Khandekar et al., 2018 - Google Patents
Noncanonical agonist PPARγ ligands modulate the response to DNA damage and sensitize cancer cells to cytotoxic chemotherapyKhandekar et al., 2018
View HTML- Document ID
- 13684635871355869125
- Author
- Khandekar M
- Banks A
- Laznik-Bogoslavski D
- White J
- Choi J
- Kazak L
- Lo J
- Cohen P
- Wong K
- Kamenecka T
- Griffin P
- Spiegelman B
- Publication year
- Publication venue
- Proceedings of the National Academy of Sciences
External Links
Snippet
The peroxisome-proliferator receptor-γ (PPARγ) is expressed in multiple cancer types. Recently, our group has shown that PPARγ is phosphorylated on serine 273 (S273), which selectively modulates the transcriptional program controlled by this protein. PPARγ ligands …
- 108010016731 PPAR gamma 0 title abstract description 131
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/5011—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing antineoplastic activity
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay
- G01N33/574—Immunoassay; Biospecific binding assay for cancer
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Khandekar et al. | Noncanonical agonist PPARγ ligands modulate the response to DNA damage and sensitize cancer cells to cytotoxic chemotherapy | |
Nilsson et al. | A YAP/FOXM1 axis mediates EMT-associated EGFR inhibitor resistance and increased expression of spindle assembly checkpoint components | |
Echeverria et al. | Resistance to neoadjuvant chemotherapy in triple-negative breast cancer mediated by a reversible drug-tolerant state | |
Zhang et al. | Inhibition of chemotherapy resistant breast cancer stem cells by a ROR1 specific antibody | |
Januario et al. | PRC2-mediated repression of SMARCA2 predicts EZH2 inhibitor activity in SWI/SNF mutant tumors | |
Xu et al. | Targetable BET proteins-and E2F1-dependent transcriptional program maintains the malignancy of glioblastoma | |
Venere et al. | The mitotic kinesin KIF11 is a driver of invasion, proliferation, and self-renewal in glioblastoma | |
Lin et al. | Mapping the molecular determinants of BRAF oncogene dependence in human lung cancer | |
Rebello et al. | Therapeutic approaches targeting MYC-driven prostate cancer | |
Weiler et al. | mTOR target NDRG1 confers MGMT-dependent resistance to alkylating chemotherapy | |
Genini et al. | Mitochondrial dysfunction induced by a SH2 domain-targeting STAT3 inhibitor leads to metabolic synthetic lethality in cancer cells | |
Kashatus et al. | Erk2 phosphorylation of Drp1 promotes mitochondrial fission and MAPK-driven tumor growth | |
Gujral et al. | Hippo pathway mediates resistance to cytotoxic drugs | |
Schito et al. | Hypoxia-inducible factor 1-dependent expression of platelet-derived growth factor B promotes lymphatic metastasis of hypoxic breast cancer cells | |
Wang et al. | Polyploidy road to therapy‐induced cellular senescence and escape | |
Halliday et al. | In vivo radiation response of proneural glioma characterized by protective p53 transcriptional program and proneural-mesenchymal shift | |
Zirath et al. | MYC inhibition induces metabolic changes leading to accumulation of lipid droplets in tumor cells | |
Zhang et al. | Digoxin and other cardiac glycosides inhibit HIF-1α synthesis and block tumor growth | |
Janghorban et al. | Targeting c-MYC by antagonizing PP2A inhibitors in breast cancer | |
Furic et al. | eIF4E phosphorylation promotes tumorigenesis and is associated with prostate cancer progression | |
Shackelford et al. | mTOR and HIF-1α-mediated tumor metabolism in an LKB1 mouse model of Peutz-Jeghers syndrome | |
Woditschka et al. | DNA double-strand break repair genes and oxidative damage in brain metastasis of breast cancer | |
Abe et al. | Hedgehog signaling overrides p53-mediated tumor suppression by activating Mdm2 | |
Xu et al. | BCL6 promotes glioma and serves as a therapeutic target | |
Zhang et al. | TRIM39 regulates cell cycle progression and DNA damage responses via stabilizing p21 |