Influencers on thyroid cancer onset: molecular genetic basis

genes G C A T T A C G G C A T Review Influencers on Thyroid Cancer Onset: Molecular Genetic Basis Berta Luzón-Toro 1,2, Raquel María Fernández 1,2, Leticia Villalba-Benito 1,2, Ana Torroglosa 1,2, Guillermo Antiñolo 1,2 and Salud Borrego 1,2,* 1 Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain; [email protected] (B.L.-T.); [email protected] (R.M.F.); [email protected] (L.V.-B.); ana.torr[email protected] (A.T.); [email protected] (G.A.) 2Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain *Correspondence: [email protected]; Tel.: +34-955-012641 Received: 3 September 2019; Accepted: 6 November 2019; Published: 8 November 2019   Abstract: Thyroid cancer, a cancerous tumor or growth located within the thyroid gland, is the most common endocrine cancer. It is one of the few cancers whereby incidence rates have increased in recent years. It occurs in all age groups, from children through to seniors. Most studies are focused on dissecting its genetic basis, since our current knowledge of the genetic background of the different forms of thyroid cancer is far from complete, which poses a challenge for diagnosis and prognosis of the disease. In this review, we describe prevailing advances and update our understanding of the molecular genetics of thyroid cancer, focusing on the main genes related with the pathology, including the different noncoding RNAs associated with the disease. Keywords: thyroid cancer; genetics; epigenetics; mutation 1. Introduction Thyroid cancer is the most common endocrine cancer, with an increasing overall incidence in recent decades of about two fold in the last 25 years and accounting for 2% of all cancers [ 1 ]. Thyroid cancer is the sixth most common cancer in women, who are three times more likely to have thyroid cancer than men. About 2% of cases occur in children and teens. Overall, the 5-year survival rate of thyroid cancer is 98%. However, survival rates depend on many factors, such as the specific type of thyroid cancer and stage of disease [2] Several types and histological subtypes can be found depending on the cells from which the tumor derives, and each one presents different characteristics and prognoses. Non-medullary thyroid cancer (NMTC) originates from follicular cells and is responsible for ~95% of all the cases. At the same time, NMTC is divided into four groups (also known as well differentiated thyroid cancer): (1) papillary thyroid cancer (PTC), which represents more than 85% of cases, (2) follicular thyroid cancer (FTC; 10% of total cases), (3) poorly differentiated thyroid cancer (PDTC, which accounts for only 1–15% of all thyroid cancers), constitutes a more aggressive follicular-derived thyroid cancer than differentiated thyroid cancer (PTC and FTC), and (4) anaplastic cancer (ATC) (<1%) [3]. Of the total number of cases, 10% of NMTCs occur during the first two decades of life [ 4 ]. Around 5% present as familial forms and the remaining 95% are sporadic. Analysis (genome-wide association study or genome-wide linkage analysis) has led to the identification of some genes associated with non-syndromic familial forms, although additional populations are needed for further validations [ 5 – 9 ]. In either case, the studies carried out to date are quite inconclusive, and thus new approaches should be carried out for the identification of new loci associated with FNMTC. Genes 2019,10, 913; doi:10.3390/genes10110913 www.mdpi.com/journal/genes Genes 2019,10, 913 2 of 27 In addition, only ~5% of cases of thyroid cancer are derived from parafollicular cells and this type is named medullary thyroid cancer (MTC) [ 4 , 10 ]. About 75% of all MTCs are believed to be sporadic (sMTC), and the remaining 25% correspond to inherited cancer syndromes known as multiple endocrine neoplasia type 2 (MEN2). MEN2 includes three clinically differentiable types: MEN2A (OMIM #171400), MEN2B (OMIM #162300), and FMTC (OMIM #155240; which may be a variant of MEN 2A) [ 11 , 12 ]. FNMTC is a rare form of thyroid cancer (only 3–9% of all cases). Moreover, just 5% of the family forms are included in specific syndromes: Cowden (OMIM #158350), Gardner (OMIM #175100), Werner (OMIM #277700), Li-Fraumeni (OMIM #151623), McCune-Albright (OMIM #174800), Carney complex (OMIM #160980), or DICER 1 (OMIM #138800) syndromes [ 5 , 6 ]). This review summarizes the current knowledge about molecular bases of thyroid cancer: from genes to ncRNAs, to provide the reader an overview of the main genetic and epigenetic factors that can influence the develop of thyroid cancer. 