{"id":4827,"date":"2020-10-23T02:54:59","date_gmt":"2020-10-22T23:54:59","guid":{"rendered":"https:\/\/groupflorence.com\/ro\/?page_id=4827"},"modified":"2020-12-16T17:25:33","modified_gmt":"2020-12-16T14:25:33","slug":"molecular-oncology-and-genetics","status":"publish","type":"page","link":"https:\/\/groupflorence.com\/ro\/centers-treatments\/oncology-center\/molecular-oncology-and-genetics\/","title":{"rendered":"Oncologie Molecular\u0103 \u015fi Genetic\u0103"},"content":{"rendered":"<section id=\"bt_section69eb70ba37343\"  class=\"boldSection gutter\" ><div class=\"port\"><div class=\"boldCell\"><div class=\"boldCellInner\"><div class=\"boldRow  \" ><div class=\"boldRowInner\"><div class=\"rowItem col-md-4 col-ms-12 btTextLeft\"  ><div class=\"rowItemContent\" ><div class=\"btClear btSeparator topSpaced noBorder\" ><hr><\/div><div class=\"btCustomMenu treatment-sidebar\" ><div class=\"menu-oncology-center-container\"><ul id=\"menu-oncology-center\" class=\"menu\"><li id=\"menu-item-3501\" class=\"menu-item menu-item-type-post_type menu-item-object-page menu-item-has-children menu-item-3501\"><a href=\"https:\/\/groupflorence.com\/ro\/centers-treatments\/\">Centre &#038; 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Testele genetice pot fi folosite pentru a ajuta la diagnostic, modificarea procedurii de urm\u0103rire, predic\u021bia prognosticului \u0219i selectarea medicamentului potrivit pentru pacien\u021bii oncologici. Tulbur\u0103rile care cauzeaz\u0103 cancer, muta\u021bii genetice, cre\u0219terea genelor, \u0219tergerea, translocarea \u0219i alte anomalii sunt detectate cu teste genetice.<\/p>\n<p>\u00cen Centrul nostru de Diagnostic Genetic, care este licen\u021biat de Ministerul S\u0103n\u0103t\u0103\u021bii \u0219i care de\u021bine certificatele Serviciului Na\u021bional de Evaluare a Calit\u0103\u021bii Externe al Regatului Unit (UKNEQAS), M\u00fcnchen Ludwig Maximilian University (LMU) toate testele citogenetice, moleculocitogenetica si genetica moleculara pentru diagnosticarea cancerului, tratament \u0219i prognostic, care sunt reglementate de Re\u021beaua Na\u021bional\u0103 de Cancer Comferensiv (NCCN), sunt rulate din s\u00e2nge, m\u0103duv\u0103 osoas\u0103, cultur\u0103 celular\u0103, \u021besut tumoral proasp\u0103t \u0219i blocuri de parafin\u0103.<\/p>\n<h3>Teste genetice personalizate\/personalizate<\/h3>\n<p>Toate anomaliile cromozomiale, transloc\u0103rile, \u0219tergerile care cauzeaz\u0103 cancer hematologic sunt detectate prin metode citogenetice \u0219i citomoleculare conven\u021bionale la Centrul de Boli Genetice \u0219i Diagnostic. Mai mult, efectu\u0103m \u201esecven\u0163ierea direct\u0103 a ADN-ului\u201d pentru a defini orice muta\u0163ii distincte sau indistincte pentru bolile oncologice \u015fi genetice.<\/p>\n<p>\u00cempreun\u0103 cu cancerul hematologic, efectu\u0103m analize genetice pentru cancerul de s\u00e2n, colorectal, pulmonar \u0219i prostat\u0103. \u00cencerc\u0103m s\u0103 definim nu numai factorii genetici de diagnostic, ci \u0219i prognostic (factori care vor afecta succesul tratamentului \u0219i rezultatul pacientului) \u00eenainte de planificarea tratamentului.