Literature DB >> 20818337

Biologic profiling of lymph node negative breast cancers by means of microRNA expression.

Emiel A M Janssen1, Aida Slewa, Einar Gudlaugsson, Kristin Jonsdottir, Ivar Skaland, Håvard Søiland, Jan P A Baak.   

Abstract

Breast cancer is a heterogeneous disease. Different subgroups can be recognized on the basis of the steroid receptors, HER-2, cytokeratin expression and proliferation patterns. As a result of mRNA-profiling studies, five major groups can be recognized, of which the triple-negative and basal-like tumors have the worst prognosis. Many of these tumors have a high proliferation that has the strongest prognostic value in node negative breast cancer. In the current study we analyzed the microRNA pattern in 103 lymph node negative breast cancers and compared these profiles with different biological characteristics and clinicopathological features. Unsupervised hierarchical cluster analysis divides the patients into four main groups, of which the basal-like/triple-negative group is the most prominent (11% of all cases), the luminal A cancers containing the Her2 negative and estrogen receptor/progesterone receptor-positive tumors is the largest group (57%), and the group of luminal B (32%) is more heterogeneous and contains the Her2 positive/estrogen receptor-negative patients as well. The highest overall classification values by analysis of variance followed by cross validation (leave one sample out and reselect genes) were found for cytokeratin 5 and 6, triple-negative and estrogen receptor, with 97, 90 and 90% accuracy, respectively. MiR-106b gene is prominent in all of these signatures and correlates strongest with high proliferation. Other interesting observations are the presence of several microRNAs (miR532-5p, miR-500, miR362-5p, and miR502-3p) located at Xp11.23 in cancers with a triple-negative signature, and the upregulation of several miR-17 cluster members in estrogen receptor-negative tumors. The current study shows that estrogen receptor negativity and cytokeratin 5 and 6 expression are important, and specific biological processes in lymph node negative breast cancer, as microRNA signatures are strongest in these subgroups.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20818337     DOI: 10.1038/modpathol.2010.177

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  31 in total

1.  Clinical and biological impact of miR-18a expression in breast cancer after neoadjuvant chemotherapy.

Authors:  Ginés Luengo-Gil; Elena García-Martínez; Asunción Chaves-Benito; Pablo Conesa-Zamora; Esther Navarro-Manzano; Enrique González-Billalabeitia; Elisa García-Garre; Alberto Martínez-Carrasco; Vicente Vicente; Francisco Ayala de la Peña
Journal:  Cell Oncol (Dordr)       Date:  2019-05-21       Impact factor: 6.730

Review 2.  Integrating contextual miRNA and protein signatures for diagnostic and treatment decisions in cancer.

Authors:  Lorenzo F Sempere
Journal:  Expert Rev Mol Diagn       Date:  2011-11       Impact factor: 5.225

Review 3.  Predictive and Prognostic Value of Non-Coding RNA in Breast Cancer.

Authors:  Navid Sobhani; Richard Chahwan; Raheleh Roudi; Rachel Morris; Stefano Volinia; Dafei Chai; Alberto D'Angelo; Daniele Generali
Journal:  Cancers (Basel)       Date:  2022-06-15       Impact factor: 6.575

4.  Functions and regulation of MUC13 mucin in colon cancer cells.

Authors:  Brij K Gupta; Diane M Maher; Mara C Ebeling; Phillip D Stephenson; Susan E Puumala; Michael R Koch; Hiroyuki Aburatani; Meena Jaggi; Subhash C Chauhan
Journal:  J Gastroenterol       Date:  2013-10-07       Impact factor: 7.527

5.  MicroRNA signature in the chemoprevention of functionally-enriched stem and progenitor pools (FESPP) by Active Hexose Correlated Compound (AHCC).

Authors:  Émilie A Graham; Jean-François Mallet; Majed Jambi; Hiroshi Nishioka; Kohei Homma; Chantal Matar
Journal:  Cancer Biol Ther       Date:  2017-09-08       Impact factor: 4.742

Review 6.  MicroRNAs in brain metastases: big things come in small packages.

Authors:  Ryan McDermott; Patrik Gabikian; Purvaba Sarvaiya; Ilya Ulasov; Maciej S Lesniak
Journal:  J Mol Med (Berl)       Date:  2012-11-09       Impact factor: 4.599

7.  Validation of expression patterns for nine miRNAs in 204 lymph-node negative breast cancers.

Authors:  Kristin Jonsdottir; Susanne R Janssen; Fabiana C Da Rosa; Einar Gudlaugsson; Ivar Skaland; Jan P A Baak; Emiel A M Janssen
Journal:  PLoS One       Date:  2012-11-07       Impact factor: 3.240

8.  Expression profiling of cancerous and normal breast tissues identifies microRNAs that are differentially expressed in serum from patients with (metastatic) breast cancer and healthy volunteers.

Authors:  Eleni van Schooneveld; Maartje Ca Wouters; Ilse Van der Auwera; Dieter J Peeters; Hans Wildiers; Peter A Van Dam; Ignace Vergote; Peter B Vermeulen; Luc Y Dirix; Steven J Van Laere
Journal:  Breast Cancer Res       Date:  2012-02-21       Impact factor: 6.466

9.  Global microRNA expression profiling identifies MiR-210 associated with tumor proliferation, invasion and poor clinical outcome in breast cancer.

Authors:  Françoise Rothé; Michail Ignatiadis; Carole Chaboteaux; Benjamin Haibe-Kains; Naïma Kheddoumi; Samira Majjaj; Bassam Badran; Hussein Fayyad-Kazan; Christine Desmedt; Adrian L Harris; Martine Piccart; Christos Sotiriou
Journal:  PLoS One       Date:  2011-06-29       Impact factor: 3.240

10.  Integrated microRNA and mRNA signatures associated with survival in triple negative breast cancer.

Authors:  Luciano Cascione; Pierluigi Gasparini; Francesca Lovat; Stefania Carasi; Alfredo Pulvirenti; Alfredo Ferro; Hansjuerg Alder; Gang He; Andrea Vecchione; Carlo M Croce; Charles L Shapiro; Kay Huebner
Journal:  PLoS One       Date:  2013-02-06       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.