Rac1 activates non-oxidative pentose phosphate pathway to induce chemoresistance of breast cancer

Nat Commun. 2020 Mar 19;11(1):1456. doi: 10.1038/s41467-020-15308-7.

Abstract

Resistance development to one chemotherapeutic reagent leads frequently to acquired tolerance to other compounds, limiting the therapeutic options for cancer treatment. Herein, we find that overexpression of Rac1 is associated with multi-drug resistance to the neoadjuvant chemotherapy (NAC). Mechanistically, Rac1 activates aldolase A and ERK signaling which up-regulates glycolysis and especially the non-oxidative pentose phosphate pathway (PPP). This leads to increased nucleotides metabolism which protects breast cancer cells from chemotherapeutic-induced DNA damage. To translate this finding, we develop endosomal pH-responsive nanoparticles (NPs) which deliver Rac1-targeting siRNA together with cisplatin and effectively reverses NAC-chemoresistance in PDXs from NAC-resistant breast cancer patients. Altogether, our findings demonstrate that targeting Rac1 is a potential strategy to overcome acquired chemoresistance in breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Biopsy, Large-Core Needle
  • Breast / pathology
  • Breast / surgery
  • Cell Line, Tumor
  • Chemotherapy, Adjuvant / methods
  • Cisplatin / pharmacology
  • Cisplatin / therapeutic use
  • DNA Damage / drug effects
  • Datasets as Topic
  • Doxorubicin / pharmacology
  • Doxorubicin / therapeutic use
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm*
  • Female
  • Follow-Up Studies
  • Fructose-Bisphosphate Aldolase / metabolism
  • Gene Knockdown Techniques
  • Glycolysis
  • Humans
  • MAP Kinase Signaling System
  • Mastectomy
  • Mice
  • Middle Aged
  • Neoadjuvant Therapy / methods
  • Nucleotides / metabolism
  • Pentose Phosphate Pathway*
  • RNA, Small Interfering / metabolism
  • Treatment Outcome
  • Triple Negative Breast Neoplasms / metabolism
  • Triple Negative Breast Neoplasms / mortality
  • Triple Negative Breast Neoplasms / pathology
  • Triple Negative Breast Neoplasms / therapy*
  • Up-Regulation
  • Xenograft Model Antitumor Assays
  • rac1 GTP-Binding Protein / metabolism*

Substances

  • Nucleotides
  • RAC1 protein, human
  • RNA, Small Interfering
  • Doxorubicin
  • rac1 GTP-Binding Protein
  • Fructose-Bisphosphate Aldolase
  • Cisplatin