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RORγ is a targetable master regulator of cholesterol biosynthesis in a cancer subtype

Nature communications, 2019-10, Vol.10 (1), p.4621-17, Article 4621

2019

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Natural compounds ursolic acid and digoxin exhibit inhibitory activities to cancer cells in RORγ-dependent and -independent manner

Frontiers in pharmacology, 2023-04, Vol.14, p.1146741

2023

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A Single Enhanced Dual-Energy CT Scan May Distinguish Lung Squamous Cell Carcinoma From Adenocarcinoma During the Venous phase

Academic radiology, 2020-05, Vol.27 (5), p.624-629

2020

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Preparation of palladium membrane by bio-membrane assisted electroless plating for hydrogen separation

International journal of hydrogen energy, 2014-04, Vol.39 (13), p.7069-7076

2014

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Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin

Acta pharmaceutica Sinica. B, 2020-12, Vol.10 (12), p.2313-2322

2020

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Pd–silicalite-1 composite membrane for direct hydroxylation of benzene

Chemical communications (Cambridge, England), 2009 (39), p.5898

2009

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RORγ is a context-specific master regulator of cholesterol biosynthesis and an emerging therapeutic target in cancer and autoimmune diseases

Biochemical pharmacology, 2022-02, Vol.196 (C), p.114725-114725, Article 114725

2022

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A Study of the Function of RORγ in Cancer Using Synthetic and Natural Small-Molecule Modulators

Zou, Hongye

2024

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Nuclear receptor RORγ inverse agonists/antagonists display tissue- and gene-context selectivity through distinct activities in altering chromatin accessibility and master regulator SREBP2 occupancy

Pharmacological research, 2022-08, Vol.182, p.106324-106324, Article 106324

2022

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Value of Cardiac Magnetic Resonance Fractal Analysis Combined With Myocardial Strain in Discriminating Isolated Left Ventricular Noncompaction and Dilated Cardiomyopathy

Journal of magnetic resonance imaging, 2019-07, Vol.50 (1), p.153-163

2019

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Abstract 4918: Natural compounds ursolic acid and digoxin exhibit anti-cancer effects through nuclear receptor RORγ-dependent and -independent mechanisms

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.4918-4918

2023

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Growth inhibition of breast cancer by two flexible heteroarotinoid enantiomers

The FASEB journal, 2018-04, Vol.32 (S1), p.804.35-804.35

2018

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Abstract 113: Evaluating the anticancer activity of two flexible heteroarotinoid analogs on breast cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.113-113

2017

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Abstract 2090: Targeting estrogen receptor negative breast cancer cells using diarylthiourea analogs of SHetA2

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.2090-2090

2017

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Enantiomer of the novel flexible heteroarotinoid, SL-1-09, blocks cell cycle progression in breast cancer cells

European journal of pharmacology, 2019-11, Vol.862, p.172634-172634, Article 172634

2019

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Novel flexible heteroarotinoid, SL-1-39, inhibits HER2-positive breast cancer cell proliferation by promoting lysosomal degradation of HER2

Cancer letters, 2019-02, Vol.443, p.157-166

2019

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Pd-silicalite-1 composite membrane for direct hydroxylation of benzene

Chemical communications (Cambridge, England), 2009-10 (39), p.5898-5900

2009

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Novel flexible heteroarotinoid, SL-1-18, promotes ERα degradation to inhibit breast cancer cell growth

Cancer letters, 2017-11, Vol.408, p.82-91

2017

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Tumor mitochondrial oxidative phosphorylation stimulated by the nuclear receptor RORγ represents an effective therapeutic opportunity in osteosarcoma

Cell reports. Medicine, 2024-05, Vol.5 (5), p.101519-101519, Article 101519

2024

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Rorγ Targeting Promotes Apoptosis and Ferroptosis in Osteosarcoma by Reprogramming Mitochondrial Oxidative Phosphorylation

SSRN Electronic Journal

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Chemotherapy significantly improves long-term survival of small lesion node negative metaplastic breast carcinoma in T1c population rather than T1a and T1b