<\/p>\n<h3>Cancerul de s\u00e2n<\/h3>\n<p>BRCA1 \u015fi BRCA2 sunt genele relevante pentru riscul de cancer mamar \u015fi ovar. Este cunoscut faptul c\u0103 existen\u021ba unei muta\u021bii pe aceste gene cre\u0219te riscul de cancer mamar \u0219i overy \u0219i cu o por\u021biune inferioar\u0103, cancer de colon \u0219i pancreas \u00een r\u00e2ndul femeilor \u0219i riscurile de cancer de s\u00e2n \u0219i de prostat\u0103 \u00een r\u00e2ndul b\u0103rba\u021bilor. Riscul de cancer mamar pe tot parcursul vie\u021bii \u00een r\u00e2ndul tuturor femeilor din societate este calculat ca% 13.2, pe de alt\u0103 parte, acela\u0219i risc este calculat ca% 36-85 \u00een r\u00e2ndul femeilor care poart\u0103 formele mutante ale genelor BRCA1 sau BRCA2. \u00cen centrul nostru, existen\u021ba muta\u021biei cunoscute sau necunoscute este analizat\u0103 prin scanarea axonului apar\u021bin\u00e2nd genelor prin metoda \u201esecven\u021biere direct\u0103 a ADN-ului\u201d. Pe\u0219tele \u0219i amplificarea Her2 Neu Gen sunt operate din blocul de parafin\u0103 de \u021besut mamar.<\/p>\n<h3>Cancer colorectal<\/h3>\n<p>K-RAS este un proto-oncogenic. K-ras gena se conecteaz\u0103 la GTP cu un stimul extern care stimuleaz\u0103 cre\u0219terea \u0219i diviziunea celular\u0103 \u0219i joac\u0103 un rol fiziologic \u00een cre\u0219terea \u0219i diviziunea celulelor, devenind activ \u0219i transfer\u00e2nd stimulul la linia de mesaj intracelular. A c\u00e2\u0219tigat importan\u021b\u0103 determinarea metodei de tratament \u00een func\u021bie de examinarea zonei genetice Kras const\u00e2nd din 7 p\u0103r\u021bi \u0219i dup\u0103 examinarea dac\u0103 modific\u0103rile genetice se g\u0103sesc sau nu la pacien\u021bii cu cancer de colon. Se determin\u0103 c\u0103 muta\u021bia p\u0103r\u021bii numite kodon 12 \u0219i 13 \u0219i situat\u0103 \u00een primul exo al genei Kras conduce rezisten\u021ba la medicament la pacien\u021bi. Din acest motiv, examinarea acestei zone \u00eenainte de tratament determin\u0103 abordarea tratamentului. \u00cen consecin\u021b\u0103, se subliniaz\u0103 faptul c\u0103 abordarea similar\u0103 este important\u0103 pentru pacien\u021bii cu cancer la nivelul capului \u0219i g\u00e2tului.<\/p>\n<h3>Cancerul pulmonar<\/h3>\n<p>Muta\u0163iile somatice ale receptorilor factorului de cre\u015ftere epidermic\u0103 (EGFR) \u00een cancerele pulmonare non- mici sunt cunoscute ca factor de cre\u015ftere a biodisponibilit\u0103\u0163ii tratamentului cu \u201egefinitib\u201d utilizat ca inhibitor al EGFR. Conform faptului c\u0103 analiza ADN-ului EGFR este capabil\u0103 s\u0103 conduc\u0103 protocolul de tratament la pacien\u021bii cu cancer pulmonar \u0219i pancreatic \u0219i \u00een func\u021bie de data \u0219tiin\u021bific\u0103 ob\u021binut\u0103 din studii, muta\u021biile exist\u0103 frecvent la 18, 19, 20 \u0219i 21 exon. Au fost proiectate grunduri \u0219i optimizarea a fost realizat\u0103 pentru a putea face analiza secven\u021bial\u0103 a acestor patru exoni importan\u021bi. \u00cen centrul nostru, muta\u021biile pot fi detectate prin investigarea analizei secven\u021bei acestor patru exoni importan\u021bi. EGFR, amplificarea ROS1 \u0219i ALK EML\/ALK t (2; 5) translocarea\/fuziunea sunt privite cu pe\u0219tii.<\/p>\n<p>MDR1, MDR2, MRP1, MRP2, cittidin\u0103 deaminaz\u0103, timdilat sintaz\u0103 Analiza expresiei genelor: Celulele tumorale pot dezvolta rezisten\u021b\u0103 la unul sau mai multe citostatice cu diferite mecanisme. Rezisten\u0163a apare \u00een general din muta\u0163iile spontane ale celulelor canceroase. Fenotipul rezistent iese din perioada timpurie c\u00e2nd nu poate fi determinat \u00een clinic\u0103. Tratamentele \u00een care medicamentele cu mecanism de afectare diferit sunt utilizate \u00een combina\u0163ie \u015fi realizate \u00eentr-o perioad\u0103 timpurie \u00eenainte de apari\u0163ia popula\u0163iilor de celule rezistente cresc succesul tratamentului cancerului. Rezisten\u021ba la medicamente este cel mai important handicap pentru succesul tratamentului at\u00e2t al cancerului pulmonar cu celule mici, c\u00e2t \u0219i al celui cu celule mici. Un rol important \u00een mecanismul de rezisten\u0163\u0103 joac\u0103 genele MDR1, MDR2, MRP1, MRP2, citdin\u0103 deaminaz\u0103, timidilat sintaz\u0103 care sunt responsabile pentru rezisten\u0163a la medicamente multiple \u00een cancerul pulmonar. \u00cen centrul nostru expresia genei apar\u021bin\u00e2nd tuturor acestor gene poate fi analizat\u0103 cantitativ.