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Updated: Jan 4, 2026

Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
Published on: November 28, 2015
Neutral effect of Glioma-associated oncogene-1 expression on survival in myelofibrosis
Marko Lucijanic1, Ana Livun2, Katarina Marija Tupek2
1Hematology Department, University Hospital Dubrava, Av. Gojka Suska 6, 10000, Zagreb, Croatia. markolucijanic@yahoo.com.
Abstract:
This study retrospectively analyzed glioma-associated oncogene 1 (GLI‑1) mRNA expression in unfractionated bone marrow aspirates of 32 patients with myelofibrosis and 16 controls. It was found that GLI‑1 expression did not significantly differ between primary, secondary myelofibrosis and controls (median difference in threshold cycles ∆CT 7.2, 7.3 and 6.9, respectively; P = 0.864), as well as that survival curves of myelofibrosis patients with higher/lower GLI‑1 expression showed multiple overlaps and overall comparable course (P = 0.651). The results suggest that general upregulation of GLI‑1 does not seem to be a feature of the disease and are in line with modest biological and clinical effects observed with inhibitors of Hedgehog signaling pathway in patients with myelofibrosis.
Insights
Glioma-associated oncogene 1 (GLI-1) mRNA expression was similar in myelofibrosis patients and controls. Higher or lower GLI-1 levels did not impact myelofibrosis patient survival, suggesting GLI-1 is not a disease hallmark.
Area of Science:
- Oncology
- Hematology
- Molecular Biology
Background:
- Myelofibrosis is a serious bone marrow disorder.
- The role of Hedgehog signaling pathway, including GLI-1, in myelofibrosis is not fully understood.
- Investigating GLI-1 expression may reveal therapeutic targets.
Purpose of the Study:
- To investigate the expression levels of glioma-associated oncogene 1 (GLI-1) mRNA in patients with myelofibrosis.
- To determine if GLI-1 expression correlates with disease type or patient survival.
- To assess the potential of GLI-1 as a biomarker or therapeutic target in myelofibrosis.
Main Methods:
- Retrospective analysis of bone marrow aspirates from 32 myelofibrosis patients and 16 controls.
- Quantification of GLI-1 mRNA expression using quantitative real-time PCR (qRT-PCR).
- Statistical comparison of GLI-1 levels between patient groups and controls, and correlation with survival data.
Main Results:
- No significant difference in GLI-1 mRNA expression was observed between primary myelofibrosis, secondary myelofibrosis, and control groups (P=0.864).
- Survival analysis showed comparable outcomes for myelofibrosis patients with higher versus lower GLI-1 expression (P=0.651).
- These findings indicate that GLI-1 is not generally upregulated in myelofibrosis.
Conclusions:
- General upregulation of GLI-1 is not a characteristic feature of myelofibrosis.
- The modest clinical effects of Hedgehog signaling pathway inhibitors in myelofibrosis align with these findings.
- GLI-1 may not serve as a significant prognostic marker or direct therapeutic target in myelofibrosis based on expression levels.
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