Id: | acc1737 |
Group: | 2sens |
Protein: | STAT3 |
Gene Symbol: | STAT3 |
Protein Id: | P40763 |
Protein Name: | STAT3_HUMAN |
PTM: | phosphorylation |
Site: | Ser727 |
Site Sequence: | CSNTIDLPMSPRTLDSLMQFG |
Disease Category: | Cancer |
Disease: | Melanoma |
Disease Subtype: | |
Disease Cellline: | SK-Mel-28 |
Disease Info: | |
Drug: | NHWD-870 |
Drug Info: | "NHWD-870 is a highly potent, orally active, and selective BET family bromodomain inhibitor that specifically targets BRD2, BRD3, BRD4 (IC50 = 2.7 nM), and BRDT, demonstrating robust antitumor efficacy by suppressing cancer cell proliferation, inducing apoptosis, and inhibiting tumor-associated macrophage interactions. " |
Effect: | inhibit |
Effect Info: | "The cytarabine drug reduces the phosphorylation of STAT3 protein, thereby reducing the expression of SPP1 and promoting the inhibition of tumor progression by BRTi inhibitors." |
Note: | |
Score: | 5.0 |
Pubmed(PMID): | 35184394 |
Sentence Index: | 35184394_8-9 |
Sentence: | "Mechanistically, we demonstrated that EEF2K upregulates the phosphorylation of STAT3 (p-STAT3) at Tyr705, which binds to the promoter region of SPP1 and enhances its transcription, thus facilitating melanoma progression. Transfection-induced re-expression of SPP1 partly negated the inhibitory effect of EEF2K silencing on melanoma, whereas inhibition of SPP1 or STAT3 significantly abolished the efficacy of EEF2K on melanoma cells." |
Sequence & Structure:
MAQWNQLQQLDTRYLEQLHQLYSDSFPMELRQFLAPWIESQDWAYAASKESHATLVFHNLLGEIDQQYSRFLQESNVLYQHNLRRIKQFLQSRYLEKPMEIARIVARCLWEESRLLQTAATAAQQGGQANHPTAAVVTEKQQMLEQHLQDVRKRVQDLEQKMKVVENLQDDFDFNYKTLKSQGDMQDLNGNNQSVTRQKMQQLEQMLTALDQMRRSIVSELAGLLSAMEYVQKTLTDEELADWKRRQQIACIGGPPNICLDRLENWITSLAESQLQTRQQIKKLEELQQKVSYKGDPIVQHRPMLEERIVELFRNLMKSAFVVERQPCMPMHPDRPLVIKTGVQFTTKVRLLVKFPELNYQLKIKVCIDKDSGDVAALRGSRKFNILGTNTKVMNMEESNNGSLSAEFKHLTLREQRCGNGGRANCDASLIVTEELHLITFETEVYHQGLKIDLETHSLPVVVISNICQMPNAWASILWYNMLTNNPKNVNFFTKPPIGTWDQVAEVLSWQFSSTTKRGLSIEQLTTLAEKLLGPGVNYSGCQITWAKFCKENMAGKGFSFWVWLDNIIDLVKKYILALWNEGYIMGFISKERERAILSTKPPGTFLLRFSESSKEGGVTFTWVEKDISGKTQIQSVEPYTKQQLNNMSFAEIIMGYKIMDATNILVSPLVYLYPDIPKEEAFGKYCRPESQEHPEADPGSAAPYLKTKFICVTPTTCSNTIDLPMSPRTLDSLMQFGNNGEGAEPSAGGQFESLTFDMELTSECATSPM
Select PDB:
Target | Drug name | MOA | Phase | Status | Disease | Source |
---|---|---|---|---|---|---|
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 2 | Recruiting | head and neck squamous cell carcinoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 2 | Active, not recruiting | non-small cell lung carcinoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 2 | Completed | non-small cell lung carcinoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Completed | hepatocellular carcinoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Active, not recruiting | head and neck squamous cell carcinoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Completed | diffuse large B-cell lymphoma | ClinicalTrials ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Active, not recruiting | neoplasm | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Active, not recruiting | non-small cell lung carcinoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Completed | non-Hodgkins lymphoma | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Active, not recruiting | urinary bladder cancer | ClinicalTrials |
STAT3 | DANVATIRSEN | STAT-3 mRNA 3'UTR antisense inhibitor | 1 | Completed | cancer | ClinicalTrials |
Note: Only show clinically investigational or approved drugs with protein targets.
