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Volumn 32, Issue 19, 2007, Pages 2051-2055

Inhibition of curcumin on histone deacetylase and expression promotion of P21WAF1/CIP1 in HepG2 cells

Author keywords

Curcumin; Cyclin dependent kinase inhibitor; HepG2 cell; Histone deacetylase

Indexed keywords

CDKN1A PROTEIN, HUMAN; CURCUMIN; CYCLIN DEPENDENT KINASE INHIBITOR 1A; HISTONE DEACETYLASE; MESSENGER RNA; UNCLASSIFIED DRUG;

EID: 36949025488     PISSN: 10015302     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (9)
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    • Curcumin induces the degradation of cyclin E expression through ubiquitin-dependent pathway and upregulates cyclin-dependent kinase inhibitors p21 and p27 in multiple human tumor cell lines[J]
    • Aggarwal B B, Banerjee S, Bhardwaj U, et al. Curcumin induces the degradation of cyclin E expression through ubiquitin-dependent pathway and upregulates cyclin-dependent kinase inhibitors p21 and p27 in multiple human tumor cell lines[J]. Biochemical Pharmacology, 2006,12:10.
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    • Curcumin (diferuloylmethane) inhibits constitutive active NF-kappaB, leading to suppression of cell growth of human T-cell leukemia virus type I-infected T-cell lines and primary adult T-cell leukemia cells[J]
    • Tomita Manko, Kawakami Hirochika, Uchihara Jun-nosuke, et al. Curcumin (diferuloylmethane) inhibits constitutive active NF-kappaB, leading to suppression of cell growth of human T-cell leukemia virus type I-infected T-cell lines and primary adult T-cell leukemia cells[J]. Cancer, 2006,118(3):765.
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    • Curcumin, a potent anti-tumor reagent, is a novel histone deacetylase inhibitor regulating B-NHL cell line Raji proliferation [J]
    • Liu Hong-qi, Chen Yan, Cui Guo-hui, et al. Curcumin, a potent anti-tumor reagent, is a novel histone deacetylase inhibitor regulating B-NHL cell line Raji proliferation [J]. Acta pharmacological Sinica, 2005,26(5):603.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.