1.Burman KD., Ringel MD., Wartofsky L. Unusual types of thyroid neoplasms. Endocrinol Metab Clin North Am. 1996. 25:49–68.
Article
2.Riesco-Eizaguirre G., Santisteban P. New insights in thyroid follicular cell biology and its impact in thyroid cancer therapy. Endocr Relat Cancer. 2007. 14:957–77.
Article
3.Wreesmann V., Singh B. Clinical impact of molecular analysis on thyroid cancer management. Surgical Oncology Clinics of North America. 2008. 17:1–35.
Article
4.El-Shabrawi Y., Mangge H., Hermann J. Anti-tumour necrosis factor alpha treatment in chronic recurrent inflammation of the anterior segment of the eye in patients resistant to standard immunomodulatory treatment. Ann Rheum Dis. 2003. 62:1243–4.
5.Roque L., Rodrigues R., Pinto A., Moura-Nunes V., Soares J. Chromosome imbalances in thyroid follicular neoplasms: a comparison between follicular adenomas and carcinomas. Genes Chromosomes Cancer. 2003. 36:292–302.
Article
6.Kitamura Y., Shimizu K., Ito K., Tanaka S., Emi M. Allelotyping of follicular thyroid carcinoma: frequent allelic losses in chromosome arms 7q, 11p, and 22q. J Clin Endocrinol Metab. 2001. 86:4268–72.
Article
7.Castro P., Eknaes M., Teixeira MR., Danielsen HE., Soares P., Lothe RA, et al. Adenomas and follicular carcinomas of the thyroid display two major patterns of chromosomal changes. J Pathol. 2005. 206:305–11.
Article
8.Wreesmann VB., Ghossein RA., Hezel M., Banerjee D., Shaha AR., Tuttle RM, et al. Follicular variant of papillary thyroid carcinoma: genome-wide appraisal of a controversial entity. Genes Chromosomes Cancer. 2004. 40:355–64.
Article
9.Roque L., Nunes VM., Ribeiro C., Martins C., Soares J. Karyotypic characterization of papillary thyroid carcinomas. Cancer. 2001. 92:2529–38.
Article
10.Singh B., Lim D., Cigudosa JC., Ghossein R., Shaha AR., Poluri A, et al. Screening for genetic aberrations in papillary thyroid cancer by using comparative genomic hybridization. Surgery. 2000. 128:888–93. discussion 93-4.
Article
11.Kjellman P., Lagercrantz S., Hoog A., Wallin G., Larsson C., Zedenius J. Gain of 1q and loss of 9q21.3-q32 are associated with a less favorable prognosis in papillary thyroid carcinoma. Genes Chromosomes Cancer. 2001. 32:43–9.
Article
12.Roque L., Soares J., Castedo S. Cytogenetic and fluorescence in situ hybridization studies in a case of anaplastic thyroid carcinoma. Cancer Genet Cytogenet. 1998. 103:7–10.
Article
13.Mark J., Ekedahl C., Dahlenfors R., Westermark B. Cytogenetical observations in five human anaplastic thyroid carcinomas. Hereditas. 1987. 107:163–74.
Article
14.Jenkins RB., Hay ID., Herath JF., Schultz CG., Spurbeck JL., Grant CS, et al. Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinoma. Cancer. 1990. 66:1213–20.
Article
15.Rodrigues RF., Roque L., Krug T., Leite V. Poorly differentiated and anaplastic thyroid carcinomas: chromosomal and oligo-array profile of five new cell lines. Br J Cancer. 2007. 96:1237–45.
Article
16.Smallridge RC., Marlow LA., Copland JA. Anaplastic thyroid cancer: molecular pathogenesis and emerging therapies. Endocr Relat Cancer. 2009. 16:17–44.
Article
17.Rapp UR., Goldsborough MD., Mark GE., Bonner TI., Groffen J., Reynolds FH Jr, et al. Structure and biological activity of v-raf, a unique oncogene transduced by a retrovirus. Proc Natl Acad Sci U S A. 1983. 80:4218–22.
