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Hepatocyte growth factor receptor
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<h2 id="gene">Gene</h2> <p><i>MET</i> proto-oncogene (<a href="https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4233&ordinalpos=1&itool=EntrezSystem2.PEntrez.Gene.Gene_ResultsPanel.Gene_RVDocSum">GeneID: 4233</a>) has a total length of 125,982 bp, and it is located in the 7q31 locus of chromosome 7.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> <i>MET</i> is transcribed into a 6,641 bp mature mRNA, which is then translated into a 1,390 amino-acid MET protein. </p> <h2 id="protein">Protein</h2> <p>MET is a <a href="/facts/Receptor_tyrosine_kinase/1oNWIdV8">receptor tyrosine kinase</a> (RTK) that is produced as a single-chain precursor. The precursor is proteolytically cleaved at a <a href="/facts/Furin/0U9X0rKX">furin</a> site to yield a highly glycosylated extracellular α-subunit and a transmembrane β-subunit, which are linked together by a <a href="/facts/Disulfide_bridge/eDx5Xtlg">disulfide bridge</a>.<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a> </p> <h3>Extracellular</h3> <ul><li>Region of homology to <a href="/facts/Semaphorin/327okAXu">semaphorins</a> (Sema domain), which includes the full α-chain and the N-terminal part of the β-chain</li> <li>Cysteine-rich MET-related sequence (MRS domain)</li> <li>Glycine-proline-rich repeats (G-P repeats)</li> <li>Four immunoglobulin-like structures (Ig domains), a typical protein-protein interaction region.<a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a></li></ul> <h3>Intracellular</h3> <p>A juxtamembrane segment that contains: </p> <ul><li>A serine residue (Ser 985), which inhibits the receptor kinase activity upon phosphorylation<a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a></li> <li>A tyrosine residue (Tyr 1003), which is responsible for MET <a href="/facts/Polyubiquitination/hpulmU3m">polyubiquitination</a>, <a href="/facts/Endocytosis/NJjChLNj">endocytosis</a>, and degradation upon interaction with the <a href="/facts/Ubiquitin_ligase/8xmNaWW3">ubiquitin ligase</a> CBL<a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a></li> <li>Tyrosine kinase domain, which mediates MET biological activity. Following MET activation, transphosphorylation occurs on Tyr 1234 and Tyr 1235</li> <li>C-terminal region contains two crucial tyrosines (Tyr 1349 and Tyr 1356), which are inserted into the multisubstrate docking site, capable of recruiting downstream adapter proteins with <a href="/facts/SH2_domain/1kEmHvzY">Src homology-2</a> (SH2) domains.<a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a> The two tyrosines of the docking site have been reported to be necessary and sufficient for the signal transduction both <i>in vitro</i>.<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a><a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a></li></ul> <h2 id="met-signaling-pathway">MET signaling pathway</h2> <p>MET activation by its ligand <a href="/facts/Hepatocyte_growth_factor/7WLEIPn4">HGF</a> induces MET kinase catalytic activity, which triggers transphosphorylation of the tyrosines Tyr 1234 and Tyr 1235. These two tyrosines engage various signal transducers,<a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a> thus initiating a whole spectrum of biological activities driven by MET, collectively known as the invasive growth program. The transducers interact with the intracellular multisubstrate docking site of MET either directly, such as <a href="/facts/GRB2/uaFzqAbM">GRB2</a>, <a href="/facts/Src_homology_2_domain-containing/1kEmHvzY">SHC</a>,<a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a> <a href="/facts/Src_(gene)/5SCJqCU4">SRC</a>, and the p85 regulatory subunit of phosphatidylinositol-3 kinase (<a href="/facts/PI3K/e5rtq0VG">PI3K</a>),<a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a> or indirectly through the scaffolding protein Gab1<a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a> </p><p>Tyr 1349 and Tyr 1356 of the multisubstrate docking site are both involved in the interaction with GAB1, SRC, and SHC, while only Tyr 1356 is involved in the recruitment of GRB2, phospholipase C γ (PLC-γ), p85, and SHP2.<a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a> </p><p>GAB1 is a key coordinator of the cellular responses to MET and binds the MET intracellular region with high <a href="/facts/Avidity/zrA1tXeI">avidity</a>, but low <a href="/facts/Receptor_affinity/uvaKXf26">affinity</a>.<a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a> Upon interaction with MET, GAB1 becomes phosphorylated on several tyrosine residues which, in turn, recruit a number of signalling effectors, including <a href="/facts/PI3K/e5rtq0VG">PI3K</a>, SHP2, and PLC-γ. GAB1 phosphorylation by MET results in a sustained signal that mediates most of the downstream signaling pathways.