A simple and cost-effective method of DNA extraction from small formalin-fixed paraffin-embedded tissue for molecular oncologic testing
© Snow et al.; licensee BioMed Central Ltd. 2014
Received: 12 March 2014
Accepted: 1 July 2014
Published: 7 July 2014
Extraction of DNA from formalin-fixed, paraffin-embedded (FFPE) tissue is a critical step in molecular oncologic testing. As molecular oncology testing becomes more important for prognostic and therapeutic decision making and tissue specimens become smaller due to earlier detection of suspicious lesions and the use of fine needle aspiration methods for tissue collection, it becomes more challenging for the typical molecular pathology laboratory to obtain reliable test results. We developed a DNA extraction method to obtain sufficient quantity and high quality genomic DNA from limited FFPE tissue for molecular oncology testing using a combination of H&E stained slides, a matrix capture method and the Qiagen DNA column.
Three DNA extraction methods were compared: our standard procedure of manually scraping tissue from unstained slides followed by DNA extraction using the QIAamp FFPE column (Qiagen, Valencia, CA), a glue capture method (Pinpoint Solution, Zymo Research Corp, Inc) on H&E stained slides followed by DNA extraction using either the QIAamp column or the column included with the Pinpoint kit (Zymo Research). The DNA extraction protocol was optimized. Statistical analysis was performed using the paired two-sample student’s t-test.
The combination of the matrix capture method with the QIAamp column gave an equivalent amount of DNA as our standard extraction method using the unstained slides and a 4.6-fold higher DNA yield than using the Zymo column included in the Pinpoint Slide Solution kit. Several molecular tests were performed and DNA purified using the new method gave the same results as for the previous methods.
Using H&E stained slides allows visual confirmation of tumor cells during microdissection. The Pinpoint solution made removal of specific tissue from the slides easier and reduced the risk of contamination and tissue loss. This DNA extraction method is simple, cost-effective, and blends with our current workflow requiring no additional equipment.
KeywordsGenomic DNA extraction Matrix capture FFPE tissue Molecular oncologic tests
Isolating genomic DNA (gDNA) from formalin-fixed, paraffin-embedded (FFPE) tissue is a critical step in molecular oncologic testing [1–6]. In most molecular diagnostic laboratories, this is done by cutting one or two hematoxylin and eosin (H&E) stained slides and 5-10 unstained sections, 6-10 microns in thickness, from FFPE tissue blocks. The H&E slide is reviewed by a pathologist; the area of interest is circled; and the slide is used to guide macro- or microdissection of the tissue from the unstained sections for tumor enrichment [7–10]. When resection specimens with large areas of tumor are available, this technique is facile. Increasingly though, molecular analysis from small biopsies or fine needle aspirates (FNA) is requested due to improved tolerance by patients and decreased invasiveness of the procedure. Since fewer tumor cells are available in these specimens, it can be very challenging to obtain enough DNA for testing, particularly in testing for the spectrum of epidermal growth factor  exons 18-21 mutations from small transbronchial lung biopsies. Additional challenges to obtain adequate genetic material, irrespective of the tissue fragment size, include contamination of tumor cells with surrounding necrosis, mucin pools, inflammatory cells, and other non-neoplastic cells. Laser capture microdissection (LCM) [12, 13] is an alternative; but it requires special equipment and special training for the medical technologists. It is also cost and space prohibitive for many laboratories to invest in an LCM system.
Another obstacle during specimen processing in the molecular diagnostic laboratory is accurate microdissection of marked tumor cell clusters from unstained slides. Tumor cells present in the H&E reference slide may be decreased or absent in the deeper unstained sections leading to a falsely negative result. Accurate morphological visualization is essential in microdissection of small biopsies . Several groups have explored the possibility of using histochemically stained slides for DNA extraction and have reported adverse consequences of the staining on DNA amplification [14–18]. Recently, Morikawa et al  extensively studied the effects of H&E staining on DNA testing and showed that neither the DNA yield nor molecular oncologic test results were affected by the stains.
