Literature DB >> 21138954

Molecular stratification of triple-negative breast cancers.

Charles M Perou1.   

Abstract

Research focused on the analysis and classification of breast tumors, primarily using DNA microarrays and patterns of gene expression, has resulted in distinct tumor subtypes. Although no knowledge of patient survival or outcomes was used to derive these gene descriptions, these different classes based upon patterns of gene expression have important prognostic implications. Predictive markers in estrogen receptor-negative and triple-negative disease will be particularly important because in the absence of therapy, these tumor subtypes tend to have a poor prognosis. In addition, the claudin-low subgroup has been found to be common within the triple-negative cancers and may have further prognostic and therapeutic implications. Patients with triple-negative breast cancer do benefit from chemotherapy, but better treatment options are needed that are less toxic, reduce the risk of disease progression, and are more targeted to this patient population. Potential treatments include poly (ADP-ribose) polymerase inhibitors, and therapies that target cancer stem cells could also have an important impact in these patients. This article will focus on the molecular stratification of triple-negative breast cancers and the therapeutic implications of these classifications.

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Year:  2010        PMID: 21138954     DOI: 10.1634/theoncologist.2010-S5-39

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  87 in total

1.  How do I treat "triple-negative" disease.

Authors:  Christos Vaklavas; Andres Forero-Torres
Journal:  Curr Treat Options Oncol       Date:  2011-12

2.  Exploring molecular pathways of triple-negative breast cancer.

Authors:  Valeria Ossovskaya; Yipeng Wang; Adam Budoff; Qiang Xu; Alexander Lituev; Olga Potapova; Gordon Vansant; Joseph Monforte; Nikolai Daraselia
Journal:  Genes Cancer       Date:  2011-09

3.  Metformin attenuates transforming growth factor beta (TGF-β) mediated oncogenesis in mesenchymal stem-like/claudin-low triple negative breast cancer.

Authors:  Reema Wahdan-Alaswad; J Chuck Harrell; Zeying Fan; Susan M Edgerton; Bolin Liu; Ann D Thor
Journal:  Cell Cycle       Date:  2016       Impact factor: 4.534

4.  The epigenetic silencing of the estrogen receptor (ER) by hypermethylation of the ESR1 promoter is seen predominantly in triple-negative breast cancers in Indian women.

Authors:  Jyothi S Prabhu; Kanu Wahi; Aruna Korlimarla; Marjorrie Correa; Suraj Manjunath; N Raman; B S Srinath; T S Sridhar
Journal:  Tumour Biol       Date:  2012-02-24

Review 5.  Insights into Molecular Classifications of Triple-Negative Breast Cancer: Improving Patient Selection for Treatment.

Authors:  Ana C Garrido-Castro; Nancy U Lin; Kornelia Polyak
Journal:  Cancer Discov       Date:  2019-01-24       Impact factor: 39.397

Review 6.  Targeting autophagy in breast cancer.

Authors:  Paola Maycotte; Andrew Thorburn
Journal:  World J Clin Oncol       Date:  2014-08-10

7.  Thioridazine inhibits self-renewal in breast cancer cells via DRD2-dependent STAT3 inhibition, but induces a G1 arrest independent of DRD2.

Authors:  Matthew Tegowski; Cheng Fan; Albert S Baldwin
Journal:  J Biol Chem       Date:  2018-08-21       Impact factor: 5.157

8.  P4 medicine: how systems medicine will transform the healthcare sector and society.

Authors:  Mauricio Flores; Gustavo Glusman; Kristin Brogaard; Nathan D Price; Leroy Hood
Journal:  Per Med       Date:  2013       Impact factor: 2.512

9.  Effective Targeting of Estrogen Receptor-Negative Breast Cancers with the Protein Kinase D Inhibitor CRT0066101.

Authors:  Sahra Borges; Edith A Perez; E Aubrey Thompson; Derek C Radisky; Xochiquetzal J Geiger; Peter Storz
Journal:  Mol Cancer Ther       Date:  2015-04-07       Impact factor: 6.261

10.  MicroRNA 9-3p targets β1 integrin to sensitize claudin-low breast cancer cells to MEK inhibition.

Authors:  Jon S Zawistowski; Kazuhiro Nakamura; Joel S Parker; Deborah A Granger; Brian T Golitz; Gary L Johnson
Journal:  Mol Cell Biol       Date:  2013-03-25       Impact factor: 4.272

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