<a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a> </p> <h3>Activation of signal transduction</h3> <p>MET engagement activates multiple <a href="/facts/Signal_transduction/1bs0Me6w">signal transduction</a> pathways: </p> <ul><li>The <a href="/facts/Ras_(protein)/JB883YoM">RAS</a> pathway mediates HGF-induced <a href="/facts/Scattering/nMou7lEH">scattering</a> and <a href="/facts/Cell_growth/wbArMaJU">proliferation</a> signals, which lead to <a href="/facts/Branching_morphogenesis/zHJh8Eae">branching morphogenesis</a>.<a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a> Of note, HGF, differently from most <a href="/facts/Mitogens/AyjRuS2a">mitogens</a>, induces sustained RAS activation, and thus prolonged <a href="/facts/Mitogen-activated_protein_kinase/YdDS5KkU">MAPK</a> activity.<a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a></li> <li>The <a href="/facts/Phosphoinositide_3-kinase/e5rtq0VG">PI3K</a> pathway is activated in two ways: PI3K can be either downstream of RAS, or it can be recruited directly through the multifunctional docking site.<a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a> Activation of the PI3K pathway is currently associated with <a href="/facts/Cell_motility/5ySAMquQ">cell motility</a> through remodeling of adhesion to the extracellular matrix as well as localized recruitment of transducers involved in cytoskeletal reorganization, such as <a href="/facts/RAC1/4tNQpMVA">RAC1</a> and <a href="/facts/PAK1/zSG1FeKH">PAK</a>. PI3K activation also triggers a survival signal due to activation of the <a href="/facts/AKT/S0Dz4fkr">AKT</a> pathway.<a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a></li> <li>The <a href="/facts/STAT_protein/E4L08eEa">STAT</a> pathway, together with the sustained MAPK activation, is necessary for the HGF-induced <a href="/facts/Branching_morphogenesis/zHJh8Eae">branching morphogenesis</a>. MET activates the <a href="/facts/STAT3/8NS3V4Mj">STAT3</a> <a href="/facts/Transcription_factor/wro0DPHe">transcription factor</a> directly, through an <a href="/facts/SH2_domain/1kEmHvzY">SH2 domain</a>.<a class="footnote-ref" id="fnref:27" href="#fn:27"><sup>27</sup></a></li> <li>The <a href="/facts/Beta-catenin/5eQzonk1">beta-catenin</a> pathway, a key component of the <a href="/facts/Wnt_signaling_pathway/7wxpKrjy">Wnt signaling pathway</a>, translocates into the nucleus following MET activation and participates in transcriptional regulation of numerous genes.<a class="footnote-ref" id="fnref:28" href="#fn:28"><sup>28</sup></a></li> <li>The <a href="/facts/Notch_signaling_pathway/5sVkTc0A">Notch</a> pathway, through transcriptional activation of <a href="/facts/Delta_(ligand)/5sVkTc0A">Delta ligand</a> (see <a href="/facts/DLL3/rd1G01Qt">DLL3</a>).<a class="footnote-ref" id="fnref:29" href="#fn:29"><sup>29</sup></a><a class="footnote-ref" id="fnref:30" href="#fn:30"><sup>30</sup></a></li></ul> <h2 id="role-in-development">Role in development</h2> <p>MET mediates a complex program known as invasive growth.<a class="footnote-ref" id="fnref:31" href="#fn:31"><sup>31</sup></a> Activation of MET triggers <a href="/facts/Mitogenesis/AyjRuS2a">mitogenesis</a>, and <a href="/facts/Morphogenesis/zHJh8Eae">morphogenesis</a>.<a class="footnote-ref" id="fnref:32" href="#fn:32"><sup>32</sup></a><a class="footnote-ref" id="fnref:33" href="#fn:33"><sup>33</sup></a> </p><p>During <a href="/facts/Embryonic_development/1lFY4EoW">embryonic development</a>, transformation of the flat, two-layer <a href="/facts/Germinal_disc/QkE7W7Y5">germinal disc</a> into a three-dimensional body depends on transition of some cells from an <a href="/facts/Epithelium/ecKHcHC3">epithelial</a> <a href="/facts/Phenotype/vxWXKGLj">phenotype</a> to spindle-shaped cells with motile behaviour, a <a href="/facts/Mesenchymal_stem_cell/W0jeK2a3">mesenchymal</a> <a href="/facts/Phenotype/vxWXKGLj">phenotype</a>. This process is referred to as <a href="/facts/Epithelial-mesenchymal_transition/7fTxEBlb">epithelial-mesenchymal transition</a> (EMT).<a class="footnote-ref" id="fnref:34" href="#fn:34"><sup>34</sup></a> Later in embryonic development, MET is crucial for <a href="/facts/Gastrulation/kN8X10mK">gastrulation</a>, <a href="/facts/Angiogenesis/h0HF9IUd">angiogenesis</a>, <a href="/facts/Myoblast/Vc6sxQvR">myoblast</a> migration, <a href="/facts/Bone_remodeling/eoanghIb">bone remodeling</a>, and <a href="/facts/Nerve/q7GsAfYV">nerve</a> sprouting among others.<a class="footnote-ref" id="fnref:35" href="#fn:35"><sup>35</sup></a> MET is essential for <a href="/facts/Embryogenesis/1lFY4EoW">embryogenesis</a>, because <i>MET</i> −/− mice die <i>in utero</i> due to severe defects in placental development.