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7-Epitaxol induces apoptosis in cisplatin-resistant head and neck squamous cell carcinoma via suppression of AKT and MAPK signalling

Yang Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan|
Jiunn-Liang (7402678479) | Ming-Ju (56520882800); Ko | Hsin-Yu (55929540200); Hsieh Department of Medical Oncology and Chest Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan| Yi-Ching (57143613400); Ho Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan| Yu-Sheng (57143546500); Chuang Ph.D. Program in Tissue Engineering and Regenerative Medicine, College of Medicine, National Chung Hsing University, Taichung, Taiwan| Chia-Chieh (57193152481); Lo Oral Cancer Research Center, Changhua Christian Hospital, Changhua, Taiwan| Mu-Kuan (8428112400); Lin Department of Otorhinolaryngology, Head and Neck Surgery, Changhua Christian Hospital, Changhua, Taiwan| Bharath Kumar (55946560300); Chen Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City, Viet Nam| Hui-Ju (57955613200); Velmurugan Department of Dermatology, Changhua Christian Hospital, Changhua, Taiwan|

Journal of Cellular and Molecular Medicine Số 23, năm 2022 (Tập 26, trang 5807-5819)

ISSN: 15821838

ISSN: 15821838

DOI:

Tài liệu thuộc danh mục:

Article

English

Tóm tắt tiếng anh
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide. Although cisplatin-based chemotherapy is commonly used in HNSCC, frequent development of cisplatin resistance is a potential cause of poor HNSCC prognosis. In the present study, we investigated the anticancer efficacy of a major paclitaxel metabolite namely 7-Epitaxol in cisplatin-resistant HNSCC. The findings revealed that 7-Epitaxol exerts cytotoxic effects in cisplatin-resistant HNSCC cell lines by inducing cell cycle arrest and intrinsic and extrinsic apoptotic pathways. Specifically, 7-Epitaxol increased Fas, TNF-R1, DR5, DcR3 and DcR2 expressions, reduced Bcl-2 and Bcl-XL (anti-apoptotic proteins) expressions, and increased Bid and Bim L/S (pre-apoptotic proteins) expressions, leading to activation of caspase-mediated cancer cell apoptosis. At the upstream cell signalling level, 7-Epitaxol reduced the phosphorylation of AKT, ERK1/2 and p38 to trigger apoptosis. In vivo results showed that animals treated with 7-Epitaxol show antitumor growth compared to control animals. Taken together, the study demonstrates the potential anticancer efficacy of 7-Epitaxol in inducing apoptosis of cisplatin-resistant HNSCC cells through the suppression of AKT and MAPK signalling pathways. � 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.

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