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Acetylshikonin suppressed growth of colorectal tumour tissue and cells by inhibiting the intracellular kinase, T-lymphokine-activated killer cell-originated protein kinase.
Zhao, Ran; Choi, Bu Young; Wei, Lixiao; Fredimoses, Mangaladoss; Yin, Fanxiang; Fu, Xiaorong; Chen, Hanyong; Liu, Kangdong; Kundu, Joydeb Kumar; Dong, Zigang; Lee, Mee-Hyun.
Afiliação
  • Zhao R; Department of Pathophysiology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Choi BY; China-US (Henan) Hormel Cancer Institute, Zhengzhou, China.
  • Wei L; Department of Pharmaceutical Science and Engineering, School of Convergence Bioscience and Technology, Seowon University, Chungbuk, South Korea.
  • Fredimoses M; China-US (Henan) Hormel Cancer Institute, Zhengzhou, China.
  • Yin F; China-US (Henan) Hormel Cancer Institute, Zhengzhou, China.
  • Fu X; Department of Pathophysiology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Chen H; China-US (Henan) Hormel Cancer Institute, Zhengzhou, China.
  • Liu K; Department of Pathophysiology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Kundu JK; China-US (Henan) Hormel Cancer Institute, Zhengzhou, China.
  • Dong Z; The Hormel Institute, University of Minnesota, Austin, Minnesota.
  • Lee MH; Department of Pathophysiology, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China.
Br J Pharmacol ; 177(10): 2303-2319, 2020 05.
Article em En | MEDLINE | ID: mdl-31985814
ABSTRACT
BACKGROUND AND

PURPOSE:

Overexpression or aberrant activation of the T-lymphokine-activated killer cell-originated protein kinase (TOPK) promotes gene expression and growth of solid tumours, implying that TOPK would be a rational target in developing novel anticancer drugs. Acetylshikonin, a diterpenoid compound isolated from Lithospermum erythrorhizon root, exerts a range of biological activities. Here we have investigated whether acetylshikonin, by acting as an inhibitor of TOPK, can attenuate the proliferation of colorectal cancer cells and the growth of patient-derived tumours, in vitro and in vivo. EXPERIMENTAL

APPROACH:

Targets of acetylshikonin, were identified using kinase profiling analysis, kinetic/binding assay, and computational docking analysis and knock-down techniques. Effects of acetylshikonin on colorectal cancer growth and the underlying mechanisms were evaluated in cell proliferation assays, propidium iodide and annexin-V staining analyses and western blots. Patient-derived tumour xenografts in mice (PDX) and immunohistochemistry were used to assess anti-tumour effects of acetylshikonin. KEY

RESULTS:

Acetylshikonin directly inhibited TOPK activity, interacting with the ATP-binding pocket of TOPK. Acetylshikonin suppressed cell proliferation by inducing cell cycle arrest at the G1 phase, stimulated apoptosis, and increased the expression of apoptotic biomarkers in colorectal cancer cell lines. Mechanistically, acetylshikonin diminished the phosphorylation and activation of TOPK signalling. Furthermore, acetylshikonin decreased the volume of PDX tumours and reduced the expression of TOPK signalling pathway in xenograft tumours. CONCLUSION AND IMPLICATIONS Acetylshikonin suppressed growth of colorectal cancer cells by attenuating TOPK signalling. Targeted inhibition of TOPK by acetylshikonin might be a promising new approach to the treatment of colorectal cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Células Matadoras Ativadas por Linfocina Limite: Animals / Humans Idioma: En Revista: Br J Pharmacol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Células Matadoras Ativadas por Linfocina Limite: Animals / Humans Idioma: En Revista: Br J Pharmacol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China