Survivin as a Novel Biomarker in the Pathogenesis of Acne Vulgaris and Its Correlation to Insulin-Like Growth Factor-I.
Hanan A AssafWafaa M Abdel-MagedBakheet E M ElsadekMohammed H HassanMohamed A AdlySoher A AliPublished in: Disease markers (2016)
Survivin, a member of the inhibitor of apoptosis protein family, has an important role in cell cycle regulation. Insulin-like growth factor-I (IGF-I) is a polypeptide hormone with wide range of biologic effects including stimulation of lipogenesis in sebaceous glands. Their overexpression in some fibrotic disorders suggests a possible implication of both IGF-I and survivin in the pathogenesis of acne and/or acne scars. The current study aimed to assess and correlate serum levels of IGF-I and survivin in patients with active acne vulgaris and postinflammatory acne scars and to evaluate their lesional expressions in comparison to healthy controls. Serum IGF-I and survivin were estimated using commercially available ELISA kits and their tissues expressions were investigated using Western blotting. Our findings suggest that IGF-I and survivin could play potential roles in the pathogenesis of active acne vulgaris and more importantly in postinflammatory acne scars with significant positive correlation coefficient between serum levels of IGF-I and survivin which support IGF-I-/PI3K-/AKT-mediated downregulation of nuclear expression of FoxO transcription factors resulting in enhanced survivin expression.
Keyphrases
- pi k akt
- cell proliferation
- signaling pathway
- cell cycle arrest
- binding protein
- cell cycle
- growth hormone
- hidradenitis suppurativa
- transcription factor
- poor prognosis
- gene expression
- rheumatoid arthritis
- oxidative stress
- magnetic resonance
- adipose tissue
- climate change
- magnetic resonance imaging
- long non coding rna
- platelet rich plasma
- risk assessment
- systemic sclerosis
- protein protein
- single molecule
- metabolic syndrome