| Literature DB >> 33321953 |
Sathishbabu Paranthaman1, Meghana Goravinahalli Shivananjegowda1, Manohar Mahadev1, Afrasim Moin2, Shivakumar Hagalavadi Nanjappa3, Nandakumar Nanjaiyah4, Saravana Babu Chidambaram5, Devegowda Vishakante Gowda1.
Abstract
A paradigm shift in treating the most aggressive and malignant form of glioma is continuously evolving; however, these strategies do not provide a better life and survival index. Currently, neurosurgical debulking, radiotherapy, and chemotherapy are the treatment options available for glioma, but these are non-specific in action. Patients invariably develop resistance to these therapies, leading to recurrence and death. Receptor Tyrosine Kinases (RTKs) are among the most common cell surface proteins in glioma and play a significant role in malignant progression; thus, these are currently being explored as therapeutic targets. RTKs belong to the family of cell surface receptors that are activated by ligands which in turn activates two major downstream signaling pathways via Rapidly Accelerating Sarcoma/mitogen activated protein kinase/extracellular-signal-regulated kinase (Ras/MAPK/ERK) and phosphatidylinositol 3-kinase/a serine/threonine protein kinase/mammalian target of rapamycin (PI3K/AKT/mTOR). These pathways are critically involved in regulating cell proliferation, invasion, metabolism, autophagy, and apoptosis. Dysregulation in these pathways results in uncontrolled glioma cell proliferation, invasion, angiogenesis, and cancer progression. Thus, RTK pathways are considered a potential target in glioma management. This review summarizes the possible risk factors involved in the growth of glioblastoma (GBM). The role of RTKs inhibitors (TKIs) and the intracellular signaling pathways involved, small molecules under clinical trials, and the updates were discussed. We have also compiled information on the outcomes from the various endothelial growth factor receptor (EGFR)-TKIs-based nanoformulations from the preclinical and clinical points of view. Aided by an extensive literature search, we propose the challenges and potential opportunities for future research on EGFR-TKIs-based nanodelivery systems.Entities:
Keywords: epidermal growth factor receptor; glioblastoma; nanoformulations; receptor tyrosine kinases; small molecule inhibitors
Year: 2020 PMID: 33321953 PMCID: PMC7763629 DOI: 10.3390/pharmaceutics12121198
Source DB: PubMed Journal: Pharmaceutics ISSN: 1999-4923 Impact factor: 6.321