A method currently used by thousands of laboratories across the nation to preserve tissue could render samples useless over time for a common test to assess gene activity.
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- In his new study @HopkinsMedicine’s Dr. De Marzo discovered how a method of tissue preservation may render samples useless over time – Click to Tweet
*Correction: This news release was updated March 15, 2018 to correct several errors related to the methodology, including tissue storage temperatures.
A method currently used by thousands of laboratories across the country to preserve tissue could render samples useless over time for a common test to assess gene activity, a study led by Johns Hopkins researchers suggests. The findings, published in the November 2, 2017 American Journal of Clinical Pathology, could eventually lead to significant changes in how tissues are stored for clinical and research purposes.
For more than a century, biomedical scientists have been preserving some tissue samples harvested from patients and research animals in the same way: by soaking these tissues in the preservative formalin and then embedding them in blocks of a wax called paraffin. Perhaps more than a billion of these blocks containing formalin-fixed paraffin-embedded (FFPE) tissues are thought to be housed in labs around the world.
“We have a warehouse of these blocks at Johns Hopkins that go back to at least the 1918 flu pandemic,” says study leader Angelo M. De Marzo, M.D., Ph.D., professor of pathology at the Johns Hopkins University School of Medicine and associate director of cancer research pathology at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.
The gold standard has been to leave these FFPE blocks at room temperature. Then, when laboratories are ready to use the samples, they cut thin slices of the embedded tissue and place them on slides to stain for the presence of various molecules. One test that’s become increasingly useful is RNA in situ hybridization (RISH), which assesses the activity of particular genes. Those findings might be able to tell doctors or researchers whether certain viruses are present in tissue or how a patient’s cells responded to particular therapies, for example.
Several years ago, De Marzo, who studies prostate cancer, and his colleagues noticed that prostate tissue samples that should have roughly the same amount of activity in specific genes had wide variations in those genes’ RISH signals. “It occurred to us that the blocks stored for longer might be producing less signal because their RNA was degrading,” he says.
To test that theory, one of the study’s authors, Qizhi Zheng, collected 25 FFPE blocks containing tissue samples taken from radical prostatectomies of prostate cancer patients. When the researchers performed RISH on these slides to look at the activity of four prostate and prostate cancer-relevant genes, they found a significantly lower visible signal in the slides obtained from the older FFPE blocks compared to the younger ones.
To confirm these findings, the study’s lead authors, Javier A. Baena-Del Valle, along with Zheng, performed a similar test on tissue microarrays (TMAs)—multiple small cores of tissue embedded in the same block. This time, they used computer image analysis to get an unbiased assessment. Once again, the signal strength for the probed genes declined over time.
The researchers performed additional tests with TMAs containing tissue from human patients grown in mice—a technique called patient-derived xenografts, often used in cancer research—and obtained from samples sent from colleagues at the University of Washington. All showed the same age-weakening results.
However, when De Marzo and his colleagues compared fresh tissues that were flash-frozen and stored at -80 degrees Celsius (an approach used on a small subset of tissues at specialized research institutions to preserve tissues) right when they were harvested from patients 10 years ago to adjacent tissue from the same patients that was embedded in FFPE blocks over the decade, they found a dramatic difference in RISH signal—while those stored in the freezer produced a strong signal for the probed genes, those stored at room temperature showed a markedly weaker signal. Additional tests showed similarly strong RISH signals for sections of newly-acquired tissue that were cut and placed on slides before being frozen for five years at -20 degrees Celsius (about the same temperature as most household freezers) compared to FFPE tissue blocks from the same patient that were stored at room temperature and cut onto slides five years later.
Finally, the authors prepared a TMA using new FFPE tissue blocks and cut the TMA slides and stored them for up to two years, either at room temperature or -20 degrees Celsius. They found that those stored in the freezer showed significantly higher levels of RISH signals compared with those stored at room temperature.
Together, these findings suggest that storing tissues at room temperature could weaken RISH signals over time, a finding that could give misleading results. For example, De Marzo explains, RISH results might reveal low or no activity of targeted genes in older tissue samples even though activity of those genes was high at harvest.
“There’s no reason to think that this isn’t happening around the world with the millions of tissue samples that are harvested every year,” he says. “These blocks are thought to be a treasure trove of data, but with every year that goes by, they might lose their effectiveness for this technique.”
Although freezing does appear to preserve function for RISH, De Marzo adds, the long-term answer won’t be to freeze every tissue sample—there isn’t room or other resources to house these numerous tissue samples. Thus, he says, researchers may want to start freezing select samples they predict to be especially useful rather than storing them at room temperature.
Other researchers who participated in this study include Javier A. Baena-Del Valle, Qizhi Zheng, Jessica L. Hicks, Helen Fedor, Bruce J. Trock, Toby C. Cornish, and Karen S. Sfanos, all of Johns Hopkins, and Colm Morrissey and Eva Corey, of the University of Washington, Seattle.
This work was supported by the US Department of Defense (DoD) (PCRP W81XWH-10-2-0056, PCRP W81XWH-10-2-0046), Prostate Cancer Biorepository Network, and National Cancer Institute/National Institutes of Health (Prostate SPORE P50CA58236, 5P30CA006973).