The Pinpoint Slide DNA Isolation System (Zymo Research Corp, Irvine, CA) is a matrix capture method which allows lifting of tissue from the slides with ease and minimizes the potential for tissue loss and contamination from flaking of tissue during scraping of the slides (http://www.zymoresearch.com/dna-purification/genomic-dna/solid-ffpe-tissue-dna/pinpoint-slide-dna-isolation-system).
In this study, we compared our standard procedure of manually microdissecting tissue from unstained FFPE tissue on glass slides with a new method using the application of Pinpoint solution (Zymo Research Corp) on non-coversliped H&E stained slides. We also optimized the DNA column purification steps by comparing the column that came with the Pinpoint Slide Solution kit (Zymo Research Corp) and the QIAamp DNA FFPE Tissue kit (Qiagen, Valencia, CA).
Comparison of tissue harvest and DNA extraction methods
To evaluate different tissue harvesting and DNA extraction methods, the specimens were divided into three groups. The first group used the standard method in the laboratory (U-SQ), in which unstained FFPE tissue was scraped with a razor blade followed by extraction with the QIAamp kit. The second and third groups employed deparaffinization and H&E staining of the slides followed by tissue harvest using the Pinpoint reagent. The specimen was then divided into two parts for extraction of gDNA, one half with the Qiagen kit (Pinpoint harvest with QIAamp column extraction, H-PQ) and the other half with the Zymo kit (Pinpoint harvest with Zymo column extraction, H-PZ) as described above. The tissue harvested for each test group was taken from different levels of the same region on the slide to minimize variation in cellular density.
Comparison of different tissue harvesting and extraction methods
Average DNA yield (ng/mm2)
260 nm/280 nm
We routinely cut 10 sections and the number of squares (1 mm2 in size) was recorded and the DNA yield was expressed as ng per mm2. Using the optimized protocol (H-PQ), we also evaluated DNA yield from a 1 mm2 square from a single section. When the percentage of cells in the area was close to 100%, the average DNA yield was 430 ng/mm2.
Assessment of DNA amplification and mutation detection
Molecular oncology assays have varying limits of detection and sensitivity to contaminating substances. The Morikawa group  demonstrated that DNA obtained from H&E stained tissue did not interfere with multiple subsequent molecular testing. We assessed the ability to amplify DNA obtained from all three methods for microsatellite instability allelic discrimination and variant detection using the more sensitive primer extension assay and the less sensitive Sanger cycle sequencing. Although these methods are not quantitative, they do provide a relative assessment of mutation sequence representation within the sample.
FFPE tissue is the most commonly used source for molecular oncology tests . Obtaining gDNA of sufficient quality and quantity from FFPE tissue is a critical step in ensuring reliable test results. This process involves selecting the right tissue block, marking area(s) with the highest tumor content and least contaminating materials by a pathologist, and microdissection of the marked area to enrich tumor content. There are multiple methods available for gDNA extraction from FFPE tissues from the traditional phenol-chloroform extraction [21–23] to column purifications using either filter or silica-based matrix [24–26]. Extraction of DNA from cellular tumors with a solid growth pattern and little contaminating, non-neoplastic tissue is relatively easy, as with gastrointestinal stromal tumors for identification of the KIT mutations. In contrast, increasing numbers of tests are requested on small biopsies which usually contain small nests of tumor cells surrounded by non-tumor tissue creating a challenge in obtaining adequate material. Identifying small areas with tumor on unstained slides adds a layer of uncertainty to the process.
Traditionally, most clinical laboratories use unstained slides for DNA extraction and H&E stained slides only as a reference. Morikawa’s group  improved the specimen processing significantly by assessing the DNA quality and assay performance of over 1000 H&E stained FFPE cases. They showed that H&E stain had no effect on DNA extraction. Based on their findings, in this study, we H&E stained all the sections in the experimental groups. Each section was examined by a pathologist and the areas with tumor were circled on the back of the slides.
