3Biyospesmen and süreç Biyospesmen Bilgilerinin Derleme ve Analizi HastaEdinim/Acquisitionİşlem/ProsesSaklamaDağıtımBilimselAnalizTıbbi/CerrahiProsedürlerArtanıStoklamaBiyospesmen BilgilerininDerleme ve AnaliziBilimsel BilgilerinDerleme ve AnaliziKlinik/Klinik Araştırma Çıktıları
9Preanalitik faktörler I: Sıvı Biyospesmen AntikoagülanlarSitrat-DNA, RNAEDTA-DNAHeparin-Sitolojik testlerStabilizör/İnhibitörlerProtein:Proteaz inhibitörleriRNA:Beta-merkaptoetanol (stabilizör)RNaz inhibitörleriDNA:Stabildir-Örn. Guthrie testiSaklama sıcaklığıPMSF, Leupeptin, pepstatin, aprotinin2-Mercaptoethanol is used in some RNA isolation procedures to eliminate ribonuclease released during cell lysis. Numerous disulfide bonds make ribonucleases very stable enzymes, so 2-mercaptoethanol is used to reduce these disulfide bonds and irreversibly denature the proteins. This prevents them from digesting the RNA during its extraction procedure
11Antikoagulanlar Aditif Renk Testler Yok Kırmızı Biyokimya, Seroloji, immünoloji, serumSodium heparin (freeze dried)YeşilImmünoloji, viroloji testleriSodium heparinKahverengiSitogenetik testler, moleküler testlerTripotassium EDTA (7.5-15% solution)MorVirology, molecular biologyAcid citrate dextrose (ACD) solutionSarıMoleküler biyoloji
12Preanalitik faktörler II: Solid Biyospesmen Kanser hücrelerinde genomik değişiklikler düşük frekanstadırKantite sorunuBiyopsi materyaliKalite sorunuBiyopsi materyalleri formalinle fiksedir.DNA izolasyonu özel protokole tabidirPürite sorunu (Tümör heterogenitesi)Normal hücreler ile karışıktırKanserin kendisinde heterogenite (farklı klonlar)RNAlater RNA Stabilization Reagent immediately stabilizes RNA in tissue samples to preserve the gene expression profile, and is supplied in 50 ml or 250 ml bottles. For stabilization of DNA, RNA, and protein in tissue samples, Allprotect Tissue Reagent can be used.
13FFPE (formalin-fixed, paraffin-embedded) örnekler Fiksasyon süresiParafine gömme sıcaklığıDoku takip işlemiParafin blokları saklama şartlarıDNA intak değildirKovalen addükler oluşurPCR 300 bp fragmandifferences (characteristics of formalin fixation; duration of fixation, type of tissue processing, temperature of paraffin embedding, storage conditions of paraffin blocks)For many retrospective studies, formalin-fixed and paraffin-embedded ... fail to allow for effective amplification of DNA fragments beyond 300 bpHowever, nucleic acids isolated from FFPE tissues are severely degraded and contain mainly small fragments, generally less than 300 bp. These fragments represent a poor substrate for molecular biological methods, e.g. PCR [1,2]. Furthermore, formalin-fixation leads to the formation of DNA-protein crosslinks, which are not completely removed by common lysis protocols . Crosslinks increase the sensitivity of DNA to mechanical stress and decrease the accessibility for enzymes. In addition, formalin is oxidized to formic acid which causes DNA depurination and DNA strand breaks.Fresh or fresh frozen tissue samples are the best material for isolation DNA of high quality and quantity. However, storage of frozen tissue samples is expensive and time-consuming. For many retrospective studies, formalin-fixed and paraffin-embedded (FFPE) material is, therefore, the only available tissue for DNA analysis.Isolation of sufficient amounts of intact DNA from FFPE tissue samples is challenging. One major problem is DNA-protein cross-linking caused by formalin fixation that must be broken up during the extraction process.3,8 Furthermore, the low pH in unbuffered fixatives leads to degradation of most DNA molecules into fragments of 200 bp or less.3 A number of approaches have been published to deal with these problems that hinder the use of FFPE for genomic analysis.1,2,5–7,9 These protocols use expensive DNA extraction kits,2,5,7,9 have low DNA yield,2,6 have suboptimal purity of DNA,1 or fail to allow for effective amplification of DNA fragments beyond 300 bp.1,2,5,6
