TY - JOUR
T1 - The biospecimen preanalytical variables program a multiassay comparison of effects of delay to fixation and fixation duration on nucleic acid quality
AU - Carithers, Latarsha J.
AU - Agarwal, Rachana
AU - Guan, Ping
AU - Odeh, Hana
AU - Sachs, Michael C.
AU - Engel, Kelly B.
AU - Greytak, Sarah R.
AU - Barcus, Mary
AU - Soria, Conrado
AU - Lih, Chih Jian
AU - Mickey Williams, P.
AU - Branton, Philip A.
AU - Sobin, Leslie
AU - Fombonne, Benjamin
AU - Bocklage, Therese
AU - Andry, Chris
AU - Duffy, Elizabeth R.
AU - Sica, Gabriel
AU - Dhir, Rajiv
AU - Jewell, Scott
AU - Roche, Nancy
AU - Moore, Helen M.
N1 - Publisher Copyright:
© 2019 College of American Pathologists. All rights reserved.
PY - 2019
Y1 - 2019
N2 - Context.—Despite widespread use of formalin-fixed, paraffin-embedded (FFPE) tissue in clinical and research settings, potential effects of variable tissue processing remain largely unknown. Objective.—To elucidate molecular effects associated with clinically relevant preanalytical variability, the National Cancer Institute initiated the Biospecimen Preanalytical Variables (BPV) program. Design.—The BPV program, a well-controlled series of systematic, blind and randomized studies, investigated whether a delay to fixation (DTF) or time in fixative (TIF) affects the quantity and quality of DNA and RNA isolated from FFPE colon, kidney, and ovarian tumors in comparison to case-matched snap-frozen controls. Results.—DNA and RNA yields were comparable among FFPE biospecimens subjected to different DTF and TIF time points. DNA and RNA quality metrics revealed assay- and time point–specific effects of DTF and TIF. A quantitative reverse transcription–polymerase chain reaction (qRT-PCR) assay was superior when assessing RNA quality, consistently detecting differences between FFPE and snap-frozen biospecimens and among DTF and TIF time points. RNA Integrity Number and DV200 (representing the percentage of RNA fragments longer than 200 nucleotides) displayed more limited sensitivity. Differences in DNA quality (Q-ratio) between FFPE and snap-frozen biospecimens and among DTF and TIF time points were detected with a qPCR-based assay. Conclusions.—DNA and RNA quality May be adversely affected in some tumor types by a 12-hour DTF or a TIF of 72 hours. Results presented here as well as those of additional BPV molecular analyses underway will aid in the identification of acceptable delays and optimal fixation times, and quality assays that are suitable predictors of an FFPE biospecimen’s fit-for-purpose.
AB - Context.—Despite widespread use of formalin-fixed, paraffin-embedded (FFPE) tissue in clinical and research settings, potential effects of variable tissue processing remain largely unknown. Objective.—To elucidate molecular effects associated with clinically relevant preanalytical variability, the National Cancer Institute initiated the Biospecimen Preanalytical Variables (BPV) program. Design.—The BPV program, a well-controlled series of systematic, blind and randomized studies, investigated whether a delay to fixation (DTF) or time in fixative (TIF) affects the quantity and quality of DNA and RNA isolated from FFPE colon, kidney, and ovarian tumors in comparison to case-matched snap-frozen controls. Results.—DNA and RNA yields were comparable among FFPE biospecimens subjected to different DTF and TIF time points. DNA and RNA quality metrics revealed assay- and time point–specific effects of DTF and TIF. A quantitative reverse transcription–polymerase chain reaction (qRT-PCR) assay was superior when assessing RNA quality, consistently detecting differences between FFPE and snap-frozen biospecimens and among DTF and TIF time points. RNA Integrity Number and DV200 (representing the percentage of RNA fragments longer than 200 nucleotides) displayed more limited sensitivity. Differences in DNA quality (Q-ratio) between FFPE and snap-frozen biospecimens and among DTF and TIF time points were detected with a qPCR-based assay. Conclusions.—DNA and RNA quality May be adversely affected in some tumor types by a 12-hour DTF or a TIF of 72 hours. Results presented here as well as those of additional BPV molecular analyses underway will aid in the identification of acceptable delays and optimal fixation times, and quality assays that are suitable predictors of an FFPE biospecimen’s fit-for-purpose.
UR - https://www.scopus.com/pages/publications/85065336228
UR - https://www.scopus.com/inward/citedby.url?scp=85065336228&partnerID=8YFLogxK
U2 - 10.5858/arpa.2018-0172-OA
DO - 10.5858/arpa.2018-0172-OA
M3 - Article
C2 - 30785788
AN - SCOPUS:85065336228
SN - 0003-9985
VL - 143
SP - 1106
EP - 1118
JO - Archives of Pathology and Laboratory Medicine
JF - Archives of Pathology and Laboratory Medicine
IS - 9
ER -