H&E stain allowed us to visualize the presence of tumor cells on the slides during microdissection and reduce the risk of false negative results. In a significant portion of the cases, changes in tumor location and/or content were observed (data not shown). In fact, some laboratories routinely stain the first and last sections of the tissue block in order to minimize the false negative result. A drawback for H&E stained sections is the tissue tends to flake off in a dry powder while scraping. We therefore explored the Pinpoint matrix capture solution (Zymo Research Corp) for tissue harvest. The Pinpoint solution kept the cells together and allowed easy harvesting of minute tumor clusters surrounded by non-neoplastic cells. It also minimized potential contamination from tissue flakes in the work area and loss of valuable tumor tissue.
The advance in high throughput technology such as massively parallel sequencing [27–29] and the multiplexed genotyping method developed by Sequenom (Sequenom Inc., San Diego, CA) [30, 31] allows multiple tests to be run at the same time with much less input DNA. DNAs obtained by our new extraction method worked well on the Ion Torrent AmpliSeq™ Cancer Hotspot Panel v2 (Life Technologies, Carlsbad, CA, data not shown). Both NGS and the Sequenom platforms require extensive test validation, strong bioinformatic support and a reasonable test volume to bring them on board. In small and medium sized clinical laboratories, Sanger sequencing and other low-throughput methods, which requires more input DNA, are still and will be used for oncology testing for a period of time. Our newly developed DNA extraction method allows us to obtain sufficient DNA from minute foci of tumor (1-2 mm2).
Test performance with DNA isolated with the new method was evaluated. Equivalent performance was observed on all assays tested in comparison with using DNA extracted by the standard method in the laboratory. Aberrations detected included BRAF V600E mutation in melanomas, colon cancer and histiocytosis by primer extension assay, deletion and SNP in the EGFR gene from lung adenocarcinomas by Sanger cycle sequencing, G12D mutation in the KRAS gene from a metastatic colon cancer using primer extension assay, and a multiplex PCR-based assay for microsatellite instability test from a colon biopsy with clusters of signet ring cells in a pool of mucin. The new method also yield good quality DNA based on the finding that the test performance was not affected.
An additional advantage of the new method is the reduced cost. The Leica machine used in our histology laboratory can automatically deparaffinize the slides without changing the frequency of reagent replenishment. The savings came from eliminating the need for buying xylene, ethanol, centrifuge tubes, and 1 ml pipet tips which were all needed for the manual deparaffinization procedure.
We developed a simple and cost-effective method for gDNA extraction from minute FFPE tissue. The combination of H&E stain with matrix capture method and the QIAamp column yielded an equivalent quantity of DNA as our standard extraction method without compromising the qualitative test results. This method also reduced the cost, blended into our work flow nicely and required no additional equipment. It is a practical method for obtaining high quality and quantity DNA from small, challenging specimens for molecular oncologic testing in the clinical laboratories.
This is a retrospective study based on data from clinical test development. The study was approved by the Institutional Review Board of University of Iowa.
Cases included in this study were selected from de-identified FFPE tissues that have been previously tested in the Molecular Pathology Laboratory at our institution since October, 2012. Special attention was paid to select cases that represented the spectrum of tissue and assays used for oncology testing. Among them, there were 19 cases of colorectal carcinomas for KRAS testing, 23 cases of lung adenocarcinomas for EGFR exons 18-21 mutational analysis, 9 cases for BRAF V600E testing (5 melanomas, 2 colon carcinomas, 1 papillary thyroid carcinoma and 1 Langerhans histiocytosis), and 1 case of colorectal carcinoma with matched normal tissue for microsatellite instability analysis.