Scientific reports, 2022-01, Vol.12 (1), p.871-11, Article 871

2022

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Circular RNA hsa_circ_0043280 inhibits cervical cancer tumor growth and metastasis via miR-203a-3p/PAQR3 axis

Cell death & disease, 2021-09, Vol.12 (10), p.888-888, Article 888

2021

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Construction and validation of a risk prediction model for clinical axillary lymph node metastasis in T1-2 breast cancer

Scientific reports, 2022-01, Vol.12 (1), p.687-11, Article 687

2022

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β-elemene inhibits tumor-promoting effect of M2 macrophages in lung cancer

Biochemical and biophysical research communications, 2017-08, Vol.490 (2), p.514-520

2017

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Functional characterization of two efficient glycosyltransferases catalysing the formation of rutin from Sophora japonica L

Organic & biomolecular chemistry, 2023-10, Vol.21 (39), p.7913-7916

2023

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RORγ is a targetable master regulator of cholesterol biosynthesis in a cancer subtype

Natural compounds ursolic acid and digoxin exhibit inhibitory activities to cancer cells in RORγ-dependent and -independent manner

A Single Enhanced Dual-Energy CT Scan May Distinguish Lung Squamous Cell Carcinoma From Adenocarcinoma During the Venous phase

Preparation of palladium membrane by bio-membrane assisted electroless plating for hydrogen separation

Targeting castration-resistant prostate cancer with a novel RORγ antagonist elaiophylin

Pd–silicalite-1 composite membrane for direct hydroxylation of benzene

RORγ is a context-specific master regulator of cholesterol biosynthesis and an emerging therapeutic target in cancer and autoimmune diseases

A Study of the Function of RORγ in Cancer Using Synthetic and Natural Small-Molecule Modulators

Nuclear receptor RORγ inverse agonists/antagonists display tissue- and gene-context selectivity through distinct activities in altering chromatin accessibility and master regulator SREBP2 occupancy

Value of Cardiac Magnetic Resonance Fractal Analysis Combined With Myocardial Strain in Discriminating Isolated Left Ventricular Noncompaction and Dilated Cardiomyopathy

Abstract 4918: Natural compounds ursolic acid and digoxin exhibit anti-cancer effects through nuclear receptor RORγ-dependent and -independent mechanisms

Growth inhibition of breast cancer by two flexible heteroarotinoid enantiomers

Abstract 113: Evaluating the anticancer activity of two flexible heteroarotinoid analogs on breast cancer

Abstract 2090: Targeting estrogen receptor negative breast cancer cells using diarylthiourea analogs of SHetA2

Enantiomer of the novel flexible heteroarotinoid, SL-1-09, blocks cell cycle progression in breast cancer cells

Novel flexible heteroarotinoid, SL-1-39, inhibits HER2-positive breast cancer cell proliferation by promoting lysosomal degradation of HER2

Pd-silicalite-1 composite membrane for direct hydroxylation of benzene

Novel flexible heteroarotinoid, SL-1-18, promotes ERα degradation to inhibit breast cancer cell growth

Tumor mitochondrial oxidative phosphorylation stimulated by the nuclear receptor RORγ represents an effective therapeutic opportunity in osteosarcoma

Rorγ Targeting Promotes Apoptosis and Ferroptosis in Osteosarcoma by Reprogramming Mitochondrial Oxidative Phosphorylation

Chemotherapy significantly improves long-term survival of small lesion node negative metaplastic breast carcinoma in T1c population rather than T1a and T1b

Circular RNA hsa_circ_0043280 inhibits cervical cancer tumor growth and metastasis via miR-203a-3p/PAQR3 axis

Construction and validation of a risk prediction model for clinical axillary lymph node metastasis in T1-2 breast cancer

β-elemene inhibits tumor-promoting effect of M2 macrophages in lung cancer

Functional characterization of two efficient glycosyltransferases catalysing the formation of rutin from Sophora japonica L

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