Apigenin Induced Apoptosis by Downregulating Sulfiredoxin Expression in Cutaneous Squamous Cell Carcinoma

Author:

Wang Wenhua123,Liu Xin12,Zhang Zhibao12,Yin Mingzhu124,Chen Xiang124,Zhao Shuang124ORCID,Wu Lisha1245ORCID

Affiliation:

1. Department of Dermatology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008 Hunan, China

2. Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008 Hunan, China

3. Department of Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, Hunan 410013, China

4. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008 Hunan, China

5. Institute of Medical Sciences, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, 410008 Hunan, China

Abstract

Cutaneous squamous cell carcinoma (cSCC) is the second carcinoma in nonmelanoma skin cancer (NMSC). Sulfiredoxin (Srx) is an antioxidant protein with a role in maintaining redox homeostasis. And Srx has an oncogenic role in skin tumorigenesis. In the current study, we found that apigenin, as a natural flavonoid, downregulated the expression of Srx protein in cSCC cell lines. Apigenin also inhibited the ability of cell proliferation and migration and induced apoptosis in cSCC cell lines. Our results also showed that apigenin induced apoptosis via the activation of the mitogen-activated protein kinase (MAPK) signaling pathway, as well as downregulated Srx expression in cSCC cell lines. Importantly, the effect of downregulation Srx by apigenin has been rescued with the inhibitor of the MAPK signaling pathway intervention. And induced apoptosis by apigenin was partially attenuated by the addition of MAPK inhibitor, Binimetinib. Our research revealed that apigenin induced apoptosis by downregulation of Srx expression through regulating the MAPK signaling pathway in cSCC cells, thus providing evidence of its applicability as a potentially effective therapeutic agent for cSCC treatment.

Funder

Central South University

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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