Potential Role of Carbon Nanomaterials in the Treatment of Malignant Brain Gliomas.
Maria CaffoAntonello CurcioKumar RajivGerardo CarusoMario VenzaAntonino GermanòPublished in: Cancers (2023)
Malignant gliomas are the most common primary brain tumors in adults up to an extent of 78% of all primary malignant brain tumors. However, total surgical resection is almost unachievable due to the considerable infiltrative ability of glial cells. The efficacy of current multimodal therapeutic strategies is, furthermore, limited by the lack of specific therapies against malignant cells, and, therefore, the prognosis of these in patients is still very unfavorable. The limitations of conventional therapies, which may result from inefficient delivery of the therapeutic or contrast agent to brain tumors, are major reasons for this unsolved clinical problem. The major problem in brain drug delivery is the presence of the blood-brain barrier, which limits the delivery of many chemotherapeutic agents. Nanoparticles, thanks to their chemical configuration, are able to go through the blood-brain barrier carrying drugs or genes targeted against gliomas. Carbon nanomaterials show distinct properties including electronic properties, a penetrating capability on the cell membrane, high drug-loading and pH-dependent therapeutic unloading capacities, thermal properties, a large surface area, and easy modification with molecules, which render them as suitable candidates for deliver drugs. In this review, we will focus on the potential effectiveness of the use of carbon nanomaterials in the treatment of malignant gliomas and discuss the current progress of in vitro and in vivo researches of carbon nanomaterials-based drug delivery to brain.
Keyphrases
- drug delivery
- high grade
- induced apoptosis
- resting state
- white matter
- cancer therapy
- cell cycle arrest
- end stage renal disease
- randomized controlled trial
- ejection fraction
- newly diagnosed
- magnetic resonance
- chronic kidney disease
- gene expression
- functional connectivity
- oxidative stress
- blood brain barrier
- endoplasmic reticulum stress
- combination therapy
- signaling pathway
- pi k akt
- patient reported
- prognostic factors