Literature DB >> 18575772

RhoA protein expression in primary breast cancers and matched lymphocytes is associated with progression of the disease.

Antonia Bellizzi1, Anita Mangia, Annalisa Chiriatti, Stella Petroni, Michele Quaranta, Francesco Schittulli, Andrea Malfettone, Rosa Angela Cardone, Angelo Paradiso, Stephan Joel Reshkin.   

Abstract

RhoA protein is over-expressed in breast cancer and other solid tumors and has been used in tumor biopsies as a quantitative tumor marker for progression, stage and prognosis in molecular detection strategies. Measuring protein markers in plasma or blood cells is preferred to tumor biopsies as it represents a minimally invasive, repeatable measurement that can be followed over time. In this study we evaluated the hypothesis that quantitative RhoA protein expression in circulatory lymphocytes is identically associated with the same tumor clinico-pathological features found in biopsies. RhoA protein levels were analyzed by Western blotting in circulating lymphocytes isolated from 52 consecutive patients with breast cancer and in 34 paired breast tumor biopsies from the same case study, and compared with the following clinico-pathological features of the patients: histological grade, tumor size, steroid receptor status, lymphonode status, proliferative activity and prognosis [Nottingham Prognostic Index (NPI)]. We observed that the level of circulatory, peripheral lymphocyte RhoA expression reflected that found in the matched biopsy of the same patient. Furthermore, similarly to previous reports regarding breast cancer tissue biopsies, the level of RhoA protein expression in both biopsies and in circulatory lymphocytes was positively associated with tumor size, grade, proliferative activity of the tumor biopsy and NPI, while there was no significant association of RhoA protein expression with either estrogen- or progesterone-receptor expression. Our study demonstrated that the association of lymphocyte RhoA protein expression with classical clinico-pathological parameters closely corresponded with that observed for RhoA protein expression in the tumor biopsies. We propose that measurement of RhoA expression in the circulatory lymphocytes of breast cancer patients can be used to predict breast cancer occurrence, progression and prognosis and may prove valuable in the management of cancer patients.

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Year:  2008        PMID: 18575772

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  30 in total

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Journal:  Chem Biol       Date:  2012-06-22

Review 2.  Forcing form and function: biomechanical regulation of tumor evolution.

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Journal:  Trends Cell Biol       Date:  2010-10-01       Impact factor: 20.808

3.  LMO7 mediates cell-specific activation of the Rho-myocardin-related transcription factor-serum response factor pathway and plays an important role in breast cancer cell migration.

Authors:  Qiande Hu; Chun Guo; Yali Li; Bruce J Aronow; Jinsong Zhang
Journal:  Mol Cell Biol       Date:  2011-06-13       Impact factor: 4.272

4.  Deciphering the transcriptional complex critical for RhoA gene expression and cancer metastasis.

Authors:  Szu-Wei Lee; Chien-Feng Li; Chia-Hsin Chan; Jing Wang; Wei-Lei Yang; Ching-Yuan Wu; Juan Wu; Keiichi I Nakayama; Hong-Yo Kang; Hsuan-Ying Huang; Mien-Chie Hung; Pier Paolo Pandolfi; Hui-Kuan Lin
Journal:  Nat Cell Biol       Date:  2010-04-11       Impact factor: 28.824

Review 5.  Transcriptional and post-transcriptional regulation of the genes encoding the small GTPases RhoA, RhoB, and RhoC: implications for the pathogenesis of human diseases.

Authors:  Eirini Nomikou; Melina Livitsanou; Christos Stournaras; Dimitris Kardassis
Journal:  Cell Mol Life Sci       Date:  2018-03-02       Impact factor: 9.261

Review 6.  Pleiotropic functions of Rho GTPase signaling: a Trojan horse or Achilles' heel for breast cancer treatment?

Authors:  P R McHenry; T Vargo-Gogola
Journal:  Curr Drug Targets       Date:  2010-09       Impact factor: 3.465

Review 7.  The hypoxic tumor microenvironment: A driving force for breast cancer progression.

Authors:  Gregg L Semenza
Journal:  Biochim Biophys Acta       Date:  2015-06-14

Review 8.  The CASZ1/Egfl7 transcriptional pathway is required for RhoA expression in vascular endothelial cells.

Authors:  Marta S Charpentier; Joan M Taylor; Frank L Conlon
Journal:  Small GTPases       Date:  2013-10-22

9.  RhoA and RhoC differentially modulate estrogen receptor α recruitment, transcriptional activities, and expression in breast cancer cells (MCF-7).

Authors:  Emilie Malissein; Elise Meunier; Isabelle Lajoie-Mazenc; Claire Médale-Giamarchi; Florence Dalenc; Sophie F Doisneau-Sixou
Journal:  J Cancer Res Clin Oncol       Date:  2013-10-06       Impact factor: 4.553

10.  The SmgGDS splice variant SmgGDS-558 is a key promoter of tumor growth and RhoA signaling in breast cancer.

Authors:  Andrew D Hauser; Carmen Bergom; Nathan J Schuld; Xiuxu Chen; Ellen L Lorimer; Jian Huang; Alexander C Mackinnon; Carol L Williams
Journal:  Mol Cancer Res       Date:  2013-11-06       Impact factor: 5.852

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