<\/p>\n<h3>Tumorile cerebrale<\/h3>\n<p>Amplific\u0103ri EGFR \u00een conformitate cu tipul de cancer sau 1p,19q Co \u0219tergeri cu Fish.<\/p>\n<p>\n<\/div><div class=\"btClear btSeparator topSemiSpaced noBorder\" ><hr><\/div><div class=\"boldRow boldInnerRow  \" ><div class=\"rowItem rowInnerItem col-md-4  btTextCenter inherit btNoPadding\" style=\"border: 1px solid #999;background-color: rgba(241, 241, 241, 1);\" ><div class=\"rowItemContent\"><div class=\"bpgPhoto btTextCenter\" ><div class=\"btImage\"><img decoding=\"async\" src=\"https:\/\/groupflorence.com\/ro\/wp-content\/uploads\/2020\/10\/Kanay-Yararbas\u0327.jpg\" alt=\"\" title=\"\"><\/div><\/div><div class=\"btIconImageRow btIconsHalfHoverPosition\" ><\/div><div class=\"btClear btSeparator topSmallSpaced noBorder\" ><hr><\/div><div class=\"btText\" ><\/p>\n<h4><a href=\"https:\/\/groupflorence.com\/ro\/doctors\/kanay-yararbas\/\">Assoc. Prof. Kanay Yararba\u015f, MD<\/a><\/h4>\n<p>\n<\/div><div class=\"btClear btSeparator bottomExtraSmallSpaced noBorder\" ><hr><\/div><a href=\"https:\/\/groupflorence.com\/ro\/doctors\/kanay-yararbas\/\" class=\"btBtn btBtn btnFilledStyle btnLightColor btnSmall btnNormalWidth btnRightPosition btnNoIcon\"  target=\"_blank\"><span class=\"btnInnerText\">VIEW CV<\/span><\/a><div class=\"btClear btSeparator topExtraSmallSpaced bottomSmallSpaced noBorder\" ><hr><\/div><\/div><\/div><div class=\"rowItem rowInnerItem col-md-4  btTextCenter inherit btNoPadding\" style=\"background-color: rgba(241, 241, 241, 1);\" ><div class=\"rowItemContent\"><\/div><\/div><div class=\"rowItem rowInnerItem col-md-4  btTextCenter inherit btNoPadding\" style=\"background-color: rgba(241, 241, 241, 1);\" ><div class=\"rowItemContent\"><\/div><\/div><\/div><div class=\"btClear btSeparator topSemiSpaced noBorder\" ><hr><\/div><header class=\"header btClear medium btDash bottomDash  btAccentDash\" ><div class=\"dash\"><h3><span class=\"headline\"><em>Contact Us Now<\/em><\/span><\/h3><\/div><\/header><div class=\"btClear btSeparator bottomSmallSpaced noBorder\" ><hr><\/div><div class=\"btText\" >\n<div class=\"wpcf7 no-js\" id=\"wpcf7-f2891-o1\" lang=\"tr-TR\" dir=\"ltr\" data-wpcf7-id=\"2891\">\n<div class=\"screen-reader-response\"><p role=\"status\" aria-live=\"polite\" aria-atomic=\"true\"><\/p> <ul><\/ul><\/div>\n<form action=\"\/ro\/wp-json\/wp\/v2\/pages\/4827#wpcf7-f2891-o1\" method=\"post\" class=\"wpcf7-form init wpcf7-acceptance-as-validation\" aria-label=\"\u0130leti\u015fim Formu\" novalidate=\"novalidate\" data-status=\"init\">\n<fieldset class=\"hidden-fields-container\"><input type=\"hidden\" name=\"_wpcf7\" value=\"2891\" \/><input type=\"hidden\" name=\"_wpcf7_version\" value=\"6.1.5\" \/><input type=\"hidden\" name=\"_wpcf7_locale\" value=\"tr_TR\" \/><input type=\"hidden\" name=\"_wpcf7_unit_tag\" value=\"wpcf7-f2891-o1\" \/><input type=\"hidden\" name=\"_wpcf7_container_post\" value=\"0\" \/><input type=\"hidden\" name=\"_wpcf7_posted_data_hash\" value=\"\" \/>\n<\/fieldset>\n<p style=\"margin-bottom:30px !important;\">\u00cen timp ce completa\u021bi formularul de contact de mai jos, pute\u021bi, de asemenea, s\u0103 ne trimite\u021bi fi\u0219ierele medicale ale pacientului\/dumneavoastr\u0103 prin <strong>transfer<\/strong>. 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