Andreas Waha
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View article: PATH-57. The GLIOSCREEN trial: Feasibility, genomic landscape, and clinical impact of prospective comprehensive molecular profiling in newly diagnosed glioma
PATH-57. The GLIOSCREEN trial: Feasibility, genomic landscape, and clinical impact of prospective comprehensive molecular profiling in newly diagnosed glioma Open
BACKGROUND Advances in molecular profiling have significantly improved the diagnostic precision of diffuse gliomas. However, translating genomic data into individualized clinical strategies remains challenging due to the heterogeneity of g…
View article: P01.24.B CORE2EDGE: A HUMAN GLIOBLASTOMA ORGANOID AND BRAIN SLICE CO-CULTURE MODEL CAPTURING TUMOR INFILTRATION AND TRANSCRIPTIONAL HETEROGENEITY FROM CORE TO SINGLE-CELL DISPERSION
P01.24.B CORE2EDGE: A HUMAN GLIOBLASTOMA ORGANOID AND BRAIN SLICE CO-CULTURE MODEL CAPTURING TUMOR INFILTRATION AND TRANSCRIPTIONAL HETEROGENEITY FROM CORE TO SINGLE-CELL DISPERSION Open
BACKGROUND Glioblastomas function as intricate cellular networks that extend into the surrounding brain tissue enabling long distance communication. This malignant connectivity spans from the tumor core to remote infiltration zones, suppor…
View article: Flow cytometry protocol for cell death analysis in glioblastoma organoids: A technical note
Flow cytometry protocol for cell death analysis in glioblastoma organoids: A technical note Open
Tumor organoid models have emerged as a promising tool in cancer research. By preserving intra- and intertumoral heterogeneity and structural integrity they provide a physiologically relevant platform for drug-response studies. However, va…
View article: Pitfalls in the evaluation of CDKN2A copy number status in meningioma
Pitfalls in the evaluation of CDKN2A copy number status in meningioma Open
View article: MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade glioma
MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade glioma Open
Pediatric high-grade glioma (pedHGG) can occur as first manifestation of cancer predisposition syndromes resulting from pathogenic germline variants in the DNA mismatch repair (MMR) genes MSH2 , MSH6 , MLH1 , and PMS2 . The aim of this stu…
View article: Tonabersat enhances temozolomide‐mediated cytotoxicity in glioblastoma by disrupting intercellular connectivity through connexin 43 inhibition
Tonabersat enhances temozolomide‐mediated cytotoxicity in glioblastoma by disrupting intercellular connectivity through connexin 43 inhibition Open
Glioblastoma cells rely on connexin 43 (Cx43)‐based gap junctions (GJs) for intercellular communication, enabling them to integrate into a widely branched malignant network. Although there are promising prospects for new targeted therapies…
View article: Cerebellar glioblastoma in adults: a comparative single-center matched pair analysis and systematic review of the literature
Cerebellar glioblastoma in adults: a comparative single-center matched pair analysis and systematic review of the literature Open
View article: Melanoma Brain Metastases Patient-Derived Organoids: An In Vitro Platform for Drug Screening
Melanoma Brain Metastases Patient-Derived Organoids: An In Vitro Platform for Drug Screening Open
Background and aims: Brain metastases are prevalent in the late stages of malignant melanoma. Multimodal therapy remains challenging. Patient-derived organoids (PDOs) represent a valuable pre-clinical model, faithfully recapitulating key a…
View article: Cerebellar glioblastoma in adults: a comparative single-center matched pair analysis and systematic review of the literature
Cerebellar glioblastoma in adults: a comparative single-center matched pair analysis and systematic review of the literature Open
Purpose The rarity of cerebellar glioblastoma presents a significant challenge in clinical practice due to the lack of extensive prognostic data on long-term survival rates, rendering it an underrepresented entity compared to its supratent…
View article: Melanoma Brain Metastases Patient-Derived Organoids: an <em>in Vitro</em> Platform for Drug Screening
Melanoma Brain Metastases Patient-Derived Organoids: an <em>in Vitro</em> Platform for Drug Screening Open
Background and aims: Brain metastases are prevalent in the late stages of malignant melanoma. Multimodal therapy remains challenging. Patient-derived organoids (PDOs) represent a valuable pre-clinical model, faithfully recapitulating key a…
View article: HGG-26. MLH1, MSH2, MSH6, AND PMS2 IMMUNOHISTOCHEMISTRY REPRESENTS A HIGHLY SENSITIVE SCREENING METHOD FOR MISMATCH REPAIR DEFICIENCY SYNDROMES IN PEDIATRIC HIGH-GRADE GLIOMA
HGG-26. MLH1, MSH2, MSH6, AND PMS2 IMMUNOHISTOCHEMISTRY REPRESENTS A HIGHLY SENSITIVE SCREENING METHOD FOR MISMATCH REPAIR DEFICIENCY SYNDROMES IN PEDIATRIC HIGH-GRADE GLIOMA Open
BACKGROUND Pediatric central nervous system (CNS) tumors can occur as first manifestations of cancer predisposition syndromes (CPS) resulting from pathogenic variants in DNA mismatch repair (MMR) genes MLH1, MSH2, MSH6, and PMS2. Early det…
