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Harnessing immune cells to leverage PARP inhibitors

  • Tian Li Wang*
  • , Ie Ming Shih
  • *Corresponding author for this work
  • Johns Hopkins University

Research output: Contribution to journalComment/debate

2 Scopus citations

Abstract

Homologous-recombination deficiency in DNA repair characterizes a unique group of cancers that are vulnerable to PARP inhibitors and cytotoxic chemotherapy. In this issue of Cell, Luo et al., demonstrated that this genetic attribute in cancer cells may reprogram tumor immune microenvironment and show promise of targeting effector-Treg cells.

Original languageEnglish
Pages (from-to)4829-4830
Number of pages2
JournalCell
Volume187
Issue number18
DOIs
StatePublished - 05 09 2024

Bibliographical note

Copyright © 2024 Elsevier Inc. All rights reserved.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Poly(ADP-ribose) Polymerase Inhibitors/therapeutic use
  • Humans
  • Tumor Microenvironment
  • Neoplasms/drug therapy
  • T-Lymphocytes, Regulatory/immunology
  • Animals

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