Molecular alterations in triple-negative breast cancer-the road to new treatment strategies.
By Carsten Denkert, C. Liedtke, Andrew Tutt, G. von Minckwitz. The Lancet, 2017
699 citations recorded by the source corpus.
Subfields: Cancer Research, Oncology
View Paper: https://www.semanticscholar.org/paper/3b21ff2e1d2617d644809d7d80377339f5a9b768
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In Oncology
Citations in the corpus
- Breast cancer development and progression: Risk factors, cancer stem cells, signaling pathways, genomics, and molecular pathogenesis (2018, methodology): “The diagnosis of TNBC relies on the accurate determination of ER and PR protein levels by immunohistochemistry (IHC) and of HER2 by IHC and/or fluorescence in situ hybridization (FISH).(286,287) Such accurate assessment is crucial to avoid false diagnosis of ERnegative and/or HER2-negative disease i”
- Recent advances in therapeutic strategies for triple-negative breast cancer (2022, background): “It is worth mentioning that a deficiency in homologous recombination, which is partly associated with the loss of breast cancer susceptibility gene (BRCA) function in BC, is correlated with a good response to cisplatin treatment [11].”
- A Structured Tumor-Immune Microenvironment in Triple Negative Breast Cancer Revealed by Multiplexed Ion Beam Imaging (2018, neutral): “Experimental model and subject details Samples of TNBC patients of no special type (ER and PR positivity less than 1%, HER2 unamplified and Her2 not 3), as well as tonsil, lymph node, placenta, gastrointestinal tract and breast carcinoma controls were obtained from Stanford Pathology department.”