<a class="footnote-ref" id="fnref:36" href="#fn:36"><sup>36</sup></a> Along with <a href="/facts/Ectodysplasin_A/GdVqbVDk">Ectodysplasin A</a>, it has been shown to be involved in the differentiation of anatomical placodes, precursors of scales, feathers and hair follicles in vertebrates.<a class="footnote-ref" id="fnref:37" href="#fn:37"><sup>37</sup></a> Furthermore, MET is required for such critical processes as <a href="/facts/Liver/Rtp4Fk2b">liver</a> regeneration and <a href="/facts/Wound_healing/3NlzV5Qn">wound healing</a> during adulthood.<a class="footnote-ref" id="fnref:38" href="#fn:38"><sup>38</sup></a> </p><p>HGF/MET axis is also involved in <a href="/facts/Myocardial_development/caNyAldT">myocardial development</a>. Both HGF and MET receptor mRNAs are co-expressed in <a href="/facts/Cardiomyocyte/fE40oTQz">cardiomyocytes</a> from E7.5, soon after the heart has been determined, to E9.5. Transcripts for HGF ligand and receptor are first detected before the occurrence of cardiac beating and looping, and persist throughout the looping stage, when heart morphology begins to elaborate.<a class="footnote-ref" id="fnref:39" href="#fn:39"><sup>39</sup></a> In avian studies, HGF was found in the myocardial layer of the atrioventricular canal, in a developmental stage in which the epithelial to mesenchymal transformation (EMT) of the <a href="/facts/Endocardial_cushion/r7sYpXgN">endocardial cushion</a> occurs.<a class="footnote-ref" id="fnref:40" href="#fn:40"><sup>40</sup></a> However, MET is not essential for heart development, since α-MHCMet-KO mice show normal heart development.<a class="footnote-ref" id="fnref:41" href="#fn:41"><sup>41</sup></a> </p> <h2 id="expression">Expression</h2> <h3>Tissue distribution</h3> <p>MET is normally expressed by <a href="/facts/Epithelial_cells/ecKHcHC3">epithelial cells</a>.<a class="footnote-ref" id="fnref:42" href="#fn:42"><sup>42</sup></a> However, MET is also found on <a href="/facts/Endothelial_cells/L4ENFVnw">endothelial cells</a>, <a href="/facts/Neurons/G7CyTVdH">neurons</a>, <a href="/facts/Hepatocytes/USpvDz1n">hepatocytes</a>, <a href="/facts/Hematopoietic/VRDwMymd">hematopoietic</a> cells, <a href="/facts/Melanocytes/z8KowoXP">melanocytes</a> and neonatal cardiomyocytes.<a class="footnote-ref" id="fnref:43" href="#fn:43"><sup>43</sup></a><a class="footnote-ref" id="fnref:44" href="#fn:44"><sup>44</sup></a> HGF expression is restricted to cells of <a href="/facts/Mesenchymal/3QDGRD1C">mesenchymal</a> origin.<a class="footnote-ref" id="fnref:45" href="#fn:45"><sup>45</sup></a> </p> <h3>Transcriptional control</h3> <p><i>MET</i> transcription is activated by HGF and several <a href="/facts/Growth_factors/D1xnRbcH">growth factors</a>.<a class="footnote-ref" id="fnref:46" href="#fn:46"><sup>46</sup></a> <i>MET</i> <a href="/facts/Promoter_(genetics)/YDYBzLfg">promoter</a> has four putative binding sites for <a href="/facts/ETS_transcription_factor_family/wkE1y5hk">Ets</a>, a family of <a href="/facts/Transcription_factors/wro0DPHe">transcription factors</a> that control several invasive growth genes.<a class="footnote-ref" id="fnref:47" href="#fn:47"><sup>47</sup></a> <a href="/facts/ETS1/4IkJXB5u">ETS1</a> activates <i>MET</i> transcription <i>in vitro</i>.<a class="footnote-ref" id="fnref:48" href="#fn:48"><sup>48</sup></a> <i>MET</i> transcription is activated by <a href="/facts/Hypoxia-inducible_factor_1/t149wfy6">hypoxia-inducible factor 1</a> (HIF1), which is activated by low concentration of intracellular oxygen.<a class="footnote-ref" id="fnref:49" href="#fn:49"><sup>49</sup></a> HIF1 can bind to one of the several <a href="/facts/Hypoxia_(medical)/JWV04G89">hypoxia</a> <a href="/facts/Response_element/WnzQeY3B">response elements</a> (HREs) in the <i>MET</i> promoter.<a class="footnote-ref" id="fnref:50" href="#fn:50"><sup>50</sup></a> Hypoxia also activates transcription factor <a href="/facts/AP-1_transcription_factor/jryICv0m">AP-1</a>, which is involved in <i>MET</i> transcription.<a class="footnote-ref" id="fnref:51" href="#fn:51"><sup>51</sup></a> </p> <h2 id="clinical-significance">Clinical significance</h2> <h3>Role in cancer</h3> <p>MET pathway plays an important role in the development of cancer through: </p> <ul><li>activation of key oncogenic pathways (<a href="/facts/Ras_(protein)/JB883YoM">RAS</a>, <a href="/facts/Phosphoinositide_3-kinase/e5rtq0VG">PI3K</a>, <a href="/facts/STAT3/8NS3V4Mj">STAT3</a>, <a href="/facts/Beta-catenin/5eQzonk1">beta-catenin</a>);</li> <li><a href="/facts/Angiogenesis/h0HF9IUd">angiogenesis</a> (sprouting of new blood vessels from pre-existing ones to supply a tumor with nutrients);</li> <li>scatter (cells dissociation due to <a href="/facts/Metalloprotease/ShDT6dbf">metalloprotease</a> production), which often leads to <a href="/facts/Metastasis/4dadbm6z">metastasis</a>.