Determination of abnormally expressed microRNAs in bone marrow smears from patients with follicular lymphomas
© Takei et al.; licensee Springer. 2014
Received: 31 March 2014
Accepted: 29 May 2014
Published: 7 June 2014
The abnormal expression of microRNAs (miRNAs) is implicated in various human diseases, including cancers. Accordingly, miRNA expressions have been examined in many cancer tissues and blood, but there have been few studies examining smear samples from bone marrow (BM) or peripheral blood. Here we successfully isolated small RNAs from BM smears using a mirVana miRNA Isolation Kit with our original modifications. The isolated small RNAs were then used to measure the levels of representative miRNAs such as miR-155, let-7a, and U6 via real-time PCR with a specific TaqMan probe, although peaks for the ribosomal RNAs (18S, and 28S) were not identified. The PCR curves of the miRNAs were indistinguishable from those from BM living cells from the same donor. Finally, our method for BM smears identified numerous abnormally altered miRNAs (significantly decreased, 39 miRNAs; significantly increased, 27 miRNAs) in follicular lymphomas (FL) compared with normal donors via TaqMan real-time PCR miRNA array. The array indicated that miR-451 showed the greatest decrease in FL (a 345-fold decrease), while miR-338-5p showed the greatest increase in FL (172-fold) relative to normal donors. The miRNAs identified by our study might serve as markers to predict the invasion of FL cells into BM without biopsy. Furthermore, our method will provide a new avenue for the analysis of miRNAs in BM smear samples from various hematologic diseases.
MicroRNAs (miRNAs), which are short non-coding single-stranded RNAs of 18–24 mer in length, negatively regulate the target gene expression at the post-transcriptional stage (Bartel2004; Ambros2004). miRNAs act to inhibit protein translation or degrade transcripts of the target gene (Bartel2009). Many studies have demonstrated that abnormal expression of miRNAs is implicated in a variety of human diseases, including cancers (Calin and Croce2006; Takei et al.2011). Accordingly, the levels of various miRNAs have been measured in body fluids such as blood (serum or plasma), urine, cerebrospinal fluid, and ascites of patients with cancer (Cortez et al.2011; Etheridge et al.2011). Based on these measurements, some of the circulating miRNAs have been regarded as beneficial biomarkers to efficiently diagnose cancers. Recent reports have indicated that circulating miRNAs are quite stable even in an extracellular ribonuclease(s)-ubiquitous environment, such as in blood or other body fluids (Grasedieck et al.2012), since most of the miRNAs there are packaged into exosomes or microvesicles (Hunter et al.2008; Skog et al.2008), into lipoprotein particles with high density (Vickers et al.2011), or into apoptotic bodies (Zernecke et al.2009). These molecular packaging mechanisms protect the miRNAs in body fluids from degradation, and thus, particularly in hematological cancers, some blood-circulating miRNAs can become excellent biomarkers to directly mirror the origin of cancers (Grasedieck et al.2013).
Microscopic bone marrow (BM) examination is performed to diagnose many blood diseases, including leukemia, lymphoma, and multiple myeloma (Ryan2010). The BM generates the cells in blood, including red blood cells, white blood cells, and platelets. BM samples are ordinarily acquired by aspiration or trephine biopsy, and much information can be derived from the blood cells in BM. Like peripheral blood smears, the BM samples are often stored as smears at room temperature (Miura et al.2011). These smears also can be transported anywhere while remaining at room temperature, and thus are convenient for use in diagnoses.
Here we successfully isolated the small RNA fractions from BM smears, and showed that these fractions could be used to quantitate miRNAs via a typical real-time PCR method. In addition, we applied the small RNA fractions to a TaqMan real-time PCR miRNA array, and thereby identified many miRNAs whose levels were significantly altered in follicular lymphoma (FL), compared with the BM smears from normal donors. To our knowledge, this is the first report in which disease-associated miRNAs were identified from BM smears.
Materials and methods
A list of normal donors and FL patients with (B cell type) in the study
The extent of BM infiltration by lymphoma cells
Age of the BM smears from the preparation up to use (Stock time at room temperature)
Jul 9, 2008
2 years and 10 months
Jul 19, 2006
4 years and 10 months
Apr 16, 2008
3 years and 1 month
FL Patient 1
Aug 11, 2006
4 years and 9 months
FL Patient 2
Aug 29, 2008
2 years and 9 months
FL Patient 3
Apr 5, 2006
5 years and 1 month
FL Patient 4
Sep 5, 2008
2 years and 10 months
FL Patient 5
Sep 15, 2006
4 years and 10 months
Preparation of BM smears
BM samples were obtained via an aspiration and biopsy. BM smears were made by placing a drop of BM on a glass slide by the previously described method (Ryan2010). Table 1 provides a list of BM smears from patients with FL (B cell type) and normal donors, along with the date of sampling and preparation of smears. We also showed each age of the BM smears (a stock time from the preparation up to use). All of the BM smears without fixation were kept at room temperature until use.
