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Targeting Cancer Heterogeneity with Immune Responses Driven by Oncolytic Peptides

Journal

TRENDS IN CANCER
Volume 7, Issue 6, Pages 557-572

Publisher

CELL PRESS
DOI: 10.1016/j.trecan.2020.12.012

Keywords

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Categories

Funding

  1. Associazione Italiana per la Ricerca sul Cancro (AIRC) [IG 2017 20417]
  2. Italian Institute for Genomic Medicine (Candiolo, Turin, Italy)
  3. Compagnia di San Paolo (Torino, Italy)
  4. National Institute of Health/National Cancer Institute (NIH/NCI) [CA198533, CA201246]
  5. Breakthrough Level 3 grant from the US Department of Defense (DoD) Breast Cancer Research Program (BRCP) [BC180595P1]
  6. Breast Cancer Research Foundation (BCRF) grant [BCRF-20-053]
  7. Breakthrough Level 2 grant fromthe US DoD BRCP [BC180476P1]
  8. 2019 Laura Ziskin Prize in Translational Research from the Stand Up to Cancer (SU2C) [ZP-6177]
  9. Mantle Cell Lymphoma Research Initiative (MCL-RI) grant from the Leukemia and Lymphoma Society (LLS)
  10. Department of Radiation Oncology at Weill Cornell Medicine (New York, USA)
  11. Rapid Response Grant from the Functional Genomics Initiative (New York, USA)
  12. Lytix Biopharma (Oslo, Norway)
  13. Phosplatin (New York, USA)
  14. CDMRP [BC180476P1, 1102090] Funding Source: Federal RePORTER

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The high heterogeneity among malignant cells poses a significant obstacle to the success of cancer therapy, calling for the development of approaches that can operate despite such intratumoral heterogeneity. Oncolytic peptides, with their ability to induce immunogenic cell death and robust anticancer immune responses independently of intratumoral heterogeneity, show promise as therapeutic tools.
Accumulating preclinical and clinical evidence indicates that high degrees of heterogeneity among malignant cells constitute a considerable obstacle to the success of cancer therapy. This calls for the development of approaches that operate - or enable established treatments to operate - despite such intratumoral heterogeneity (ITH). In this context, oncolytic peptides stand out as promising therapeutic tools based on their ability to drive immunogenic cell death associated with robust anticancer immune responses independently of ITH. We review the main molecular and immunological pathways engaged by oncolytic peptides, and discuss potential approaches to combine these agents with modern immunotherapeutics in support of superior tumor-targeting immunity and efficacy in patients with cancer.

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