In my view ... Fetal cell carcinogenesis: A new hypothesis for better understanding of thyroid carcinoma

被引:50
作者
Takano, T
Amino, N
机构
[1] Osaka Univ, Grad Sch Med, Dept Lab Med, Osaka 5650871, Japan
[2] Kuma Hosp, Chuo Ku, Kobe, Hyogo, Japan
关键词
D O I
10.1089/thy.2005.15.432
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Modern advances in molecular technology have given us the chance to establish a new insight into thyroid carcinogenesis. Gene expression in thyroid malignancies usually reveals highly consistent profiles, which leads to questioning of the classic concept of multistep carcinogenesis, in which cancer cells are produced from well-differentiated benign cells by transformation caused by accumulating damage to their genome. We propose a novel hypothesis of thyroid carcinogenesis, the fetal cell carcinogenesis hypothesis, in which cancer cells are derived from the remnants of three types of fetal thyroid cells, instead of normal thyroid follicular cells. This hypothesis explains well the clinical and biologic features and recent molecular evidence of thyroid carcinoma. It suggests the importance of clarifying the molecular mechanism of thyroid development and the identification of fetal thyroid cells, especially thyroid stem cells (TSCs), because Such data will lead to better understanding of thyroid carcinogenesis and thyroid regeneration.
引用
收藏
页码:432 / 438
页数:7
相关论文
共 47 条
[1]   Anaplastic thyroid carcinoma: Behavior, biology, and therapeutic approaches [J].
Ain, KB .
THYROID, 1998, 8 (08) :715-726
[2]  
Barden CB, 2003, CLIN CANCER RES, V9, P1792
[3]  
BOCIANSOBKOWSKA J, 1992, HISTOL HISTOPATHOL, V7, P415
[4]  
BocianSobkowska J, 1997, HISTOL HISTOPATHOL, V12, P79
[5]  
Bouras M, 1995, ANN BIOL CLIN-PARIS, V53, P549
[6]   FOLLICULAR AND HURTHLE CELL-CARCINOMA OF THE THYROID [J].
COOPER, DS ;
SCHNEYER, CR .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1990, 19 (03) :577-591
[7]   MALIGNANT AND BENIGN NEOPLASMS OF THYROID IN PATIENTS TREATED FOR HYPERTHYROIDISM - REPORT OF COOPERATIVE THYROTOXICOSIS THERAPY FOLLOW-UP STUDY [J].
DOBYNS, BM ;
SHELINE, GE ;
WORKMAN, JB ;
TOMPKINS, EA ;
MCCONAHEY, WM ;
BECKER, DV .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1974, 38 (06) :976-998
[8]   Stem cells in normal breast development and breast cancer [J].
Dontu, G ;
Al-Hajj, M ;
Abdallah, WA ;
Clarke, MF ;
Wicha, MS .
CELL PROLIFERATION, 2003, 36 :59-72
[9]   PHYSIOLOGICAL AND PATHOLOGICAL REGULATION OF THYROID-CELL PROLIFERATION AND DIFFERENTIATION BY THYROTROPIN AND OTHER FACTORS [J].
DUMONT, JE ;
LAMY, F ;
ROGER, P ;
MAENHAUT, C .
PHYSIOLOGICAL REVIEWS, 1992, 72 (03) :667-697
[10]   Involvement of the PAX8/peroxisome proliferator-activated receptor γ rearrangement in follicular thyroid tumors [J].
Dwight, T ;
Thoppe, SR ;
Foukakis, T ;
Lui, WO ;
Wallin, G ;
Höög, A ;
Frisk, T ;
Larsson, C ;
Zedenius, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (09) :4440-4445