2. Molecular Genetics of Thyroid Cancer Alterations on some genes and pathways have been described to be associated with the different forms of thyroid cancer. The most relevant are summarized in the current review (Figure 1). Thyroid tumorigenesis and progression are closely linked to somatic point mutations on BRAF (B-rapidly accelerated fibrosarcoma), RAS,RET, and NTRK1/3genes that promote the activation of mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase (PI3K) signaling pathways [ 13 , 14 ]. Interestingly, there is a strong relationship between the oncogenic genotype and histopathologic phenotype, mutations in BRAF,PAX8, and PPARG genes being common in FTC and RAS mutations either in FTC and PTC (follicular variant, fvPTC) [ 15 – 19 ]. The global analysis of genomic variants, gene and miRNA expression, aberrant methylation, and proteomic profiles unraveled that mutations in BRAF and RAS, together with RET-PTC fusions, are the most common genetic alterations in both FTC and PTC. It is worth mentioning The Cancer Genome Atlas (TCGA) project outcomes, where a comprehensive and multiplatform approach to analyze multidimensional molecular data of 496 PTCs (excluding both poorly and undifferentiated carcinomas to compile all tumor-initiating alterations) was performed. Such a cohort led to classification into molecular subtypes (including tumor cluster, histology, genotype, signaling, and risk assessment) to associate them with clinically relevant parameters and improve the management of patients. They mainly distinguish two types of PTC tumors: PTCs with RAS mutations (RL-PTCs) and BRAFV600E-driven tumors (BVL-PTCs). Both are basically different in their genomic, epigenomic, and proteomic profiles, which is in concordance with their histological differences [20]. 3. The RET Proto-Oncogene Role In 1993 RET proto-oncogene was demonstrated to be the causative event for MTC [ 21 ]. Since then, several mutations have been described in MEN2 series. Thus, the RET genetic screening is a crucial diagnostic and prognostic procedure for MTC [22]. 3.1. Somatic RET Mutations 3.1.1. RET Gene Rearrangements The Rearranged During Transfection (RET) gene encodes a single transmembrane receptor, which is a tyrosine kinase implicated in the cellular signaling of members of the glial derived neurotrophic factors family [23]. In PTC, RET rearrangements (RET-PTC) seem to be an early event in carcinogenesis, with 10–20% of RET fusions being detected in PTC patients. RET-PTC fusions used to be associated with sporadic and radiation-induced PTC [ 24 , 25 ]. In addition, coiled-coil domain containing 6-RET rearrangements are also commonly found in this type of tumor [ 26 , 27 ]. The presence or higher expression of a RET fusion protein has been linked to regional invasion and lymph node metastasis [28]. Genes 2019,10, 913 3 of 27 Figure 1. Progression of thyroid cancer and the main genetic alterations involved in such process. ( A ) Picture depicting thyroid cancer hystotypes and their causative genetic events. PTCs present BRAF (V600E substitution), RAS mutations, and/or RET/PTC rearrangements. FTCs display PPARc/Pax8 rearrangements, RAS mutations, and PTEN inactivating mutations or deletions. ATCs are characterized by PTEN and CTNNB1 mutations and p53 inactivation. ( B ) Schema shows the key molecular signaling pathways involved in thyroid cancer. On the left (inside the circle with dashed blue line): MAPK