Laboratory standard protocol for isolation of genomic DNA from FFPE tissue
All cases were reviewed by a pathologist and the optimal block was selected for molecular testing. One H&E stained slide along with 10 unstained sections (6 microns in thickness) were cut. Areas of interest were circled on the H&E slide by a pathologist and corresponding areas from the unstained slides were manually microdissected using a razor blade. The paraffin flakes were placed in a 1.5 ml microcentrifuge tube, deparaffinized with 1200 μL of xylene, vortexed, and centrifuged at 16,000 g × 5 min. The tissue pellet was washed with 95% ethanol twice before proceeding with the extraction. Genomic DNA was isolated from the microdissected FFPE sections using the QIAamp DNA FFPE Tissue kit (Qiagen) which will be referred to as U-SQ (Unstained slides, Scraped harvest method, Qiagen extraction column). The deparaffinized tissue was resuspended in 180 μl of Buffer ATL, followed by 50 μl of Proteinase K (600 mAU/ML) digestion at 56°C overnight till the specimen was completely lysed. The lysate was incubated at 90°C for one hour to partially reverse the formaldehyde modification of nucleic acids. After briefly centrifugation of the tube to remove drops from the inside of the lid, 200 μl of Buffer AL was added, and the mixture was vortexed for 15 seconds. 200 μl of ethanol (96-100%) was added and mixed by vertexing for 15 seconds. The mixture was incubated for 5 min at room temperature, briefly centrifuged and the entire lysate was transferred to the QIAamp MinElute column. DNA was extracted according to the manufacturer’s instruction included in the kit.
One H&E slide with cover-slip and 10 unstained sections were obtained as described above. The unstained slides were deparaffinized and H&E stained in our histology laboratory using a standard protocol on the Leica ST5020. This automated instrument submerges the slides through three changes of xylene followed by a gradient of washes with 100% ethanol, 95% ethanol, 70% ethanol, and water. After deparaffinization, the slides were processed through the H&E staining wells. No coverslip was placed. The underside of the uncover-slipped slides was marked by a pathologist and the pinpoint matrix capture solution (Zymo Research Corp) was applied to the slide and allowed to air dry. Tissue bound to the dried solution was removed from the slide using a razor blade (Figure 1). After proteinase K digestion at 55°C for 24 hours, the sample was divided into two aliquots for genomic DNA isolation either by the QIAamp DNA FFPE Tissue kit (Qiagen) as described earlier or the Pinpoint Slide DNA Isolation kit (Zymo Research Corp). Genomic DNA extraction using the Zymo kit was performed as follows: 50 μl of Extraction Buffer and 5 μl Proteinase K were added to the tube of recovered tissue. The tube was incubated at 55°C overnight, followed by heat-inactivation at 98°C for 10 minutes. The tube was placed immediately on ice, vortexed vigorously for 15 seconds and centrifuged at 16,000 g × 5 min. The supernatant was transferred to a clean tube. The DNA concentration was measured by the NanoDrop spectrophotometer (NanoDrop, Westlake Village, CA) and the quality of gDNA was assessed by the ratio of absorbance at 260 nm and 280 nm. These two methods were designated as H-PZ for H&E stained slides, Pinpoint matrix capture and Zymo Slide DNA Isolation kit and H-PQ for H&E stained slides, Pinpoint matrix capture with the Qiagen QIAamp DNA FFPE column purification.
Comparison of tissue harvest and DNA extraction methods
The specimens were divided into three groups. The first group used the standard method in the laboratory (U-SQ). In this method, unstained FFPE tissue was scraped with a razor blade followed by extraction with the QIAamp kit as described above. The second and third groups employed deparaffinization and H&E staining of the slides followed by tissue harvest using the Pinpoint reagent. The specimen was then divided into two parts for extraction of gDNA, one half with the Qiagen kit (Pinpoint harvest with QIAamp column extraction, H-PQ) and the other half with the Zymo kit (Pinpoint harvest with Zymo column extraction, H-PZ) as described above. The tissue harvested for each test group was taken from different levels of the same region on the slide to minimize variation in cellular density.
Molecular tests performed
BRAF codon V600 mutation analysis by primer extension assay
BRAF exon 15 was PCR amplified using primers 5′-GATCCCTTTACTTACTACACCTCAG-3′ and 5′-GATCGTAACTCAGCAGCATCTC-3′. Mutations in codon V600 were examined by single nucleotide primer extension assay using the Snapshot Multiplex kit (Applied Biosystems, Foster City, CA). The V600 codon was interrogated with a sense probe consisting of deoxy-thymidine monophosphate homopolymers of varied sizes for discrimination of different mutation products  (See reference  for probe sequences). After amplification, the product was subjected to probe annealing and addition of a single, fluorescently labeled dideoxynucleotide. The primer extension products were analyzed by capillary electrophoresis.