<a class="footnote-ref" id="fnref:52" href="#fn:52"><sup>52</sup></a></li></ul> <p>Coordinated down-regulation of both MET and its downstream effector extracellular signal-regulated kinase 2 (ERK2) by <a href="/facts/Mir-199_microRNA_precursor/ptIyJ4rn">miR-199a*</a> may be effective in inhibiting not only cell proliferation but also motility and invasive capabilities of tumor cells.<a class="footnote-ref" id="fnref:53" href="#fn:53"><sup>53</sup></a> </p><p>MET amplification has emerged as a potential biomarker of the <a href="/facts/Clear_cell_adenocarcinoma/NmTAg4z8">clear cell tumor</a> subtype.<a class="footnote-ref" id="fnref:54" href="#fn:54"><sup>54</sup></a> </p><p>The amplification of the <a href="/facts/Cell_surface_receptor/0YGSjDdL">cell surface receptor</a> MET often drives resistance to <a href="/facts/EGFR_inhibitors/NLmnXKYY">anti-EGFR therapies</a> in <a href="/facts/Colorectal_cancer/nV592sW7">colorectal cancer</a>.<a class="footnote-ref" id="fnref:55" href="#fn:55"><sup>55</sup></a> </p> <h3>Role in autism</h3> <p>The SFARIgene database lists MET with an <a href="/facts/Autism/6MTwMNoJ">autism</a> score of 2.0, which indicates that it is a strong candidate for playing a role in cases of autism. The database also identifies at least one study that found a role for MET in cases of <a href="/facts/Schizophrenia/FMP4lQ57">schizophrenia</a>. The gene was first implicated in autism in a study that identified a polymorphism in the promoter of the MET gene.<a class="footnote-ref" id="fnref:56" href="#fn:56"><sup>56</sup></a> The polymorphism reduces transcription by 50%. Further, the variant as an autism risk polymorphism has been replicated, and shown to be enriched in children with autism and gastrointestinal disturbances.<a class="footnote-ref" id="fnref:57" href="#fn:57"><sup>57</sup></a> A rare mutation has been found that appears in two family members, one with autism and the other with a social and communication disorder.<a class="footnote-ref" id="fnref:58" href="#fn:58"><sup>58</sup></a> The role of the receptor in brain development is distinct from its role in other developmental processes. Activation of the MET receptor regulates synapse formation<a class="footnote-ref" id="fnref:59" href="#fn:59"><sup>59</sup></a><a class="footnote-ref" id="fnref:60" href="#fn:60"><sup>60</sup></a><a class="footnote-ref" id="fnref:61" href="#fn:61"><sup>61</sup></a><a class="footnote-ref" id="fnref:62" href="#fn:62"><sup>62</sup></a><a class="footnote-ref" id="fnref:63" href="#fn:63"><sup>63</sup></a> and can impact the development and function of circuits involved in social and emotional behavior.<a class="footnote-ref" id="fnref:64" href="#fn:64"><sup>64</sup></a> </p> <h3>Role in heart function</h3> <p>In adult mice, MET is required to protect cardiomyocytes by preventing age-related <a href="/facts/Oxidative_stress/HX7dfUUb">oxidative stress</a>, <a href="/facts/Apoptosis/8dVzSm4y">apoptosis</a>, fibrosis and cardiac dysfunction.<a class="footnote-ref" id="fnref:65" href="#fn:65"><sup>65</sup></a> Moreover, MET inhibitors, such as <a href="/facts/Crizotinib/NGkt526c">crizotinib</a> or PF-04254644, have been tested by short-term treatments in cellular and preclinical models, and have been shown to induce cardiomyocytes death through ROS production, activation of <a href="/facts/Caspase/YPl75Q9B">caspases</a>, metabolism alteration and blockage of <a href="/facts/Ion_channel/A46LARFH">ion channels</a>.<a class="footnote-ref" id="fnref:66" href="#fn:66"><sup>66</sup></a><a class="footnote-ref" id="fnref:67" href="#fn:67"><sup>67</sup></a> </p><p>In the injured heart, HGF/MET axis plays important roles in cardioprotection by promoting pro-survival (anti-apoptotic and anti-<a href="/facts/Autophagic/kJC4QM9l">autophagic</a>) effects in cardiomyocytes, angiogenesis, inhibition of fibrosis, anti-inflammatory and immunomodulatory signals, and regeneration through activation of <a href="/facts/Endogenous_cardiac_stem_cell/G73doLg6">cardiac stem cells</a>.<a class="footnote-ref" id="fnref:68" href="#fn:68"><sup>68</sup></a><a class="footnote-ref" id="fnref:69" href="#fn:69"><sup>69</sup></a> </p> <h2 id="interaction-with-tumour-suppressor-genes">Interaction with tumour suppressor genes</h2> <h3><i>PTEN</i></h3> <p><i><a href="/facts/PTEN_(gene)/Xg6MAcHm">PTEN</a></i> (phosphatase and tensin homolog) is a <a href="/facts/Tumor_suppressor_gene/Awte4S51">tumor suppressor gene</a> encoding a protein PTEN, which possesses lipid and protein phosphatase-dependent as well as phosphatase-independent activities.