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Autophagy in combination therapy of temozolomide and IFN-γ in C6-induced glioblastoma: role of non-coding RNAs.

Abstract
Aim: We predicted the modulation of autophagy and apoptosis in response to temozolomide (TMZ) and IFN-γ based on changes in the expression of non-coding RNAs in C6-induced glioblastoma (GBM). Materials & methods: Each rat received an intraperitoneal injection of TMZ (7.5 mg/kg) and/or IFN-γ (50,000 IU). Results: The reduced expression of H19 and colorectal neoplasia differentially expressed (CRNDE) was associated with a reduction in autophagy in response to TMZ, IFN-γ and TMZ + IFN-γ therapy, whereas the decreased level of miR-29a (proapoptotic miRNA) was associated with an increase in apoptosis. Conclusion: It appears that H19 promotes switching from autophagy to apoptosis in response to combination therapy of TMZ and IFN-γ through the miR-29a/autophagy-related protein 9A (ATG9A) pathway in C6-induced GBM.
AuthorsHamideh Bashiri, Maryam Moazam-Jazi, Mohammad Reza Karimzadeh, Saeideh Jafarinejad-Farsangi, Amirhossein Moslemizadeh, Marziyeh Lotfian, Zahra Miri Karam, Reza Kheirandish, Mohammad Mojtaba Farazi
JournalImmunotherapy (Immunotherapy) Vol. 15 Issue 14 Pg. 1157-1169 (10 2023) ISSN: 1750-7448 [Electronic] England
PMID37584216 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Temozolomide
  • MicroRNAs
  • Antineoplastic Agents, Alkylating
Topics
  • Rats
  • Animals
  • Temozolomide (therapeutic use, pharmacology)
  • Glioblastoma (drug therapy)
  • Brain Neoplasms (drug therapy, genetics)
  • MicroRNAs (genetics)
  • Autophagy
  • Apoptosis
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm (genetics)
  • Antineoplastic Agents, Alkylating (pharmacology, therapeutic use)

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