» Articles » PMID: 37940743

The Value of GLI1 and P16 Immunohistochemistry in the Premolecular Screening for GLI1-altered Mesenchymal Neoplasms

Abstract

Mesenchymal neoplasms with GLI1 alterations have recently been reported in several anatomic locations. Their morphology and immunohistochemistry (IHC) are nonspecific, making their recognition a true challenge. To assess the diagnostic value of GLI1 and p16 IHC for identifying GLI1-altered neoplasms, we evaluated 12 such neoplasms (6 GLI1-amplified and 6 with GLI1-fusions) using the GLI1 IHC. Additionally, we evaluated some of their morphological and molecular mimickers, including glomangiomas, Ewing sarcomas (ES), myxoid liposarcomas, and MDM2/CDK4-amplified sarcomas (well-differentiated liposarcoma/WDLPS, dedifferentiated liposarcoma/DDLPS, and intimal sarcoma). All successfully tested GLI1-altered tumors (11/11) demonstrated at least moderate/strong nuclear and/or cytoplasmic GLI1 IHC positivity. GLI1-amplified tumors exhibited a moderate/strong predominantly nuclear staining, compared to a moderate, patchy, and predominantly cytoplasmic GLI1 positivity in GLI1-fusion tumors. Among their mimics, GLI1 immunoreactivity, either cytoplasmic or nuclear, was observed in intimal sarcoma (3/3) and WDLPS/DDLPS (22/25). GLI1 IHC demonstrated 92% sensitivity and 90.8% specificity in diagnosing GLI1-altered neoplasms. Strong/moderate nuclear/cytoplasmic p16 immunoexpression was noted in all GLI1-amplified tumors compared to none of fused cases. Overall, the GLI1/p16 combination demonstrated a sensitivity and specificity of 100% and 93% for GLI1-amplified tumors. In conclusion, we confirm that GLI1 IHC represents a good, quick, and cheap helpful screening tool. The inclusion of p16 may aid in pre-screening for potential GLI1-amplified neoplasms and provide insights on which tumors warrant further molecular testing.

Citing Articles

-Rearranged Enteric Tumors: Updates on Clinicopathologic and Molecular Genetics Features.

Younes A, Mejbel H Cells. 2025; 14(2).

PMID: 39851545 PMC: 11763425. DOI: 10.3390/cells14020118.


GLI1::FOXO4-rearranged kidney tumors: a potentially distinct renal subtype within the spectrum of GLI1-altered tumors?.

Pancsa T, Klubickova N, Dashti N, Machado I, Llombart-Bosch A, Linos K Virchows Arch. 2024; .

PMID: 39688667 DOI: 10.1007/s00428-024-03998-z.


The Combined Immunohistochemical Expression of GLI1 and BCOR in Synovial Sarcomas for the Identification of Three Risk Groups and Their Prognostic Outcomes: A Study of 52 Patients.

Giner F, Medina-Ceballos E, Lopez-Reig R, Machado I, Lopez-Guerrero J, Navarro S Int J Mol Sci. 2024; 25(14).

PMID: 39062853 PMC: 11276717. DOI: 10.3390/ijms25147615.


Molecularly defined sinonasal malignancies: an overview with focus on the current WHO classification and recently described provisional entities.

Skalova A, Agaimy A, Bradova M, Vander Poorten V, Hanna E, Guntinas-Lichius O Virchows Arch. 2024; 484(6):885-900.

PMID: 38491228 PMC: 11186917. DOI: 10.1007/s00428-024-03775-y.


Soft Tissue Sarcomas with Chromosomal Alterations in the 12q13-15 Region: Differential Diagnosis and Therapeutic Implications.

Lavernia J, Claramunt R, Romero I, Lopez-Guerrero J, Llombart-Bosch A, Machado I Cancers (Basel). 2024; 16(2).

PMID: 38275873 PMC: 10814159. DOI: 10.3390/cancers16020432.

References
1.
Liu Y, Huang J, Sun J, Su M, Yang D, Zhao M . GLI1 amplified/fused mesenchymal tumor: A case report and review of the literature. Oral Oncol. 2022; 129:105897. DOI: 10.1016/j.oraloncology.2022.105897. View

2.
Agaram N, Zhang L, Sung Y, Singer S, Stevens T, Prieto-Granada C . GLI1-amplifications expand the spectrum of soft tissue neoplasms defined by GLI1 gene fusions. Mod Pathol. 2019; 32(11):1617-1626. PMC: 6821565. DOI: 10.1038/s41379-019-0293-x. View

3.
Mosquera J, Sboner A, Zhang L, Chen C, Sung Y, Chen H . Novel MIR143-NOTCH fusions in benign and malignant glomus tumors. Genes Chromosomes Cancer. 2013; 52(11):1075-87. PMC: 3889711. DOI: 10.1002/gcc.22102. View

4.
Rollins B, Cassarino D, Lindberg M . Primary cutaneous epithelioid mesenchymal neoplasm with ACTB-GLI1 fusion: a case report. J Cutan Pathol. 2021; 49(3):284-287. DOI: 10.1111/cup.14152. View

5.
Dahlen A, Fletcher C, Mertens F, Fletcher J, Perez-Atayde A, Hicks M . Activation of the GLI oncogene through fusion with the beta-actin gene (ACTB) in a group of distinctive pericytic neoplasms: pericytoma with t(7;12). Am J Pathol. 2004; 164(5):1645-53. PMC: 1615655. DOI: 10.1016/s0002-9440(10)63723-6. View