Article
18.Nucera C., Goldfarb M., Hodin R., Parangi S. Role of B-Raf (V600E) in differentiated thyroid cancer and preclinical validation of compounds against B-Raf (V600E). Biochim Biophys Acta. 2009. 1795:152–61.
19.Leicht DT., Balan V., Kaplun A., Singh-Gupta V., Kaplun L., Dobson M, et al. Raf kinases: function, regulation and role in human cancer. Biochim Biophys Acta. 2007. 1773:1196–212.
Article
20.Emuss V., Garnett M., Mason C., Marais R. Mutations of C-RAF are rare in human cancer because C-RAF has a low basal kinase activity compared with B-RAF. Cancer Res. 2005. 65:9719–26.
Article
21.Davies H., Bignell GR., Cox C., Stephens P., Edkins S., Clegg S, et al. Mutations of the BRAF gene in human cancer. Nature. 2002. 417:949–54.
Article
22.Kumar R., Angelini S., Czene K., Sauroja I., Hahka-Kemppinen M., Pyrhonen S, et al. BRAF mutations in metastatic melanoma: a possible association with clinical outcome. Clin Cancer Res. 2003. 9:3362–8.
23.Nikiforova MN., Stringer JR., Blough R., Medvedovic M., Fagin JA., Nikiforov YE. Proximity of chromosomal loci that participate in radiation-induced rearrangements in human cells. Science. 2000. 290:138–41.
Article
24.Wan PT., Garnett MJ., Roe SM. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell. 2004. 116:855–67.
Article
25.Nikiforova MN., Kimura ET., Gandhi M., Biddinger PW., Knauf JA., Basolo F, et al. BRAF mutations in thyroid tumors are restricted to papillary carcinomas and anaplastic or poorly differentiated carcinomas arising from papillary carcinomas. J Clin Endocrinol Metab. 2003. 88:5399–404.
Article
26.Xing M. BRAF mutation in thyroid cancer. Endocr Relat Cancer. 2005. 12:245–62.
Article
27.Chung KW., Yang SK., Lee GK., Kim EY., Kwon S., Lee SH, et al. Detection of BRAFV600E mutation on fine needle aspiration specimens of thyroid nodule refines cyto-pathology diagnosis, especially in BRAF600E mutation-prevalent area. Clin Endocrinol (Oxf). 2006. 65:660–6.
28.Jo YS., Li S., Song JH., Kwon KH., Lee JC., Rha SY, et al. Influence of the BRAF V600E mutation on expression of vascular endothelial growth factor in papillary thyroid cancer. J Clin Endocrinol Metab. 2006. 91:3667–70.
Article
29.Xing M., Vasko V., Tallini G., Larin A., Wu G., Udelsman R, et al. BRAF T1796A transversion mutation in various thyroid neoplasms. J Clin Endocrinol Metab. 2004. 89:1365–8.
Article
30.Xing M., Westra WH., Tufano RP., Cohen Y., Rosenbaum E., Rhoden KJ, et al. BRAF mutation predicts a poorer clinical prognosis for papillary thyroid cancer. J Clin Endocrinol Metab. 2005. 90:6373–9.
Article
31.Kim TY., Kim WB., Rhee YS., Song JY., Kim JM., Gong G, et al. The BRAF mutation is useful for prediction of clinical recurrence in low-risk patients with conventional papillary thyroid carcinoma. Clin Endocrinol (Oxf). 2006. 65:364–8.
Article
32.Riesco-Eizaguirre G., Gutierrez-Martinez P., Garcia-Cabezas MA., Nistal M., Santisteban P. The oncogene BRAF V600E is associated with a high risk of recurrence and less differentiated papillary thyroid carcinoma due to the impairment of Na+/I-targeting to the membrane. Endocr Relat Cancer. 2006. 13:257–69.
33.Fecher LA., Cummings SD., Keefe MJ., Alani RM. Toward a molecular classification of melanoma. J Clin Oncol. 2007. 25:1606–20.
