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Ardinata, Dedi, Alferraly, Tengku Ibnu, Yosi, Ariyati, Pase, Muhammad Aron. (1405). Insulin Resistance and Cutaneous Squamous Cell Carcinoma: A Narrative Review of Molecular Mechanisms. سامانه مدیریت نشریات علمی, (), -. doi: 10.30476/ijms.2025.106644.4091
Dedi Ardinata; Tengku Ibnu Alferraly; Ariyati Yosi; Muhammad Aron Pase. "Insulin Resistance and Cutaneous Squamous Cell Carcinoma: A Narrative Review of Molecular Mechanisms". سامانه مدیریت نشریات علمی, , , 1405, -. doi: 10.30476/ijms.2025.106644.4091
Ardinata, Dedi, Alferraly, Tengku Ibnu, Yosi, Ariyati, Pase, Muhammad Aron. (1405). 'Insulin Resistance and Cutaneous Squamous Cell Carcinoma: A Narrative Review of Molecular Mechanisms', سامانه مدیریت نشریات علمی, (), pp. -. doi: 10.30476/ijms.2025.106644.4091
Ardinata, Dedi, Alferraly, Tengku Ibnu, Yosi, Ariyati, Pase, Muhammad Aron. Insulin Resistance and Cutaneous Squamous Cell Carcinoma: A Narrative Review of Molecular Mechanisms. سامانه مدیریت نشریات علمی, 1405; (): -. doi: 10.30476/ijms.2025.106644.4091

Insulin Resistance and Cutaneous Squamous Cell Carcinoma: A Narrative Review of Molecular Mechanisms

Iranian Journal of Medical Sciences
مقالات آماده انتشار، اصلاح شده برای چاپ، انتشار آنلاین از تاریخ 16 تیر 1405    اصل مقاله (724.35 K)
نوع مقاله: Review Article
شناسه دیجیتال (DOI): 10.30476/ijms.2025.106644.4091
نویسندگان
Dedi Ardinata1؛ Tengku Ibnu Alferraly* 2؛ Ariyati Yosi3؛ Muhammad Aron Pase4
1Department of Physiology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia
2Department of Anatomic Pathology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia
3Department of Dermatology and Venereology, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia
4Department of Internal Medicine, Faculty of Medicine, Universitas Sumatera Utara, Medan, Indonesia
چکیده
Although the association between diabetes and cutaneous squamous cell carcinoma (cSCC) is well recognized, the specific role of insulin resistance (IR) as an independent driver of cSCC pathogenesis remains underexplored. This review synthesized emerging evidence on the ultraviolet (UV)-independent molecular mechanisms by which IR promotes cSCC initiation and progression. Hyperinsulinemia activates the insulin-like growth factor-1 receptor (IGF-1R), which triggers both the mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) and phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) pathways, stimulating keratinocyte proliferation and suppressing apoptosis. In parallel, hyperglycemia-driven formation of advanced glycation end products (AGEs) and oxidative stress cause deoxyribonucleic acid (DNA) damage and impair tumor suppressor functions, notably that of tumor protein p53 (TP53). The resulting reactive oxygen species (ROS) activate nuclear factor-kappa B (NF-κB), establishing a chronic inflammatory milieu that remodels the tumor microenvironment through cytokines, including interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α), and by upregulating matrix metalloproteinases (MMPs). These processes collectively facilitate the malignant transformation of actinic keratosis (AK) to invasive cSCC. The analysis in the present study identified novel therapeutic targets and reaffirmed the importance of further studies on microbiome interactions and lifestyle interventions for IR-associated cSCC.

تازه های تحقیق

Dedi Ardinata (Google Scholar)
Tengku Ibnu Alferraly (Google Scholar)

کلیدواژه‌ها
Insulin resistance؛ Keratinocytes؛ Oxidative stress؛ Squamous cell؛ Carcinoma
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