Prostate specific membrane antigen (PSMA): a novel modulator of p38 for proliferation, migration, and survival in prostate cancer cells (Q28281777)

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Tao Du

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Jieqing Chen

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Wei Wang

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Kewei Xu

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Tianxin Lin

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Hai Huang

Mapping, genomic organization and promoter analysis of the human prostate-specific membrane antigen gene

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language of work or name

English

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publication date

June 2013

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published in

The Prostate

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volume

73

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issue

8

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page(s)

835-41

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cites work

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Tumor target prostate specific membrane antigen (PSMA) and its regulation in prostate cancer

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A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells

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Mechanisms and functions of p38 MAPK signalling.

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Selective activation of p38 mitogen-activated protein (MAP) kinase isoforms by the MAP kinase kinases MKK3 and MKK6

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Mechanism of p38 MAP kinase activation in vivo.

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pp60(v-src) induction of cyclin D1 requires collaborative interactions between the extracellular signal-regulated kinase, p38, and Jun kinase pathways. A role for cAMP response element-binding protein and activating transcription factor-2 in pp60(v-

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Hepatocyte growth factor/scatter factor activates proliferation in melanoma cells through p38 MAPK, ATF-2 and cyclin D1.

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A novel cell type-specific role of p38α in the control of autophagy and cell death in colorectal cancer cells

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Phosphorylation by p38 MAPK as an alternative pathway for GSK3beta inactivation.

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Non-classical p38 map kinase functions: cell cycle checkpoints and survival

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Signal integration by JNK and p38 MAPK pathways in cancer development

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p38alpha and p38delta mitogen-activated protein kinase isoforms regulate invasion and growth of head and neck squamous carcinoma cells

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Oncogenic K-Ras down-regulates Rac1 and RhoA activity and enhances migration and invasion of pancreatic carcinoma cells through activation of p38.

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Activation of p38 has opposing effects on the proliferation and migration of endothelial cells

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Lentivirus-mediated RNAi knockdown of prostate-specific membrane antigen suppresses growth, reduces migration ability and the invasiveness of prostate cancer cells.

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Identifiers

DOI

10.1002/PROS.22627

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Consolidated OpenCitations Corpus – April 2017

4778512

4778512

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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