Article
34.Ugolini C., Giannini R., Lupi C., Salvatore G., Miccoli P., Proietti A, et al. Presence of BRAF V600E in very early stages of papillary thyroid carcinoma. Thyroid. 2007. 17:381–8.
Article
35.Kim TY., Kim WB., Song JY., Rhee YS., Gong G., Cho YM, et al. The BRAF mutation is not associated with poor prognostic factors in Korean patients with conventional papillary thyroid microcarcinoma. Clin Endocrinol (Oxf). 2005. 63:588–93.
37.Curtin JA., Fridlyand J., Kageshita T., Patel HN., Busam KJ., Kutzner H, et al. Distinct sets of genetic alterations in melanoma. N Engl J Med. 2005. 353:2135–47.
Article
36.Mitsutake N., Miyagishi M., Mitsutake S., Akeno N., Mesa C Jr., Knauf JA, et al. BRAF mediates RET/PTC-induced mitogen-activated protein kinase activation in thyroid cells: functional support for requirement of the RET/PTC-RAS-BRAF pathway in papillary thyroid carcinogenesis. Endocrinology. 2006. 147:1014–9.
Article
38.Frasca F., Nucera C., Pellegriti G., Gangemi P., Attard M., Stella M, et al. BRAF (V600E) mutation and the biology of papillary thyroid cancer. Endocr Relat Cancer. 2008. 15:191–205.
39.Guan H., Ji M., Bao R., Yu H., Wang Y., Hou P, et al. Association of high iodine intake with the T1799A BRAF mutation in papillary thyroid cancer. J Clin Endocrinol Metab. 2009. 94:1612–7.
Article
40.Suarez HG. Molecular basis of epithelial thyroid tumorigenesis. C R Acad Sci III. 2000. 323:519–28.
Article
41.Takahashi M., Ritz J., Cooper GM. Activation of a novel human transforming gene, ret, by DNA rearrangement. Cell. 1985. 42:581–8.
Article
42.Fusco A., Grieco M., Santoro M., Berlingieri MT., Pilotti S., Pierotti MA, et al. A new oncogene in human thyroid papillary carcinomas and their lymph-nodal metastases. Nature. 1987. 328:170–2.
Article
43.Grieco M., Santoro M., Berlingieri MT., Melillo RM., Donghi R., Bongarzone I, et al. PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thyroid papillary carcinomas. Cell. 1990. 60:557–63.
Article
44.Santoro M., Dathan NA., Berlingieri MT., Bongarzone I., Paulin C., Grieco M, et al. Molecular characterization of RET/PTC3; a novel rearranged version of the RETproto-oncogene in a human thyroid papillary carcinoma. Oncogene. 1994. 9:509–16.
45.Miyagi E., Braga-Basaria M., Hardy E., Vasko V., Burman KD., Jhiang S, et al. Chronic expression of RET/PTC 3 enhances basal and insulin-stimulated PI3 kinase/AKT signaling and increases IRS-2 expression in FRTL-5 thyroid cells. Mol Carcinog. 2004. 41:98–107.
Article
46.Ouyang B., Knauf JA., Smith EP., Zhang L., Ramsey T., Yusuff N, et al. Inhibitors of Raf kinase activity block growth of thyroid cancer cells with RET/PTC or BRAF mutations in vitro and in vivo. Clin Cancer Res. 2006. 12:1785–93.
47.Nikiforov YE. RET/PTC rearrangement in thyroid tumors. Endocr Pathol. 2002. 13:3–16.
Article
48.Nikiforov YE. Radiation-induced thyroid cancer: what we have learned from chernobyl. Endocr Pathol. 2006. 17:307–17.
Article
49.Thomas GA., Bunnell H., Cook HA., Williams ED., Nerovnya A., Cherstvoy ED, et al. High prevalence of RET/PTC rearrangements in Ukrainian and Belarussian post-Chernobyl thyroid papillary carcinomas: a strong correlation between RET/PTC3 and the solid-follicular variant. J Clin Endocrinol Metab. 1999. 84:4232–8.