KRAS codon 12, 13, and 61 mutation analysis by primer extension assay
This assay was performed with a similar procedure to that described for the BRAF V600 primer extension assay above. In this assay, exons 2 and 3 of the KRAS gene were amplified using specific primers in a multiplex reaction (see reference 32 for primer sequences). The primer extension probes were designed with varying lengths of deoxythymidine monophosphate homopolymers ranging from 30 to 76 bases to allow for discrimination of the products by size. The sense probes were designed to end one base 5′ of the following positions: c.35, c.38, and c.182. The antisense probes were designed to end one base 5′ of the following positions: c.34, c.37, c.57, c.181, and c.183. These probes allowed for the detection of common variants present in codons 12, 13, and 61 of the KRAS gene.
EGFR mutation analysis by Sanger sequencing
Exons 18-21 of the EGFR gene were PCR amplified using primers designed to produce one amplicon per exon. Primer sequences were: 5′-TCTGGCACTGCTTTCCAGC-3′ and 5′-TCCCAAACACTCAGTGAAACAAA-3′ for exon 18; 5′-ACCCAG ATC ACTGGGCAGC-3′ and 5′-AGCAGCTGCCAGACATGAG-3′ for exon 19; 5′-CTGGCCACCATGCGAAGCC-3′ and 5′-ATCCTGGCTCCTTATCTCC-3′ for exon 20; and 5′-CCCATGATGATCTGTCCCT-3′ and 5′-TGGTCCCTGGTGTCAGGAA-3′ for exon 21. 25 to 150 ng of gDNA was used as the starting material in each amplification reaction. The PCR thermocycling conditions were as follows: 94°C for 2 minutes, followed by 30 cycles of 94°C for 15 seconds, 58°C for 30 seconds, and 72°C for 30 seconds. The amplification products were purified using the Qiagen QIAquick PCR purification kit (Qiagen). Cycle sequencing was performed using the ABI Big Dye Terminator Mix, version 3.1 and the products were separated by capillary electrophoresis on an ABI 3130 Genetic Analyzer (Applied Biosystems).
Microsatellite instability testing by PCR followed by capillary electrophoresis
The National Cancer Institute (NCI) recommended five-marker panel (two mononucleotide markers, BAT25 and BAT26 and three dinucleotide markers, D2S123, D5S346 and D17S250) were used for microsatellite instability testing in two multiplexed reactions with fluorescently labeled primers. Genomic DNA extracted from tumor and paired normal tissue from the same patient was used. The amplicons were then analyzed using capillary electrophoresis.
Comparison of 4-hour versus overnight proteinase K digestion
Three samples with uniform cellularity were selected. Ten slides were prepared by deparaffinization and H&E staining without placement of coverslips. Areas with the greatest cellular uniformity were marked by a pathologist using a 2 mm × 2 mm template. The pinpoint reagent was applied and the dried matrix was removed as described above. The matrix pellet was digested with proteinase K at 55°C for 4 hours and then divided into two aliquots: one was extracted immediately using the QIAamp FFPE kit (Qiagen); the other one was subjected to continued proteinase K digestion overnight and DNA was extracted using the same column type the next day. Optical densitometry was performed after extraction and the mean concentration values were compared statistically.
Statistical analysis was performed using the paired two-sample student’s t-test. A significant difference is defined as p value less than .05.
Unstained slides, Scraped harvest method, Qiagen extraction column
H&E stained slides, Pinpoint matrix capture and Zymo Slide DNA Isolation kit
H&E stained slides, Pinpoint matrix capture with the Qiagen QIAamp DNA FFPE column.
The authors thank Jason Hackman, CLS, Matthew Zubcic, CLS, and Sue Forde, CLS at the Molecular Genetic Pathology Laboratory and Melissa Jans, CLS at the Histology Laboratory at University of Iowa Hospitals and Clinics for their technical support.
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