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Inhibition of Glutathione S-Transferase M1 by New Gabosine Analogues Is Essential for Overcoming Cisplatin Resistance in Lung Cancer Cells
- Source :
- Journal of Medicinal Chemistry. 54:8574-8581
- Publication Year :
- 2011
- Publisher :
- American Chemical Society (ACS), 2011.
-
Abstract
- A new class of human GST inhibitors has been identified via rational design approach; we report their discovery, synthesis, inhibitory activity, and synergetic effect in combination with cisplatin against A549 lung cancer cell line. The results of this effort show that the lead 4-O-decyl-gabosine D (24) has optimum synergetic effect in A549 human lung adenocarcinoma epithelial cell and that this activity involves inhibition of glutathione S-transferase M1, apparently consistent with siRNA-mediated knockdown of GSTM1 gene.
- Subjects :
- Lung Neoplasms
Cell Survival
Antineoplastic Agents
Structure-Activity Relationship
chemistry.chemical_compound
Cell Line, Tumor
Drug Discovery
medicine
Humans
RNA, Small Interfering
Lung cancer
Glutathione Transferase
Cisplatin
Gene knockdown
biology
Cyclohexanones
Rational design
Drug Synergism
Glutathione
respiratory system
medicine.disease
respiratory tract diseases
Isoenzymes
Glutathione S-transferase
chemistry
Drug Resistance, Neoplasm
biology.protein
Cancer research
Molecular Medicine
Adenocarcinoma
GSTM1 Gene
Drug Screening Assays, Antitumor
medicine.drug
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 54
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....6f38af1465d1fbbef7fe24467f7ac055
- Full Text :
- https://doi.org/10.1021/jm201131n