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Prognostic Role of Monocytic Myeloid-Derived Suppressor Cells in Advanced Non-Small-Cell Lung Cancer: Relation to Different Hematologic Indices
Author(s) -
Asmaa M. Zahran,
‏Helal F. Hetta,
Zeinab Albadry M. Zahran,
Alaa Rashad,
Amal Rayan,
Dalia O. Mohamed,
Zeinab Ahmed Abd Elhameed,
Salah Khallaf,
Gaber ElSaber Batiha,
Yasir Waheed,
Khalid Muhammad,
Hanaa NafadyHego
Publication year - 2021
Publication title -
journal of immunology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.315
H-Index - 83
eISSN - 2314-8861
pISSN - 2314-7156
DOI - 10.1155/2021/3241150
Subject(s) - medicine , lung cancer , cancer , myeloid derived suppressor cell , immunosuppression , stage (stratigraphy) , immune system , platelet , oncology , radiation therapy , tumor microenvironment , gastroenterology , chemotherapy , immunology , suppressor , biology , paleontology
Methods We recruited 40 cases of advanced NSCLC, stages III and IV, aged > 18–<70 years old, and eligible to receive chemotherapy with or without radiotherapy, along with 20 healthy controls of comparable age and sex; after diagnosis and staging of patients, blood samples were collected for flow cytometric detection of Mo-MDSCs.Results Significant accumulation of Mo-MDSCs in patients compared to their controls ( p < 0.0001). Furthermore, these cells accumulated significantly in stage IV compared to stage III ( p = 0.006) and correlated negatively with overall survival ( r = −0.471, p = 0.002), lymphocyte to monocyte ratio ( r = −0.446, p = 0.004), and mean platelet volume to platelet count ratio (MPV/PC) ( r = −0.464, p = 0.003), patients with Mo‐MDSCs < 13% had significantly better survival than those with Mo‐MDSCs ≥ 13% ( p = 0.041).Conclusion Mo-MDSCs represent one of the key mechanisms in the immunosuppressive tumor microenvironment (TME) to play major roles not only in the carcinogenesis of lung cancer but also in disease progression and prognosis and, in addition, predict the efficacy of immune checkpoint inhibitors; our results provided some support to target Mo-MDSCs and needed to be augmented by further studies.

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