Article
50.Ishizaka Y., Kobayashi S., Ushijima T., Hirohashi S., Sugimura T., Nagao M. Detection of retTPC/PTC transcripts in thyroid adenomas and adenomatous goiter by an RT-PCR method. Oncogene. 1991. 6:1667–72.
51.Nikiforova MN., Caudill CM., Biddinger P., Nikiforov YE. Prevalence of RET/PTC rearrangements in Hashimoto's thyroiditis and papillary thyroid carcinomas. Int J Surg Pathol. 2002. 10:15–22.
Article
52.Wirtschafter A., Schmidt R., Rosen D., Kundu N., Santoro M., Fusco A, et al. Expression of the RET/PTC fusion gene as a marker for papillary carcinoma in Hashimoto's thyroiditis. Laryngoscope. 1997. 107:95–100.
53.Sheils OM., O'Eary JJ., Uhlmann V., Lattich K., Sweeney EC. Ret/PTC-1 Activation in hashimoto thyroiditis. Int J Surg Pathol. 2000. 8:185–9.
Article
54.Elisei R., Romei C., Vorontsova T., Cosci B., Veremeychik V., Kuchinskaya E, et al. RET/PTC rearrangements in thyroid nodules: studies in irradiated and not irradiated, malignant and benign thyroid lesions in children and adults. J Clin Endo-crinol Metab. 2001. 86:3211–6.
Article
55.Fenton CL., Lukes Y., Nicholson D., Dinauer CA., Francis GL., Tuttle RM. The ret/PTC mutations are common in sporadic papillary thyroid carcinoma of children and young adults. J Clin Endocrinol Metab. 2000. 85:1170–5.
56.Adeniran AJ., Zhu Z., Gandhi M., Steward DL., Fidler JP., Giordano TJ, et al. Correlation between genetic alterations and microscopic features, clinical manifestations, and prognostic characteristics of thyroid papillary carcinomas. Am J Surg Pathol. 2006. 30:216–22.
Article
57.Zhu Z., Ciampi R., Nikiforova MN., Gandhi M., Nikiforov YE. Prevalence of RET/PTC rearrangements in thyroid papillary carcinomas: effects of the detection methods and genetic heterogeneity. J Clin Endocrinol Metab. 2006. 91:3603–10.
58.Chung KW., Chang MC., Noh DY., Oh SK., Choe KJ., Youn YK. RET oncogene expression of papillary thyroid carcinoma in Korea. Surg Today. 2004. 34:485–92.
Article
59.Chung JH., Hahm JR., Min YK., Lee MS., Lee MK., Kim KW, et al. Detection of RET/PTC oncogene rearrangements in Korean papillary thyroid carcinomas. Thyroid. 1999. 9:1237–43.
Article
60.Knauf JA., Kuroda H., Basu S., Fagin JA. RET/PTC-induced dedifferentiation of thyroid cells is mediated through Y1062 signaling through SHC-RAS-MAP kinase. Oncogene. 2003. 22:4406–12.
Article
61.Harvey JJ. An unidentified virus which causes the rapid production of tumours in mice. Nature. 1964. 204:1104–5.
Article
62.Kirsten WH., Mayer LA. Morphologic responses to a murine erythroblastosis virus. J Natl Cancer Inst. 1967. 39:311–35.
63.Garcia-Rostan G., Zhao H., Camp RL., Pollan M., Herrero A., Pardo J, et al. ras mutations are associated with aggressive tumor phenotypes and poor prognosis in thyroid cancer. J Clin Oncol. 2003. 21:3226–35.
Article
64.Nikiforov YE. Genetic alterations involved in the transition from well-differentiated to poorly differentiated and anaplastic thyroid carcinomas. Endocr Pathol. 2004. 15:319–27.
Article
65.Lemoine NR., Mayall ES., Wyllie FS., Farr CJ., Hughes D., Padua RA, et al. Activated ras oncogenes in human thyroid cancers. Cancer Res. 1988. 48:4459–63.
66.Namba H., Rubin SA., Fagin JA. Point mutations of ras oncogenes are an early event in thyroid tumorigenesis. Mol Endocrinol. 1990. 4:1474–9.
