TY - JOUR
T1 - Understanding Neovascularization in Glioblastoma: Insights from the Current Literature
AU - Ballato, M.
AU - Germana, E.
AU - Ricciardi, G.
AU - Giordano, W. G.
AU - Tralongo, P.
AU - Buccarelli, M.
AU - Castellani, G.
AU - Ricci-Vitiani, L.
AU - D'Alessandris, Quintino Giorgio
AU - Giuffre, G.
AU - Pizzimenti, C.
AU - Fiorentino, V.
AU - Zuccala, V.
AU - Ieni, A.
AU - Caffo, M.
AU - Fadda, G.
AU - Martini, M.
PY - 2025
Y1 - 2025
N2 - Glioblastomas (GBMs), among the most aggressive and resilient brain tumors, characteristically exhibit high angiogenic potential, leading to the formation of a dense yet aberrant vasculature, both morphologically and functionally. With these premises, numerous expectations were initially placed on anti-angiogenic therapies, soon dashed by their limited efficacy in concretely improving patient outcomes. Neovascularization in GBM soon emerged as a complex, dynamic, and heterogeneous process, hard to manage with the classical standard of care. Growing evidence has revealed the existence of numerous non-canonical strategies of angiogenesis, variously exploited by GBM to meet its ever-increasing metabolic demand and differently involved in tumor progression, recurrence, and escape from treatments. In this review, we provide an accurate description of each neovascularization mode encountered in GBM tumors to date, highlighting the molecular players and signaling cascades primarily involved. We also detail the key architectural and functional aspects characteristic of the GBM vascular compartment because of an intricate crosstalk between the different angiogenic networks. Additionally, we explore the repertoire of emerging therapies against GBM that are currently under study, concluding with a question: faced with such a challenging scenario, could combined therapies, tailored to the patient’s genetic signatures, represent an effective game changer?
AB - Glioblastomas (GBMs), among the most aggressive and resilient brain tumors, characteristically exhibit high angiogenic potential, leading to the formation of a dense yet aberrant vasculature, both morphologically and functionally. With these premises, numerous expectations were initially placed on anti-angiogenic therapies, soon dashed by their limited efficacy in concretely improving patient outcomes. Neovascularization in GBM soon emerged as a complex, dynamic, and heterogeneous process, hard to manage with the classical standard of care. Growing evidence has revealed the existence of numerous non-canonical strategies of angiogenesis, variously exploited by GBM to meet its ever-increasing metabolic demand and differently involved in tumor progression, recurrence, and escape from treatments. In this review, we provide an accurate description of each neovascularization mode encountered in GBM tumors to date, highlighting the molecular players and signaling cascades primarily involved. We also detail the key architectural and functional aspects characteristic of the GBM vascular compartment because of an intricate crosstalk between the different angiogenic networks. Additionally, we explore the repertoire of emerging therapies against GBM that are currently under study, concluding with a question: faced with such a challenging scenario, could combined therapies, tailored to the patient’s genetic signatures, represent an effective game changer?
KW - aberrant angiogenesis
KW - emerging therapies
KW - glioblastoma (GBM)
KW - pro-angiogenic factors
KW - strategies of neovascularization
KW - aberrant angiogenesis
KW - emerging therapies
KW - glioblastoma (GBM)
KW - pro-angiogenic factors
KW - strategies of neovascularization
UR - https://publicatt.unicatt.it/handle/10807/314246
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=105001132546&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105001132546&origin=inward
U2 - 10.3390/ijms26062763
DO - 10.3390/ijms26062763
M3 - Article
SN - 1422-0067
VL - 26
SP - 2763
EP - 2763
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 6
ER -