Caspase 3 and Cleaved Caspase 3 Expression in Tumorogenesis and Its Correlations with Prognosis in Head and Neck Cancer: A Systematic Review and Meta-Analysis.
Fábio França-Vieira E SilvaMaría Elena Padín-IruegasVito Carlo Alberto CaponioAlejandro Ismael Lorenzo-PousoPaula Saavedra-NievesCintia Micaela Chamorro-PetronacciJose Manuel Suaréz-PeñarandaMário Pérez-SayánsPublished in: International journal of molecular sciences (2022)
Head and neck cancer (HNC) is an ascending and agressive disease. The search for new molecular markers is emerging to solve difficulties in diagnosis, risk management, prognosis and effectiveness of treatments. Proteins related to apoptotic machinery have been identified as potential biomarkers. Caspase 3 is the main effector caspase and has a key role in apoptosis. The objective of this systematic review and meta-analysis is to review studies that analyze changes in Caspase 3 and Cleaved Caspase 3 expression both in oral premalignant disorders (OPMD) as well as in head and neck cancer (HNC). This study also proposes to review the prognostic values associated with HNC according to the expression of Caspase 3. Medline (via PubMed), EMBASE, Scopus, Cochrane, Web of Science and Grey Literature Database were screened from inception to june of 2022 and 18 studies were selected and 8 were included in the prognostic meta-analysis. Results related to the comparison of Caspase 3 expression demonstrated similar expression of Caspase 3 in HNC, with an average of 51.9% (9.5-98.1) showing high/moderate expression compared to 45.7% (14.6-84.7) in OPMD. Of interest, Cleaved Caspase 3 resulted incresed in HNC when compared with OPMD, being 73.3% (38.6-88.3) versus 22.9% (7.1-38.7). Pooled Fixed effect of HR values (95% CI) for OS related to Caspase 3 IHC expression in HNC patients was 1.48 (95% CI 0.95-2.28); also, the rate of heterogeneity was low, as revealed by I 2 = 31%. For DFS was 1.07 (95% CI 0.79-1.45) with I 2 = 0% and DSS showed a HR of 0.88 (95% CI 0.69-1.12) with I 2 = 37%. Caspase 3 and Cleaved Caspase 3 expression could be linked with malignancy progression, but the expression of Caspase 3 did not influence the prognosis of patients with HNC.
Keyphrases
- cell death
- poor prognosis
- induced apoptosis
- systematic review
- cell cycle arrest
- binding protein
- endoplasmic reticulum stress
- public health
- randomized controlled trial
- emergency department
- clinical trial
- dendritic cells
- end stage renal disease
- ejection fraction
- signaling pathway
- chronic kidney disease
- single cell
- cell proliferation
- multiple sclerosis
- pulmonary arterial hypertension
- peritoneal dialysis
- study protocol
- pulmonary artery
- regulatory t cells