Literature DB >> 29861174

Roles of p53, NF-κB and the androgen receptor in controlling NGAL expression in prostate cancer cell lines.

William H Chappell1, Saverio Candido2, Stephen L Abrams3, Suzanne Russo4, Roger Ove4, Alberto M Martelli5, Lucio Cocco5, Giulia Ramazzotti5, Melchiorre Cervello6, Giuseppe Montalto7, Linda S Steelman3, Xiaohong Leng8, Ralph B Arlinghaus8, Massimo Libra2, James A McCubrey9.   

Abstract

Neutrophil gelatinase-associated lipocalin (NGAL a.k.a lipocalin 2, lnc2) is a secreted protein which can form a complex with matrix metalloproteinase-9 (MMP9). This MMP9/NGAL complex has been associated with metastasis. MMP9 and NGAL are detected in the urine of patients afflicted with many different types of cancer, including prostate cancer. The effects of p53, NF-κB and the androgen receptor (AR) on the expression of NGAL was examined in four prostate cancer cell lines. Prostate cancer cell lines that are AR negative and expressed either mutant or no p53 (DU145 and PC3) displayed higher levels of NGAL expression compared to the prostate cancer cell lines (LNCaP and 22Rv-1) which are AR positive and express wild type (WT) p53. Introduction of WT-p53 into the PC3 prostate cancer cell line, resulted in reduction of the levels of NGAL expression. Conversely, introduction of dominant negative (DN) p53 or a retroviral construct expressing NF-κB into LNCaP cells increased NGAL expression. NGAL expression had functional effects on the ability of the cells to form colonies in soft agar. Whereas suppression of WT-53 in LNCaP cells increased NGAL expression, the introduction of WT-p53 suppressed NGAL transcription activity in PC3 prostate cells which normally express high level of NGAL. NF-κB and p53 were determined to regulate NGAL expression by positive and negative mechanisms, respectively. Our data indicate that prostate cancer growth, progression and sensitivity to chemotherapeutic drugs are regulated in part by NGAL and may involve complex interactions between NGAL, MMP9, NF-κB and p53.
Copyright © 2018 Elsevier Ltd. All rights reserved.

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Year:  2018        PMID: 29861174     DOI: 10.1016/j.jbior.2018.05.002

Source DB:  PubMed          Journal:  Adv Biol Regul        ISSN: 2212-4926


  8 in total

1.  Wild type and gain of function mutant TP53 can regulate the sensitivity of pancreatic cancer cells to chemotherapeutic drugs, EGFR/Ras/Raf/MEK, and PI3K/mTORC1/GSK-3 pathway inhibitors, nutraceuticals and alter metabolic properties.

Authors:  James A McCubrey; Akshaya K Meher; Shaw M Akula; Stephen L Abrams; Linda S Steelman; Michelle M LaHair; Richard A Franklin; Alberto M Martelli; Stefano Ratti; Lucio Cocco; Fulvio Barbaro; Przemysław Duda; Agnieszka Gizak
Journal:  Aging (Albany NY)       Date:  2022-04-27       Impact factor: 5.682

2.  Influences of TP53 and the anti-aging DDR1 receptor in controlling Raf/MEK/ERK and PI3K/Akt expression and chemotherapeutic drug sensitivity in prostate cancer cell lines.

Authors:  William H Chappell; Saverio Candido; Stephen L Abrams; Shaw M Akula; Linda S Steelman; Alberto M Martelli; Stefano Ratti; Lucio Cocco; Melchiorre Cervello; Giuseppe Montalto; Ferdinando Nicoletti; Massimo Libra; James A McCubrey
Journal:  Aging (Albany NY)       Date:  2020-06-03       Impact factor: 5.682

Review 3.  Iron in the Tumor Microenvironment-Connecting the Dots.

Authors:  Christa Pfeifhofer-Obermair; Piotr Tymoszuk; Verena Petzer; Günter Weiss; Manfred Nairz
Journal:  Front Oncol       Date:  2018-11-26       Impact factor: 6.244

Review 4.  The Metabolism Symbiosis Between Pancreatic Cancer and Tumor Microenvironment.

Authors:  Ying Li; Ju Zhang; Jie Xu; Shanglong Liu
Journal:  Front Oncol       Date:  2021-12-16       Impact factor: 6.244

Review 5.  NGAL as a Potential Target in Tumor Microenvironment.

Authors:  Elvira Crescenzi; Antonio Leonardi; Francesco Pacifico
Journal:  Int J Mol Sci       Date:  2021-11-15       Impact factor: 5.923

Review 6.  Thromboinflammatory Processes at the Nexus of Metabolic Dysfunction and Prostate Cancer: The Emerging Role of Periprostatic Adipose Tissue.

Authors:  Ibrahim AlZaim; Aya Al-Saidi; Safaa H Hammoud; Nadine Darwiche; Yusra Al-Dhaheri; Ali H Eid; Ahmed F El-Yazbi
Journal:  Cancers (Basel)       Date:  2022-03-25       Impact factor: 6.639

Review 7.  The Integration of Metabolomics with Other Omics: Insights into Understanding Prostate Cancer.

Authors:  Eleazer P Resurreccion; Ka-Wing Fong
Journal:  Metabolites       Date:  2022-05-27

8.  Lipocalin-2 (LCN2) Deficiency Leads to Cellular Changes in Highly Metastatic Human Prostate Cancer Cell Line PC-3.

Authors:  Sarah K Schröder; Manuela Pinoé-Schmidt; Ralf Weiskirchen
Journal:  Cells       Date:  2022-01-13       Impact factor: 6.600

  8 in total

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