The Expression of FAP in Hepatocellular Carcinoma Cells is Induced by Hypoxia and Correlates with Poor Clinical Outcomes

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The Expression of FAP in Hepatocellular Carcinoma Cells is Induced by Hypoxia and Correlates with Poor Clinical Outcomes

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

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The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

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The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

@en

The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

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The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

@en

The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

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P1476

The Expression of FAP in Hepat ...... es with Poor Clinical Outcomes

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P2093

Baimeng Zhang

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Baojia Zou

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Bibesh Pokhrel

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Chaonong Cai

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Jiafan Chen

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Jian Li

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Jianxu Chen

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Lei Ding

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Linjuan Zeng

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Peiping Li

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P2860

Expression patterns of seprase, a membrane serine protease, in cervical carcinoma and cervical intraepithelial neoplasm

Management of hepatocellular carcinoma

Downregulation of FAP suppresses cell proliferation and metastasis through PTEN/PI3K/AKT and Ras-ERK signaling in oral squamous cell carcinoma.

FAP-α (Fibroblast activation protein-α) is involved in the control of human breast cancer cell line growth and motility via the FAK pathway.

Selective approach to major hepatic resection for hepatocellular carcinoma in chronic liver disease.

Increased expression of CCN2, epithelial membrane antigen, and fibroblast activation protein in hepatocellular carcinoma with fibrous stroma showing aggressive behavior.

Tissue injury and hypoxia promote malignant progression of prostate cancer by inducing CXCL13 expression in tumor myofibroblasts.

Hypoxia induces epithelial-mesenchymal transition via activation of SNAI1 by hypoxia-inducible factor -1α in hepatocellular carcinoma.

Fibroblast activation protein-α, a stromal cell surface protease, shapes key features of cancer associated fibroblasts through proteome and degradome alterations

C14orf166 is a high-risk biomarker for bladder cancer and promotes bladder cancer cell proliferation.

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3278-3286

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scholarly article

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10.7150/JCA.25775

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English

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P478

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P577

2018-01-01T00:00:00Z

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P698

30271487

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P921

hypoxia

P932

6160687

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