Cited by 303Cytokine Signaling Pathways and InteractionsBreast Cancer Treatment StudiesImmune cells in cancer

The DOI matches its Crossref record; 134 of the 136 references it cites were found in a registry or an index.

The significant role of interleukin-6 and its signaling pathway in the immunopathogenesis and treatment of breast cancer

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Masjedi, Ali, Hashemi, Vida, Hojjat-Farsangi, Mohammad, Ghalamfarsa, Ghasem, Azizi, Gholamreza, Yousefi, Mehdi, Jadidi-Niaragh, Farhad·2018·Biomedicine & Pharmacotherapy

Abstract

Despite remarkable improvements in cancer treatment approaches, breast cancer is still the main cause of cancer-related death in women. Its principal cause is the resistance of the cancer cells against conventional anticancer therapeutics, mainly in advanced disease stages. It has been shown that chronic inflammation in the tumor microenvironment facilitates tumor growth and induces resistance toward chemo- and radiotherapy. Overexpression of interleukin-6 (IL-6) cytokine in the tumor microenvironment has been demonstrated in numerous tumors including breast cancer. Tumor cells and tumor-associated fibroblasts are the major sources of IL-6 secretion in the tumor microenvironment. Several studies have demonstrated the immunopathogenic function of IL-6 and its signaling in the tumor growth, metastasis, and therapeutic resistance in the breast cancer. Therefore, it seems that targeting IL-6 and/or its receptor in combination with other potent anticancer therapies may be a potent therapeutic approach for breast cancer therapy.

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Crossref · 10.1016/j.biopha.2018.09.177

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Research works printed but not linked: 5

  1. Kozlowski, 2003, Concentration of interleukin-6 (IL-6), interleukin-8 (IL-8) and interleukin-10 (IL-10) in blood serum of breast cancer patients, Rocz. Akad. Med. Bialymst., 48, 82
  2. Jiang, 2011, Down-regulation of expression of interleukin-6 and its receptor results in growth inhibition of MCF-7 breast cancer cells, Anticancer Res., 31, 2899
  3. Chiu, 1996, Interleukin 6 acts as a paracrine growth factor in human mammary carcinoma cell lines, Clin. Cancer Res., 2, 215
  4. Sa-Nguanraksa, 2016, Association of Estrogen Receptor Alpha and Interleukin 6 Polymorphisms with Lymphovascular Invasion, Extranodal Extension, and Lower Disease-Free Survival in Thai Breast Cancer Patients, Asian Pac. J. Cancer Prev., 17, 2935
  5. Tawara, 2011, Clinical significance of interleukin (IL)-6 in cancer metastasis to bone: potential of anti-IL-6 therapies, Cancer Manag. Res., 3, 177

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Metadata

Authors
Masjedi, A., Hashemi, V., Hojjat-Farsangi, M., Ghalamfarsa, G., Azizi, G., Yousefi, M., & Jadidi-Niaragh, F.
Affiliations
  • Tabriz University of Medical Sciences (IR)
  • University of Maragheh (IR)
  • Yasuj University of Medical Sciences (IR)
  • Alborz University of Medical Sciences (IR)
Venue
Biomedicine & Pharmacotherapy
Publisher
Elsevier BV
Published
2018-12
Volume
108
Pages
1415-1424
ISSN
0753-3322 (ISSN-L)
OpenAlex
W2894776217
Cited by
303
References
136
Citations by year
2026: 20 · 2025: 33 · 2024: 32 · 2023: 60 · 2022: 67 · 2021: 41 · 2020: 39 · 2019: 9 · 2018: 1
FWCI
2.37
Type
journal article
Language
en
Open access
Locations
  • Biomedicine & Pharmacotherapy (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Funders
National Institute for Medical Research Development
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
  • Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
Keywords
interleukin-6, IL-6 signaling, breast cancer, tumor microenvironment, chronic inflammation, cancer-associated fibroblasts, chemoresistance, radioresistance (biology), metastasis, immunopathogenesis, combination therapy
MeSH terms
Janus Kinase Inhibitors, Interleukin-6 Inhibitors, Antibodies, Monoclonal, Breast Neoplasms, Female, Humans, Signal Transduction, Interleukin-6, Receptors, Interleukin-6, Tumor Microenvironment, Antibodies, Monoclonal, Humanized

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