<a class="footnote-ref" id="fnref:70" href="#fn:70"><sup>70</sup></a> PTEN protein <a href="/facts/Phosphatase/LBJs1fXx">phosphatase</a> is able to interfere with MET signaling by dephosphorylating either PIP3 generated by <a href="/facts/PI3K/e5rtq0VG">PI3K</a>, or the p52 isoform of <a href="/facts/SHC1/toWBWWMQ">SHC</a>. SHC dephosphorylation inhibits recruitment of the <a href="/facts/GRB2/uaFzqAbM">GRB2</a> adapter to activated MET.<a class="footnote-ref" id="fnref:71" href="#fn:71"><sup>71</sup></a> </p> <h3><i>VHL</i></h3> <p>There is evidence of correlation between inactivation of <i><a href="/facts/VHL/X9zbh0vx">VHL</a></i> <a href="/facts/Tumor_suppressor_gene/Awte4S51">tumor suppressor gene</a> and increased MET signaling in <a href="/facts/Renal_cell_carcinoma/rRXSrA63">renal cell carcinoma</a> (RCC) and also in malignant transformations of the heart.<a class="footnote-ref" id="fnref:72" href="#fn:72"><sup>72</sup></a><a class="footnote-ref" id="fnref:73" href="#fn:73"><sup>73</sup></a> </p> <h2 id="cancer-therapies-targeting-hgfmet">Cancer therapies targeting HGF/MET</h2> <p>Since tumor invasion and metastasis are the main cause of death in cancer patients, interfering with MET signaling appears to be a promising therapeutic approach. A comprehensive list of HGF and MET targeted experimental therapeutics for oncology now in human clinical trials can be found <a href="https://ccrod.cancer.gov/confluence/display/CCRHGF/Home">here</a>. </p> <h3>MET kinase inhibitors</h3> <p class="note">Further information: <a href="/facts/C-Met_inhibitor/z5kp9NQt">c-Met inhibitor</a></p> <p>Kinase inhibitors are low molecular weight molecules that prevent <a href="/facts/Adenosine_triphosphate/nB9bwgcU">ATP</a> binding to MET, thus inhibiting receptor transphosphorylation and recruitment of the downstream effectors. The limitations of kinase inhibitors include the facts that they only inhibit kinase-dependent MET activation, and that none of them is fully specific for MET. </p> <ul><li><a href="/facts/K252a/Lc4j0Pm0">K252a</a> (<a href="/facts/Fermentek/f18vo6lQ">Fermentek</a> Biotechnology) is a <a href="/facts/Staurosporine/0IXu5c1P">staurosporine</a> analogue isolated from <i>Nocardiopsis</i> sp. soil <a href="/facts/Fungi/BHo5DP59">fungi</a>, and it is a potent inhibitor of all <a href="/facts/Receptor_tyrosine_kinases/1oNWIdV8">receptor tyrosine kinases</a> (RTKs). At nanomolar concentrations, K252a inhibits both the <a href="/facts/Wild_type/Rr0vGvM0">wild type</a> and the mutant (M1268T) MET function.<a class="footnote-ref" id="fnref:74" href="#fn:74"><sup>74</sup></a></li> <li>SU11274 (<a href="/facts/SUGEN/99t500wb">SUGEN</a>) specifically inhibits MET kinase activity and its subsequent signaling. SU11274 is also an effective inhibitor of the M1268T and H1112Y MET mutants, but not the L1213V and Y1248H mutants.<a class="footnote-ref" id="fnref:75" href="#fn:75"><sup>75</sup></a> SU11274 has been demonstrated to inhibit HGF-induced motility and invasion of epithelial and carcinoma cells.<a class="footnote-ref" id="fnref:76" href="#fn:76"><sup>76</sup></a></li> <li>PHA-665752 (<a href="/facts/Pfizer/1ADDanWs">Pfizer</a>) specifically inhibits MET kinase activity, and it has been demonstrated to represses both HGF-dependent and constitutive MET phosphorylation.<a class="footnote-ref" id="fnref:77" href="#fn:77"><sup>77</sup></a> Furthermore, some tumors harboring <i>MET</i> amplifications are highly sensitive to treatment with PHA-665752.<a class="footnote-ref" id="fnref:78" href="#fn:78"><sup>78</sup></a></li> <li><a href="/facts/Tivantinib/vJRuBpIY">Tivantinib</a> (ArQule) is a promising selective inhibitor of MET, which entered a phase 2 clinical trial in 2008. (Failed a phase 3 in 2017)</li> <li><a href="/facts/Foretinib/sDM8eynf">Foretinib</a> (XL880, Exelixis) targets multiple <a href="/facts/Receptor_tyrosine_kinases/1oNWIdV8">receptor tyrosine kinases</a> (RTKs) with growth-promoting and angiogenic properties. The primary targets of foretinib are MET, <a href="/facts/VEGFR2/m1Yd5IUY">VEGFR2</a>, and <a href="/facts/Kinase_insert_domain_receptor/m1Yd5IUY">KDR</a>. Foretinib has completed a phase 2 clinical trials with indications for papillary <a href="/facts/Renal_cell_carcinoma/rRXSrA63">renal cell carcinoma</a>, <a href="/facts/Gastric_cancer/HJjYtkqS">gastric cancer</a>, and <a href="/facts/Head_and_neck_cancer/v8T8bNs7">head and neck cancer</a></li> <li>SGX523 (SGX Pharmaceuticals) specifically inhibits MET at low nanomolar concentrations.</li> <li>MP470 (SuperGen) is a novel inhibitor of <a href="/facts/C-KIT/Lku3gt0m">c-KIT</a>, MET, <a href="/facts/PDGFR/Wmj7CSw1">PDGFR</a>, Flt3, and <a href="/facts/AXL_receptor_tyrosine_kinase/jCzJrUW6">AXL</a>. Phase I clinical trial of MP470 had been announced in 2007.</li> <li><a href="/facts/Vebreltinib/5s1btX2Q">Vebreltinib</a>, approved in China for the treatment of non-small-cell lung cancer.