Isolation of small RNAs from BM smears
Isolation of small RNAs, including miRNAs from BM smears, was performed using a mirVana miRNA Isolation Kit, or an RNAqueous-Micro Kit (a protocol for laser-captured microdissection samples) (Life Technologies Japan, Tokyo, Japan). We modified the manufacturer’s protocol for adequate isolation from BM smears.
For the isolation using the mirVana miRNA Isolation Kit, one BM smear slide was placed on a clean 100 mm dish, and lysis/binding buffer (300 μl) from the kit was dropped on the slide. Using a clean cell scraper and a pipette with a 1-ml tip, the dried smear component on the slide could be resolved but with high viscosity. The lysate from two BM smear slides was collected into a 2-ml tube, and the liquid volume was measured. A one-tenth volume (miRNA Homogenate Additive) of the lysate was added, and then the solution was mixed and incubated on ice for 10 minutes. An equal volume (acid-phenol chloroform) of the lysate was added, and then the solution was mixed with a vortex for 5 minutes, and centrifuged (10,000 rpm for 5 minutes). This extraction step can be repeated two or three times; the repetition was particularly effective for the already-stained BM smears. The water-phase was collected, and its liquid volume measured. Ethanol (a 1.25-times volume of the water-phase) was added, and the solution was mixed. All of the mixture was applied onto a micro-filter cartridge and centrifuged (the flow-through liquid was discarded). After washing the filter cartridge with Wash Solution 1 and 2/3, 100 μl of an elution solution heated at 95°C was added to the column, and 5 minutes later the desired solution was recovered by centrifugation.
For the isolation using the RNAqueous-Micro Kit, Lysis Solution (300 μl) from the kit was added onto one BM smear slide, and scraped using a clean cell scraper. For another BM smear slide, we repeated the procedure. The lysate (total 600 μl from two BM smear slides) was incubated at 42°C for 30 minutes, and then the supernatant by centrifugation was collected. Fifteen μl of LCM Additive from the kit was added to the supernatant (500 μl) and the solution was vigorously mixed, and then ethanol (1.25-times volume of the supernatant) was added with mixing. All of the mixture was applied onto a micro-filter cartridge and centrifuged (the flow-through liquid was discarded). After washing the cartridge with Wash Solution 1 and 2/3, 10 μl of an elution solution heated at 95°C was added to the column, and 5 minutes later the desired solution was recovered. The elution was repeated using another 10 μl of elution solution. Finally, 20 μl of the eluted solution was obtained.
Our modified methods are just matched for two BM smear slides (e.g., each liquid volume and handling, and column and tube size). The isolated small RNAs from two BM slides are enough to carry out several examinations such as qPCR, and array analysis. The critical points for the effective isolation are on ‘acid-phenol chloroform step’ to prevent and regulate high viscosity, which is peculiar to BM smears. The repetition of the step reduced their viscosity.
The RNA concentration of the eluted solution was determined by a NanoDrop ND-1000 spectrophotometer (Invitrogen), and its quality was examined using an Agilent 2100 Bioanalyzer (Agilent Technologies).
Quantitative reverse transcription-PCR (qRT-PCR) for miRNA
Small RNAs isolated from BM smears were subjected to qRT-PCR for miRNAs such as U6, miR-155, and let-7a. Each RNA sample (10 ng) was reverse-transcribed using a TaqMan MicroRNA RT Kit and TaqMan MicroRNA Assay (Applied Biosystems), and the obtained cDNA was analyzed using specific TaqMan probes (U6, Assay ID 001973; miR-155, Assay ID 000479; and let-7a Assay ID 000377) and TaqMan Universal PCR Master Mix as described previously (Takei et al.2011). All of the reactions and analyses were performed using a StepOne Real-Time PCR System (Applied Biosystems).
TaqMan real-time PCR miRNA array
Quality check of the isolated RNAs from normal donors and FL patients according to our proposed method
RNA concentration (ng/μl)
Total yield (μg)
FL Patient 1
FL Patient 2
FL Patient 3
FL Patient 4
FL Patient 5
Statistical analysis on TaqMan real-time PCR miRNA array was performed using the Mann-Whitney U test. Probability values were shown in each table and the values less than 0.01 (1 × 10-2) were considered to indicate significant differences.
Successful isolation of small RNAs from BM smears
Successful quantitative PCR analysis for miRNAs in small RNA fractions from BM smears
Using the isolated small RNA fractions, we performed quantitative PCR analysis for three representative miRNAs (U6, let-7a, and miR-155) with TaqMan probes. All three miRNAs were successfully amplified (Figure 1C), demonstrating that the miRNAs from BM smears can be quantified by PCR. The PCR curves were not notably different between the two kits, suggesting both small RNAs were equally functional. We decided to use the mirVana miRNA Isolation Kit for further study due to its simplicity.
