Recent advances in the biology of germ cell tumors: Implications for the diagnosis and treatment

被引:21
作者
Chieffi, P. [1 ]
Chieffi, S. [2 ]
Franco, R. [3 ]
Sinisi, A. A. [4 ]
机构
[1] Univ Naples 2, Dept Psychol, Caserta, Italy
[2] Univ Naples 2, Dept Expt Med, Naples, Italy
[3] Ist Nazl Tumori Fdn G Pascale, Naples, Italy
[4] Univ Naples 2, Dept Cardiothorac & Resp Sci, Naples, Italy
关键词
Aurora B; gonocytes; GPR30; HMGA; PATZ1; seminoma; teratoma; testis; testicular cancer; testicular germ cells tumors; HUMAN TESTICULAR SEMINOMAS; ENDOTHELIAL GROWTH-FACTOR; CARCINOMA-IN-SITU; AURORA-B EXPRESSION; C-KIT; CLINICAL-IMPLICATIONS; MOLECULAR TARGETS; RANA-ESCULENTA; RECEPTOR-BETA; STEM-CELLS;
D O I
10.3275/8716
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Testicular germ cell tumors (TGCT), are the most frequent solid malignant tumors in men 20-40 yr of age, and the most frequent cause of death from solid tumors in this age group. TGCT can be subdivided into seminoma and non-seminoma germ cell tumors (NSGCT), including embryonal cell carcinoma, choriocarcinoma, yolk sac tumor, and teratoma. Seminomas and NSGCT do not only present distinctive clinical features, but they also show significant differences as far as therapy and prognosis are concerned. Many novel markers have given further advantages to discriminate between histological subgroups. In addition, therapeutic approaches for the treatment of TGCT have been proposed: humanized antibodies against receptors/surface molecules on cancer cells, inhibitors of serine-threonine, and tyrosine kinases, and others. The review will focus on the recent advances in the research of molecular alterations identified in TGCT and on novel targeted anti-neoplastic strategies that might help to treat chemotherapy-resistant TGCT. (J. Endocrinol. Invest. 35: 1015-1020, 2012) (C) 2012, Editrice Kurtis
引用
收藏
页码:1015 / 1020
页数:6
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