Neuroendocrine differentiation in the progression of prostate cancer

被引:109
作者
Komiya, Akira [1 ,2 ]
Suzuki, Hiroyoshi [2 ]
Imamoto, Takashi [2 ]
Kamiya, Naoto [2 ]
Nihei, Naoki [2 ]
Naya, Yukio [2 ]
Ichikawa, Tomohiko [2 ]
Fuse, Hideki [1 ]
机构
[1] Toyama Univ, Grad Sch Med & Pharmaceut Sci Res, Dept Urol, Toyama, Japan
[2] Chiba Univ, Grad Sch Med, Dept Urol, Chiba, Japan
关键词
androgen-independent; hormone-refractory prostate cancer; hormone therapy; neuroendocrine differentiation; prostate cancer; GASTRIN-RELEASING-PEPTIDE; SMALL-CELL-CARCINOMA; INTERMITTENT ANDROGEN SUPPRESSION; OBJECTIVE CLINICAL-RESPONSES; NEOPLASTIC HUMAN PROSTATE; PRETREATMENT SERUM-LEVEL; NEURON-SPECIFIC ENOLASE; PLASMA CHROMOGRANIN-A; KI67 LABELING INDEX; SOMATOSTATIN ANALOG;
D O I
10.1111/j.1442-2042.2008.02175.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Neuroendocrine (NE) cells originally exist in the normal prostate acini and duct, regulating prostatic growth, differentiation and secretion. Clusters of malignant NE cells are found in most prostate cancer (PCa) cases. NE differentiation (NED) is the basic character of the prostate, either benign or malignant. NE cells hold certain peptide hormones or pro-hormones, which affect the target cells by endocrine, paracrine, autocrine and neuroendocrine transmission in an androgen-independent fashion due to the lack of androgen receptor. NED is accessed by immunohistochemical staining or measurement of serum levels of NE markers. The extent of NED is associated with progression and prognosis of PCa. Chromogranin A (CGA) is the most important NE marker. In metastatic PCa, pretreatment serum CGA levels can be a predictor for progression and survival after endocrine therapy. It is recommended to measure longitudinal change in serum CGA. The NE pathway can also be a therapeutic target.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 125 条
[91]   Morphologic and molecular prognostic markers in prostate cancer [J].
Ross, JS ;
Sheehan, CE ;
Dolen, EM ;
Kallakury, BVS .
ADVANCES IN ANATOMIC PATHOLOGY, 2002, 9 (02) :115-128
[92]   Changes in chromogranin A serum levels during endocrine therapy in metastatic prostate cancer patients [J].
Sasaki, T ;
Komiya, A ;
Suzuki, H ;
Shimbo, M ;
Ueda, T ;
Akakura, K ;
Ichikawa, T .
EUROPEAN UROLOGY, 2005, 48 (02) :224-230
[93]   Intermittent androgen suppression for locally advanced and metastatic prostate cancer: Preliminary report of a prospective multicenter study [J].
Sato, N ;
Akakura, K ;
Isaka, S ;
Nakatsu, H ;
Tanaka, M ;
Ito, H ;
Masai, M .
UROLOGY, 2004, 64 (02) :341-345
[94]  
SCHALLY AV, 1988, CANCER RES, V48, P6977
[95]   Somatostatin analogues and estrogens in the treatment of androgen ablation refractory prostate adenocarcinoma [J].
Sciarra, A ;
Bosman, C ;
Monti, G ;
Gentile, V ;
Gomez, AMA ;
Ciccariello, M ;
Pastore, A ;
Salvatori, G ;
Fattore, F ;
Di Silverio, F .
JOURNAL OF UROLOGY, 2004, 172 (05) :1775-1783
[96]   Effect of nonsteroidal antiandrogen monotherapy versus castration therapy on neuroendocrine differentiation in prostate carcinoma [J].
Sciarra, A ;
Di Silverio, F .
UROLOGY, 2004, 63 (03) :523-527
[97]   Variation in chromogranin A serum levels during intermittent versus continuous androgen deprivation therapy for prostate adenocarcinoma [J].
Sciarra, A ;
Monti, S ;
Gentile, V ;
Mariotti, G ;
Cardi, A ;
Voria, G ;
Lucera, R ;
Di Silverio, F .
PROSTATE, 2003, 55 (03) :168-179
[98]  
Shimura S, 2000, CANCER RES, V60, P5857
[99]   The role of serotonin (5-hydroxytryptamine1A and 1B) receptors in prostate cancer cell proliferation [J].
Siddiqui, Emad J. ;
Shabbir, Majid ;
Mikhailidis, Dimitri P. ;
Thompson, Cecil S. ;
Mumtaz, Faiz H. .
JOURNAL OF UROLOGY, 2006, 176 (04) :1648-1653
[100]  
SOLOWAY MS, 1988, CANCER-AM CANCER SOC, V61, P195, DOI 10.1002/1097-0142(19880101)61:1<195::AID-CNCR2820610133>3.0.CO