Danvatirsen
Based on 1 Customer Validation
Danvatirsen (AZD9150) is an antisense oligonucleotide targeting STAT3. Danvatirsen reduces the viability and promotes apoptosis of leukemia cell lines. Danvatirsen inhibits the expression of endogenous STAT3 and its downstream target genes, and reduces the proliferation and tumorigenicity of neuroblastoma and lymphoma cells. Danvatirsen inhibited tumor growth in mouse models of neuroblastoma, lymphoma, and non-small cell lung cancer. Danvatirsen achieves STAT3 mRNA and protein depletion in a mouse model of epidermoid carcinoma. Danvatirsen can be used in research related to lymphoma, myelodysplastic syndrome, acute myeloid leukemia, neuroblastoma and non-small cell lung cancer.
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- Pureza : 99.12%
- No. CAS: 1402357-06-5
- Peso molecular:5422.00
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Almacenamiento:
-20°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
Actividad biológica
Descripciòn
In Vitro
Danvatirsen (2.5-10 μM) significantly reduces STAT3 mRNA levels in KG1a, CMK, MOLM13 and KT1 leukemia cell lines[2].
Danvatirsen (1-10 μM; 24-72 h) significantly reduces the viability of leukemia/myelodysplastic syndrome (MDS) cell lines including NB4, MOLM14, MDS-L, MV411, KG1a, MOLM13, KT1 and CMK[2].
Danvatirsen (5 μM for CMK, 10 μM for KT1 and U937; 48 h) significantly increases the apoptosis levels of CMK, KT1 and U937 leukemia cell lines[2].
Danvatirsen (2.5-10 μM; 24 h) significantly reduces STAT3 mRNA levels in primary MDS/AML stem cells[2].
Danvatirsen (10 μM; 14 days) enhances erythroid and myeloid differentiation of primary myelodysplastic syndrome (MDS) stem/progenitor cells[2].
Danvatirsen (10 μM; 24 h) downregulates STAT3 and its downstream oncogenic target genes (IL1RAP, MSI2, MCL1, IL8, CXCR2) at the mRNA level, and reduces the protein levels of STAT3, phosphorylated STAT3 and MCL1 in CMK leukemia cells[2].
Danvatirsen induces dose-dependent apoptosis in primary TP53-mutant MDS/AML stem/progenitor cells and reduces the replating efficiency of primary AML stem and progenitor cells in colony-forming assays[2].
Danvatirsen (0.25-10 μM; 6 days) dose-dependently inhibits STAT3 mRNA expression in SK-N-AS, NGP and IMR32 neuroblastoma cells, with IC50 values of 0.69, 0.64 and 0.76 μM, respectively[3].
Danvatirsen (0.25-10 μM; 6 days) dose-dependently inhibits the expression of total STAT3 protein and phosphorylated STAT3 protein in SK-N-AS, NGP and IMR32 neuroblastoma cells, with IC50 values of 0.99 μM, 0.97 μM and 0.98 μM, respectively[3].
Danvatirsen (1 μM; 6 days) significantly reduces the mRNA and protein expression levels of multiple STAT3 target genes in SK-N-AS, NGP and IMR32 neuroblastoma cells[3].
Danvatirsen (1 μM; 4 weeks) significantly inhibits the proliferation of SK-N-AS, NGP and IMR32 neuroblastoma cells, reducing the maximum cell confluence by up to 38%, 37% and 34% respectively during continuous incubation. It also suppresses the anchorage-independent colony formation of the cells, decreasing the number of colonies by 20%, 43% and 67% respectively[3].
Danvatirsen (1 μM; 6 days) significantly enhances the sensitivity of SK-N-AS, NGP and IMR32 neuroblastoma cells to Cisplatin (HY-17394), reduces the IC50 value of Cisplatin by up to 2-fold, and attenuates the activation of Cisplatin-induced DNA damage response pathways[3].
Danvatirsen (0.005-5 μM; 5 days) dose-dependently inhibits the proliferation of STAT3-dependent human lymphoma cell lines KARPAS299 and SUP-M2 via free uptake[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
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Cell Line:NB4, MOLM14, MDS-L, MV411, KG1a, MOLM13, KT1, CMK leukemic/MDS cell lines
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Concentration:10 μM
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Incubation Time:24 h, 48 h, 72 h
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Result:Induced a significant, dose-dependent decrease in cell viability across all tested cell lines.
Showed greater inhibition at higher concentrations.
