Pathogenetic mechanisms in thyroid follicular-cell neoplasia

被引:696
作者
Kondo, T
Ezzat, S
Asa, SL [1 ]
机构
[1] Univ Toronto, Dept Pathol, Univ Hlth Network, Toronto, ON M5G 2C4, Canada
[2] Univ Toronto, Dept Pathol, Toronto Med Labs, Toronto, ON M5G 2C4, Canada
[3] Univ Toronto, Toronto Med Labs, Toronto, ON M5G 2C4, Canada
[4] Univ Toronto, Dept Lab Med & Pathol, Toronto, ON M5G 2C4, Canada
[5] Freeman Ctr Endocrine Oncol, Toronto, ON M5G 2M9, Canada
[6] Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
[7] Mt Sinai Hosp, Dept Med, Toronto, ON M5G 1X5, Canada
[8] Univ Toronto, Toronto, ON M5G 1X5, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1038/nrc1836
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thyroid cancer is one of the few malignancies that are increasing in incidence. Recent advances have improved our understanding of its pathogenesis; these include the identification of genetic alterations that activate a common effector pathway involving the RET-Ras-BRAF signalling cascade, and other unique chromosomal rearrangements. Some of these have been associated with radiation exposure as a pathogenetic mechanism. Defects in transcriptional and post-transcriptional regulation of adhesion molecules and cell-cycle control elements seem to affect tumour progression. This information can provide powerful ancillary diagnostic tools and can also be used to identify new therapeutic targets.
引用
收藏
页码:292 / 306
页数:15
相关论文
共 235 条
  • [1] The GDNF family: Signalling, biological functions and therapeutic value
    Airaksinen, MS
    Saarma, M
    [J]. NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) : 383 - 394
  • [2] AKSLEN LA, 1995, CANCER, V76, P1643, DOI 10.1002/1097-0142(19951101)76:9<1643::AID-CNCR2820760922>3.0.CO
  • [3] 2-#
  • [4] Papillary and follicular thyroid carcinomas show distinctly different microarray expression profiles and can be distinguished by a minimum of five genes
    Aldred, MA
    Huang, Y
    Liyanarachchi, S
    Pellegata, NS
    Gimm, O
    Jhiang, S
    Davuluri, RV
    de La Chapelle, A
    Eng, C
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (17) : 3531 - 3539
  • [5] *AM CANC SOC, 2005, FACTS FIG 2005
  • [6] Retinoblastoma expression in thyroid neoplasms
    Anwar, F
    Emond, MJ
    Schmidt, RA
    Hwang, HC
    Bronner, MP
    [J]. MODERN PATHOLOGY, 2000, 13 (05) : 562 - 569
  • [7] CLONALITY OF THYROID-NODULES IN SPORADIC GOITER
    APEL, RL
    EZZAT, S
    BAPAT, BV
    PAN, N
    LIVOLSI, VA
    ASA, SL
    [J]. DIAGNOSTIC MOLECULAR PATHOLOGY, 1995, 4 (02) : 113 - 121
  • [8] My approach to oncocytic tumours of the thyroid
    Asa, SL
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2004, 57 (03) : 225 - 232
  • [9] EPIDERMAL GROWTH-FACTOR STIMULATES CELL-PROLIFERATION AND INHIBITS IODIDE UPTAKE OF FRTL-5 CELLS IN-VITRO
    ASMIS, LM
    GERBER, H
    KAEMPF, J
    STUDER, H
    [J]. JOURNAL OF ENDOCRINOLOGY, 1995, 145 (03) : 513 - 520
  • [10] Cyclin D1 overexpression in thyroid carcinomas: Relation with clinico-pathological parameters, retinoblastoma gene product, and Ki67 labeling index
    Basolo, F
    Caligo, MA
    Pinchera, A
    Fedeli, F
    Baldanzi, A
    Miccoli, P
    Iacconi, P
    Fontanini, G
    Pacini, F
    [J]. THYROID, 2000, 10 (09) : 741 - 746