Antagonist of Growth Hormone-Releasing Hormone Potentiates the Antitumor Effect of Pemetrexed and Cisplatin in Pleural Mesothelioma.
Cell Line, Tumor
Cisplatin
/ pharmacology
Cyclin D1
Cyclooxygenase 2
Growth Hormone-Releasing Hormone
HMGB1 Protein
Humans
Insulin-Like Growth Factor I
/ therapeutic use
Matrix Metalloproteinase 2
Matrix Metalloproteinase 9
/ genetics
Mesothelioma
/ drug therapy
Mesothelioma, Malignant
NF-kappa B
/ metabolism
Pemetrexed
/ pharmacology
Pleural Neoplasms
/ drug therapy
Vascular Endothelial Growth Factor A
/ metabolism
GHRH antagonists
chemotherapeutic drugs
pleural mesothelioma
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
24 Sep 2022
24 Sep 2022
Historique:
received:
13
08
2022
revised:
15
09
2022
accepted:
20
09
2022
entrez:
14
10
2022
pubmed:
15
10
2022
medline:
18
10
2022
Statut:
epublish
Résumé
Pleural mesothelioma (PM) is an aggressive cancer with poor prognosis and no effective therapies, mainly caused by exposure to asbestos. Antagonists of growth hormone-releasing hormone (GHRH) display strong antitumor effects in many experimental cancers, including lung cancer and mesothelioma. Here, we aimed to determine whether GHRH antagonist MIA-690 potentiates the antitumor effect of cisplatin and pemetrexed in PM. In vitro, MIA-690, in combination with cisplatin and pemetrexed, synergistically reduced cell viability, restrained cell proliferation and enhanced apoptosis, compared with drugs alone. In vivo, the same combination resulted in a strong growth inhibition of MSTO-211H xenografts, decreased tumor cell proliferation and increased apoptosis. Mechanistically, MIA-690, particularly with chemotherapeutic drugs, inhibited proliferative and oncogenic pathways, such as MAPK ERK1/2 and cMyc, and downregulated cyclin D1 and B1 mRNAs. Inflammatory pathways such as NF-kB and STAT3 were also reduced, as well as oxidative, angiogenic and tumorigenic markers (iNOS, COX-2, MMP2, MMP9 and HMGB1) and growth factors (VEGF and IGF-1). Overall, these findings strongly suggest that GHRH antagonists of MIA class, such as MIA-690, could increase the efficacy of standard therapy in PM.
Identifiants
pubmed: 36232554
pii: ijms231911248
doi: 10.3390/ijms231911248
pmc: PMC9569772
pii:
doi:
Substances chimiques
HMGB1 Protein
0
NF-kappa B
0
Vascular Endothelial Growth Factor A
0
Pemetrexed
04Q9AIZ7NO
Cyclin D1
136601-57-5
Insulin-Like Growth Factor I
67763-96-6
Growth Hormone-Releasing Hormone
9034-39-3
Cyclooxygenase 2
EC 1.14.99.1
Matrix Metalloproteinase 2
EC 3.4.24.24
Matrix Metalloproteinase 9
EC 3.4.24.35
Cisplatin
Q20Q21Q62J
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Italian Ministry of Instruction and Research PRIN 2017
ID : 2017HRTZYA
Organisme : Italian Ministry of Instruction and Research PRIN 2017
ID : 2017S55RXB_002
Organisme : Fondazione Buzzi Unicem
ID : 2019-2022
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