Updates on Molecular Targeted Therapies for CNS Tumors

The challenges in identifying effective therapies for CNS tumors continue to be daunting. Potentially effective targeted therapies must be able to penetrate the blood-brain barrier to reach the tumor and, in sufficient concentrations, to result in meaningful treatment responses. Moreover, molecular...

Full description

Saved in:
Bibliographic Details
Other Authors: Pan, Edward (Editor)
Format: Electronic Book Chapter
Language:English
Published: MDPI - Multidisciplinary Digital Publishing Institute 2023
Subjects:
MET
NF1
PFA
PFB
GBM
LPS
n/a
Online Access:DOAB: download the publication
DOAB: description of the publication
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000naaaa2200000uu 4500
001 doab_20_500_12854_113964
005 20230911
003 oapen
006 m o d
007 cr|mn|---annan
008 20230911s2023 xx |||||o ||| 0|eng d
020 |a books978-3-0365-8529-1 
020 |a 9783036585284 
020 |a 9783036585291 
040 |a oapen  |c oapen 
024 7 |a 10.3390/books978-3-0365-8529-1  |c doi 
041 0 |a eng 
042 |a dc 
072 7 |a M  |2 bicssc 
072 7 |a MJCL  |2 bicssc 
100 1 |a Pan, Edward  |4 edt 
700 1 |a Pan, Edward  |4 oth 
245 1 0 |a Updates on Molecular Targeted Therapies for CNS Tumors 
260 |b MDPI - Multidisciplinary Digital Publishing Institute  |c 2023 
300 |a 1 electronic resource (368 p.) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
506 0 |a Open Access  |2 star  |f Unrestricted online access 
520 |a The challenges in identifying effective therapies for CNS tumors continue to be daunting. Potentially effective targeted therapies must be able to penetrate the blood-brain barrier to reach the tumor and, in sufficient concentrations, to result in meaningful treatment responses. Moreover, molecular targets must be key drivers in the growth and progression of CNS tumors. Numerous potentially efficacious therapies have failed in randomized clinical trials due to other factors, including subclonal genetic intratumoral heterogeneity (particularly within malignant gliomas), epigenetic heterogeneity, and failure to target important factors involved in the tumor microenvironment. Developing effective targeted therapies requires a thorough fundamental understanding of the genetic and epigenetic factors driving tumor progression, the interactions between CNS tumor cells and the tumor microenvironment, and the key mechanisms of tumor treatment resistance. In this Special Issue, experts in the field of CNS tumors will highlight the most promising molecular targets in the development of treatments for patients with CNS tumors. 
540 |a Creative Commons  |f https://creativecommons.org/licenses/by/4.0/  |2 cc  |4 https://creativecommons.org/licenses/by/4.0/ 
546 |a English 
650 7 |a Medicine  |2 bicssc 
650 7 |a Oncology  |2 bicssc 
653 |a glioblastoma molecular classification 
653 |a ERK/MAPK pathway 
653 |a PI3K/PTEN pathway 
653 |a receptor tyrosine kinase 
653 |a EGFR 
653 |a PDGFRA 
653 |a FGFR3 
653 |a MET 
653 |a EPHB2 
653 |a NF1 
653 |a immunotherapy 
653 |a glioblastoma 
653 |a blood-brain barrier 
653 |a central nervous system 
653 |a T cells 
653 |a T lymphocytes 
653 |a PCNSL 
653 |a CNS lymphoma 
653 |a methotrexate 
653 |a novel therapies 
653 |a novel therapeutics 
653 |a neurofibromatosis 
653 |a low grade glioma 
653 |a plexiform neurofibroma 
653 |a vestibular schwannoma 
653 |a glioma 
653 |a tumor mutation burden 
653 |a neoantigen 
653 |a immune score 
653 |a germline mutation 
653 |a antigen processing and presentation 
653 |a ependymoma 
653 |a subependymoma 
653 |a RELA 
653 |a YAP1 
653 |a ZFTA 
653 |a PFA 
653 |a PFB 
653 |a MYCN 
653 |a Group A 
653 |a Group B 
653 |a myxopapillary 
653 |a targeted therapy 
653 |a diffuse midline gliomas 
653 |a molecular targets 
653 |a potential therapy development 
653 |a intraparenchymal metastases 
653 |a CNS disease 
653 |a metastatic disease 
653 |a tyrosine kinase inhibitors 
653 |a monoclonal antibodies 
653 |a Warburg effect 
653 |a mass spectrometry 
653 |a isotope labeling 
653 |a cancer metabolism 
653 |a pediatric brain tumor 
653 |a adenosine 
653 |a tumor microenvironment 
653 |a A2AAR antagonist 
653 |a immune evasion 
653 |a adenosine receptors 
653 |a bevacizumab 
653 |a temozolomide 
653 |a progression 
653 |a biomarker 
653 |a neoplastic 
653 |a meningitis 
653 |a leptomeningeal 
653 |a chemotherapy 
653 |a radiotherapy 
653 |a intrathecal 
653 |a GBM 
653 |a U87MG 
653 |a A172 
653 |a Metformin 
653 |a LPS 
653 |a antioxidant 
653 |a cell cycle arrest 
653 |a apoptosis 
653 |a low-grade glioma 
653 |a preclinical models 
653 |a IDH-mutant glioma 
653 |a patient avatars 
653 |a methylation 
653 |a methylomics 
653 |a G-CIMP 
653 |a MGMT 
653 |a DNMT 
653 |a ATRX 
653 |a H3K27M 
653 |a CpG island 
653 |a tumor suppressor 
653 |a methyltransferases 
653 |a histone acetylation 
653 |a brain tumor 
653 |a brain metastasis 
653 |a lung cancer 
653 |a lung malignancy 
653 |a progression-free survival 
653 |a epidermal growth factor receptor 
653 |a lung carcinoma 
653 |a molecular therapy 
653 |a whole-brain radiation therapy 
653 |a stereotactic radiosurgery 
653 |a KIF11 
653 |a n/a 
856 4 0 |a www.oapen.org  |u https://mdpi.com/books/pdfview/book/7808  |7 0  |z DOAB: download the publication 
856 4 0 |a www.oapen.org  |u https://directory.doabooks.org/handle/20.500.12854/113964  |7 0  |z DOAB: description of the publication