Similar results were obtained in living cells of BM
The already-stained BM smears could also be used for quantitative PCR of the miRNAs
miRNAs with significant abnormal alterations were found in the smears from the patients with FL compared with normal donors
Significantly altered miRNAs (Top 20) in the patients with FL, compared with normal donors
2.6 × 10-6
1.6 × 10-5
1.7 × 10-5
5.1 × 10-5
6.7 × 10-5
5.2 × 10-5
4.5 × 10-5
1.8 × 10-4
2.3 × 10-4
7.1 × 10-5
1.1 × 10-4
2.4 × 10-4
5.1 × 10-5
3.3 × 10-4
2.2 × 10-5
3.4 × 10-5
5.4 × 10-5
6.2 × 10-4
5.0 × 10-5
7.4 × 10-4
3.2 × 10-5
6.4 × 10-5
6.0 × 10-5
4.9 × 10-5
3.5 × 10-4
5.9 × 10-5
6.2 × 10-4
5.8 × 10-4
3.9 × 10-5
3.2 × 10-4
5.3 × 10-4
6.0 × 10-5
5.4 × 10-4
7.5 × 10-5
5.1 × 10-5
8.8 × 10-4
2.9 × 10-4
5.2 × 10-4
2.3 × 10-4
2.0 × 10-4
Smear samples are easy to store and to transport at room temperature. Thus, they are handy to use. They provide much information for the diagnosis of many diseases, including hematologic diseases, and particularly hematological malignancies. In the present study, we successfully isolated small RNAs from BM smears of FL patients, and according to TaqMan real-time PCR miRNA array, we also successfully determined many miRNAs that were significantly altered in the patients compared with normal donors (Table 3 and Additional file1). To our knowledge, this is the first report in which disease-associated miRNAs were identified from BM smears.
The abnormal expression of miRNAs has been implicated in a variety of human diseases, including cancers. Circulating miRNAs have thus received much attention for their potential as stable blood-based biomarkers for detecting cancers Grasedieck et al.2013; Mitchell et al.2008; Hessvik et al.2013). Circulating miRNAs in body fluids are much stable due to their packaging into exosomes, microvesicles, or lipoproteins (Hunter et al.2008; Skog et al.2008; Vickers et al.2011). Regarding hematologic malignancies, the use of miRNA profiling for cancer biopsy samples from patients with FL has been reported (Roehle et al.2008; Lawrie et al.2009; Wang et al.2012; Leich et al.2011). However, circulating miRNAs in the BM of FL patients, especially in their BM smears, have not yet been reported. Based on a comparison of the previous reports (FL tissues; refs. Roehle et al.2008; Lawrie et al.2009; Wang et al.2012; Leich et al.2011) and our present report (BM smears from FL), the miRNAs that showed significant alterations in both cancer tissues and BM smears from FL compared with normal donors were as follows: the significantly decreased common miRNAs were miR-202 (Rank 18), and miR-139-5p (Rank 37); and the significantly increased miRNAs were miR-338-5p (Rank 1), miR-9 (Rank 21), and miR-330-3p (Rank 24). All of the other altered miRNAs in BM smears from FL patients, as shown in Table 3 and Additional file1, were newly identified in our study.
FL is regarded as one of the malignant lymphomas that actively invade into BM; however, we currently have no ideas for appropriate marker(s) to detect such invasion without biopsy. Further, the mechanism(s) by which FL cells so readily invade into BM remains poorly understood. The results of the present study suggest that the measurement of some miRNA expression level(s) in BM smears can be used to correctively predict and diagnose FL without lymph node biopsy, although much investigation remains to be performed prior to the actual application for simple diagnosis of FL.
The stability of miRNAs in formalin-fixed paraffin-embedded (FFPE) tissues has already been reported, and thus many studies have shown that archived FFPE tissue samples can be used for PCR-based miRNA analysis (Li et al.2007; Xi et al.2007; Doleshal et al.2008; Kolbert et al.2013), or next-generation sequencing (Kelly et al.2013; Meng et al.2013). Here, the RIN of RNA fractions isolated from FFPE tissues was generally low (approximately 2.4–2.6), indicating that the RNAs were heavily fragmented. This, in turn, means that the small RNAs isolated from BM smears and FFPE tissues are quite similar to each other, and they might be suitable for miRNA quantitation rather than gene expression analysis. Indeed, our BM smears are not suitable for determining mRNA expression levels via quantitative RT-PCR (data not shown).
Our isolation method provides a new avenue for the analysis of miRNAs in BM smear samples from patients with various diseases, particularly blood malignancies. Using this method, numerous miRNAs with potential as diagnostic markers in BM may be identified in the near future.
We thank Drs. Kazuo Kita, Takayuki Okubo, and Kaori Yasuda for their helpful suggestions regarding the experiments and the manuscript. We also thank Ms. Naomi Maruyama for her excellent technical assistance.
This work was supported in part by a grant from the Research Institute for Radiation Biology and Medicine, Hiroshima University, and by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (17016030) and from the Japan Society for the Promotion of Science (21590305 and 24590348).
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