Current Perspective on the Natural Compounds and Drug Delivery Techniques in Glioblastoma Multiforme.
Tarapati RanaAditi SharmaLalit SharmaAayush SehgalSukhbir SinghNeelam SharmaGokhan ZenginSimona Gabriela BungauMirela Marioara TomaDaniela GiteaElena Emilia BabesClaudia Teodora Judea PustaAdrian Gheorghe BumbuPublished in: Cancers (2021)
Glioblastoma multiforme (GBM) is one of the debilitating brain tumors, being associated with extremely poor prognosis and short median patient survival. GBM is associated with complex pathogenesis with alterations in various cellular signaling events, that participate in cell proliferation and survival. The impairment in cellular redox pathways leads to tumorigenesis. The current standard pharmacological regimen available for glioblastomas, such as radiotherapy and surgical resection following treatment with chemotherapeutic drug temozolomide, remains fatal, due to drug resistance, metastasis and tumor recurrence. Thus, the demand for an effective therapeutic strategy for GBM remains elusive. Hopefully, novel products from natural compounds are suggested as possible solutions. They protect glial cells by reducing oxidative stress and neuroinflammation, inhibiting proliferation, inducing apoptosis, inhibiting pro-oncogene events and intensifying the potent anti-tumor therapies. Targeting aberrant cellular pathways in the amelioration of GBM could promote the development of new therapeutic options that improve patient quality of life and extend survival. Consequently, our review emphasizes several natural compounds in GBM treatment. We also assessed the potential of drug delivery techniques such as nanoparticles, Gliadel wafers and drug delivery using cellular carriers which could lead to a novel path for the obliteration of GBM.
Keyphrases
- drug delivery
- poor prognosis
- oxidative stress
- cancer therapy
- induced apoptosis
- signaling pathway
- cell proliferation
- free survival
- cell cycle arrest
- long non coding rna
- endoplasmic reticulum stress
- cell death
- early stage
- traumatic brain injury
- dna damage
- pi k akt
- spinal cord injury
- neuropathic pain
- risk assessment
- combination therapy
- locally advanced
- ischemia reperfusion injury
- spinal cord
- brain injury
- climate change
- human health
- electronic health record
- adverse drug
- replacement therapy