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Image Search Results
Journal: Journal of Clinical Oncology
Article Title: Identification of Clinical and Biologic Correlates Associated With Outcome in Children With Adrenocortical Tumors Without Germline TP53 Mutations: A St Jude Adrenocortical Tumor Registry and Children’s Oncology Group Study
doi: 10.1200/JCO.2017.74.2460
Figure Lengend Snippet: Somatic TP53 mutations in patients with adrenocortical tumors (ACTs) without TP53 mutations. (A) Schematic diagram of acquired TP53 mutations. (B) Kaplan-Meier estimates for progression-free survival (B) in pediatric patients with ACTs with or without acquired TP53 mutations and (C) by TP53 status and disease stage. After discriminating for disease stage and including stage IV disease in the Cox regression model, presence of somatic TP53 mutations was no longer associated with outcome (P = .21). hom, homozygous.
Article Snippet: Large deletions of TP53 and ATRX were assessed using commercial
Techniques:
Journal: Journal of Clinical Oncology
Article Title: Identification of Clinical and Biologic Correlates Associated With Outcome in Children With Adrenocortical Tumors Without Germline TP53 Mutations: A St Jude Adrenocortical Tumor Registry and Children’s Oncology Group Study
doi: 10.1200/JCO.2017.74.2460
Figure Lengend Snippet: Somatic CTNNB1 mutations in patients with adrenocortical tumors (ACTs) without TP53 mutations. (A) Schematic diagram of activating CTNNB1 mutations. (B) Immunohistochemical analysis of β-catenin and yes-associated protein 1 (YAP1) in pediatric ACTs. YAP serves as a surrogate marker for β-catenin expression. Moderate nuclear immunostaining of (i) β-catenin and (ii) YAP in a tumor with the S45P mutation in CTNNB1. Strong nuclear immunoreactivity for (iii) β-catenin and (iv) YAP in a pediatric patient with unknown CTNNB1 molecular status. These results are indicative of Wnt signaling pathway activation. Size bars represent 50 μm. (C) Kaplan-Meier estimates for progression-free survival by CTNNB1 status (P = .80).
Article Snippet: Large deletions of TP53 and ATRX were assessed using commercial
Techniques: Immunohistochemical staining, Marker, Expressing, Immunostaining, Mutagenesis, Activation Assay
Journal: Journal of Clinical Oncology
Article Title: Identification of Clinical and Biologic Correlates Associated With Outcome in Children With Adrenocortical Tumors Without Germline TP53 Mutations: A St Jude Adrenocortical Tumor Registry and Children’s Oncology Group Study
doi: 10.1200/JCO.2017.74.2460
Figure Lengend Snippet: (A) Hematoxylin and eosin staining and Ki-67 labeling index (LI) in pediatric adrenocortical tumors without TP53 mutations: (i, ii) tumor with a high (≥ 15%) Ki-67 labeling index (LI; red arrows indicate mitotic figures), (iii, iv) tumor with a low (< 5%) LI. Size bars represent 50 μm. (B) Kaplan-Meier estimates for progression-free survival (PFS) according to Ki-67 LI showing that Ki-67 LI < 15% was significantly associated with longer PFS (P = .002). (C) Kaplan-Meier estimates for PFS according to Ki-67 LI and disease stage. Ki-67 LI remained significantly associated with outcome after adjusting for disease stage (P = .0048).
Article Snippet: Large deletions of TP53 and ATRX were assessed using commercial
Techniques: Staining, Labeling
Journal: Journal of Clinical Oncology
Article Title: Identification of Clinical and Biologic Correlates Associated With Outcome in Children With Adrenocortical Tumors Without Germline TP53 Mutations: A St Jude Adrenocortical Tumor Registry and Children’s Oncology Group Study
doi: 10.1200/JCO.2017.74.2460
Figure Lengend Snippet: Characteristics of Patients With ACTs Harboring Mutations or No Mutations in TP53
Article Snippet: Large deletions of TP53 and ATRX were assessed using commercial
Techniques: