Docetaxel Upregulates HMGB1 Levels in Non-small Cell Lung Cancer.
A549 Cells
Antineoplastic Agents
CD11 Antigens
/ metabolism
Carcinoma, Non-Small-Cell Lung
/ drug therapy
Cell Line, Tumor
Chemokines
/ metabolism
Combined Modality Therapy
Cytokines
/ metabolism
Docetaxel
/ pharmacology
Epidermal Growth Factor
/ antagonists & inhibitors
ErbB Receptors
/ antagonists & inhibitors
Female
HMGB1 Protein
/ blood
Humans
Integrin alpha Chains
/ metabolism
Male
Mutation
Protein Kinase Inhibitors
/ pharmacology
Protein-Tyrosine Kinases
/ antagonists & inhibitors
Transcriptional Activation
/ drug effects
cancer immunotherapy
docetaxel
high-mobility group box 1 (HMGB1)
non-small cell lung cancer (NSCLC)
Journal
Biological & pharmaceutical bulletin
ISSN: 1347-5215
Titre abrégé: Biol Pharm Bull
Pays: Japan
ID NLM: 9311984
Informations de publication
Date de publication:
2020
2020
Historique:
entrez:
3
3
2020
pubmed:
3
3
2020
medline:
25
9
2020
Statut:
ppublish
Résumé
Immune checkpoint inhibitors (ICIs) exert beneficial effects in non-small cell lung cancer (NSCLC) patients. However, ICIs are only advantageous for a limited population of NSCLC patients. Therefore to enhance their effects, combination therapies with ICIs have been developed. To identify preferable chemotherapy to combine with ICIs against lung cancer, we examined immunological effects of docetaxel compared with epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI). We found no difference in peripheral lymphocyte counts and ratio of their subpopulations in lung cancer patients before and after both treatments. On the other hand, plasma levels of high-mobility group box 1 (HMGB1), a damage-associated molecular pattern (DAMP) protein, showed significant increase after docetaxel treatment. Furthermore, we investigated effects of HMGB1 on tumor-infiltrating immune cells obtained from surgically resected tumor tissue from NSCLC patients. When the tumor infiltrating cells were stimulated with HMGB1, CD11c
Identifiants
pubmed: 32115500
doi: 10.1248/bpb.b19-00702
doi:
Substances chimiques
Antineoplastic Agents
0
CD11 Antigens
0
Chemokines
0
Cytokines
0
HMGB1 Protein
0
HMGB1 protein, human
0
ITGAD protein, human
0
Integrin alpha Chains
0
Protein Kinase Inhibitors
0
Docetaxel
15H5577CQD
Epidermal Growth Factor
62229-50-9
ErbB Receptors
EC 2.7.10.1
Protein-Tyrosine Kinases
EC 2.7.10.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM