., Fine J. 13-year outcomes following treatment for clinically localized prostate cancer in a population based cohort J Urol 2007 ;  177 (3) : 932-936 [cross-ref]
 
Luzzi K.J., MacDonald I.C., Schmidt E.E., et al. Multistep nature of metastatic inefficiency: dormancy of solitary cells after successful extravasation and limited survival of early micrometastases Am J Pathol 1998 ;  153 : 865-873 [cross-ref]
 
Rosol T.J., Tannehill-Gregg S.H., LeRoy B.E., Mandl S., Contag C.H. Animal models of bone metastasis Cancer 2003 ;  97 : 748-757 [cross-ref]
 
Vartanian R.K., Weidner N. Endothelial cell proliferation in prostatic carcinoma and prostatic hyperplasia: correlation with Gleason’s score, microvessel density, and epithelial cell proliferation Lab Invest 1995 ;  73 : 844-850
 
Brawer M.K., Deering R.E., Brown M., Preston S.D., Bigler S.A. Predictors of pathologic stage in prostatic carcinoma: the role of neovascularity Cancer 1994 ;  73 : 678-687 [cross-ref]
 
Bostwick D.G., Wheeler T.M., Blute M., et al. Optimized microvessel density analysis improves prediction of cancer stage from prostate needle biopsies Urology 1996 ;  48 : 47-57 [inter-ref]
 
Yancopoulos G.D., Davis S., Gale N.W., Rudge J.S., Wiegand S.J., Holash J. Vascular-specific growth factors in blood vessel formation Nature 2000 ;  407 : 242-248 [cross-ref]
 
Zeng Y., Opeskin K., Baldwin M.E., et al. Expression of vascular endothelial growth factor receptor-3 by lymphatic endothelial cells is associated with lymph node metastasis in prostate cancer Clin Cancer Res 2004 ;  10 : 5137-5144 [cross-ref]
 
Lin J., Lalani A.S., Harding T.C., et al. Inhibition of lymphogenous metastasis using adeno-associated virus-mediated gene transfer of a soluble VEGFR-3 decoy receptor Cancer Res 2005 ;  65 : 6901-6909 [cross-ref]
 
Bussemakers M.J., Van Bokhoven A., Tomita K., Jansen C.F., Schalken J.A. Complex cadherin expression in human prostate cancer cells Int J Cancer 2000 ;  85 : 446-450 [cross-ref]
 
Day M.L., Zhao X., Vallorosi C.J., et al. Ecadherin mediates aggregation-dependent survival of prostate and mammary epithelial cells through the retinoblastoma cell cycle control pathway J Biol Chem 1999 ;  274 : 9656-9664 [cross-ref]
 
Tran N.L., Nagle R.B., Cress A.E., Heimark R.L. N-Cadherin expression in human prostate carcinoma cell lines: an epithelial–mesenchymal transformation mediating adhesion with stromal cells Am J Pathol 1999 ;  155 : 787-798 [cross-ref]
 
Bryden A.A., Hoyland J.A., Freemont A.J., Clarke N.W., Schembri Wismayer D., George N.J. E-cadherin and beta-catenin are downregulated in prostatic bone metastases BJU Int 2002 ;  89 (4) : 400-403 [cross-ref]
 
Sanda M.G., Restifo N.P., Walsh J.C., et al. Molecular characterization of defective antigen processing in human prostate cancer J Nat Cancer Inst 1995 ;  87 : 280-285 [cross-ref]
 
Borsig L., Wong R., Feramisco J., Nadeau D.R., Varki N.M., Varki A. Heparin and cancer revisited: mechanistic connections involving platelets, P-selectin, carcinoma mucins, and tumor metastasis Proc Natl Acad Sci U S A 2001 ;  98 : 3352-3357 [cross-ref]
 
Stoelcker B, Hafner M, Orosz P, Nieswandt B, Männel DN. Role of adhesion molecules and platelets in TNF-induced adhesion of tumor cells to endothelial cells: implications for experimental metastasis. J Inflamm 1995-1996;46(3):155-67.
 
Chay C.H., Cooper C.R., Gendernalik J.D., et al. A functional thrombin receptor (PAR1) is expressed on bone-derived prostate cancer cell lines Urology 2002 ;  60 : 760-765 [inter-ref]
 
Trikha M., Nakada M.T. Platelets and cancer: implications for antiangiogenic therapy Semin Thromb Hemost 2002 ;  28 : 39-44 [cross-ref]
 
Batson O.V. Function of vertebral veins and their role in spread of metastases Ann Surg 1940 ;  112 : 138-149 [cross-ref]
 
Al-Mehdi A.B., Tozawa K., Fisher A.B., Shientag L., Lee A., Muschel R.J. Intravascular origin of metastasis from the proliferation of endothelium-attached tumor cells: a new model for metastasis Nat Med 2000 ;  6 : 100-102 [cross-ref]
 
Koeneman K.S., Yeung F., Chung L.W. Osteomimetic properties of prostate cancer cells: a hypothesis supporting the predilection of prostate cancer metastasis and growth in the bone environment Prostate 1999 ;  39 : 246-261 [cross-ref]
 
Zhau H.E., Li C.L., Chung L.W. Establishment of human prostate carcinoma skeletal metastasis models Cancer 2000 ;  88 (Suppl 12) : 2995-3001 [cross-ref]
 
Ritchie C.K., Andrews L.R., Thomas K.G., Tindall D.J., Fitzpatrick L.A. The effects of growth factors associated with osteoblasts on prostate carcinoma proliferation and chemotaxis: implications for the development of metastatic disease Endocrinology 1997 ;  138 : 1145-1150 [cross-ref]
 
Cohen P., Peehl D.M., Lamson G., Rosenfeld R.G. Insulin-like growth factors (IGFs), IGF receptors, and IGF-binding proteins in primary cultures of prostate epithelial cells J Clin Endocrinol Metab 1991 ;  73 : 401-407 [cross-ref]
 
Arya M., Bott S.R., Shergill I.S., Ahmed H.U., Williamson M., Patel H.R. The metastatic cascade in prostate cancer Surg Oncol 2006 ;  15 (3) : 117-128 [cross-ref]
 
Varambally S., Yu J., Laxman B., et al. Integrative genomic and proteomic analysis of prostate cancer reveals signatures of metastatic progression Cancer Cell 2005 ;  8 : 393-406 [cross-ref]
 
Taylor B.S., Varambally S., Chinnaiyan A.M. A systems approach to model metastatic progression Cancer Res 2006 ;  66 : 5537-5539 [cross-ref]
 
   
 
 
   

 

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