许培扬
砒霜治疗白血病:美国NIH资助国际科研项目(81项)
2013-2-15 09:28
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标签:美国, 国际, 白血病

砒霜治疗白血病:美国NIH资助国际科研项目(81项)

检索策略:leukemia   and  arsenic trioxide

(("leukaemia"[All Fields] OR "leukemia"[MeSH Terms] OR "leukemia"[All Fields]) AND ("arsenic trioxide"[Supplementary Concept] OR "arsenic trioxide"[All Fields])) AND Research Support, N I H, Extramural[ptyp]


检索结果见:pubmed_result 81.txt


检索数据库:http://www.ncbi.nlm.nih.gov/pubmed

研究项目实例:

 2005 May;12(5):523-31.
Triterpenoid CDDO-Im downregulates PML/RARalpha expression in acute promyelocytic leukemia cells.
Source

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.

Abstract

The triterpenoid 2-cyano-3,12-dioxooleana-1,9-dien-28-oic acid (CDDO) induces differentiation and apoptosis of diverse human tumor cells. In the present study, we examined the effects of the CDDO imidazolide imide (CDDO-Im) on the NB4 acute promyelocytic leukemia (APL) cell line and primary APL cells. The results show that CDDO-Im selectively downregulates expression of the PML/retinoic receptor alpha fusion protein by a caspase-dependent mechanism and sensitizes APL cells to the differentiating effects of all-trans retinoic acid (ATRA). CDDO-Im treatment of APL cells was also associated with disruption of redox balance and activation of the extrinsic apoptotic pathway. In concert with these results, CDDO-Im sensitizes APL cells to arsenic trioxide (ATO)-induced apoptosis. Our findings indicate that CDDO-Im may be effective in the treatment of APL by: (i) downregulation of PML/RARalpha; (ii) enhancement of ATRA-induced differentiation; and (iii) sensitization of ATO-induced APL cell death.

PMID: 15746941 [PubMed - indexed for MEDLINE] Free full text

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