14İnce iğne biyopsi materyalleri Taze doku örnekleriPatolog gözetiminde çalışılmalıdırİnce iğne biyopsi materyalleriHücre sayısı yetersiz olabilir
15Saklama koşulları- DNA NumunelerKan, Kemik iliği, Vücut sıvıları<1 gün, 23°C; 3 gün, 4°CWBC, >1 year, -20°C or -70°CDoku<1 gün, 4°C>2 hafta, -20°C>2 yıl, -70°CIzole DNA<26 hafta, 2-25°C1-3 yıl, 4°C (Southern blot için 1 yıl)<7 yıl, -20°C, -70°C (not frost-free)
16Saklama koşulları- RNA NumunelerKan, Kemik iliği, vücut sıvıları<2 saat, 23°C or 4°C5 gün, 23°C; 7 gün 4°C denaturan’da1-2 hafta, -70°C denaturan’daWBC, 2-4 hafta, -20°C; >6 ay, -70°CDoku<2 saat, 4°Csnap frozen, -70°C, >2 yılnitrogen vapor -140°C– -150°C, >2 yearsIzole RNA<30 gün, -20°C DEPC-treated su içinde<30 gün, -70°C DEPC-treated su içinde>6 ay, -70°C ethanol içinde
17Preanalitik faktörler III: Moleküler lab Benç ve ekipmanlarFizik alan olarak ayrı bir laboratuvar olmalıTek-yönlü iş akışı olmalıLaminer flow kabin kullanılmalıEldivensiz çalışılmamalıGiriş-çıkışlar sınırlı olmalıEkipman ve malzemeler laboratuvara özel olmalı; asla dışarı çıkarılmamalıDNaz-free ve RNaz-free çalışma ortamı sağlanmalıRNase ZAP (yüzey dekontaminasyonu),RNase AWAY (plastik ve cam malzemeler) gibi solüsyonlar kullanılabilir1-RNaseZap® RNase Decontamination Solution is a surface decontamination solution that destroys RNases on contact. You simply spray RNaseZap® Solution 2-RNase AWAY® Reagent is a ready-to-use solution for eliminating RNase and DNA contamination from labware. Apply it evenly over the surface of glassware or plasticware to be treated and then rinse it away with distilled water. Unwanted RNase and DNA contamination are eliminated. RNase AWAY® Reagent is nonabrasive, noncarcinogenic, and nonbiologically corrosive.
18Sarflar Reaktifler Filtreli pipet ucu kullanılmalı DNaz-free ve RNaz-free sertifikalı olmalıCam malzemeler 0.1% diethyl pyrocarbonate (DEPC) ile yıkanmalıReaktiflerOtoklav yetersizdirKimyasal ve sarflar, DNaz-free ve RNaz-free sertifikalı olmalı,DEPC iyi bir RNaz inhibitörüdürSu, reaktif ve solusyonlar mutlaka DEPC içermeli,0.05–0.1% DEPC ilave edilebilir (Tris ve EDTA tamponlar hariç)DEPC will react with primary amines and cannot be used directly to treat Tris buffers.Diethylpyrocarbonate (DEPC) treatment is the most commonly used method for eliminating RNase contamination from water, buffers, and other solutions. DEPC destroys enzymatic activity by modifying -NH, -SH and -OH groups in RNases and other proteins. When DEPC breaks down during autoclaving, a small amount of ethanol is produced.Reagents containing primary amine groups (e.g., Tris and EDTA) and some reagents containing secondary or tertiary amines (e.g., HEPES) cannot be DEPC-treated. The amine groups tend to react with and "sop up" the DEPC, making it unavailable for inactivating RNases