View article: <i>FH</i>-mutant glioma displaying the epigenetic signature of <i>IDH</i>-mutant astrocytomas
<i>FH</i>-mutant glioma displaying the epigenetic signature of <i>IDH</i>-mutant astrocytomas Open
View article: <scp> <i>TRIM28</i> </scp> inactivation in epithelial nephroblastoma is frequent and often associated with predisposing <scp> <i>TRIM28</i> </scp> germline variants
<span> <i>TRIM28</i> </span> inactivation in epithelial nephroblastoma is frequent and often associated with predisposing <span> <i>TRIM28</i> </span> germline variants Open
Wilms tumors (WTs) are histologically diverse childhood cancers with variable contributions of blastema, stroma, and epithelia. A variety of cancer genes operate in WTs, including the tripartite‐motif‐containing‐28 gene ( TRIM28 ). Case re…
View article: Downregulation of MGMT expression by targeted editing of DNA methylation enhances temozolomide sensitivity in glioblastoma
Downregulation of MGMT expression by targeted editing of DNA methylation enhances temozolomide sensitivity in glioblastoma Open
Glioblastoma is the most common and aggressive primary tumor of the central nervous system with poor outcome. Current gold standard treatment is surgical resection followed by a combination of radio- and chemotherapy. Efficacy of temozolom…
View article: Supplemental Figure 4 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 4 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Full-length blots presented in this study.
View article: Supplementary legend from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplementary legend from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Supplementary legend
View article: Supplemental Table 3 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Table 3 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Killer plate® compounds and screening data.
View article: Supplemental Figure 3 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 3 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Cell cycle analysis of pGBM #046 after niclosamide exposure.
View article: Supplemental Table 2 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Table 2 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
List of pGBMs and their respective passage numbers used for the various experimental paradigms in this study.
View article: Supplemental Figure 1 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 1 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Niclosamide dose-response curves.
View article: Supplemental Table 3 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Table 3 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Killer plate® compounds and screening data.
View article: Supplemental Figure 2 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 2 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Niclosamide dose-response curves, supplementing data presented in Figure 2B.
View article: Data from Anticancer Effects of Niclosamide in Human Glioblastoma
Data from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Purpose: Glioblastoma is a highly malignant, invariably fatal brain tumor for which effective pharmacotherapy remains an unmet medical need.Experimental Design: Screening of a compound library of 160 synthetic and natural tox…
View article: Data from Anticancer Effects of Niclosamide in Human Glioblastoma
Data from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Purpose: Glioblastoma is a highly malignant, invariably fatal brain tumor for which effective pharmacotherapy remains an unmet medical need.Experimental Design: Screening of a compound library of 160 synthetic and natural tox…
View article: Supplemental Figure 2 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 2 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Niclosamide dose-response curves, supplementing data presented in Figure 2B.
View article: Supplemental Figure 3 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 3 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Cell cycle analysis of pGBM #046 after niclosamide exposure.
View article: Supplemental Table 1 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Table 1 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Patient data.
View article: Supplemental Figure 4 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Figure 4 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Full-length blots presented in this study.
View article: Supplemental Table 2 from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplemental Table 2 from Anticancer Effects of Niclosamide in Human Glioblastoma Open
List of pGBMs and their respective passage numbers used for the various experimental paradigms in this study.
View article: Supplementary legend from Anticancer Effects of Niclosamide in Human Glioblastoma
Supplementary legend from Anticancer Effects of Niclosamide in Human Glioblastoma Open
Supplementary legend