Dedifferentiated thyroid cancer: A therapeutic challenge

被引:90
作者
Antonelli, Alessandro [1 ]
Fallahi, Poupak [1 ]
Ferrari, Silvia Martina [1 ]
Carpi, Angelo [2 ]
Berti, Piero [3 ]
Materazzi, Gabriele [3 ]
Minuto, Michele [3 ]
Guastalli, Mario [1 ]
Miccoli, Paolo [3 ]
机构
[1] Univ Pisa, Dept Internal Med, Sch Med, I-56100 Pisa, Italy
[2] Univ Pisa, Sch Med, Dept Reprod & Ageing, I-56100 Pisa, Italy
[3] Univ Pisa, Dept Surg, I-56100 Pisa, Italy
关键词
Thyroid cancer; Targeted therapy; Thiazolidinediones;
D O I
10.1016/j.biopha.2008.07.056
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Human papillary dedifferentiated thyroid cancer (HPDTC) represents a therapeutic dilemma. Targeted therapy (RET proto-oncogene or BRAF-targeting drugs) are promising treatments for HPDTC. Also PPARg agonists are another exciting field for redifferentiating therapy of HPDTC. However, even if many new approaches for the therapy of HPDTC are emerging, until now a significant clinical impact on survival by the use of these drugs is still lacking. In the future, the identification of patients who are likely to benefit from each therapeutic option will be important. In this view particular importance should be given to development of primary cells from the single patient by fine needle aspiration samples, as recently observed in anaplastic thyroid cancer. In fact, chemosensitivity tests in primary tumoral cells may help in detecting responsive patients and in preventing the administration of inactive drugs to those unresponsive. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:559 / 563
页数:5
相关论文
共 44 条
[1]   Interferon-γ-inducible α-chemokine CXCL10 involvement in Graves' ophthalmopathy:: Modulation by peroxisome proliferator-activated receptor-γ agonists [J].
Antonelli, A ;
Rotondi, M ;
Ferrari, SM ;
Fallahi, P ;
Romagnani, P ;
Franceschini, SS ;
Serio, M ;
Ferrannini, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (02) :614-620
[2]  
ANTONELLI A, 2008, CLIN ENDOCRINOL 0110
[3]  
BOUGHTON D, 2006, ASCO M ATL GEORG US
[4]   Mutant Ras-induced proliferation of human thyroid epithelial cells requires three effector pathways [J].
Bounacer, A ;
McGregor, A ;
Skinner, J ;
Bond, J ;
Poghosyan, Z ;
Wynford-Thomas, D .
ONCOGENE, 2004, 23 (47) :7839-7845
[5]   Beyond radioiodine: A review of potential new therapeutic approaches for thyroid cancer [J].
Braga-Basaria, M ;
Ringel, MD .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (05) :1947-1960
[6]   Expression of angiogenesis stimulators and inhibitors in human thyroid tumors and correlation with clinical pathological features [J].
Bunone, G ;
Vigneri, P ;
Mariani, L ;
Butó, S ;
Collini, P ;
Pilotti, S ;
Pierotti, MA ;
Bongarzone, I .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (06) :1967-1976
[7]   BAY 43-9006 inhibition of oncogenic RET mutants [J].
Carlomagno, F ;
Anaganti, S ;
Guida, T ;
Salvatore, G ;
Troncone, G ;
Wilhelm, SM ;
Santoro, M .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (05) :326-334
[8]   Valproic acid induces apoptosis and cell cycle arrest in poorly differentiated thyroid cancer cells [J].
Catalano, MG ;
Fortunati, N ;
Pugliese, M ;
Costantino, L ;
Poli, R ;
Bosco, O ;
Boccuzzi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (03) :1383-1389
[9]   Angiogenesis and lymphangiogenesis in thyroid proliferative lesions: relationship to type and tumour behaviour [J].
de la Torre, N. Garcia ;
Buley, I. ;
Wass, J. A. H. ;
Turner, H. E. .
ENDOCRINE-RELATED CANCER, 2006, 13 (03) :931-944
[10]   How thyroid tumors start and why it matters: kinase mutants as targets for solid cancer pharmacotherapy [J].
Fagin, JA .
JOURNAL OF ENDOCRINOLOGY, 2004, 183 (02) :249-256