Dopamine and cAMP-regulated phosphoprotein 32 kDa (DARPP-32) and survival in breast cancer: a retrospective analysis of protein and mRNA expression.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
18 11 2019
Historique:
received: 25 03 2019
accepted: 21 10 2019
entrez: 20 11 2019
pubmed: 20 11 2019
medline: 3 11 2020
Statut: epublish

Résumé

Dopamine and cAMP regulated phosphoprotein 32 kDa (DARPP-32) also known as phosphoprotein phosphatase-1 regulatory subunit 1B and encoded by the PPP1R1B gene is an inhibitor of protein phosphatase-1 and protein kinase A. DARPP-32 is expressed in a wide range of epithelial cells and some solid tumours; however, its role in breast cancer is only partially defined. DARPP-32 expression was determined using immunohistochemistry in two independent cohorts of early stage invasive breast cancer patients (discovery n = 1352; validation n = 1655), and 112 HER2 positive breast cancer patients treated with trastuzumab and adjuvant chemotherapy. PPP1R1B mRNA expression was assessed in the METABRIC cohort (n = 1980), using artificial neural network analysis to identify associated genes. In the discovery cohort, low nuclear expression of DARPP-32 was significantly associated with shorter survival (P = 0.041), which was independent of other prognostic variables (P = 0.019). In the validation cohort, low cytoplasmic and nuclear expression was significantly associated with shorter survival (both P = 0.002), with cytoplasmic expression independent of other prognostic variables (P = 0.023). Stronger associations with survival in oestrogen receptor (ER) positive disease were observed. In patients treated with trastuzumab, low nuclear expression was significantly associated with adverse progression-free survival (P = 0.031). In the METABRIC cohort, low PPP1R1B expression was associated with shortened survival of ER positive patients. Expression of CDC42 and GRB7, amongst others, were associated with PPP1R1B expression. This data suggests a role for DARPP-32 as a prognostic marker with clinical utility in breast cancer.

Identifiants

pubmed: 31740718
doi: 10.1038/s41598-019-53529-z
pii: 10.1038/s41598-019-53529-z
pmc: PMC6861271
doi:

Substances chimiques

Dopamine and cAMP-Regulated Phosphoprotein 32 0
PPP1R1B protein, human 0
RNA, Messenger 0
Trastuzumab P188ANX8CK

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16987

Références

Cancer Res. 2002 Jul 15;62(14):4061-4
pubmed: 12124342
Nat Commun. 2015 Dec 07;6:10099
pubmed: 26639316
J Neurosci. 1984 Jan;4(1):84-98
pubmed: 6319627
J Biol Chem. 2009 Oct 2;284(40):27533-43
pubmed: 19651774
Cancer. 2003 Oct 1;98(7):1547-51
pubmed: 14508844
Lancet Oncol. 2016 Jul;17(7):1004-1018
pubmed: 27312051
Mol Cancer. 2010 Sep 13;9:240
pubmed: 20836878
Int Surg. 2015 Feb;100(2):213-20
pubmed: 25692420
Commun Biol. 2018;1:43
pubmed: 29782621
Oncogene. 2014 Nov 13;33(46):5341-7
pubmed: 24276243
Nature. 1983 Jan 6;301(5895):69-71
pubmed: 6296685
Oncotarget. 2015 Oct 20;6(32):33134-45
pubmed: 26430732
Mol Cancer Res. 2006 Jul;4(7):449-55
pubmed: 16849520
Biochem Pharmacol. 2019 Feb;160:71-79
pubmed: 30552871
Nature. 1984 Aug 9-15;310(5977):503-5
pubmed: 6087160
J Biol Chem. 1984 Jul 10;259(13):8080-3
pubmed: 6330098
Oncotarget. 2016 Jul 26;7(30):47927-47937
pubmed: 27323818
AAPS J. 2005 Oct 05;7(2):E353-60
pubmed: 16353915
Clin Cancer Res. 2018 Mar 1;24(5):1216-1226
pubmed: 29180608
Br J Cancer. 2005 Aug 22;93(4):387-91
pubmed: 16106245
Mol Cancer. 2014 Aug 15;13:192
pubmed: 25128420
Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):1186-91
pubmed: 24395794
Br J Cancer. 2004 Jul 5;91(1):119-23
pubmed: 15188007
PLoS One. 2009 Jul 13;4(7):e6220
pubmed: 19593441
Exp Cell Res. 2006 Dec 10;312(20):4011-8
pubmed: 17027969
Clin Cancer Res. 2008 Jul 15;14(14):4564-71
pubmed: 18579663
Clin Cancer Res. 2004 Nov 1;10(21):7252-9
pubmed: 15534099
J Neurosci. 1984 Jan;4(1):99-110
pubmed: 6319628
Breast Cancer Res Treat. 2010 Feb;120(1):47-57
pubmed: 19301121
Pathol Oncol Res. 2013 Apr;19(2):329-43
pubmed: 23250732
Oncotarget. 2018 May 25;9(40):25946-25956
pubmed: 29899833
J Neurosci. 1984 Jan;4(1):111-24
pubmed: 6319625
BMC Cancer. 2014 Dec 23;14:995
pubmed: 25539577
Mol Cancer Res. 2013 Jan;11(1):86-94
pubmed: 23160836
J Am Coll Cardiol. 2006 Apr 18;47(8):1544-52
pubmed: 16630989
Cell Signal. 2017 Dec;40:53-61
pubmed: 28867659

Auteurs

Shreeya Kotecha (S)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Marie N Lebot (MN)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Bhudsaban Sukkarn (B)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Graham Ball (G)

John van Geest Cancer Research Centre, School of Science and Technology, Nottingham Trent University, Clifton Campus, Nottingham, NG1 4BU, UK.

Paul M Moseley (PM)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Stephen Y Chan (SY)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Andrew R Green (AR)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Emad Rakha (E)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Ian O Ellis (IO)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Stewart G Martin (SG)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK.

Sarah J Storr (SJ)

Nottingham Breast Cancer Research Centre, Division of Cancer and Stem Cells, School of Medicine, University of Nottingham, Nottingham City Hospital, Nottingham, NG5 1PB, UK. sarah.storr@nottingham.ac.uk.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH