Literature DB >> 27987320

Association between AXL, Hippo Transducers, and Survival Outcomes in Male Breast Cancer.

Anna Di Benedetto1, Marcella Mottolese1, Francesca Sperati2, Cristiana Ercolani1, Luigi Di Lauro3, Laura Pizzuti3, Patrizia Vici3, Irene Terrenato2, Abeer M Shaaban4, Matthew P Humphries5, Sreekumar Sundara-Rajan5, Maddalena Barba3,6, Valerie Speirs5, Ruggero De Maria7, Marcello Maugeri-Saccà3,6.   

Abstract

Male breast cancer (MBC) is an uncommon malignancy. We have previously reported that the expression of the Hippo transducers TAZ/YAP and their target CTGF was associated with inferior survival in MBC patients. Preclinical evidence demonstrated that Axl is a transcriptional target of TAZ/YAP. Thus, we herein assessed AXL expression to further investigate the significance of active TAZ/YAP-driven transcription in MBC. For this study, 255 MBC samples represented in tissue microarrays were screened for AXL expression, and 116 patients were included. The association between categorical variables was verified by the Pearson's Chi-squared test of independence (2-tailed) or the Fisher Exact test. The relationship between continuous variables was tested with the Pearson's correlation coefficient. The Kaplan-Meier method was used for estimating survival curves, which were compared by log-rank test. Factors potentially impacting 10-year and overall survival were verified in Cox proportional regression models. AXL was positively associated with the TAZ/CTGF and YAP/CTGF phenotypes (P = 0.001 and P = 0.002, respectively). Patients with TAZ/CTGF/AXL- or YAP/CTGF/AXL-expressing tumors had inferior survival compared with non-triple-positive patients (log rank P = 0.042 and P = 0.048, respectively). The variables TAZ/CTGF/AXL and YAP/CTGF/AXL were adverse factors for 10-year survival in the multivariate Cox models (HR 2.31, 95%CI:1.02-5.22, P = 0.045, and HR 2.27, 95%CI:1.00-5.13, P = 0.050). Nearly comparable results were obtained from multivariate analyses of overall survival. The expression pattern of AXL corroborates the idea of the detrimental role of TAZ/YAP activation in MBC. Overall, Hippo-linked biomarkers deserve increased attention in this rare disease. J. Cell. Physiol. 232: 2246-2252, 2017.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

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Year:  2017        PMID: 27987320     DOI: 10.1002/jcp.25745

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  5 in total

1.  The Hippo Transducer YAP/TAZ as a Biomarker of Therapeutic Response and Prognosis in Trastuzumab-Based Neoadjuvant Therapy Treated HER2-Positive Breast Cancer Patients.

Authors:  Jia-Qi Yuan; Nian-Hua Ding; Zhi Xiao
Journal:  Front Pharmacol       Date:  2020-08-27       Impact factor: 5.810

Review 2.  The Role of the Hippo Pathway in Breast Cancer Carcinogenesis, Prognosis, and Treatment: A Systematic Review.

Authors:  Anastasios Kyriazoglou; Michalis Liontos; Roubini Zakopoulou; Maria Kaparelou; Anna Tsiara; Alkistis Maria Papatheodoridi; Rebecca Georgakopoulou; Flora Zagouri
Journal:  Breast Care (Basel)       Date:  2020-05-12       Impact factor: 2.860

3.  Analysis of the ATR-Chk1 and ATM-Chk2 pathways in male breast cancer revealed the prognostic significance of ATR expression.

Authors:  Anna Di Benedetto; Cristiana Ercolani; Marcella Mottolese; Francesca Sperati; Laura Pizzuti; Patrizia Vici; Irene Terrenato; Abeer M Shaaban; Matthew P Humphries; Luigi Di Lauro; Maddalena Barba; Ilio Vitale; Gennaro Ciliberto; Valerie Speirs; Ruggero De Maria; Marcello Maugeri-Saccà
Journal:  Sci Rep       Date:  2017-08-14       Impact factor: 4.379

Review 4.  The role of Hippo signal pathway in breast cancer metastasis.

Authors:  Changran Wei; Ying Wang; Xiangqi Li
Journal:  Onco Targets Ther       Date:  2018-04-17       Impact factor: 4.147

Review 5.  AXL as a Target in Breast Cancer Therapy.

Authors:  Sierra A Colavito
Journal:  J Oncol       Date:  2020-02-14       Impact factor: 4.375

  5 in total

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