This paper performs a cross-species transcriptome meta-analysis to identify conserved gene expression changes following anterior cruciate ligament rupture. It integrates datasets from human, mouse, dog, and rabbit studies using rigorous differential expression methods ().
The authors highlight genes such as CEMIP, VMP1, ADAMTS12, and TOP2A as robustly altered across species, suggesting their potential as translational biomarkers.
This paper () leverages publicly available RNA-seq datasets to address a significant clinical and translational challenge in orthopedics.
The study identified a panel of 210 genes with consistent expression changes. Notably, high Stouffer values were reported for genes including:
| Gene | Stouffer Value | Std Deviation | p Adjusted |
|---|---|---|---|
| CEMIP | 25.3357199 | 9.71226471 | 2.71 Γ 10^-139 |
| VMP1 | 23.057659 | 9.14444267 | 8.63 Γ 10^-116 |
| ADAMTS12 | 22.5712722 | 9.84778032 | 4.36 Γ 10^-111 |
| TOP2A | 21.1795111 | 4.02365932 | 6.20 Γ 10^-98 |
| ASPM | 20.2395895 | 3.78516438 | 1.54 Γ 10^-89 |
| FAP | 19.6239809 | 8.77073799 | 2.89 Γ 10^-84 |
| OLFML2B | 19.4848792 | 9.73187037 | 3.87 Γ 10^-83 |
| BUB1B | 18.7945286 | 4.77117528 | 1.95 Γ 10^-77 |
| MKI67 | 18.4529349 | 4.88371517 | 1.04 Γ 10^-74 |
| CCNB2 | 17.9602446 | 3.21936435 | 7.62 Γ 10^-71 |
This table clearly illustrates the statistical robustness of the key genes, underpinning the hypothesis that conserved molecular responses drive ACL rupture pathology across species.
The study robustly identifies conserved gene expression changes following ACL rupture. Its findings underscore the potential utility of animal models to guide translational research and therapeutic target discovery in human ACL injuries. However, further experimental validation is warranted to address dataset heterogeneity and species-specific variability.
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