19Reaksiyonlar Lab temizliği Cross-kontaminasyon önlenmeli RNasin eklenmeliBlank tüp/kuyu kullanılmalıİnternal kontrol kullanılmalıMümkünse kapalı sistemler tercih edilmeliLab temizliğiÇalışma öncesi kabinlerde UV kullanılmalıHer çalışmadan sonra dekontaminasyon yapılmalıYüzeyler önce %10 hipoklorit sonra %70 etanol ileRNaz kontaminasyonu düzenli kontrol edilmeliRNaseAlert kitWipe testRNasin® Plus RNase Inhibitor is a recombinant mammalian RNase inhibitor that is expressed as a soluble protein in E. coli, allowing easy purification through a combination of ion exchange and hydrophobic interaction chromatography. The protein is capable of inhibiting eukaryotic RNases (e.g., RNase A and RNase B) similarly to human placental RNase inhibitor. RNasin® Plus RNase Inhibitor is tested in RT-PCR and is compatible with enzymes such as AMV, M-MLV and ImProm-II™ Reverse Transcriptases or Taq and Tfl DNA PolymerasesAmbion® RNaseAlert® Lab Test kit is a Patent-pending technology detects RNase activity in a convenient and sensitive assay that delivers results in real time. Suitable for testing small sample numbers and can be used to ensure that solutions, tubes, tips, etc. are RNase-free; the kit contains sufficient reagents for 25 reactions.Wipe test
24Platformlar-DNA Ekstraksiyon/Pürifikasyon Array-CGH CGH Dizi analizi ElektroforezFISHIn situ hibridizasyonPCR/LCR/RT-PCR/RFLPSNP assayDoku mikroarrayMicroarray-based comparative genomic hybridization (array CGH) is a type of genetic testing. This technology evaluates important areas of a patient’s chromosomes to see if there are extra or missing DNA segments that could be the cause of the person’s medical problems.Comparative genomic hybridization is a molecular cytogenetic method for analysing copy number variations (CNVs) relative to ploidy level in the DNA of a test sample compared to a reference sample, without the need for culturing cells. The aim of this technique is to quickly and efficiently compare two genomic DNA samples arising from two sources, which are most often closely related,Fluorescence In Situ Hybridization
25Platformlar-RNA Ekstraksiyon/Pürifikasyon cDNA mikroarray In situ hibridizationElektroforezNorthern blot analiziRT-PCRDoku mikroarray
26Platformlar-Protein Ekstraksiyon/Pürifikasyon 1D/2D gel elektroforezleriAntikor mikroarrayİmmunohistokimyaKütle spektrometreMALDI-TOFSELDI-TOFDoku mikroarrayWestern blot analizi
27Preanalitik faktörler IV: Edinim (Acquisition) ÖnceSonraWarm iskemiCold iskemiAntibiyotiklerOda ısısında kalma süresiDiğer ilaçlarOdanın sıcaklığıAnestezi tipiFiksatif tipiAnestezinin süresiFiksatifin sıcaklığıTurnike zamanıFiksatifte kalma süresiKan basınç değişimleriDondurma yöntemiIntra-Op kan kaybıDondurmanın hızıIntra-Op kan verilmesiAlikotlama volümüIntra-Op sıvı verilmesiÖrnek kabının tipiCerrahi/Tıbbi tedavi tipiEkstraksiyon yöntemiVarolan rahatsızlıklarıSaklama sıcaklığı ve süresiHastanın cinsi (K/E)Vakumlu saklama
28Edinim (Acquisition) Warm iskemi (Intra-op) Cold iskemi (Post-op) Cold ischemiaTime interval between tissue removal and stabilization (HERE: formalin fixation)Warm ischemiaTime interval between ischemia-relevant vessel ligation/clamping (e.g. for stomach: ligation of Arteria gastricasinistra and Arteria gastroepiploica) and tissue removalWarm iskemi(Intra-op)Cold iskemi(Post-op)
36Sistematik-SPREC-01 Standard Preanalytical Coding for Biospecimens Each biospecimen is assigned a seven-element-long code that corresponds to seven preanalytical variables and contains a string of 11 (for fluids) or 13 (for solid tissues) letters in a defined order, separated by six hyphens. Wherever possible, we make use of the existing Laboratory Data Management System (LDMS) codes (5) for the sample types and the primary container types.Cancer Epidemiology Biomarkersand Prevention 2010;19:
37Örnekler Sıvı spesmen Serum Plazma İdrar SSS Sample type SER PL2 U24 CSFType of containerSSTSEDPIXPPTPrecentrifugation delayABCentrifugationECSecond centrifugationNPostcentrifugation delayStorageGJSER-SST-A-E-N-A-G. This corresponds to a serum (SER) specimen that has been collected from a serum collection tube (SST), whose precentrifugation delay is <2 hours at room temperature (A); centrifugation has been done at ambient temperature at 3,000 to 6,000 g with braking (E). Only one centrifugation step was done (N) and the delay between centrifugation and freezing was <1 hour at 3°C to 7°C (A). Serum was stored in straws at a temperature between −85°C and −60°C (G).Plasma specimenPL2-SED-B-B-E-A-G. This corresponds to a double spun plasma (PL2) specimen that has been collected from a sodium EDTA vacutainer collection tube (SED), whose precentrifugation delay is <2 hours at 3°C to 7°C (B); first centrifugation has been done at ambient temperature at <3,000 g with braking (B) and second centrifugation has been done at ambient temperature at 3,000 to 6,000 g with braking (E). The delay between centrifugation and freezing was <1 hour at 3-7°C (A). Plasma was stored in straws at a temperature between −85°C and −60°C (G).Urine specimenU24-PIX-B-A-N-A-J. This corresponds to a 24-hour urine (U24) specimen that has been collected in a collection tube with protease inhibitors (PIX), whose precentrifugation delay is <2 hours at 3°C to 7°C (B); centrifugation has been done at ambient temperature at <3,000 g without braking (A). Only one centrifugation step was done (N) and the delay between centrifugation and freezing was <1 hour at 3°C to 7°C (A). Urine was stored in >5-mL polypropylene tubes at a temperature between −85°C and −60°C (J).CSF SpecimenCSF-PPS-B-C-N-A-A. This corresponds to a cerebrospinal fluid (CSF) specimen that has been collected in a sterile polypropylene collection tube (PPS), whose precentrifugation delay is <2 hours at 3°C to 7°C (B); centrifugation has been done at 3°C to 7°C at <3,000 g without braking (C). Only one centrifugation step was done (N) and the delay between centrifugation and freezing was <1 hour at 3°C to 7°C (A). CSF was stored in 0.5- to 2-mL polypropylene tubes at a temperature between −85°C and −60°C (A).
38Solid spesmen Solid doku Sample type TIS Type of collection BPS Warm ischemiaNCold ischemiaBFixation typeRNLFixation timeAStorageSolid tissue or cytologic SpecimenTIS-BPS-N-B-RNL-A-A. This corresponds to a solid tissue (TIS) specimen that has been collected as a biopsy (BPS), with no warm ischemia (N), with cold ischemia of <10 minutes (B), fixed in RNALater (RNL) for <15 minutes (A) and stored in a 0.5- to 2-mL polypropylene tube at a temperature between −85°C and −60°C (A). Biopsies, obtained either at time of traditional surgery, laparoscopy, or puncture, and cytologic specimens such as fine needle aspirates, are assigned the same SPREC.Warm ischemia: Intra-surgical ischemiaCold ischemia: Post-surgical ischemiaRNAlater RNA Stabilization Reagent immediately stabilizes RNA in tissue samples to preserve the gene expression profile, and is supplied in 50 ml or 250 ml bottles. For stabilization of DNA, RNA, and protein in tissue samples, Allprotect Tissue Reagent can be used.
