Protein Kinase CK2 Inhibition Represents a Pharmacological Chance for the Treatment of Skin Diseases
Michele Scuruchi, Desirèe Speranza, Giuseppe Bruschetta, Federico Vaccaro, Mariarosaria Galeano, Giovanni Pallio, Mario Vaccaro, Francesco Borgia, Federica Li Pomi, Massimo Collino, Natasha Irrera

TL;DR
This paper reviews how inhibiting the protein kinase CK2 could offer new treatments for skin diseases like psoriasis and skin cancer.
Contribution
The paper highlights CK2 as a novel pharmacological target for dermatological therapies and summarizes preclinical evidence for its inhibition.
Findings
CK2 overactivation contributes to psoriasis through STAT3 and Akt pathways.
CK2 inhibitors like CX-4945 show therapeutic potential in preclinical models of skin diseases.
Combination therapies with CK2 inhibitors may enhance treatment efficacy and reduce side effects.
Abstract
Protein kinase CK2 has emerged as a pivotal regulator of cellular processes involved in skin homeostasis, including cell proliferation, differentiation and inflammatory response regulation. In fact, CK2 activity dysregulation is implicated in the pathogenesis of different skin diseases, such as psoriasis, cancer and inflammatory dermatoses. CK2 overactivation fosters keratinocyte proliferation and pro-inflammatory cytokine production through the STAT3 and Akt pathways in psoriasis, thus contributing to epidermal hyperplasia and inflammation. In the realm of oncology, CK2 overexpression correlates with tumor progression, facilitating cell survival and metastasis in melanoma and non-melanoma skin cancers. Pharmacological inhibition of CK2 has demonstrated therapeutic potential, with CX-4945 (Silmitasertib) as the most studied adenosine triphosphate-competitive inhibitor (ATP-competitive…
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Taxonomy
TopicsPsoriasis: Treatment and Pathogenesis · PI3K/AKT/mTOR signaling in cancer · NF-κB Signaling Pathways