pathway, which is activated in most thyroid cancers after a mutational event. Once thyroid cancer development is initiated, gene expression is altered, evoking cell proliferation, cell growth, angiogenesis, and loss of differentiation. On the right (inside the circle with dashed red line): pathways altered in advanced thyroid cancers, which promote tumor progression. This includes the PI3K–mTOR pathway, the p53 tumor suppressor, and alterations in the promoter for TERT. miRNAs, lncRNAs and circRNAs are also represented inside the nucleus as genetic players in thyroid cancer development. Genes 2019,10, 913 4 of 27 Thus, RET rearrangements are determinant on the evaluation of thyroid nodules with undefined cytology. The main RET/PTC oncoproteins are summarized in Table 1. Table 1. RET/PTC oncoproteins related with thyroid cancer. RET/PTC Rearrangement Fusion Partner Chromosomal Alteration Reference RET/PTC1 Coiled-coil domain-containing protein 6 (CCDC6) inv10(q11.2;q21) [29] RET/PTC2 Protein kinase, cAMP-dependent, regulatory, type I, alpha (PRKAR1A) t(10;17)(q11.2;q23) [30] RET/PTC3 Nuclear coactivator 4 (RET-fused gene, androgen receptor-associated protein 70) (NCoa4 (RFG, ARA70) inv10(q11.2;q10) [29] RET/PTC4 Nuclear coactivator 4 (RET-fused gene, androgen receptor-associated protein 70) (NCoa4 (RFG, ARA70) inv10(q11.2;q10) [31] RET/PTC5 RET-fused gene 5 (Golgin A5) (RFG5 (GOLGA5)) t(10;14)(q11.2;q32) [32] RET/PTC6 Tripartite motif-containing 24 (TRIM24) t(7;10)(q32-q34;q11.2) [33] RET/PTC7 RET-fused gene 7 (tripartite motif-containing 33 (RFG7(TRIM33)) t(1;10)(p13;q11.2) [33] RET/PTC8 Kinectin 1 (KTN1) t(10;14)(q11.2;q22.1) [34] RET/PTC9 RET-fused gene 9 (RFG9) t(10;18) (q11.2;q21-22) [35] RET/ELKS Glutamate, leucine, lysine, serine-rich sequence (RAB6-interacting protein 2) (ELKS (RAB6IP2)) t(10;12)(q11.2;p13.3) [36] RET/PCM1 Pericentriolar material 1 (PCM1) t(8;10)(q21-22;q11.2) [37] RET/RFP RET finger protein (tripartite motif-containing 27) (RFP (TRIM27)) t(6;10)(p21;q11.2) [38] RET/HOOK3 Hook homolog 3 (HOOK3) t(8;10)(p11.21;q11.2) [39] Most relevant genes in thyroid cancer: a compilation of the main genes related with the disease, indicating their location, their main type of alterations (somatic or germline mutations), and their incidence on the disease. A footnote with the main databases available to access all RET variants “with clinical relevance to date”, indicating their number registered on each database until the last access, is included. 3.1.2. Other Somatic RET Mutations The genetic bases for nearly all thyroid cancers have been solved through DNA sequencing studies. Most thyroid tumors harbor mutations that eventually activate MAPK and PI3K-AKT signaling pathways, which regulate cellular proliferation [ 3 , 40 , 41 ]. Furthermore, somatic RET mutations appear in 40–50% of sporadic MTCs and have been linked with a worse prognosis for patients. In fact, the presence of a somatic RET mutation is associated with lymph node metastases at diagnosis, which is a bad prognostic factor for complete cure for such patients [ 22 ]. Somatic RET mutations have been described in sporadic cases of MTC [ 42 ] as well as loss of heterozygosity at different loci (deletions of tumor suppressor genes) in MTC [ 21 ]. In addition, a mutation in codon 664 of the RET gene, which affects the protein kinase domain of the gene product by changing a threonine for a methionine, was found in unrelated MEN2B patients as well as in six sporadic tumors [43]. The application of new approaches has improved the knowledge of somatic RET mutations such as RET M918T mutation. A genome-wide DNA methylation profiling was performed in a large MTC series. Integration of methylation data together with mRNA and miRNA expression data revealed JAK/Stat signaling effector STAT3 as a potential therapeutic target for these tumors [44]. 3.2. Germline RET Mutations Gain-of-function RET mutations give rise to MEN2 [ 23 , 45 ]. In MEN2, mutations in the RET intracellular domains lead to activation of RET monomers while in the extracellular domain carry to dimerization [ 23 , 46 ]. Thus, MEN2 RET receptors constitutively activate signaling pathways linked to wildtype RET activity [ 47 , 48 ]. In fact, MEN2 phenotype is more severe when specific RET mutations lead to increased kinase activity [ 49 , 50 ]. Based on these observations, the clinical management Genes 2019,10, 913 5 of 27 guidelines for MEN2 patients recommend early genetic screening in at-risk individuals, in order to determine if they carry any RET mutation, which is associated with the poorest prognosis [ 50 ]. There are three American Thyroid Association categories: I) moderate-risk mutations (exon 10, exon 11 mutations other than codon 634, and exons 13 through 15), which lead to relatively late MTC onset; II) high-risk mutations (exon 11, codon 634, the classical MEN2A mutation; and exon 15, codon 883), which present intermediate risk; and III) highest-risk mutations, with the typical MEN2B mutation (exon 16, codon 918), which confer the highest risk of early MTC development and growth [ 51 ]. All updated information regarding the effect of RET mutations on sporadic and familial cases of thyroid cancer is compiled in different reviews [26,52,53]. More than 95% of MEN2 cases have germline mutations in the RET proto-oncogene, leading to a constitutive activation of the metabolic pathways of RET signaling [ 54 ]. Of those patients, 98% have mutations grouped in a hotspot composed of five cysteine codons present in the extracellular domain of the protein (C609, C611, C618, C620, C630, C634) [ 49 , 55 , 56 ]. Eighty-seven percent of MEN2A patients carry mutations affecting codon 634, C634R being the most prevalent one that has been detected [49], unlike in the Spanish population, who mostly carry the C634Y mutation [ 57 – 60 ]. In addition, although over 70 RET mutations have been described in MEN2A patients (all in the extracellular region, close to the transmembrane domain), only two RET mutations (affecting codons 918 and 883) have been linked to MEN2B [61]. Regarding FMTC missense mutations in the tyrosine kinase domain, one changes glutamate 768 for an aspartate and another one substitutes valine 804 for a leucine. In addition, there are some relevant mutations on cysteine codons and the transmembrane domain, some of them shared with MEN2A syndrome, which are updated and summarized in Figure 2. Both are gain-of-function mutations and result in aberrant signaling mediated by RET [42,62,63]. Genes 2019,10, 913 6 of 27 Figure 2. Schematic structure of RET, and mutations identified in MEN2A, MEN 2B and familial medullary thyroid carcinoma (FMTC). Modified from [64,65]. Genes 2019,10, 913 7 of 27 3.3. Susceptibility Factors A germline RET S836S variant (c.2508C>T, rs1800862) has been correlated with somatic RET M918T mutation in exon 16, which leads to a more aggressive sMTC. Furthermore, this variant was found to have a significantly higher frequency in sMTC compared to controls, which led to it being considered as the first genetic susceptibility factor for the disease [ 64 , 66 – 68 ]. Additionally, IVS1-126G>T (c.74-126G>T, rs2565206) and G691S (c.2071G>A, rs1799939, p.Gly691Ser)/S904S (c.2712C>G, rs1800863) have also been described as associated with sMTC in several populations although this finding was not replicated in a larger study [69]. The RET c*587T>C variant was restricted to the Italian population [70–73]. It has been suggested that variants in genes encoding for RET coreceptors might play a role in the pathogenesis of sMTC. A study of the German population showed that GFRA1-193C>G and c.537T>C were overrepresented in sMTC versus controls, which suggested that both variants could be in linkage disequilibrium with other locus responsible for the disease. However, such overrepresentation was not found in a similar study of the Spanish population, supporting a founder effect of both variants in Germany [74]. 