Article
67.Vitagliano D., Portella G., Troncone G., Francione A., Rossi C., Bruno A, et al. Thyroid targeting of the N-ras(Gln61Lys) oncogene in transgenic mice results in follicular tumors that progress to poorly differentiated carcinomas. Oncogene. 2006. 25:5467–74.
Article
68.Hihi AK., Michalik L., Wahli W. PPARs: transcriptional effectors of fatty acids and their derivatives. Cell Mol Life Sci. 2002. 59:790–8.
69.Kroll TG., Sarraf P., Pecciarini L., Chen CJ., Mueller E., Spiegelman BM, et al. PAX8-PPARgamma1 fusion oncogene in human thyroid carcinoma [corrected]. Science. 2000. 289:1357–60.
70.Marques AR., Espadinha C., Frias MJ., Roque L., Catarino AL., Sobrinho LG, et al. Underexpression of peroxisome proliferator-activated receptor (PPAR)gamma in PAX8/PPARgamma-negative thyroid tumours. Br J Cancer. 2004. 91:732–8.
71.French CA., Alexander EK., Cibas ES., Nose V., Laguette J., Faquin W, et al. Genetic and biological subgroups of low-stage follicular thyroid cancer. Am J Pathol. 2003. 162:1053–60.
Article
72.Nikiforova MN., Lynch RA., Biddinger PW., Alexander EK., Dorn GW 2nd., Tallini G, et al. RAS point mutations and PAX8-PPAR gamma rearrangement in thyroid tumors: evidence for distinct molecular pathways in thyroid follicular carcinoma. J Clin Endocrinol Metab. 2003. 88:2318–26.
73.Kim KY., Ahn JH., Cheon HG. Apoptotic action of peroxisome proliferator-activated receptor-gamma activation in human non small-cell lung cancer is mediated via proline oxidase-induced reactive oxygen species formation. Mol Pharmacol. 2007. 72:674–85.
74.Govindarajan R., Ratnasinghe L., Simmons DL., Siegel ER., Midathada MV., Kim L, et al. Thiazolidinediones and the risk of lung, prostate, and colon cancer in patients with diabetes. J Clin Oncol. 2007. 25:1476–81.
Article
75.Martelli ML., Iuliano R., Le Pera I., Sama I., Monaco C., Cammarota S, et al. Inhibitory effects of peroxisome poliferator-activated receptor gamma on thyroid carcinoma cell growth. J Clin Endocrinol Metab. 2002. 87:4728–35.
76.Giordano TJ., Au AY., Kuick R., Thomas DG., Rhodes DR., Wilhelm KG Jr, et al. Delineation, functional validation, and bioinformatic evaluation of gene expression in thyroid follicular carcinomas with the PAX8-PPARG translocation. Clin Cancer Res. 2006. 12:1983–93.
Article
77.Garcia-Rostan G., Costa AM., Pereira-Castro I., Salvatore G., Hernandez R., Hermsem MJ, et al. Mutation of the PIK3CA gene in anaplastic thyroid cancer. Cancer Res. 2005. 65:10199–207.
Article
78.Singh B., Reddy PG., Goberdhan A., Walsh C., Dao S., Ngai I, et al. p53 regulates cell survival by inhibiting PIK3CA in squamous cell carcinomas. Genes Dev. 2002. 16:984–93.
Article
79.Robertson GP. Functional and therapeutic significance of Akt deregulation in malignant melanoma. Cancer Metastasis Rev. 2005. 24:273–85.
Article
80.Kada F., Saji M., Ringel MD. Akt: a potential target for thyroid cancer therapy. Curr Drug Targets Immune Endocr Metabol Disord. 2004. 4:181–5.
Article
81.Ollikainen M., Gylling A., Puputti M., Nupponen NN., Abdel-Rahman WM., Butzow R, et al. Patterns of PIK3CA alterations in familial colorectal and endometrial carcinoma. Int J Cancer. 2007. 121:915–20.
