Functional Characterisation of Anticancer Activity in the Aqueous Extract of Helicteres angustifolia L. Roots

PLoS One. 2016 Mar 24;11(3):e0152017. doi: 10.1371/journal.pone.0152017. eCollection 2016.

Abstract

Helicteres angustifolia L. is a shrub that forms a common ingredient of several cancer treatment recipes in traditional medicine system both in China and Laos. In order to investigate molecular mechanisms of its anticancer activity, we prepared aqueous extract of Helicteres angustifolia L. Roots (AQHAR) and performed several in vitro assays using human normal fibroblasts (TIG-3) and osteosarcoma (U2OS). We found that AQHAR caused growth arrest/apoptosis of U2OS cells in a dose-dependent manner. It showed no cytotoxicity to TIG-3 cells at doses up to 50 μg/ml. Biochemical, imaging and cell cycle analyses revealed that it induces ROS signaling and DNA damage response selectively in cancer cells. The latter showed upregulation of p53, p21 and downregulation of Cyclin B1 and phospho-Rb. Furthermore, AQHAR-induced apoptosis was mediated by increase in pro-apoptotic proteins including cleaved PARP, caspases and Bax. Anti-apoptotic protein Bcl-2 showed decrease in AQHAR-treated U2OS cells. In vivo xenograft tumor assays in nude mice revealed dose-dependent suppression of tumor growth and lung metastasis with no toxicity to the animals suggesting that AQHAR could be a potent and safe natural drug for cancer treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Proliferation
  • Cyclin B1 / metabolism
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • DNA Damage
  • Dose-Response Relationship, Drug
  • Female
  • Fibroblasts / metabolism
  • Humans
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Malvaceae / chemistry*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Metastasis
  • Neoplasm Transplantation
  • Osteosarcoma / drug therapy*
  • Osteosarcoma / pathology
  • Plant Extracts / chemistry*
  • Plant Roots / chemistry
  • Poly(ADP-ribose) Polymerases / metabolism
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Tumor Suppressor Protein p53 / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents, Phytogenic
  • CCNB1 protein, human
  • CDKN1A protein, human
  • Cyclin B1
  • Cyclin-Dependent Kinase Inhibitor p21
  • Plant Extracts
  • Reactive Oxygen Species
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Poly(ADP-ribose) Polymerases

Grants and funding

The study was supported by grants from the Institute of Laboratory Animal Science, CAMS&PUMC (DWS201402) to RG and National Institute of Advanced Industrial Science & Technology (AIST) Special Research Fund to SCK and RW.