Cited by 159Immunotherapy and Immune ResponsesImmune Response and InflammationCell death mechanisms and regulation

Prognostic and predictive value of DAMPs and DAMP-associated processes in cancer

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Fucikova, Jitka, Moserova, Irena, Urbanova, Linda, Bezu, Lucillia, Kepp, Oliver, Cremer, Isabelle, Salek, Cyril, Strnad, Pavel +3 more·2015·Frontiers in Immunology

Abstract

It is now clear that human neoplasms form, progress, and respond to therapy in the context of an intimate crosstalk with the host immune system. In particular, accumulating evidence demonstrates that the efficacy of most, if not all, chemo- and radiotherapeutic agents commonly employed in the clinic critically depends on the (re)activation of tumor-targeting immune responses. One of the mechanisms whereby conventional chemotherapeutics, targeted anticancer agents, and radiotherapy can provoke a therapeutically relevant, adaptive immune response against malignant cells is commonly known as "immunogenic cell death." Importantly, dying cancer cells are perceived as immunogenic only when they emit a set of immunostimulatory signals upon the activation of intracellular stress response pathways. The emission of these signals, which are generally referred to as "damage-associated molecular patterns" (DAMPs), may therefore predict whether patients will respond to chemotherapy or not, at least in some settings. Here, we review clinical data indicating that DAMPs and DAMP-associated stress responses might have prognostic or predictive value for cancer patients.

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  • Loss-of-function polymorphisms in genes for immune receptors that recognize ICD-associated adjuvant-like molecules correlate with poor outcomes in breast cancer patients given anthracycline-based chemotherapy.

    “loss-of-function polymorphisms in various genes encoding immune receptors involved in the recognition of ICD-associated adjuvant-like molecules have been linked with poor disease outcome in cohorts of breast cancer patients receiving ICD-inducing anthracycline-based chemotherapy (Fucikova et al., 2015).”

    From Immunomodulation by targeted anticancer agents (2021) · cites this paper as Fucikova et al., 2015

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References 232 · Cited by 159

Authors
Fucikova, J., Moserova, I., Urbanova, L., Bezu, L., Kepp, O., Cremer, I., Salek, C., Strnad, P., Kroemer, G., Galluzzi, L., & Spisek, R.
Affiliations
  • Charles University (CZ)
  • Inserm (FR)
  • Sorbonne Paris Cité (FR)
Corresponding author
Galluzzi, Lorenzo
Venue
Frontiers in Immunology
Published
2015-08-07
Volume
6
Pages
402-402
ISSN
1664-3224 (ISSN-L)
OpenAlex
W1489012416
Cited by
159
References
232
Citations by year
2026: 6 · 2025: 13 · 2024: 12 · 2023: 25 · 2022: 13 · 2021: 8 · 2020: 22 · 2019: 16 · 2018: 11 · 2017: 14 · 2016: 16 · 2015: 3
FWCI
1.38
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Frontiers in Immunology (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, cc-by)
  • RWTH Publications (RWTH Aachen) (submittedVersion, other-oa)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • RWTH Publications (RWTH Aachen)
Funders
  • Association pour la Recherche sur le Cancer
  • E-Rare
  • European Commission
  • Agence Nationale de la Recherche (E-Rare-2)
  • Fondation pour la Recherche Médicale
  • Ligue Contre le Cancer
  • Fondation de France
  • Institut National Du Cancer
  • Labex Immuno-Oncology
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
Keywords
damage-associated molecular patterns, immunogenic cell death, cancer immunotherapy, chemotherapy response prediction, tumor immune microenvironment, prognostic factors, predictive biomarkers, radiotherapy, targeted anticancer agents

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