Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 5 min ago
Peer-reviewedCC BYJournal of cancer research and clinical oncology

Crosstalk between chemotherapeutics and tumor-associated macrophages (TAMs): implications for tumor response.

  1. 1Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdańsk University of Technology, Gabriela Narutowicza 11/12, 80-233, Gdańsk, Poland.
  2. 2Department of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Banacha 1a, 02- 097, Warsaw, Poland.
  3. 3Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdańsk University of Technology, Gabriela Narutowicza 11/12, 80-233, Gdańsk, Poland. [email protected].

Abstract

The understanding of cancer has evolved from a group of mutated cancerous cells to a complex ecosystem comprising many cellular and non-cellular components. Tumor-associated macrophages (TAMs) are one of the most abundant immune cells in the tumor microenvironment (TME). They actively contribute to cancer outcomes in two ways, either promoting its development and progression or stimulating immune response to combat tumor. Recently, TAMs have been recognized not only as prognostic markers for the outcome of anti-cancer therapy, but also as major players in shaping treatment response. It was also established that therapeutic agents may affect TAMs' phenotype, and in consequence modulate tumor's behavior. Therefore, reprogramming of TAMs in order to enhance tumor infiltration and overcome immune suppression is also currently a hot topic in preclinical research. In this review, we discuss the interactions between chemotherapeutic agents and tumor-associated macrophages and their potential consequences for tumor response.

Related

  1. Spatial single-cell landscape of tumor-associated macrophages and their crosstalk with the tumor microenvironment
    Rui-chao Nie, Guosheng Hu, Shi-qiang Cao +3
    Cell DiscoveryPeer-reviewedCC BY9 citedImmunologyOpenAlex
  2. Enhanced tumor metastasis driven by the crosstalk between melanoma cells and tumor-associated macrophages: insights into the CXCL10/CXCR3-hnRNP C-MIF axis
    Yuan Wang, Chiara Massa, Gowtham Chowdary Tammineni +6
    Journal for Immunotherapy of CancerPeer-reviewedCC BY-NC 4.0Full textImmunologyPMC
  3. Tumor-associated macrophages in glioblastoma: implications for immunotherapy
    Jianan Lei, Mei Lao, Zhuona Ni +6
    Frontiers in ImmunologyPeer-reviewedCC BY 4.0Full textImmunologyCrossrefEurope PMC
  4. Distinct Polarization of Human Macrophages in Response to Infection with the Periodontitis-Associated Bacteria Fusobacterium nucleatum, Porphyromonas gingivalis, and Tannerella forsythia
    Katharina Schwarz, Carlotta Rickert, Fabian L. Kendlbacher +4
    CellsPeer-reviewedCC BY 4.0Cell biologyCrossref
  5. Multidimensional regulation of hepatic macrophages in chronic liver disease: from metabolic reprogramming to intercellular and interorgan crosstalk
    Che Xu, Xin-Yu Zhu, Hai-Na Xie +3
    Frontiers in immunologyPeer-reviewedCC BYFull textImmunologyEurope PMC
BibTeX
@article{pezala2026crosstalk,
  title = {{Crosstalk between chemotherapeutics and tumor-associated macrophages (TAMs): implications for tumor response.}},
  author = {Bożena Pezała and Magdalena Radziszewska and Ewa Augustin},
  journal = {Journal of cancer research and clinical oncology},
  year = {2026},
  month = aug,
  doi = {10.1007/s00432-026-06575-w},
  url = {https://europepmc.org/article/MED/42967962},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Crosstalk between chemotherapeutics and tumor-associated macrophages (TAMs): implications for tumor response.
AU  - Bożena Pezała
AU  - Magdalena Radziszewska
AU  - Ewa Augustin
PY  - 2026
DA  - 2026/08/04
JO  - Journal of cancer research and clinical oncology
DO  - 10.1007/s00432-026-06575-w
UR  - https://europepmc.org/article/MED/42967962
AB  - The understanding of cancer has evolved from a group of mutated cancerous cells to a complex ecosystem comprising many cellular and non-cellular components. Tumor-associated macrophages (TAMs) are one of the most abundant immune cells in the tumor microenvironment (TME). They actively contribute to cancer outcomes in two ways, either promoting its development and progression or stimulating immune response to combat tumor. Recently, TAMs have been recognized not only as prognostic markers for the outcome of anti-cancer therapy, but also as major players in shaping treatment response. It was also established that therapeutic agents may affect TAMs' phenotype, and in consequence modulate tumor's behavior. Therefore, reprogramming of TAMs in order to enhance tumor infiltration and overcome immune suppression is also currently a hot topic in preclinical research. In this review, we discuss the interactions between chemotherapeutic agents and tumor-associated macrophages and their potential consequences for tumor response.
SN  - 0171-5216
SN  - 1432-1335
ER  -