Phospho-Akt immunoreactivity in prostate cancer: relationship to disease severity and outcome, Ki67 and phosphorylated EGFR expression (Q34469245)

2 August 2017

title

Phospho-Akt immunoreactivity in prostate cancer: relationship to disease severity and outcome, Ki67 and phosphorylated EGFR expression (English)

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2 August 2017

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2

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2 August 2017

Lars Egevad

5

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Andreas Josefsson

object named as

Andreas Josefsson

3

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Pär Stattin

4

object named as

Pär Stattin

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2 August 2017

Peter Hammarsten

1

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2 August 2017

Torvald Granfors

6

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2 August 2017

Christopher J Fowler

7

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2 August 2017

language of work or name

English

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publication date

25 October 2012

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2 August 2017

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2 August 2017

volume

7

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2 August 2017

issue

10

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2 August 2017

page(s)

e47994

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Creative Commons Attribution 4.0 International

2 August 2017

copyright license

start time

25 October 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Pathobiological implications of the expression of EGFR, pAkt, NF-κB and MIC-1 in prostate cancer stem cells and their progenies

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Frequent gene products and molecular pathways altered in prostate cancer- and metastasis-initiating cells and their progenies and novel promising multitargeted therapies

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Tumour Cannabinoid CB(1) receptor and phosphorylated epidermal growth factor receptor expression are additive prognostic markers for prostate cancer

6 July 2018

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Differential roles of ERK and Akt pathways in regulation of EGFR-mediated signaling and motility in prostate cancer cells

6 July 2018

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Stromal PDGFRbeta expression in prostate tumors and non-malignant prostate tissue predicts prostate cancer survival

6 July 2018

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Hierarchical clustering of immunohistochemical analysis of the activated ErbB/PI3K/Akt/NF-kappaB signalling pathway and prognostic significance in prostate cancer

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Phosphorylation of the androgen receptor is associated with reduced survival in hormone-refractory prostate cancer patients.

6 July 2018

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Luteolin inhibits insulin-like growth factor 1 receptor signaling in prostate cancer cells

6 July 2018

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Expression and localisation of Akt-1, Akt-2 and Akt-3 correlate with clinical outcome of prostate cancer patients

6 July 2018

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Immunohistochemical demonstration of phospho-Akt in high Gleason grade prostate cancer

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Akt suppresses androgen-induced apoptosis by phosphorylating and inhibiting androgen receptor

6 July 2018

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Increased AKT activity contributes to prostate cancer progression by dramatically accelerating prostate tumor growth and diminishing p27Kip1 expression

6 July 2018

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Interleukin-3-induced phosphorylation of BAD through the protein kinase Akt

6 July 2018

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The protein kinase encoded by the Akt proto-oncogene is a target of the PDGF-activated phosphatidylinositol 3-kinase

6 July 2018

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6 July 2018

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High levels of phosphorylated form of Akt-1 in prostate cancer and non-neoplastic prostate tissues are strong predictors of biochemical recurrence.

21 January 2018

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Phosphorylation of Akt (Ser473) is an excellent predictor of poor clinical outcome in prostate cancer.

21 January 2018

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Low endoglin vascular density and Ki67 index in Gleason score 6 tumours may identify prostate cancer patients suitable for surveillance

21 January 2018

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Natural History of Early, Localized Prostate Cancer

21 January 2018

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27 October 2018

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0047994

Prognostic value of the Gleason score in prostate cancer

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23133535

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Inhibition of the epidermal growth factor receptor enhances castration-induced prostate involution and reduces testosterone-stimulated prostate growth in adult rats

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23133535

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Low levels of phosphorylated epidermal growth factor receptor in nonmalignant and malignant prostate tissue predict favorable outcome in prostate cancer patients

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23133535

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0047994

1 reference

2 August 2017

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1 reference

2 August 2017

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