4. BRAF The most frequent mutations (60%) in PTC patients are found on the BRAF gene. Moreover, the BRAF V600E mutation (p.Val600Glu; commonly known as V600E), which is found in 95% of cases, is used as a risk biomarker in PTC [ 20 ]. Although somatic mutations in this gene are absent on benign thyroid nodules, they appear on a third of anaplastic thyroid cancers [ 75 , 76 ]. As we mentioned above, the majority of BRAF mutations implicate the activation of the kinase domain of this protein, which finally dysregulates the MAPK signaling pathway [ 77 – 79 ], thus being relevant in cellular processes implicated in cancer development such as tumorigenesis, proliferation, and progression [80,81]. 5. RAS The RAS genes (H-RAS,N-RAS,K-RAS) present somatic point mutations in follicular adenoma, FTC (40–53%), PTC (0–20%), fvPTC (17–25%), and poorly differentiated and anaplastic thyroid cancer (20–60%) [ 19 , 75 , 82 – 85 ]. A codon 61 mutation of NRAS (N2) was identified four times more frequently in follicular tumors than in papillary cancers, and it is the second most common point mutation with an incidence of 8.5% [ 20 ]. Thus, RAS mutations are associated with follicular tumors that compile from a preinvasive lesion to a true malignancy, either FTC, PTC, fvPTC, or poorly differentiated thyroid cancer [ 84 , 86 ]. RAS mutations together with TERT promoter mutations (C228T and C250T) have been associated with more aggressive and recurrent thyroid tumor and patient mortality, especially in PTC patients. Although further studies are needed, these outcomes indicate that TERT is a new oncogene in thyroid cancer and promoter mutations may be promising in clinical management of thyroid cancer, especially in combination with BRAF V600E or RAS mutations [87]. 6. PAX8-PPARG The PAX8-PPARG fusion protein is the product of a t(2;3)(q13;p25) chromosomal translocation, which used to be linked to FTC, and presents oncogenic capacity in transgenic mice [ 88 ]. PAX8-PPARG-positive tumors present a more prominent vascular and capsular invasion than RAS-positive tumors [16]. 7. Other Genes In ATC the accumulation of several oncogenic alterations is equivalent to an increased level of dedifferentiation and aggressiveness [ 89 ]. The role that P53 plays in thyroid carcinogenesis is well known, but the role of the remaining P53 family members in thyroid cancer needs further studies. Increasing evidence indicates that such family members favor the development of multiple thyroid cancer variants, and in addition they are being used as therapeutical targets [90]. Genes 2019,10, 913 8 of 27 Furthermore, there is a lack of knowledge of pathways specifically associated with each RET mutation and with non-RET-mutated sporadic MTC. A transcriptional profile assay, together with pathway enrichment analysis and gene ontology biological processes, revealed that PROM1 could be necessary for the survival of tumoral cells in this tumor [91]. In addition, a novel constitutional frameshift c.948delT mutation (p.G318Afs*22) in ESR2 was found to segregate with MTC (without any identifiable RET mutation) [ 92 ]. However, this mutation was not found in other series of patients, such as FMTC cases [93]. Rearrangements involving the anaplastic lymphoma kinase (ALK) gene with the striatin (STRN) gene have been described, which constitutively activate ALK kinase, inducing tumor formation in nude mice. Such fusion may represent a therapeutic target for patients with highly aggressive types of thyroid cancer [ 94 ]. Moreover, the ETV6-NTRK3 rearrangement, exclusively found in fvPTC, together with STRN-ALK are recurrent and absent in benign lesions, which could be useful for the diagnosis of thyroid nodules [95]. There is a thyroid specific transcription factor, FOXE1, which plays an essential role in thyroid development. Among other functions, it recognizes sites in thyroglobulin and thyroperoxidase and it also aids in maintaining cellular differentiation in the adult thyroid. Some genes increase its expression (Adamts9,Cdh1,Duox2, and S100a4) in the absence of FOXE1, while