82.Davies MA., Stemke-Hale K., Tellez C., Calderone TL., Deng W., Prieto VG, et al. A novel AKT3 mutation in melanoma tumours and cell lines. Br J Cancer. 2008. 99:1265–8.
Article
83.Liu Z., Hou P., Ji M., Guan H., Studeman K., Jensen K, et al. Highly prevalent genetic alterations in receptor tyrosine kinases and phosphatidylinositol 3-kinase/akt and mitogen-activated protein kinase pathways in anaplastic and follicular thyroid cancers. J Clin Endocrinol Metab. 2008. 93:3106–16.
Article
84.Carpten JD., Faber AL., Horn C., Donoho GP., Briggs SL., Robbins CM, et al. A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. Nature. 2007. 448:439–44.
85.Liaw D., Marsh DJ., Li J., Dahia PL., Wang SI., Zheng Z, et al. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet. 1997. 16:64–7.
Article
86.Alvarez-Nunez F., Bussaglia E., Mauricio D., Ybarra J., Vilar M., Lerma E, et al. PTEN promoter methylation in sporadic thyroid carcinomas. Thyroid. 2006. 16:17–23.
Article
87.Hou P., Liu D., Shan Y., Hu S., Studeman K., Condouris S, et al. Genetic alterations and their relationship in the phosphatidylinositol 3-kinase/Akt pathway in thyroid cancer. Clin Cancer Res. 2007. 13:1161–70.
Article
88.Halachmi N., Halachmi S., Evron E., Cairns P., Okami K., Saji M, et al. Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors. Genes Chromosomes Cancer. 1998. 23:239–43.
89.Wu G., Mambo E., Guo Z., Hu S., Huang X., Gollin SM, et al. Uncommon mutation, but common amplifications, of the PIK3CA gene in thyroid tumors. J Clin Endocrinol Metab. 2005. 90:4688–93.
90.Ringel MD., Hayre N., Saito J., Saunier B., Schuppert F., Burch H, et al. Overexpression and overactivation of Akt in thyroid carcinoma. Cancer Res. 2001. 61:6105–11.
91.Vasko V., Saji M., Hardy E., Kruhlak M., Larin A., Savchenko V, et al. Akt activation and localisation correlate with tumour invasion and oncogene expression in thyroid cancer. J Med Genet. 2004. 41:161–70.
Article
92.Yeager N., Klein-Szanto A., Kimura S., Di Cristofano A. Pten loss in the mouse thyroid causes goiter and follicular adenomas: insights into thyroid function and Cowden disease pathogenesis. Cancer Res. 2007. 67:959–66.
Article
93.Wang Y., Hou P., Yu H., Wang W., Ji M., Zhao S, et al. High prevalence and mutual exclusivity of genetic alterations in the phosphatidylinositol-3-kinase/akt pathway in thyroid tumors. J Clin Endocrinol Metab. 2007. 92:2387–90.
Article
94.Hollstein M., Sidransky D., Vogelstein B., Harris CC. p53 mutations in human cancers. Science. 1991. 253:49–53.
Article
95.Vogelstein B., Kinzler KW. p53 function and dysfunction. Cell. 1992. 70:523–6.
Article
96.Freedman DA., Wu L., Levine AJ. Functions of the MDM2 oncoprotein. Cell Mol Life Sci. 1999. 55:96–107.
Article
97.Jin S., Levine AJ. The p53 functional circuit. J Cell Sci. 2001. 114:4139–40.
Article
98.Tao W., Levine AJ. P19(ARF) stabilizes p53 by blocking nucleo-cytoplasmic shuttling of Mdm2. Proc Natl Acad Sci U S A. 1999. 96:6937–41.
Article
99.Vogelstein B., Kinzler KW. Cancer genes and the pathways they control. Nat Med. 2004. 10:789–99. 100) Donghi R, Longoni A, Pilotti S, Michieli P, Della Porta G, Pierotti MA. Gene p53 mutations are restricted to poorly differentiated and undifferentiated carcinomas of the thyroid gland. J Clin Invest 1993;91: 1753-60.
