Tumor Infiltrating Lymphocytes Affect the Outcome of Patients with Operable Triple-Negative Breast Cancer in Combination with Mutated Amino Acid Classes

Autor: Paris Kosmidis, Amanda Psyrri, Irene Nicolaou, Gerasimos Aravantinos, Flora Zagouri, George Pentheroudakis, Zoi Alexopoulou, Sotiris Lakis, Christos Papadimitriou, Evangelia Razis, Ioannis Efstratiou, George Fountzilas, Vassiliki Kotoula, Eleni Giannoulatou, Ioannis S. Vlachos, Dimitrios Pectasides, Kyriakos Chatzopoulos, Kyriaki Papadopoulou, Pavlos Papakostas, Maria Sotiropoulou, Helen Gogas
Jazyk: angličtina
Rok vydání: 2016
Předmět:
0301 basic medicine
Cancer Treatment
lcsh:Medicine
medicine.disease_cause
0302 clinical medicine
Breast Tumors
Basic Cancer Research
Medicine and Health Sciences
Medicine
Stromal tumor
lcsh:Science
Immune Response
Triple-negative breast cancer
Mutation
Multidisciplinary
hemic and immune systems
Nonsense Mutation
Genomics
Phenotype
Oncology
030220 oncology & carcinogenesis
Amino Acid Analysis
Anatomy
Research Article
Histology
Concordance
Nonsense mutation
Immunology
chemical and pharmacologic phenomena
Research and Analysis Methods
03 medical and health sciences
Breast cancer
Cancer Genomics
Genomic Medicine
Breast Cancer
Genetics
Molecular Biology Techniques
Molecular Biology
Molecular Biology Assays and Analysis Techniques
business.industry
Tumor-infiltrating lymphocytes
lcsh:R
Biology and Life Sciences
Cancers and Neoplasms
medicine.disease
030104 developmental biology
Cancer research
lcsh:Q
business
Zdroj: PLoS ONE
PLoS ONE, Vol 11, Iss 9, p e0163138 (2016)
ISSN: 1932-6203
Popis: Background Stromal tumor infiltrating lymphocytes (TILs) density is an outcome predictor in triple-negative breast cancer (TNBC). Herein we asked whether TILs are related to coding mutation load and to the chemical class of the resulting mutated amino acids, i.e., charged, polar, and hydrophobic mutations. Methods We examined paraffin tumors from TNBC patients who had been treated with adjuvant chemotherapy mostly within clinical trials (training cohort, N = 133; validation, N = 190) for phenotype concordance; TILs density; mutation load and types. Results Concordance of TNBC phenotypes was 42.1% upon local / central, and 72% upon central / central pathology assessment. TILs were not associated with mutation load, type and class of mutated amino acids. Polar and charged mutation patterns differed between TP53 and PIK3CA (p50% TILs tumors (training p = 0.003; validation p = 0.015). Conclusions TILs density is unrelated to mutation load in TNBC, which may be regarded as an unstable phenotype. If further validated, hydrophobic mutations along with TILs density may help identifying TNBC patients in higher risk for relapse.
Databáze: OpenAIRE