LINCATRA: Two-cycle method to amplify RNA for transcriptome analysis from formalin-fixed paraffin-embedded tissue

被引:0
|
作者
Bhamidimarri, Poorna Manasa [1 ]
Salameh, Laila [2 ]
Mahdami, Amena [1 ]
Abdullah, Hanan Wael [1 ]
Mahboub, Bassam [2 ,3 ]
Hamoudi, Rifat [1 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Sharjah, Res Inst Med & Hlth Sci, Sharjah, U Arab Emirates
[2] Rashid Hosp, Dubai Hlth, Dubai 4545, U Arab Emirates
[3] Univ Sharjah, Coll Med, Clin Sci Dept, Sharjah, U Arab Emirates
[4] UCL, Div Surg & Intervent Sci, London, England
[5] Univ Sharjah, Biomedically Informed Artificial Inelligence Lab, BIMAI Lab, Sharjah 27272, U Arab Emirates
[6] Univ Sharjah, Res Inst Med & Hlth Sci, Ctr Excelence Precis Med, Sharjah 27272, U Arab Emirates
关键词
Linear amplification; Formalin-fixed paraffin embedded; RNA-Seq; Degraded; Transcriptomic analysis; SEQUENCE-BASED AMPLIFICATION; READ ALIGNMENT; PROGNOSIS; SAMPLES; ASSAY; SEQ;
D O I
10.1016/j.heliyon.2024.e32896
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Whole transcriptome analysis (WTA) using RNA extracted from Formalin Fixed Paraffin Embedded (FFPE) tissue is an invaluable tool to understand the molecular pathology of disease. RNA extracted from FFPE tissue is either degraded and/or in very low quantities hampering gene expression analysis. Earlier studies described protocols applied for cellular RNA using poly-A primer-based linear amplification. The current study describes a method, LINCATRA (LINear amplifiCAtion of RNA for whole TRAnscriptome analysis). It employs random nonamer primer based method which can amplify short, fragmented RNA with high fidelity from as low as 5 ng to obtain enough material for WTA. The two-cycle method significantly amplified RNA at similar to 1000 folds (p < 0.0001) improving the mean read lengths (p < 0.05) in WTA. Overall, increased mean read length positively correlated with on-target reads (Pearson's r = 0.71, p < 0.0001) in both amplified and unamplified RNA-seq analysis. Gene expression analysis compared between unamplified and amplified group displayed substantial overlap of the differentially expressed genes (DEGs) (log2 fold change cut-off < -2 and >2, p < 0.05) identified between lung cancer and asthma cohorts validating the method developed. This method is applicable in clinical molecular pathology field for both diagnostics and elucidation of disease mechanisms.
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页数:12
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