Comparison of Two Methods of RNA Extraction from Formalin-Fixed Paraffin-Embedded Tissue Specimens

被引:16
作者
Gouveia, Gisele Rodrigues [1 ,2 ]
Ferreira, Suzete Cleusa [3 ]
Ferreira, Jerenice Esdras [1 ]
Coelho Siqueira, Sheila Aparecida [4 ]
Pereira, Juliana [5 ]
机构
[1] Univ Sao Paulos, Med Sch FMUSP, BR-05403000 Sao Paulo, Brazil
[2] Hosp Clin FMUSP, Lab Imunopatol, BR-05403000 Sao Paulo, Brazil
[3] FMUSP, Sao Paulos Blood Ctr, Fundacao Pro Sangues, Dept Mol Biol, BR-05403000 Sao Paulo, Brazil
[4] FMUSPs Hosp Clin HC, Pathol Serv, BR-05403000 Sao Paulo, Brazil
[5] FMUSP, State Sao Paulo Canc Inst ICESP, HC FMUSP Cent Inst IC, Hematol Serv, BR-05403000 Sao Paulo, Brazil
关键词
EXPRESSION; DNA; PCR; AMPLIFICATION;
D O I
10.1155/2014/151724
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The present study aimed to compare two different methods of extracting RNA from formalin-fixed paraffin-embedded (FFPE) specimens of diffuse large B-cell lymphoma (DLBCL). We further aimed to identify possible influences of variables-such as tissue size, duration of paraffin block storage, fixative type, primers used for cDNA synthesis, and endogenous genes tested-on the success of amplification from the samples. Both tested protocols used the same commercial kit for RNA extraction (the Recover All Total Nucleic Acid Isolation Optimized for FFPE Samples from Ambion). However, the second protocol included an additional step of washing with saline buffer just after sample rehydration. Following each protocol, we compared the RNA amount and purity and the amplification success as evaluated by standard PCR and real-time PCR. The results revealed that the extra washing step added to the RNA extraction process resulted in significantly improved RNA quantity and quality and improved success of amplification from paraffin-embedded specimens.
引用
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页数:5
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