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Loss of histone H3K27me3 identifies a subset of meningiomas with increased risk of recurrence

Overview of attention for article published in Acta Neuropathologica, April 2018
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  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (82nd percentile)
  • Above-average Attention Score compared to outputs of the same age and source (60th percentile)

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Title
Loss of histone H3K27me3 identifies a subset of meningiomas with increased risk of recurrence
Published in
Acta Neuropathologica, April 2018
DOI 10.1007/s00401-018-1844-9
Pubmed ID
Authors

Leah M. Katz, Thomas Hielscher, Benjamin Liechty, Joshua Silverman, David Zagzag, Rajeev Sen, Peter Wu, John G. Golfinos, David Reuss, Marian Christoph Neidert, Hans-Georg Wirsching, Peter Baumgarten, Christel Herold-Mende, Wolfgang Wick, Patrick N. Harter, Michael Weller, Andreas von Deimling, Matija Snuderl, Chandra Sen, Felix Sahm

Abstract

Epigenetic patterns on the level of DNA methylation have already been shown to separate clinically relevant subgroups of meningiomas. We here set out to identify potential prognostic implications of epigenetic modification on the level of histones with focus on H3K27 trimethylation (H3K27me3). H3K27me3 was assessed by immunohistochemistry on 232 meningiomas from 232 patients. In 194 cases, trimethylation was detected in tumor cells. In 25 cases, staining was limited to vessels while all tumor cells were negative. Finally, 13 cases yielded equivocal staining patterns. Reduced abundance of H3K27me3 in cases with staining limited to vessels was confirmed by mass spectrometry on a subset of cases. Lack of staining for H3K27me3 in all tumor cells was significantly associated with more rapid progression (p = 0.009). In line, H3K27me3-negative cases were associated with a DNA methylation pattern of the more aggressive types among the recently introduced DNA methylation groups. Also, NF2 and SUFU mutations were enriched among cases with complete lack of H3K27me3 staining in tumor cells (p < 0.0001 and p = 0.029, respectively). H3K27me3 staining pattern added significant prognostic insight into WHO grade II cases and in the compound subset of WHO grade I and II cases (p = 0.04 and p = 0.007, respectively). However, it did not further stratify within WHO grade III cases. Collectively, these data indicate that epigenetic modifications beyond DNA methylation are involved in the aggressiveness of meningioma. It also suggests that H3K27me3 immunohistochemistry might be a useful adjunct in meningioma diagnostics, particularly for cases with WHO grade II histology or at the borderline between WHO grade I and II.

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X Demographics

The data shown below were collected from the profiles of 19 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 81 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 81 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 10 12%
Researcher 8 10%
Student > Doctoral Student 7 9%
Student > Bachelor 7 9%
Other 6 7%
Other 13 16%
Unknown 30 37%
Readers by discipline Count As %
Medicine and Dentistry 30 37%
Biochemistry, Genetics and Molecular Biology 9 11%
Neuroscience 4 5%
Nursing and Health Professions 3 4%
Economics, Econometrics and Finance 1 1%
Other 2 2%
Unknown 32 40%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 12. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 02 July 2019.
All research outputs
#3,030,761
of 25,724,500 outputs
Outputs from Acta Neuropathologica
#744
of 2,550 outputs
Outputs of similar age
#59,666
of 344,245 outputs
Outputs of similar age from Acta Neuropathologica
#16
of 40 outputs
Altmetric has tracked 25,724,500 research outputs across all sources so far. Compared to these this one has done well and is in the 88th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 2,550 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 17.4. This one has gotten more attention than average, scoring higher than 70% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 344,245 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 82% of its contemporaries.
We're also able to compare this research output to 40 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 60% of its contemporaries.