A Novel Acidic Polysaccharide from Inonotus obliquus (IOP-1) Suppresses Growth and Induces Apoptosis in Non-Small

Jiaqi Zhao1, Wei Xie2, Xinze Liu1

  • 1Changchun University of Chinese Medicine Jilin Ginseng Academy Changchun China.

Abstract

Insights

An acidic polysaccharide, IOP-1, derived from Inonotus obliquus, demonstrates significant antitumor effects against non-small cell lung cancer (NSCLC). IOP-1 inhibits cancer cell proliferation and migration, offering a promising new therapeutic avenue for NSCLC treatment.

Area of Science:

  • Biochemistry
  • Pharmacology
  • Oncology

Background:

  • Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality worldwide.
  • Investigating novel therapeutic agents for NSCLC is crucial for improving patient outcomes.
  • The potential of natural compounds like polysaccharides from Inonotus obliquus warrants exploration for anticancer properties.

Purpose of the Study:

  • To investigate the antitumor effects of an acidic polysaccharide, designated IOP-1, isolated from Inonotus obliquus.
  • To elucidate the underlying mechanisms of IOP-1's action against NSCLC cells.
  • To evaluate the therapeutic potential of IOP-1 in preclinical models of NSCLC.

Main Methods:

  • Isolation and purification of acidic polysaccharide IOP-1 from Inonotus obliquus.
  • Characterization of IOP-1's functional groups and monosaccharide composition.
  • In vitro studies using NCI-H460 NSCLC cells to assess proliferation, migration, and apoptosis.
  • In vivo experiments in mice to evaluate tumor growth inhibition and relevant physiological parameters.

Main Results:

  • IOP-1 significantly inhibited proliferation and migration of NCI-H460 cells while inducing apoptosis.
  • IOP-1 treatment altered the expression of key apoptosis-related proteins (Bax, Bcl-2, P53, Cyto-c) and migration-related proteins (MMP-9, Parp-1).
  • In vivo studies demonstrated that IOP-1 effectively inhibited tumor growth, increased spleen weight, and reduced tumor blood perfusion in mice.

Conclusions:

  • IOP-1 exhibits potent antitumor activity against NSCLC by modulating apoptosis and migration pathways.
  • The findings suggest that IOP-1 is a promising candidate for the development of novel NSCLC therapeutics.
  • IOP-1 represents a new therapeutic strategy for the clinical management of non-small cell lung cancer.

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