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Cell Line:CMK, KT1, U937 leukemic cell lines
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Concentration:5 μM (CMK cells); 10 μM (KT1 and U937 cells)
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Incubation Time:48 h
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Result:Induced a significant increase in early apoptotic, late apoptotic, and necrotic cell populations compared with controls.
Showed a dose-dependent effect observed across tested concentrations.
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Cell Line:CMK leukemic cells
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Concentration:10 μM
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Incubation Time:24 h
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Result:Downregulated expression of STAT3 and oncogenic/stem cell-associated genes including IL1RAP, MSI2, MCL1, IL8, and CXCR2 at the mRNA level.
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Cell Line:CMK leukemic cells
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Concentration:10 μM
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Incubation Time:24 h
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Result:Reduced STAT3 protein, phospho-STAT3, and MCL1 protein levels.
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Cell Line:SK-N-AS, NGP, IMR32 human neuroblastoma cell lines
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Concentration:0.25-10 μM
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Incubation Time:6 days
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Result:Inhibited STAT3 mRNA levels in a dose-dependent manner.
Achieved IC50 values of 0.69 μM in SK-N-AS cells, 0.64 μM in NGP cells, and 0.76 μM in IMR32 cells.
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Cell Line:SK-N-AS, NGP, IMR32 human neuroblastoma cell lines
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Concentration:0.25-10 μM
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Incubation Time:6 days
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Result:Decreased both total and phosphorylated STAT3 (Ser727, Tyr705) protein levels in a dose-dependent manner.
Achieved IC50 values of 0.99 μM in SK-N-AS cells, 0.97 μM in NGP cells, and 0.98 μM in IMR32 cells.
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Cell Line:SK-N-AS, NGP, IMR32 human neuroblastoma cell lines
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Concentration:1 μM
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Incubation Time:continuous incubation (up to 240 hours)
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Result:Caused a significant decrease in cell growth: up to 38% decrease in SK-N-AS cells, up to 37% decrease in NGP cells, and up to 34% decrease in IMR32 cells.
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Cell Line:SK-N-AS, NGP, IMR32 human neuroblastoma cell lines
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Concentration:1 μM
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Incubation Time:3 days pre-incubation, followed by 3 days co-incubation with cisplatin
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Result:Significantly increased cisplatin sensitivity, resulting in a 2-fold decrease in cisplatin IC50 in NGP cells and IMR32 cells, and a smaller decrease in SK-N-AS cells.
Attenuated cisplatin-induced activation of the ATM and ATR DNA damage response pathways, as shown by reduced phosphorylation of ATM, Chk2, ATR, Chk1, and γH2AX.
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Cell Line:KARPAS299, SUP-M2 (human lymphoma cell lines)
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Concentration:0.005-5 μM
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Incubation Time:5 days
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Result:Induced dose-dependent inhibition of cell proliferation in KARPAS299 and SUP-M2 cells.
Showed antiproliferative effects that correlated with the degree of STAT3 depletion.
In Vivo
Combination of Danvatirsen (100 mg/kg; s.c.; 5 times per week for 3 consecutive weeks) with Cisplatin results in a maximum growth inhibition rate of 38% in neuroblastoma xenografts and significantly prolongs the survival of tumor-bearing mice[3].
Danvatirsen (25-50 mg/kg; s.c.; 5 times per week; for 3 consecutive weeks) induces potent, dose-dependent depletion of STAT3 mRNA and protein in human epidermoid carcinoma A431 xenografts, with the 25 mg/kg dose reducing tumor STAT3 mRNA levels by 90%[4].
Danvatirsen (50 mg/kg, s.c., 5 times per week for 5 weeks) inhibits the growth of human lymphoma SUP-M2 xenografts with an inhibition rate of 62%, and reduces tumor STAT3 mRNA levels by approximately 40%. It exhibits systemic anti-lymphoma activity in the disseminated SUP-M2 model, reducing tumor STAT3 mRNA by approximately 50% and decreasing plasma concentrations of sIL-2Rα and sCD30[4].
Danvatirsen (25 mg/kg; s.c.; 5 times per week; for approximately 5 weeks) inhibits the growth of PC-9 human non-small cell lung cancer xenografts by 90%, and reduces STAT3 activity and the expression of its downstream target genes[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Nonobese Diabetic Scid Gamma (NSG) (irradiated, engrafted with primary human MDS/AML peripheral blood mononuclear cells)[2]
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Dosage:50 mg/kg
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Administration:s.c.; 5 days per week; 4 weeks
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Result:Reduced MDS/AML burden, with greatly decreased fold change of human CD45+ cells in bone marrow compared with controls.
Achieved complete loss of detectable human CD45+ cells in some treated mice.
Exerted effects in both low-risk and high-risk MDS patient-derived xenografts.
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Animal Model:athymic nude mice (5-6 week-old female)[3]
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Dosage:100 mg/kg (target reagent); 2 mg/kg (Cisplatin)
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Administration:subcutaneous (target reagent; 5 times per week; 3 weeks); intraperitoneal (cisplatin; 2 times per week; 3 weeks; co-administered starting on day 11 of target reagent treatment)
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Result:Reduced neuroblastoma xenograft growth by up to 38% compared to control-treated mice.
Prolonged survival significantly compared to control-treated mice.
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Animal Model:Immunocompromised mice; NSG mice (disseminated lymphoma model)[4]
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Dosage:25 mg/kg; 37.5 mg/kg; 50 mg/kg
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Administration:5 times per week; 3 weeks (25 mg/kg, 50 mg/kg)
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Result:Reduced tumor STAT3 mRNA by approximately 90% (P=0.0001) and STAT3 protein by 93% (25 mg/kg).
Produced near-complete depletion of STAT3 protein throughout the tumor as measured by immunohistochemistry (50 mg/kg).
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Animal Model:NSG mice, Immunocompromised mice[4]
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Dosage:50 mg/kg
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Administration:5 times per week; 2, 5 weeks
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Result:Reduced STAT3 mRNA by ~50% in tumors isolated from axillary lymph nodes and peritoneal cavity vs control groups.
Reduced plasma sIL-2Rα and sCD30 concentrations.
Reduced tumor burden (and ascites formation.
Achieved 67% tumor growth inhibition (TGI).
Confirmed inhibition of human STAT3 in tumor cells and murine STAT3 in tumor-associated stromal cells via species-specific PCR.
Confirmed reduced phospho-STAT3 protein in both human tumor and mouse stromal cells via immunohistochemistry.
No associated change in body weight was observed.
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Animal Model:Immunocompromised mice[4]
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Dosage:25 mg/kg
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Administration:5 times per week; ~5 weeks
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Result:Achieved 90% tumor growth inhibition (TGI) vs control .
Reduced tumor STAT3 and phospho-STAT3 protein, and reduced expression of STAT3 target genes c-MYC, MCL-1, and VEGF.
Chemical Information
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No. CAS 1402357-06-5
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Appearance Solid
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Peso molecular 5422.00
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Color White to off-white
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SMILES
[Danvatirsen]
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Synonyms
AZD9150
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Sequence
DNA, d(P-thio)([(5′ξ)-2′,5′-anhydro-6′-deoxy-4′-C-(hydroxymethyl)-α-L-lyxo-hexofurano]m5C-(3′→4′)-[(5′ξ)-2′,5′-anhydro-6′-deoxy-4′-C-(hydroxymethyl)-α-L-lyxo-hexofurano]m5U-(3′→4′)-[(5′ξ)-2′,5′-anhydro-6′-deoxy-4′-C-(hydroxymethyl)-α-L-lyxo-hexofurano]A-T-T-T-G-G-A-T-G-T-m5C-(3′→4′)-[(5′ξ)-2′,5′-anhydro-6′-deoxy-4′-C-(hydroxymethyl)-α-L-lyxo-hexofurano]A-(3′→4′)-[(5′ξ)-2′,5′-anhydro-6′-deoxy-4′-C-(hydroxymethyl)-α-L-lyxo-hexofurano]G-(3′→4′)-[(5′ξ)-2′,5′-anhydro-6′-deoxy-4′-C-(hydroxymethyl)-α-L-lyxo-hexofurano]m5C)
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
-20°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
Solvente y solubilidad
In Vitro:
H2O : 100 mg/mL (18.44 mM; Need ultrasonic)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
In Vivo:
For the following dissolution methods, please prepare the working solution directly:
It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: PBS
Solubility: 50 mg/mL (9.22 mM); Clear solution; Need ultrasonic
Protocolo
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RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.
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Annexin V plus membrane-impermeant dye apoptosis staining
Annexin V-based apoptosis assays rely on the detection of phosphatidylserine (PS) externalization from the inner leaflet of the plasma membrane to the outer leaflet, an early biochemical hallmark of apoptosis. Fluorescently labeled Annexin V binds PS in a calcium-dependent manner, enabling identification of early apoptotic cells by flow cytometry or fluorescence microscopy. When combined with a membrane-impermeant DNA-binding dye (e. g. , propidium iodide), this approach allows discrimination between viable (Annexin V−/dye−), early apoptotic (Annexin V+/dye−), and late apoptotic or necrotic (Annexin V+/dye+) cell populations by assessing membrane integrity and PS exposure.
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Patient-Derived Orthotopic Xenograft (PDOX)
Patient-derived orthotopic xenograft (PDOX) modeling implants fresh patient tumor tissue or patient-derived tumor cells into the anatomically corresponding organ or tissue site of immunodeficient mice, usually by surgical orthotopic implantation, to preserve patient tumor histology, local microenvironmental context, invasion, metastatic behavior, and treatment-response features better than subcutaneous implantation. PDOX readouts include tumor engraftment, orthotopic tumor growth, local invasion, metastasis, recurrence after resection, histologic similarity to the donor tumor, biomarker retention, molecular concordance, survival, and response or resistance to therapy. PDOX models are used for preclinical drug testing and individualized therapy evaluation, but engraftment success varies by tumor type and specimen quality.
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
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How to Choose the Right Model Animal
Choosing the right model animal is a validity-driven decision in which the species, strain, sex, age, genetic background, disease-induction method, outcome measures, and welfare burden must match the scientific question rather than laboratory tradition or convenience. A model should be selected by judging face validity, construct validity, and predictive validity: whether it resembles the human phenotype, whether it reproduces relevant mechanisms, and whether results are likely to predict human biology or treatment response. Animal studies often fail to translate because of species differences, weak disease resemblance, poor experimental design, inadequate reporting, publication bias, and underuse of randomization, blinding, and sample-size justification. Unresolved questions include how to rank competing models objectively, how much human-disease complexity must be reproduced for a given objective, and when non-animal systems such as organoids, ex vivo tissue, or computational models
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Carcinogenicity Bioassay
A carcinogenicity bioassay detects whether long-term exposure to a test substance increases benign or malignant tumor incidence, changes tumor spectrum, or shortens tumor latency in experimental animals; the classical rodent design exposes rats and/or mice to multiple dose levels for most of their lifespan, followed by complete necropsy and histopathologic diagnosis of neoplastic and non-neoplastic lesions. The readout is tumor incidence by organ, sex, species, dose group, and survival status; interpretation requires concurrent controls, dose-response assessment, survival-adjusted tumor statistics, and pathology review because mortality, spontaneous tumor background, and body-weight effects can influence apparent tumor rates.
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Apoptosis
Apoptosis, also called programmed cell death, is generally characterized by distinct morphological characteristics.
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TUNEL staining for apoptotic DNA fragmentation
TUNEL staining detects DNA strand breaks by using terminal deoxynucleotidyl transferase to add labeled nucleotides to exposed 3′-OH DNA termini, generating either microscopic staining in fixed cells or tissue sections, or fluorescence/cytometric signal in cell suspensions. TUNEL positivity reflects DNA fragmentation but should not be interpreted alone as definitive apoptosis, because TUNEL can also label necrotic, autolytic, mechanically damaged, or DNA-repair-associated DNA breaks.
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Patient-Derived Xenograft (PDX)
Patient-derived xenograft (PDX) models are generated by engrafting primary human tumor tissue directly into immunodeficient mice, allowing in vivo propagation of patient tumor biology without initial in vitro adaptation. These models are used to preserve key histopathological and molecular characteristics of the original tumor and enable assessment of tumor growth dynamics and therapeutic response in a living organism. The biological readout is tumor engraftment and subsequent growth in the murine host, which reflects the ability of human tumor cells to survive, vascularize, and expand in an immunocompromised microenvironment.
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Apoptosis Solutions
Apoptosis is a regulated, generally non-lytic cell-death pathway that removes unwanted, damaged, infected, or abnormal cells through coordinated morphological changes, caspase activation, DNA fragmentation, and membrane remodeling. The intrinsic apoptosis pathway is controlled mainly by mitochondrial outer membrane permeabilization, BCL-2 family proteins, cytochrome c release, apoptosome formation, caspase-9 activation, and downstream executioner caspase-3/7 activation. The extrinsic apoptosis pathway is initiated by death receptors such as Fas, TNFR, and TRAIL receptors, which recruit adaptor proteins and activate caspase-8 before engaging executioner caspases or mitochondrial amplification through BID cleavage. Apoptosis is linked to many phenotypes, including cancer cell killing, tissue homeostasis, immune regulation, neurodegeneration, infection response, and treatment-induced cytotoxicity; unresolved questions include how apoptosis interacts with necroptosis, pyroptosis, ferroptos
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Soft Agar Colony Formation Assay
Soft agar colony formation assay measures anchorage-independent growth, in which transformed or tumorigenic cells proliferate as colonies in a semisolid agar matrix while many non-transformed adherent cells fail to proliferate without attachment; classic studies showed that growth in semisolid medium correlates with tumorigenicity in nude mice, and later protocol papers describe the method as a stringent in vitro assay for malignant transformation. The readout is the number, size, morphology, or signal intensity of colonies formed within agar after incubation; published formats include manual colony counting after staining, 96-well or 384-well quantitative formats, DNA-binding dye detection, MTT/tetrazolium-based detection, digital image analysis, and PCR-based marker detection from soft agar cultures.
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Subcutaneous Cell-Line-Derived Xenograft
Subcutaneous cell-line-derived xenograft (CDX) models are established by implanting cultured human cancer cell lines into immunodeficient mice, where the injected cells form localized tumors that can be monitored in vivo as a measure of tumorigenic potential, growth kinetics, and treatment response. These models are widely used in oncology research because they allow reproducible tumor formation and enable comparative assessment of tumor growth between different cell lines or genetic manipulations in a controlled in vivo microenvironment. Subcutaneous implantation of cancer cells in immunodeficient mice is a standard approach for evaluating tumor growth behavior and therapeutic response across multiple cancer types, including prostate, esophageal, pancreatic, and colon cancer models.
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Orthotopic Cell-Line Xenograft
Orthotopic cell-line xenograft models involve implantation of human cancer cell lines into the anatomically corresponding organ of immunodeficient mice to reproduce tumor growth within a native microenvironment, enabling more clinically relevant tumor behavior compared with subcutaneous models. These models are widely used because orthotopic placement better recapitulates tumor progression, including invasion and metastatic spread, which are often underrepresented in heterotopic implantation systems. Compared with conventional xenografts, orthotopic implantation is described as more technically complex but provides improved simulation of tumor-microenvironment interactions and metastatic behavior, making it particularly valuable for translational oncology research. Surgical orthotopic implantation approaches have been emphasized as enabling faithful reproduction of clinical cancer features, including metastasis and disease progression patterns that align with the tumor’s organ of origi
Pureza y Documentación
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Ficha de datos (293 KB)
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SDS (252 KB)
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Instrucciones de manejo (2242 KB)
Referencias
[1]. Reilley MJ, et al. STAT3 antisense oligonucleotide AZD9150 in a subset of patients with heavily pretreated lymphoma: results of a phase 1b trial. J Immunother Cancer. 2018;6(1):119. Published 2018 Nov 16. [Content Brief]
[2]. Shastri A, et al. Antisense STAT3 inhibitor decreases viability of myelodysplastic and leukemic stem cells. J Clin Invest. 2018;128(12):5479-5488. [Content Brief]
[3]. Odate S, et al. Inhibition of STAT3 with the Generation 2.5 Antisense Oligonucleotide, AZD9150, Decreases Neuroblastoma Tumorigenicity and Increases Chemosensitivity. Clin Cancer Res. 2017;23(7):1771-1784. [Content Brief]
[4]. Hong D, et al. AZD9150, a next-generation antisense oligonucleotide inhibitor of STAT3 with early evidence of clinical activity in lymphoma and lung cancer. Sci Transl Med. 2015;7(314):314ra185. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (stored under nitrogen). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| H2O | 1 mM | 0.1844 mL | 0.9222 mL | 1.8443 mL | 4.6108 mL |
| 5 mM | 0.0369 mL | 0.1844 mL | 0.3689 mL | 0.9222 mL | |
| 10 mM | 0.0184 mL | 0.0922 mL | 0.1844 mL | 0.4611 mL | |
| 15 mM | 0.0123 mL | 0.0615 mL | 0.1230 mL | 0.3074 mL |
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Keywords
- Danvatirsen
- 1402357-06-5
- AZD9150
- AZD 9150
- AZD-9150
- STAT
- Apoptosis
- STAT3 Inhibitor
- MOLM14 cells
- MDS-L cells
- MV411 cells
- KG1a cells
- MOLM13 cells
- KT1 cells
- CMK leukemic/MDS cell lines
- SK-N-AS cells
- NGP cells
- IMR32 cells
- lymphoma
- myelodysplastic syndrome
- acute myeloid leukemia
- neuroblastoma and non-small cell lung cancer
- Inhibitor
- inhibitor
- inhibit