Inhibition of c-MET increases the antitumour activity of PARP inhibitors in gastric cancer models

J Cell Mol Med. 2020 Sep;24(18):10420-10431. doi: 10.1111/jcmm.15655. Epub 2020 Jul 20.

Abstract

Gastric cancer is the fifth most common malignancy and the third leading cause of cancer-related death worldwide. Activation of c-MET increases tumour cell survival through the initiation of the DNA damage repair pathway. PARP is an essential key in the DNA damage repair pathway. The primary role of PARP is to detect and initiate an immediate cellular response to single-strand DNA breaks. Tumours suppressor genes such as BRCA1/2 are closely associated with the DNA repair pathway. In BRCA1/2 mutations or deficiency status, cells are more likely to develop additional genetic alterations and chromosomal instability and can lead to cancer. In this study, we investigate the role of c-MET and PARP inhibition in a gastric cancer model. We exploited functional in vitro and in vivo experiments to assess the antitumour potential of co-inhibition of c-MET (SU11274) and PARP (NU1025). This leads to a reduction of gastric cancer cells viability, especially after knockdown of BRCA1/2 through apoptosis and induction of γ-Η2ΑΧ. Moreover, in AGS xenograft models, the combinatorial treatment of NU1025 plus SU11274 reduced tumour growth and triggers apoptosis. Collectively, our data may represent a new therapeutic approach for GC thought co-inhibition of c-MET and PARP, especially for patients with BRCA1/2 deficiency tumours.

Keywords: BRCA1; BRCA2; PARP inhibitor; c-Met inhibitor; gastric cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Clone Cells
  • DNA Damage
  • Histones / metabolism
  • Humans
  • Indoles / pharmacology
  • Indoles / therapeutic use
  • Mice
  • Models, Biological*
  • Neoplasm Proteins / metabolism
  • Piperazines / pharmacology
  • Piperazines / therapeutic use
  • Poly(ADP-ribose) Polymerase Inhibitors / therapeutic use*
  • Proto-Oncogene Proteins c-met / antagonists & inhibitors*
  • Quinazolines / pharmacology
  • Quinazolines / therapeutic use
  • Stomach Neoplasms / drug therapy*
  • Stomach Neoplasms / pathology
  • Sulfonamides / pharmacology
  • Sulfonamides / therapeutic use
  • Xenograft Model Antitumor Assays

Substances

  • ((3Z)-N-(3-chlorophenyl)-3-((3,5-dimethyl-4-((4-methylpiperazin-1-yl)carbonyl)-1H-pyrrol-2-yl)methylene)-N-methyl-2-oxo-2,3-dihydro-1H-indole-5-sulfonamide)
  • Antineoplastic Agents
  • H2AX protein, human
  • Histones
  • Indoles
  • NU 1025
  • Neoplasm Proteins
  • Piperazines
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Quinazolines
  • Sulfonamides
  • Proto-Oncogene Proteins c-met