<a class="footnote-ref" id="fnref:79" href="#fn:79"><sup>79</sup></a></li></ul> <h3>HGF inhibitors</h3> <p>Since HGF is the only known ligand of MET, blocking the formation of a HGF:MET complex blocks MET <a href="/facts/Biological_activity/jJ14jyvc">biological activity</a>. For this purpose, truncated HGF, anti-HGF neutralizing antibodies, and an uncleavable form of HGF have been utilized so far. The major limitation of HGF inhibitors is that they block only HGF-dependent MET activation. </p> <ul><li>NK4 competes with HGF as it binds MET without inducing receptor activation, thus behaving as a full <a href="/facts/Antagonist/AssYgnt1">antagonist</a>. NK4 is a molecule bearing the N-terminal hairpin and the four <a href="/facts/Kringle_domain/CuCSKjpp">kringle domains</a> of HGF. Moreover, NK4 is structurally similar to <a href="/facts/Angiostatin/jrKkIoRo">angiostatins</a>, which is why it possesses anti-angiogenic activity.<a class="footnote-ref" id="fnref:80" href="#fn:80"><sup>80</sup></a></li> <li>Neutralizing anti-HGF antibodies were initially tested in combination, and it was shown that at least three <a href="/facts/Antibodies/MX8pdTdP">antibodies</a>, acting on different HGF <a href="/facts/Epitopes/PL0oBuGh">epitopes</a>, are necessary to prevent MET tyrosine kinase activation.<a class="footnote-ref" id="fnref:81" href="#fn:81"><sup>81</sup></a> More recently, it has been demonstrated that fully human <a href="/facts/Monoclonal_antibodies/4rUBWB87">monoclonal antibodies</a> can individually bind and neutralize human HGF, leading to regression of tumors in mouse models.<a class="footnote-ref" id="fnref:82" href="#fn:82"><sup>82</sup></a> Two anti-HGF antibodies are currently available: the humanized AV299 (AVEO), and the fully human AMG102 (<a href="/facts/Amgen/55tpQ4xd">Amgen</a>).</li> <li>Uncleavable HGF is an engineered form of pro-HGF carrying a single amino-acid substitution, which prevents the maturation of the molecule. Uncleavable HGF is capable of blocking MET-induced biological responses by binding MET with high affinity and displacing mature HGF. Moreover, uncleavable HGF competes with the wild-type endogenous pro-HGF for the catalytic domain of <a href="/facts/Proteases/G1ASdVat">proteases</a> that cleave HGF precursors. Local and systemic expression of uncleavable HGF inhibits tumor growth and, more importantly, prevents <a href="/facts/Metastasis/4dadbm6z">metastasis</a>.</li></ul> <h3>Decoy MET</h3> <p>Decoy MET refers to a soluble truncated MET receptor. Decoys are able to inhibit MET activation mediated by both HGF-dependent and independent mechanisms, as decoys prevent both the ligand binding and the MET receptor homodimerization. CGEN241 (<a href="/facts/Compugen_(Israeli_company)/lts6cyoI">Compugen</a>) is a decoy MET that is highly efficient in inhibiting tumor growth and preventing <a href="/facts/Metastasis/4dadbm6z">metastasis</a> in animal models.<a class="footnote-ref" id="fnref:83" href="#fn:83"><sup>83</sup></a> </p> <h3>Immunotherapy targeting MET</h3> <p>Drugs used for <a href="/facts/Immunotherapy/hgq3KQaJ">immunotherapy</a> can act either passively by enhancing the immunologic response to MET-expressing tumor cells, or actively by stimulating <a href="/facts/Immune_cells/vsDunUK0">immune cells</a> and altering differentiation/growth of tumor cells.<a class="footnote-ref" id="fnref:84" href="#fn:84"><sup>84</sup></a> </p> <h4>Passive immunotherapy</h4> <p>Administering <a href="/facts/Monoclonal_antibodies/4rUBWB87">monoclonal antibodies</a> (mAbs) is a form of passive immunotherapy. MAbs facilitate destruction of tumor cells by <a href="/facts/Complement-dependent_cytotoxicity/2tp1yUUI">complement-dependent cytotoxicity</a> (CDC) and cell-mediated cytotoxicity (<a href="/facts/Antibody-dependent_cell-mediated_cytotoxicity/A63IhhqH">ADCC</a>). In CDC, mAbs bind to specific <a href="/facts/Antigen/9JlAernG">antigen</a>, leading to activation of the <a href="/facts/Complement_cascade/vRSrQDUv">complement cascade</a>, which in turn leads to formation of pores in tumor cells. In ADCC, the Fab domain of a mAb binds to a <a href="/facts/Tumor_antigen/o0Kkwe8U">tumor antigen</a>, and Fc domain binds to Fc receptors present on effector cells (<a href="/facts/Phagocytes/1vbsR9er">phagocytes</a> and <a href="/facts/NK_cells/A3THWxrJ">NK cells</a>), thus forming a bridge between an effector and a target cells. This induces the effector cell activation, leading to <a href="/facts/Phagocytosis/eBrv2XKV">phagocytosis</a> of the tumor cell by <a href="/facts/Neutrophils/KL6oTt8b">neutrophils</a> and <a href="/facts/Macrophages/z7hkQu3o">macrophages</a>. Furthermore, <a href="/facts/NK_cells/A3THWxrJ">NK cells</a> release <a href="/facts/Cytotoxic/SQuTTLoL">cytotoxic</a> molecules, which lyse tumor cells.