Literature DB >> 21676924

Direct evidence for concurrent morphological and genetic heterogeneity in an invasive ductal carcinoma of triple-negative phenotype.

Neill Patani1, Violetta Barbashina, Maryou B K Lambros, Arnaud Gauthier, Marthe Mansour, Alan Mackay, Jorge S Reis-Filho.   

Abstract

Triple-negative breast cancers account for 12-17% of all invasive breast carcinomas and comprise a heterogeneous group of tumours, with varying histological features and clinical behaviours. Focal apocrine differentiation can be associated with a subset of these lesions. To establish whether morphological diversity is associated with divergent genetic aberrations the genomic profiles of microdissected, morphologically distinct components from an invasive ductal carcinoma of no special type with triple-negative phenotype and a region of apocrine differentiation were determined by high-resolution microarray-based comparative genomic hybridisation and validated by fluorescence in-situ hybridisation. Morphologically distinct components were found to harbour differing genetic aberrations, with the region of apocrine differentiation demonstrating genomic gains and losses on chromosome arms 9p and 9q, respectively, not present in non-apocrine areas. The results provide additional direct evidence of intra-tumour genetic heterogeneity in breast cancer and demonstrate that morphologically distinct regions can be associated with distinct genetic aberrations.

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Year:  2011        PMID: 21676924     DOI: 10.1136/jclinpath-2011-200135

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  10 in total

Review 1.  Clinical management of breast cancer heterogeneity.

Authors:  Dimitrios Zardavas; Alexandre Irrthum; Charles Swanton; Martine Piccart
Journal:  Nat Rev Clin Oncol       Date:  2015-04-21       Impact factor: 66.675

Review 2.  Beyond Genetics: Metastasis as an Adaptive Response in Breast Cancer.

Authors:  Federica Ruscitto; Niccolò Roda; Chiara Priami; Enrica Migliaccio; Pier Giuseppe Pelicci
Journal:  Int J Mol Sci       Date:  2022-06-03       Impact factor: 6.208

3.  Synchronous clear cell renal cell carcinoma and tubulocystic carcinoma: genetic evidence of independent ontogenesis and implications of chromosomal imbalances in tumor progression.

Authors:  Gabriela Quiroga-Garza; Sergio Piña-Oviedo; Karime Cuevas-Ocampo; Richard Goldfarb; Mary R Schwartz; Alberto G Ayala; Federico A Monzon
Journal:  Diagn Pathol       Date:  2012-02-27       Impact factor: 2.644

Review 4.  Breast cancer intra-tumor heterogeneity.

Authors:  Luciano G Martelotto; Charlotte K Y Ng; Salvatore Piscuoglio; Britta Weigelt; Jorge S Reis-Filho
Journal:  Breast Cancer Res       Date:  2014-05-20       Impact factor: 6.466

5.  Tumor heterogeneity at protein level as an independent prognostic factor in endometrial cancer.

Authors:  Anna Supernat; Sylwia Lapińska-Szumczyk; Hanna Majewska; Jacek Gulczyński; Wojciech Biernat; Dariusz Wydra; Anna J Zaczek
Journal:  Transl Oncol       Date:  2014-07-19       Impact factor: 4.243

Review 6.  Tumor Heterogeneity in Breast Cancer.

Authors:  Gulisa Turashvili; Edi Brogi
Journal:  Front Med (Lausanne)       Date:  2017-12-08

7.  Quantification of intrinsic subtype ambiguity in Luminal A breast cancer and its relationship to clinical outcomes.

Authors:  Neeraj Kumar; Dan Zhao; Dulal Bhaumik; Amit Sethi; Peter H Gann
Journal:  BMC Cancer       Date:  2019-03-08       Impact factor: 4.430

8.  Intratumoral heterogeneity of second-harmonic generation scattering from tumor collagen and its effects on metastatic risk prediction.

Authors:  Danielle E Desa; Robert L Strawderman; Wencheng Wu; Robert L Hill; Marcel Smid; J W M Martens; Bradley M Turner; Edward B Brown
Journal:  BMC Cancer       Date:  2020-12-10       Impact factor: 4.430

Review 9.  The Role of Genomic Profiling in Advanced Breast Cancer: The Two Faces of Janus.

Authors:  Yesim Eralp
Journal:  Transl Oncogenomics       Date:  2016-08-14

10.  Clinically relevant morphological structures in breast cancer represent transcriptionally distinct tumor cell populations with varied degrees of epithelial-mesenchymal transition and CD44+CD24- stemness.

Authors:  Evgeny V Denisov; Nikolay A Skryabin; Tatiana S Gerashchenko; Lubov A Tashireva; Jochen Wilhelm; Mikhail A Buldakov; Aleksei A Sleptcov; Igor N Lebedev; Sergey V Vtorushin; Marina V Zavyalova; Nadezhda V Cherdyntseva; Vladimir M Perelmuter
Journal:  Oncotarget       Date:  2017-05-19
  10 in total

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