Effect of PRK and SRB on Mtb H37Rv survival

Slides:



Advertisements
Similar presentations
Effects of inhibiting inflammatory cell recruitment on fracture healing Treatment with CCR2 antagonist, INCB3344, led to impaired fracture healing compared.
Advertisements

Structures of CK1 inhibitors and their effects on CK1 activity in vitro. Structures of CK1 inhibitors and their effects on CK1 activity in vitro. (A) Structures.
Loss of Hdac3 impairs Ar signaling in mouse prostate tissues and has no effect on apoptosis Loss of Hdac3 impairs Ar signaling in mouse prostate tissues.
Identification and structure of small molecules that preferentially stabilise RNA G4C2 repeat G‐quadruplexes Identification and structure of small molecules.
The HDAC3 inhibitor suppresses SPOP‐mutated prostate cancer cell growth The HDAC3 inhibitor suppresses SPOP‐mutated prostate cancer cell growth A22Rv1.
TUG‐891 increases oxygen consumption by brown adipocytes, mediated by direct UCP1 activation and mitochondrial fragmentation TUG‐891 increases oxygen consumption.
PbA‐specific CD4 T‐cell responses are maximal at day 6 post‐pRBC infection PbA‐specific CD4 T‐cell responses are maximal at day 6 post‐pRBC infection Proportion.
Functional assays confirm daf‐2‐dependent reduction in protein metabolism. Functional assays confirm daf‐2‐dependent reduction in protein metabolism. (A)
Treatment with p38γ/p38δ inhibitor shows antifungal effects in vivo
Palmitoylation of EGFR alters its cellular distribution and is crucial for growth of TKI‐resistant EGFR mutated NSCLC cells Palmitoylation of EGFR alters.
Expression levels of the transgenic DIA1(R1204X) mutant in the inner ear of TG mice Expression levels of the transgenic DIA1(R1204X) mutant in the inner.
Fstl1 promotes cardiac fibroblasts proliferation via the ERK1/2‐dependent pathway Fstl1 promotes cardiac fibroblasts proliferation via the ERK1/2‐dependent.
BRD4 is associated with poor patient survival and constitutes a promising target for NRASMut melanoma BRD4 is associated with poor patient survival and.
Quantitative mass spectrometry of proteasome pulldowns
Correlating protein to mRNA and proteins per mRNA ratios
HPV‐E7 enhances chemotherapy‐mediated cellular stress and CerS1/ceramide‐mediated lethal mitophagy HPV‐E7 enhances chemotherapy‐mediated cellular stress.
ECM 29 and Kaplan–Meier survival curves for additional datasets
Clinical testing of calcineurin inhibitors cyclosporine A and tacrolimus in autoimmune disorders Clinical testing of calcineurin inhibitors cyclosporine.
Palbociclib activates the proteasome indirectly and reduces the association of ECM29 with the proteasome Palbociclib activates the proteasome indirectly.
Inhibition of JNK signaling in breast cancer cells and lung colonization in a xenograft mouse model Inhibition of JNK signaling in breast cancer cells.
Expression of PD‐1 on PBMC and malignant exudate T cells
Characterization of oligo#5 and its derivatives
Superior potency of EnAd expressing EpCAM BiTE in partially EnAd‐resistant cancer cell line Superior potency of EnAd expressing EpCAM BiTE in partially.
Effect of VEGFA on ALDH+ population maintenance
The BET inhibitor JQ‐1 in combination with the MEK inhibitor PD synergistically impairs cell proliferation and induces apoptosis of NRAS‐mutant.
SEMA3C silencing inhibits CRPC cell growth and induces apoptosis
TR specifically inhibits NLRP3 inflammasome activation
Mitochondrial ceramide is involved in HPV‐E7‐mediated lethal mitophagy
Combination of OTX‐015 and PD does not induce overt toxicity
SPRY2 deficiency‐induced SRB1 mediates CRPC
Inhibition of CDK6 kinase activity sensitizes EOC cells to platinum in vitro Inhibition of CDK6 kinase activity sensitizes EOC cells to platinum in vitro.
Reduced ALPI expression in patients’ small intestinal biopsies
DOK7 gene therapy enhances life span and motor activity in ALS mice
BETi potentiate the efficacy of MEKi in NRAS‐mutant melanoma
Hdac3 deletion decreases AKT phosphorylation and tumor growth in Pten knockout prostate cancer Hdac3 deletion decreases AKT phosphorylation and tumor growth.
Characterization of super‐enhancers in WT and KO macrophages
BIRC6 confers resistance against cisplatin and oxaliplatin.
Akt inhibition with AZD5363 does not enhance the radiosensitivity of tumour cells in vitro Akt inhibition with AZD5363 does not enhance the radiosensitivity.
TGF‐β1 treatment induces the chromatin binding of Smad2/3/4 in 4T1 cells TGF‐β1 treatment induces the chromatin binding of Smad2/3/4 in 4T1 cells A, BWestern.
IL‐23‐induced psoriasis‐like skin disease is ameliorated in IL‐23−/− mice IL‐23‐induced psoriasis‐like skin disease is ameliorated in IL‐23−/− mice ARepresentative.
Improvement of shHBV7 specificity and efficiency by co‐expression of a TuD against the sense strand Improvement of shHBV7 specificity and efficiency by.
T55delinsRT mutation in MEK1 is responsible for resistance to vemurafenib in M032R4 Somatic mutations present in each of these metastases, revealing that.
Inhibition of NAMPT using the potent inhibitor FK866 sensitizes additional tumour cells to olaparib.A‐E.Sensitivity of the cell lines MDAMB468 (A), SUM149.
Activation of miR‐21‐3p by PPARβ/δ requires activation of the TGFβ receptor Activation of miR‐21‐3p by PPARβ/δ requires activation of the TGFβ receptor.
Characterization of MET‐addicted cells rendered resistant to MET tyrosine kinase inhibitors Characterization of MET‐addicted cells rendered resistant to.
Proteasomal inhibition suppresses palbociclib‐induced senescence phenotype Proteasomal inhibition suppresses palbociclib‐induced senescence phenotype ARepresentative.
GPR120 deficiency alters the expression of genes involved in glucose and lipid metabolism in BAT GPR120 deficiency alters the expression of genes involved.
Target engagement of the systemic Stat3 inhibitor in APP/PS1 mice
Assessment of proliferation status of PDGFRα+ cells in developing mouse lungs Assessment of proliferation status of PDGFRα+ cells in developing mouse lungs.
The HDAC3 inhibitor suppresses PTEN‐deficient prostate cancer growth
TUG‐891 increases oxygen consumption by brown adipocytes, mediated by direct UCP1 activation and mitochondrial fragmentation TUG‐891 increases oxygen consumption.
Both the number and the OX40L expression level of bronchiolar progenitors were increased by influenza infection. Wild‐type mice were intratracheally infected.
Drp1 knockdown prevents mitophagy
Therapeutic role of TR in HFD‐established diabetic mice
In vitro kinetics and binding studies of inhibitory compounds (PRK and SRB) MtArgJ In vitro kinetics and binding studies of inhibitory compounds (PRK and.
High CDK6 expression predicts poor prognosis in EOC patients
Re‐expression of the AXIN1 coding sequence re‐sensitizes VACO6R cells to PORCN inhibition Re‐expression of the AXIN1 coding sequence re‐sensitizes VACO6R.
Growth of TKI‐resistant EGFR delE746‐A750 PC‐9 NSCLC cells is associated with elevated cellular free fatty acid and expression of FASN, and is suppressed.
Etifoxine modulation of T‐cell activity during EAE
Histological and mRNA analysis of the inflammatory cytokines in the vehicle‐ or etifoxine‐treated mice at onset of clinical symptoms.A–D.At day 10 p.i.,
PKAN human neurons show altered oxidative status
P2X4R blockade increases pro‐inflammatory gene expression after EAE
Cellular stress or neuronal excitotoxic stress increases DPR levels for all C9orf72 NRE ORFs in rat cortical neurons and in patient‐derived iPS spinal.
Inhibitory effect of perhexiline on the proliferation of the HepG2 cell line A, BPerhexiline was used to mimic the effect of the l‐carnitine analog on.
FGFR1 and TGFβ signaling activity in smooth muscle cells in a mouse atherosclerosis model FGFR1 and TGFβ signaling activity in smooth muscle cells in a.
CNP520 treatment of male C57/BL6 mice for 8 weeks did not cause hair depigmentation CNP520 treatment of male C57/BL6 mice for 8 weeks did not cause hair.
SEMA3C regulates prostate cancer cell growth
Synergistic combination of valproic acid and oncolytic parvovirus H‐1PV as a potential therapy against cervical and pancreatic carcinomas H‐1PV and VPA.
GR cells are dependent upon sustained CDC25C signaling as pharmacologic or genetic inhibition of CDC25C induce synthetic lethality. GR cells are dependent.
Co‐targeting BET and MEK as salvage therapy for MAPK and checkpoint inhibitor‐resistant melanoma NRAS‐mutant melanoma cells were treated with JQ‐1 alone.
Presentation transcript:

Effect of PRK and SRB on Mtb H37Rv survival Effect of PRK and SRB on Mtb H37Rv survival ARepresentative image of Alamar blue assay employed for MIC determination.B, CMtb H37Rv cells were treated with varying concentration of inhibitors, and cell viability was determined using Alamar blue assay. MIC90 was calculated by plotting cell viability (%) against increasing concentration of inhibitors PRK and SRB.D, EHill's plot analysis of decline in Alamar blue fluorescence with increasing concentration of PRK and SRB, for IC50 determination.F, GCFU analysis of Mtb treated with PRK/SRB alone or a cocktail of Rif, Inh and Emb abbreviated as RHE and compared with a new combination of RH + PRK and RH + SRB, at two concentrations of PRK and SRB (0.1 and 1 μM), respectively. The x‐axis represents the time points post‐treatment with the inhibitors, and all the experiments were performed in triplicate and confirmed with biological duplicates at least. Statistical significance between experimental groups was determined by two‐tailed, unpaired Student's t‐test (****P < 0.0001, ***P < 0.001, **P < 0.01, *P < 0.1).Data information: (D–G). Mean and standard error (SE) determined from three technical replicates (n = 3) and at least two biological duplicates. Archita Mishra et al. EMBO Mol Med. 2018;emmm.201708038 © as stated in the article, figure or figure legend