Casp4,Creld2,Dusp5,Etv5,Hsp5a, Nr4a2, and Tm4sf1 decrease [ 96 ]. FOXE1 has been associated with hypothyroidism and PTC [ 97 ]. A single nucleotide polymorphism in FOXE1 rs965513 which has been related with differentiated thyroid cancers in Caucasian population [98] A compilation of the main genes related with the disease, indicating their location, their main type of alterations (somatic or germline mutations) and their incidence on the disease has been included in Table 2. Table 2. Most relevant genes in thyroid cancer. Gene Chromosome (Chr) Type of Alteration Origin of Mutation Disease Reference RET (*) Chr 10 RET/PTC rearrangements Somatic PTC [26–28] Point mutations Somatic sporadic MTC [43,99] Germline MEN2A [OMIM# 171400]), MEN2B [OMIM#162300]) and FMTC [OMIM# 155240]) [23,45] BRAF Chr 7 V600E mutation (p.Val600Glu) Somatic PTC [75,76] Point mutations Somatic ATC RAS (N-, K-, H-) NRAS: Chr 1; KRAS: Chr 12; HRAS: Chr 11 Point mutations Somatic follicular adenoma, FTC, PTC, fvPTC, poorly differentiated and anaplastic thyroid cancer [19,75,82–85] PTEN Chr 10 Insertions, deletions, splice site mutations and large deletions Germline Cowden syndrome 1 (CWS1, [OMIM# 158350] [100] PIK3CA Chr 3 Point mutations Somatic PTC [101] Germline Cowden syndrome 5 (CWS5, [OMIM# 615108]) [17] AKT1 Chr 14 Point mutations Germline Cowden syndrome 6 (CWS6, [OMIM# 615109] [102] TERT Promoter Chr 5 Mutations with a co-occurrence with either BRAF or RAS mutations Somatic ATC and advanced stages of FNMTC [103,104] Genes 2019,10, 913 9 of 27 Table 2. Cont. Gene Chromosome (Chr) Type of Alteration Origin of Mutation Disease Reference JAK3 Chr 19 Point mutations Somatic FTC [105] TP53 Chr 17 Point mutations Somatic ATC, PDTC [106,107] Germline Li-Fraumeni syndrome (LFS, [OMIM# 151623]) [108] CHEK2 Chr 22 Deletions and point mutations Germline Li-Fraumeni syndrome 2 (LFS2, [OMIM# 609265]) [109] MET Chr 7 Point mutations Somatic MTC [110] ALK Chr 2 Gene rearrangements Somatic PTC, PDTC and ATC [111] APC Chr 5 Point mutations Somatic PTC [112,113] Germline Gardner syndrome [OMIM# 175100] [113,114] CTNNB1 Chr 3 Point mutations Somatic PTC [115] (*) Databases including the registered RET variants up to date (October 25th, 2019): LOVD (v.3.0 Build 21c): https://databases.lovd.nl/shared/genes/RET. From the 146 RET variants reported, this database does not distinguish which ones are linked to thyroid cancer. Then, in order to see the specific variants associated with thyroid cancer, it is useful to visit https://databases.lovd.nl/shared/diseases#id=0&order=symbol%2CASC&search_name= thyroid%20cancer&page_size=100&page=1. ClinVar: https://www.ncbi.nlm.nih.gov/clinvar/?term=RET%5Bgene% 5D+thyroid+cancer. There have been reported 813 RET variants linked to any form of thyroid cancer. HGMD: http://www.hgmd.cf.ac.uk/ac/gene.php?gene=RET. From the 395 registered RET mutations in this database, 133 of them are associated to thyroid cancer. In summary, the molecular pathogenesis of differentiated thyroid cancer, with specific signaling pathways and activating point mutations, has been elucidated. When some of the specific genes mutate, the tumor become into more aggressive and advanced thyroid cancer. Some of those events, include: RAS mutations (25% in poorly differentiated thyroid cancers); activating mutations of PIK3CA; point mutation p.V600E in BRAF; mutations in CTNNB1 ( β -catenin) which is involved in Wnt signaling, and in TP53 (a tumor suppressor), which may participate in de-differentiation of these tumors [ 116 , 117 ]. In addition, copy-number gains (found in proto-oncogenes) or oncogenic gene amplifications are mostly found in poorly differentiated and anaplastic than in differentiated thyroid carcinomas, suggesting that these genetic alterations play an important role in the progression and aggressiveness of thyroid cancer. This is the case, for example, of the genes encoding receptor tyrosine kinases (RTKs) and P13K-AKT pathway members, where an increased protein expression will activate these signaling pathways [ 118 ]. Regarding ALK gene, it was found in 9% of poorly differentiated thyroid cancers, 4% of ATC and 1% of PTC [ 119 ]. While MAPK and P13K-AKT pathways are firstly involved in differentiated thyroid carcinoma, when genetic alterations accumulate, both pathways get activated and an evolution of the tumor occurs into poorly differentiated and ATC [14]. 