<a class="footnote-ref" id="fnref:85" href="#fn:85"><sup>85</sup></a> </p> <ul><li>DN30 is monoclonal anti-MET antibody that recognizes the extracellular portion of MET. DN30 induces both <a href="/facts/Proteases_in_angiogenesis/tTEJNBq1">shedding</a> of the MET <a href="/facts/Ectodomain/UJx59K7M">ectodomain</a> as well as cleavage of the intracellular domain, which is successively degraded by <a href="/facts/Proteasome/8vTtg2MI">proteasome</a> machinery. As a consequence, on one side MET is inactivated, and on the other side the shed portion of extracellular MET hampers activation of other MET receptors, acting as a decoy. DN30 inhibits tumour growth and prevents <a href="/facts/Metastasis/4dadbm6z">metastasis</a> in animal models.<a class="footnote-ref" id="fnref:86" href="#fn:86"><sup>86</sup></a></li> <li>OA-5D5 is one-armed monoclonal anti-MET antibody that was demonstrated to inhibit orthotopic pancreatic<a class="footnote-ref" id="fnref:87" href="#fn:87"><sup>87</sup></a> and <a href="/facts/Glioblastoma/hJojdA5x">glioblastoma</a><a class="footnote-ref" id="fnref:88" href="#fn:88"><sup>88</sup></a> tumor growth and to improve survival in <a href="/facts/Tumor_xenograft_model/oMTLraDj">tumor xenograft models</a>. OA-5D5 is produced as a <a href="/facts/Recombinant_protein/dT3PL7M6">recombinant protein</a> in <i><a href="/facts/Escherichia_coli/nR4Gvl56">Escherichia coli</a></i>. It is composed of murine <a href="/facts/Variable_domain/MX8pdTdP">variable domains</a> for the <a href="/facts/Immunoglobulin_heavy_chain/3H7Axuu5">heavy</a> and <a href="/facts/Immunoglobulin_light_chain/xJdoVLfK">light chains</a> with human IgG1 constant domains. The antibody blocks HGF binding to MET in a competitive fashion.</li></ul> <h4>Active immunotherapy</h4> <p><a href="/facts/Active_immunotherapy/oaCtlDTQ">Active immunotherapy</a> to MET-expressing tumors can be achieved by administering <a href="/facts/Cytokines/SdWpWABH">cytokines</a>, such as <a href="/facts/Interferons/63XfwpEh">interferons</a> (IFNs) and <a href="/facts/Interleukins/a8qBzb0E">interleukins</a> (<a href="/facts/Interleukin_2/hH1DXu2W">IL-2</a>), which triggers non-specific stimulation of numerous immune cells. IFNs have been tested as therapies for many types of cancers and have demonstrated therapeutic benefits. IL-2 has been approved by the <a href="/facts/Food_and_Drug_Administration_(United_States)/rCEnh9WB">U.S. Food and Drug Administration</a> (FDA) for the treatment of <a href="/facts/Renal_cell_carcinoma/rRXSrA63">renal cell carcinoma</a> and metastatic melanoma, which often have deregulated MET activity.<a class="footnote-ref" id="fnref:89" href="#fn:89"><sup>89</sup></a> </p> <h2 id="interactions">Interactions</h2> <p>Met has been shown to <a href="/facts/Protein-protein_interaction/etvm9Wmg">interact</a> with: </p> <ul><li><a href="/facts/CDH1_(gene)/u3MPHtKl">CDH1</a>,<a class="footnote-ref" id="fnref:90" href="#fn:90"><sup>90</sup></a></li> <li><a href="/facts/Cbl_gene/YND39pME">Cbl gene</a>,<a class="footnote-ref" id="fnref:91" href="#fn:91"><sup>91</sup></a><a class="footnote-ref" id="fnref:92" href="#fn:92"><sup>92</sup></a></li> <li><a href="/facts/GLMN/FMGfcuam">GLMN</a>,<a class="footnote-ref" id="fnref:93" href="#fn:93"><sup>93</sup></a></li> <li><a href="/facts/Grb2/uaFzqAbM">Grb2</a>,<a class="footnote-ref" id="fnref:94" href="#fn:94"><sup>94</sup></a><a class="footnote-ref" id="fnref:95" href="#fn:95"><sup>95</sup></a></li> <li><a href="/facts/Hepatocyte_growth_factor/7WLEIPn4">Hepatocyte growth factor</a>,<a class="footnote-ref" id="fnref:96" href="#fn:96"><sup>96</sup></a><a class="footnote-ref" id="fnref:97" href="#fn:97"><sup>97</sup></a></li> <li><a href="/facts/PTPRM/laX6IJdP">PTPmu</a>,<a class="footnote-ref" id="fnref:98" href="#fn:98"><sup>98</sup></a> and</li> <li><a href="/facts/RANBP9/zTqhfHqB">RANBP9</a><a class="footnote-ref" id="fnref:99" href="#fn:99"><sup>99</sup></a></li></ul> <h2 id="see-also">See also</h2> <ul><li><a href="/facts/C-Met_inhibitors/z5kp9NQt">c-Met inhibitors</a></li> <li><a href="/facts/Tpr-met_fusion_protein/hU4995US">Tpr-met fusion protein</a></li></ul> <h2 id="further-reading">Further reading</h2> <ul><li>Peruzzi B, Bottaro DP (2006). <a href="https://doi.org/10.1158%2F1078-0432.CCR-06-0818">"Targeting the c-Met signaling pathway in cancer"</a>. <i>Clin. Cancer Res</i>. 12 (12): 3657–60. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1158%2F1078-0432.CCR-06-0818">10.1158/1078-0432.CCR-06-0818</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/16778093">16778093</a>.</li> <li>Birchmeier C, Birchmeier W, Gherardi E, Vande Woude GF (December 2003). "Met, metastasis, motility and more". <i>Nat. Rev. Mol. Cell Biol</i>. 4 (12): 915–25. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2Fnrm1261">10.1038/nrm1261</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/14685170">14685170</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:19330786">19330786</a>.</li> <li>Zhang YW, Vande Woude GF (February 2003). "HGF/SF-met signaling in the control of branching morphogenesis and invasion". <i>J. Cell. Biochem</i>. 88 (2): 408–17. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1002%2Fjcb.10358">10.1002/jcb.10358</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/12520544">12520544</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:13212355">13212355</a>.</li> <li>Paumelle R, Tulasne D, Kherrouche Z, Plaza S, Leroy C, Reveneau S, et al. (April 2002). "Hepatocyte growth factor/scatter factor activates the ETS1 transcription factor by a RAS-RAF-MEK-ERK signaling pathway". <i>Oncogene</i>. 21 (15): 2309–19. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2Fsj.onc.1205297">10.1038/sj.onc.1205297</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11948414">11948414</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:22371025">22371025</a>.</li> <li>Comoglio PM (1993). "Structure, biosynthesis and biochemical properties of the HGF receptor in normal and malignant cells". <i>EXS</i>. 65: 131–65. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/8380735">8380735</a>.</li> <li>Maulik G, Shrikhande A, Kijima T, Ma PC, Morrison PT, Salgia R (2002). "Role of the hepatocyte growth factor receptor, c-Met, in oncogenesis and potential for therapeutic inhibition". <i>Cytokine Growth Factor Rev</i>. 13 (1): 41–59. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2FS1359-6101%2801%2900029-6">10.1016/S1359-6101(01)00029-6</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11750879">11750879</a>.</li> <li>Ma PC, Maulik G, Christensen J, Salgia R (2003). "c-Met: structure, functions and potential for therapeutic inhibition". <i>Cancer Metastasis Rev</i>. 22 (4): 309–25. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1023%2FA%3A1023768811842">10.1023/A:1023768811842</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/12884908">12884908</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:23542507">23542507</a>.</li> <li>Knudsen BS, Edlund M (2004). <a href="https://archive.org/details/advancesincancer0000unse_n0p5/page/31">"Prostate cancer and the met hepatocyte growth factor receptor"</a>. <i>Adv. Cancer Res</i>. Advances in Cancer Research. 91: <a href="https://archive.org/details/advancesincancer0000unse_n0p5/page/31">31–67</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2FS0065-230X%2804%2991002-0">10.1016/S0065-230X(04)91002-0</a>. <a href="/facts/ISBN_(identifier)/15AdSPa9">ISBN</a> 978-0-12-006691-9. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/15327888">15327888</a>.</li> <li>Dharmawardana PG, Giubellino A, Bottaro DP (2004). <a href="https://zenodo.org/record/894616">"Hereditary papillary renal carcinoma type I"</a>. <i>Curr. Mol. Med</i>. 4 (8): 855–68. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.2174%2F1566524043359674">10.2174/1566524043359674</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/15579033">15579033</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:10928725">10928725</a>.</li> <li>Kemp LE, Mulloy B, Gherardi E (2006). "Signalling by HGF/SF and Met: the role of heparan sulphate co-receptors". <i>Biochem. Soc. Trans</i>. 34 (Pt 3): 414–7. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1042%2FBST0340414">10.1042/BST0340414</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/16709175">16709175</a>.</li></ul> <h2 id="external-links">External links</h2> <ul><li><a href="https://meshb.nlm.nih.gov/record/ui?name=Proto-Oncogene+Proteins+c-met">Proto-Oncogene+Proteins+c-met</a> at the U.S. National Library of Medicine <a href="/facts/Medical_Subject_Headings/C57g2JuF">Medical Subject Headings</a> (MeSH)</li> <li><a href="http://www.expasy.org/uniprot/P08581">UniProtKB/Swiss-Prot entry P08581: MET_HUMAN</a>, ExPASy (Expert Protein Analysis System) proteomics server of the <a href="/facts/Swiss_Institute_of_Bioinformatics/dqAfD7qp">Swiss Institute of Bioinformatics</a> (SIB)</li> <li>A <a href="http://www.vai.org/met/">table</a> with references to significant roles of MET in cancer</li> <li>Human <a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&singleSearch=knownCanonical&position=MET"><i>MET</i></a> genome location and <a href="https://genome.ucsc.edu/cgi-bin/hgGene?db=hg38&hgg_type=knownGene&hgg_gene=MET"><i>MET</i></a> gene details page in the <a href="/facts/UCSC_Genome_Browser/kwumPyLb">UCSC Genome Browser</a>.</li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Bottaro DP, Rubin JS, Faletto DL, Chan AM, Kmiecik TE, Vande Woude GF, et al. 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