AI Article Synopsis

  • Nodular fasciitis (NF) is known to be self-limited, but its underlying mechanisms are still unclear; the study found that younger cases of NF show a higher percentage of USP6 break-apart signals compared to older cases.
  • It was shown that a higher percentage of USP6 break-apart signals correlates negatively with the lifetime of the tumor while having a positive relationship with mitotic counts, indicating a potential mechanism for NF's self-limiting behavior.
  • The research supports a negative feedback loop involving USP6 that may lead to apoptosis and cellular aging in NF tumors, highlighting the need for careful interpretation of genetic data for clinical diagnostics.

Article Abstract

The self-limited nature of nodular fasciitis (NF) is well-known but its precise mechanism has not yet been clarified. We observed that "young" NF (preoperative duration <1 month) consistently contains a higher percentage (~80%) of USP6 break-apart FISH signals than "old" NF (preoperative duration >3 months) (~20%). Thus, we hypothesized that our original observation may reflect a connection with the self-limited nature of NF. Seventeen cases with reliable data concerning the onset were selected, thus approximating the lifetime of each tumor. Besides the USP6 interphase FISH examination, we also checked the most common MYH9-USP6 fusion using RT-PCR. Because of the known pathways of the tumorigenesis of NF, the mRNA level of USP6, TRAIL, IFN-beta, JAK1, STAT1, STAT3, JUN, and CDKN2A was measured using qRT-PCR. Regarding proteins, USP6, p16, p27, TRAIL, and IFN-beta were examined using immunohistochemistry. Targeted gene panel next-generation sequencing (NGS) of three cases was additionally performed. We found a strong negative correlation (p = 0.000) between the lifetime and percentage of USP6 break-apart signals and a strong positive relationship (p = 0.000) between USP6 break-apart signals and mitotic counts. Results of immunostainings, along with qRT-PCR results, favored the previously-suggested USP6-induced negative feedback mechanism through activation of TRAIL and IFN-beta, likely resulting in apoptosis and senescence of tumor cells harboring USP6 fusions. Targeted-NGS resulted in the detection of several variants, but no additional recurrent changes in the pathogenesis of these tumors. We revealed on a cellular level the USP6-induced negative feedback mechanism. In conclusion, we emphasize that in "old" NF, the percentage of USP6 break-apart FISH signals can be as low as 14-27% which can be very important from a differential diagnostic point of view. We emphasize that a careful examination and interpretation of the NGS data is needed before clinical decision-making on treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592838PMC
http://dx.doi.org/10.1038/s41379-021-00883-xDOI Listing

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