دورية أكاديمية

Antagonist of growth hormone-releasing hormone MIA-690 attenuates the progression and inhibits growth of colorectal cancer in mice

التفاصيل البيبلوغرافية
العنوان: Antagonist of growth hormone-releasing hormone MIA-690 attenuates the progression and inhibits growth of colorectal cancer in mice
المؤلفون: Recinella, Lucia, Chiavaroli, Annalisa, Veschi, Serena, Di Valerio, Valentina, Lattanzio, Rossano, Orlando, Giustino, Ferrante, Claudio, Gesmundo, Iacopo, Granata, Riccarda, Cai, Renzhi, Sha, Wei, Schally, Andrew V, Brunetti, Luigi, Leone, Sheila
المساهمون: Recinella, Lucia, Chiavaroli, Annalisa, Veschi, Serena, Di Valerio, Valentina, Lattanzio, Rossano, Orlando, Giustino, Ferrante, Claudio, Gesmundo, Iacopo, Granata, Riccarda, Cai, Renzhi, Sha, Wei, Schally, Andrew V, Brunetti, Luigi, Leone, Sheila
سنة النشر: 2022
المجموعة: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
مصطلحات موضوعية: Apoptotic pathway, Colorectal cancer, Growth hormone-releasing hormone antagonist, Inflammation, Oncogenic pathway, Oxidative stre, Animal, Apoptosi, Carcinogenesi, Cell Proliferation, Colorectal Neoplasm, Down-Regulation, Growth Hormone-Releasing Hormone, Inflammation Mediator, Male, Mice, Inbred C57BL, Random Allocation, Up-Regulation
الوصف: Colorectal cancer (CRC) is an aggressive tumor in which new treatment options deliver negative results on cure rates and long-term survival. The anticancer effects of growth hormone-releasing hormone (GHRH) antagonists have been reported in various experimental tumors, but their activity in CRC is unknown. In the present study, we demonstrated that chronic treatment with GHRH antagonist of MIAMI class, MIA-690, promoted survival and gradually blunted tumor progression in experimentally induced colitis-associated cancer in mice, paralleled by reduced inflammation in colon tissue. In particular, MIA-690 improved disease activity index score, and reduced loss of weight and mortality, by improving the survival rates, compared with vehicle-treated group. MIA-690 was also found to reduce various inflammatory and oxidative markers, such as serotonin, prostaglandin (PG)E2 and 8-iso-PGF2α levels, as well as COX-2, iNOS, TNF-α, IL-6 and NF-kB gene expression. Moreover, MIA-690 inhibited the protein expression of c-Myc, P-AKT and Bcl-2 and upregulated p53 protein expression. In conclusion, we showed that MIA-690 suppresses CRC progression and growth by reducing inflammatory and oxidative markers and modulating apoptotic and oncogenic pathways. Further investigations are required for translating these findings into the clinics.
نوع الوثيقة: article in journal/newspaper
اللغة: English
ردمك: 978-0-7533-3222-1
0-7533-3222-1
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34923341; volume:146; issue:112554; firstpage:1; lastpage:11; numberofpages:11; journal:BIOMÉDECINE & PHARMACOTHÉRAPIE; http://hdl.handle.net/2318/1870424Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85121268310; https://www.sciencedirect.com/science/article/pii/S075333222101341X?via=ihubTest
DOI: 10.1016/j.biopha.2021.112554
الإتاحة: https://doi.org/10.1016/j.biopha.2021.112554Test
http://hdl.handle.net/2318/1870424Test
https://www.sciencedirect.com/science/article/pii/S075333222101341X?via=ihubTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.E4872CA8
قاعدة البيانات: BASE
الوصف
ردمك:9780753332221
0753332221
DOI:10.1016/j.biopha.2021.112554