8. ncRNAs The global analysis of genomic variants, gene and microRNA (miRNA) expression, aberrant methylation, and proteomic profiles revealed that mutations in BRAF and RAS, together with RET-PTC fusions, are the most common genetic alterations in both FTC and PTC. However, epigenetic modulators, such as non-coding RNAs (ncRNAs), have recently emerged as helpful factors for both the diagnosis and treatment of these thyroid carcinomas. Specifically, ncRNAs such as miRNAs, circular RNAs (circRNAs), and long non-coding RNAS (lncRNAs) have been implicated in the modulation of gene expression that regulates cellular processes such as cell differentiation, proliferation, cell cycle, apoptosis, migration, and invasion [ 120 – 123 ]. Over the past four decades, thyroid cancer has emerged as a major health issue. Thus, the identification of novel molecular therapeutic targets for prognosis and diagnosis to advance in the overall management of this malignancy is really needed. Interestingly, ncRNAs have been identified together with epistatic gene interactions in sMTC and juvenile PTC, which help to understand the genetic architecture of complex diseases and support the relevance that these elements have to explain carcinoma development and progression [124,125]. Genes 2019,10, 913 16 of 27 Finally, the correlation of molecular profile (obtained by new sequencing technologies) with clinicopathological characteristics will lead to the development of novel precision therapies, reducing morbidity and mortality in thyroid cancer patients [ 206 – 208 ]. In this sense, differential response to a mitogen-activated protein kinase inhibitor was found to be related to the thyroid cancer genotype [ 209 ]. Molecular testing of mutation hotspots, rearrangements, and gene expression is now an effective diagnostic tool to better select patients for potential thyroid surgery [210,211]. The TCGA project mentioned in this review [ 20 ] shifts the focus regarding thyroid cancer classification to a strong multidimensional genomic and integrative approach, which has relevant consequences on basic pathobiology, tumor classification, and therapies. In this manner, thyroid cancer therapy would enter the realm of precision medicine, which will favor a more personalized approach to this pathology, achieving, ultimately, greater hope and quality of life for patients. In summary, the diagnosis and treatment of thyroid cancer is nowadays influenced by the molecular characterization of thyroid cancer types. The improvement of such techniques would help to reduce unnecessary treatments in indolent thyroid cancers, as well as improve the outcomes in patients with clinically aggressive cancers. Author Contributions: B.L.-T.: draft the manuscript; R.M.F., L.V.-B., A.T., and G.A.: reviewing of the manuscript. S.B.: reviewing of the manuscript and funding acquisition. All authors have approved the submitted version and agree to be personally accountable for the author’s own contributions and for ensuring that questions related to the accuracy or integrity of any part of the work, even ones in which the author was not personally involved, are appropriately investigated, resolved, and documented in the literature. Funding: This study was supported by Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Economy and competitiveness, Spain, and co-funded by European Union (ERDF/ESF, “Investing in your future”) [PI16/0142]. CIBERER is an initiative of the ISCIII, Spanish Ministry of Economy and Competitiveness. Conflicts of Interest: The authors declare no conflicts of interest. References 1. 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