Article
101.Boltze C., Roessner A., Landt O., Szibor R., Peters B., Schneider-Stock R. Homozygous proline at codon 72 of p53 as a potential risk factor favoring the development of undifferentiated thyroid carcinoma. Int J Oncol. 2002. 21:1151–4.
Article
102.Saltman B., Singh B., Hedvat CV., Wreesmann VB., Ghossein R. Patterns of expression of cell cycle/apoptosis genes along the spectrum of thyroid carcinoma progression. Surgery. 2006. 140:899–905. discussion 05-6.
Article
103.Onel K., Cordon-Cardo C. MDM2 and prognosis. Mol Cancer Res. 2004. 2:1–8.
104.La Perle KM., Jhiang SM., Capen CC. Loss of p53 promotes anaplasia and local invasion in ret/PTC1-induced thyroid carcinomas. Am J Pathol. 2000. 157:671–7.
Article
105.Mulholland DJ., Dedhar S., Coetzee GA., Nelson CC. Interaction of nuclear receptors with the Wnt/beta-catenin/Tcf signaling axis: Wnt you like to know? Endocr Rev. 2005. 26:898–915.
106.Van Aken E., De Wever O., Correia da Rocha AS., Mareel M. Defective E-cadherin/catenin complexes in human cancer. Virchows Arch. 2001. 439:725–51.
Article
107.Garcia-Rostan G., Camp RL., Herrero A., Carcangiu ML., Rimm DL., Tallini G. Beta-catenin dysregulation in thyroid neoplasms: down-regulation, aberrant nuclear expression, and CTNNB1 exon 3 mutations are markers for aggressive tumor phenotypes and poor prognosis. Am J Pathol. 2001. 158:987–96.
108.Garcia-Rostan G., Tallini G., Herrero A., D'Aquila TG., Carcangiu ML., Rimm DL. Frequent mutation and nuclear localization of beta-catenin in anaplastic thyroid carcinoma. Cancer Res. 1999. 59:1811–5.
109.Kurihara T., Ikeda S., Ishizaki Y., Fujimori M., Tokumoto N., Hirata Y, et al. Immunohistochemical and sequencing analyses of the Wnt signaling components in Japanese anaplastic thyroid cancers. Thyroid. 2004. 14:1020–9.
Article
110.Mazzanti C., Zeiger MA., Costouros NG., Umbricht C., Westra WH., Smith D, et al. Using gene expression profiling to differentiate benign versus malignant thyroid tumors. Cancer Res. 2004. 64:2898–903.
Article
111.Weber F., Shen L., Aldred MA., Morrison CD., Frilling A., Saji M, et al. Genetic classification of benign and malignant thyroid follicular neoplasia based on a three-gene combination. J Clin Endocrinol Metab. 2005. 90:2512–21.
Article
112.Foukakis T., Gusnanto A., Au AY., Hoog A., Lui WO., Larsson C, et al. A PCR-based expression signature of malignancy in follicular thyroid tumors. Endocr Relat Cancer. 2007. 14:381–91.
Article
113.Fan C., Oh DS., Wessels L., Weigelt B., Nuyten DS., Nobel AB, et al. Concordance among gene-expression-based predictors for breast cancer. N Engl J Med. 2006. 355:560–9.
Article
114.Wang Y., Klijn JG., Zhang Y., Sieuwerts AM., Look MP., Yang F, et al. Gene-expression profiles to predict distant metastasis of lymph-node-negative primary breast cancer. Lancet. 2005. 365:671–9.
Article
115.Brown LM., Helmke SM., Hunsucker SW., Netea-Maier RT., Chiang SA., Heinz DE, et al. Quantitative and qualitative differences in protein expression between papillary thyroid carcinoma and normal thyroid tissue. Mol Carcinog. 2006. 45:613–26.
Article
116.Netea-Maier RT., Hunsucker SW., Hoevenaars BM., Helmke SM., Slootweg PJ., Hermus AR, et al. Discovery and validation of protein abundance differences between follicular thyroid neoplasms. Cancer Res. 2008. 68:1572–80.
Article