Acetyl-macrocalin B suppresses tumor growth in esophageal squamous cell carcinoma and exhibits synergistic anti-cancer effects with the Chk1/2 inhibitor AZD7762

Toxicol Appl Pharmacol. 2019 Feb 15:365:71-83. doi: 10.1016/j.taap.2019.01.005. Epub 2019 Jan 8.

Abstract

Natural products derived from herbal medicines have become a major focus of anti-cancer drug discovery studies. Acetyl-macrocalin B (A-macB) is an ent-diterpenoid isolated from Isodon silvatica. This study aimed to examine the effect and molecular action of A-macB in esophageal squamous cell carcinoma (ESCC) and explore possible drug synergistic modalities. A-macB induced cellular reactive oxygen species (ROS) generation, initiated the p38 mitogen-activated protein kinase (MAPK) signaling pathway, and triggered the caspase-9-dependent apoptosis cascade in ESCC cells. The ROS scavenger N-acetylcysteine (NAC) and the specific p38 inhibitor SB203580 reversed the effects of A-macB on the p38 network and thus rescued ESCC cells from apoptosis. The cellular ROS increase was at least partially due to the suppression of glutathione-S-transferase P1 (GSTP1) by A-macB. A-macB also upregulated the Chk1/Chk2-Cdc25C/Cdc2/Cyclin B1 axis to induce G2/M phase arrest. The cell growth inhibition induced by A-macB was further enhanced by AZD7762, a specific Chk1/Chk2 inhibitor, with a combination index (CI) of <1. Moreover, A-macB efficiently suppressed xenograft growth without inducing significant toxicity, and AZD7762 potentiated the effects of A-macB in the suppression of tumor growth in vivo. Taken together, A-macB is a promising lead compound for ESCC and exerts synergistic anti-cancer effects with AZD7762.

Keywords: Acetyl-macrocalin B; Chk1/Chk2; Esophageal squamous cell carcinoma; Reactive oxygen species; p38 MAPK.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Checkpoint Kinase 1 / antagonists & inhibitors*
  • Checkpoint Kinase 1 / metabolism
  • Checkpoint Kinase 2 / antagonists & inhibitors*
  • Checkpoint Kinase 2 / metabolism
  • Diterpenes, Kaurane / pharmacology*
  • Drug Synergism
  • Esophageal Neoplasms / drug therapy*
  • Esophageal Neoplasms / enzymology
  • Esophageal Neoplasms / pathology
  • Esophageal Squamous Cell Carcinoma / drug therapy*
  • Esophageal Squamous Cell Carcinoma / enzymology
  • Esophageal Squamous Cell Carcinoma / pathology
  • Female
  • G2 Phase Cell Cycle Checkpoints / drug effects
  • Humans
  • Mice, Inbred BALB C
  • Mice, Nude
  • Phosphorylation
  • Protein Kinase Inhibitors / pharmacology*
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects
  • Thiophenes / pharmacology*
  • Tumor Burden / drug effects
  • Urea / analogs & derivatives*
  • Urea / pharmacology
  • Xenograft Model Antitumor Assays
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • 3-(carbamoylamino)-5-(3-fluorophenyl)-N-(3-piperidyl)thiophene-2-carboxamide
  • Antineoplastic Agents, Phytogenic
  • Diterpenes, Kaurane
  • Protein Kinase Inhibitors
  • Reactive Oxygen Species
  • Thiophenes
  • acetyl-macrocalin B
  • Urea
  • Checkpoint Kinase 2
  • CHEK1 protein, human
  • CHEK2 protein, human
  • Checkpoint Kinase 1
  • p38 Mitogen-Activated Protein Kinases