Targeting PD-L1 with BMS-202 Enhances Antitumor Cytokine and Cytotoxic T-Lymphocyte Responses in C57BLx/6 Mouse Lung Carcinogenesis

These findings suggest that BMS-202 effectively promotes apoptosis and enhances immune responses in lung cancer, underscoring its potential as a therapeutic agent in treating lung carcinogenesis.

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Publication Details

Journal
Cancer Management and Research
Published
2025-12-01
DOI
https://doi.org/10.2147/cmar.s560799
Primary Topic
NF-κB Signaling Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

Targeting PD-L1 with BMS-202 Enhances Antitumor Cytokine and Cytotoxic T-Lymphocyte Responses in C57BLx/6 Mouse Lung Carcinogenesis

Kovan Faidhalla Jalal, Arash Abdolmaleki, Shang Ziyad Abdulqadir, Mustafa Fahmi Rajab et al.
Cancer Management and Research
NF-κB Signaling Pathways
article

Targeting PD-L1 with BMS-202 Enhances Antitumor Cytokine and Cytotoxic T-Lymphocyte Responses in C57BLx/6 Mouse Lung Carcinogenesis

Kovan Faidhalla Jalal, Arash Abdolmaleki, Shang Ziyad Abdulqadir, Mustafa Fahmi Rajab, Mohammad B. Ghayour, Christer Janson, Shukur Wasman Smail, Abdullah Abubaker Shareef
article en

Abstract

These findings suggest that BMS-202 effectively promotes apoptosis and enhances immune responses in lung cancer, underscoring its potential as a therapeutic agent in treating lung carcinogenesis.

Cancer Management and ResearchVol. Volume 17
Uppsala University (SE), Cihan University-Erbil (IQ), Salahaddin University-Erbil (IQ), University of Mohaghegh Ardabili (IR), Tishk International University (IQ)
Uppsala Universitet, HjärtLung Uppsala, Länsföreningen
Openalex Percentile: Top 52%
NF-κB Signaling Pathways
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