40FFPE ve saklama koşulları FFPE, Formalin-Fixed, Paraffin-Embedded (tissue).Assessment of protein immunoreactivity to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) by Western blotting. (a) Western Blot by anti-GAPDH antibody. Lane 1, RT-Vac + Drierite; lane 2, RT-HC; lane 3, 4C-Vac + Drierite; lane 4, 4C–HC; lane 5, 30C-Vac + Drierite; lane 6, 30C–HC; lane 7, 37C-Vac + Drierite; lane 8, 37C–HC. (b) Quantitative analysis of Western blot (ImageQuant Program version 5.2, Piscataway, NJ). HC, humidity chamber; RT, room temperature; Vac, vacuum packed.We hypothesize that the presence of both endogenous water and ambient water is crucial to protein degradation and diminution of immunoreactivity in FFPE tissue sections. In an attempt to test our hypothesis, we examined the impact of inadequate processing in FFPE tissues after tissue processing on antigen degradation. To determine the effect of ambient water on protein integrity and immunoreactivity, two storage conditions, vacuum-pack with desiccant and humidity chamber at different temperatures, were further investigated.J Histochem Cytochem April;59(4): 356–365.
41Warm iskemi ve gen ekspresyonu WIMA: Warm ischemia-induced metabolic activityWIRD: Warm ischemia-induced RNA degradationContribution of WIMA and WIRD to changes in gene expression within different time periods.Yi Ma , et al., Analytical Biochemistry Volume 423, Issue
42Cold iskemi ve gen ekspresyonu Genlerin yaklaşık % 20-25’i ilk 30 dakikada etkilenmiştir (Affymetrix cDNA microarray)Indivumed, Prof. Dr. Hartmut Juhl, 2nd Biospecimen Research Network SymposiumMarch 16-18, 2009Kolon kanserinde Affymetrix cDNA microarray sonuçlarıFollowing tumor resection ~ 20-25% of genes are differentially expressedwithin the first 30 minutes !Sprüssel et al, BioTechniques 2004
43Cold iskemi ve protein ekspresyonu Proteinlerin yaklaşık %25-30’u ilk 30 dakikada etkilenmiştir (SELDI-TOF)Tissue ischemia time and protein expression in colon tissue (SELDI-TOF-MS analysis)Following tumor resection ~ 25-30% of proteins are differentially expressedwithin the first 30 minutes !
44Cold iskemi ve IHC/FISH sonuçları HER2 (Human Epidermal Growth Factor Receptor 2) also known as Neu, ErbB-2, CD340 (cluster of differentiation 340) or p185 is a protein that in humans is encoded by the ERBB2 gene. HER2 is a member of the epidermal growth factor receptor (EGFR/ErbB) family. Amplification or over-expression of this gene has been shown to play an important role in the pathogenesis and progression of certain aggressive types of breast cancer and in recent years it has evolved to become an important biomarker and target of therapy for approx. 30% of breast cancer patients[
45Biyopsi lokasyonu ve kolon kanserde protein ekspresyonu Proteinlerin yaklaşık %40’ı tümör bölgesine göre değişim göstermiştir
46Biyopsi lokasyonu ve kolon kanserde VEGF ekspresyonu Farklı dokular: 61, 157, 161, 197, 249
47Sonuç ve Öneriler Sorumluluk tamamen klinisyenlere bırakılamaz; Sorumluluk büyük orandalaboratuvar uzmanına aittir;Laboratuvar uzmanı, klinisyenleridoğru yönlendirmeli,Sürekli gelişim esas olmalı,
48Klavuzlar takip edilmeli ve uygulanmalı, Literatür takip edilmeli, Kalite kontrol sistemleri uygulanmalı,Preanalitik hatalar yanlış teşhis, tedavi ve öngörüye yol açar,Sonuçta hastanın yaşam kalitesini olumsuz etkiler,Biospesmen bilimi’nin varlıgını kabul etmeliyizWhat is biospecimen science?Biospecimen Science is the multidisciplinary field of study responsible for establishing tested and proven biospecimen resource-related procedures based on experimentation in the areas of specimen collection, processing, shipping, and storageWhy is it needed?Biospecimens are composed of active and reactive living cells or cell products, making them highly complex.The collection, handling, and storage process can profoundly alter the molecular profile and quality of biospecimens.Such alterations, though artificial, can be misinterpreted as disease related or disease specific.High degrees of sensitivity and specificity in new molecular techniques raise the bar for analyte (specimen) data and quality.