Protein Tractability:
source: Open TargetsPTM Intensity:
source: CPTACSTAT3-Ser727 | |
---|---|
Cancer | Intensity |
BRCA | 1.74 |
COAD | |
HGSC | |
ccRCC | |
GBM | -1.099 |
HNSC | |
LUAD | -0.272 |
LUSC | |
non_ccRCC | -0.473 |
PDAC | 0.531 |
UCEC | -0.428 |
PTM-Disease Association:
source: PTMDResidue | Position | State | Disease | Class | PMID |
---|---|---|---|---|---|
S | 727 | D | Oral squamous epithelial carcinoma | Phosphorylation | 23733313 |
S | 727 | D | Triple-negative breast cancer | Phosphorylation | 36017196 |
S | 727 | D | Pancreatic cancer | Phosphorylation | 37548811 |
S | 727 | D | Pancreatic cancer/carcinoma/adenocarcinoma | Phosphorylation | 18519681 |
S | 727 | P | Prostate cancer/carcinoma/adenocarcinoma | Phosphorylation | 23941877 |
S | 727 | P | Breast cancer/tumor/carcinoma | Phosphorylation | 23329648 ;  23329839 |
S | 727 | P | Cancer | Phosphorylation | 23145121 |
S | 727 | P | Melanoma | Phosphorylation | 22418867 |
S | 727 | U | Chronic lymphocytic leukemia | Phosphorylation | 35595309 |
S | 727 | U | Clear cell kidney cancer | Phosphorylation | 24615012 ;  33772065 ;  37945711 |
S | 727 | U | Head and neck squamous cell carcinoma | Phosphorylation | 21281788 |
S | 727 | U | Prostate cancer | Phosphorylation | 18829527 |
S | 727 | U | Glioblastoma multiforme | Phosphorylation | 35670018 |
S | 727 | U | B-cell acute lymphoblastic leukemia | Phosphorylation | 33393494 |
S | 727 | U | Hepatocellular carcinoma | Phosphorylation | 31498440 |
S | 727 | U | Thyroid cancer/carcinoma | Phosphorylation | 17209045 |
State Note: Based on the distinct PTM states in diseases, PTMD classified all disease-associated PTMs into six classes, including whether the up-regulation (U) or down-regulation (D) of PTM levels, the absence (A) or presence (P) of PTMs, and the creation (C) or disruption (N) of PTM sites are associated with diseases.
PTM-Drug Perturbation Response:
source: DecryptMProtein | Gene | PTM | Position | Modified sequence | Cell | Drug | pEC50 | Regulation | Experiment |
---|---|---|---|---|---|---|---|---|---|
P40763 | STAT3 | P | Ser727 | FICVTPTTCSNTIDLPMS(ph)PR | MDA-MB-175 | Pertuzumab | -4.9774 | - | |
P40763 | STAT3 | P | Ser727 | FICVTPTTCSNTIDLPMS(ph)PR | MDA-MB-175 | Trastuzumab | 1.4554 | - | |
P40763 | STAT3 | P | Ser727 | TKFICVTPTTCSNTIDLPMS(ph)PR | MDA-MB-175 | Trastuzumab | -0.3231 | - | |
P40763 | STAT3 | P | Ser727 | TKFICVTPTTCSNTIDLPMS(ph)PR | SK-BR-3 | Lapatinib | 7.1426 | - | |
P40763 | STAT3 | P | Ser727 | FICVTPTTCSNTIDLPMS(ph)PR | SK-BR-3 | Lapatinib | 6.1655 | - | |
P40763 | STAT3 | P | Ser727 | FICVTPTTCSNTIDLPMS(ph)PR | SK-BR-3 | Pertuzumab | -1.7721 | - | |
P40763 | STAT3 | P | Ser727 | FICVTPTTCSNTIDLPMS(ph)PR | SK-BR-3 | Trastuzumab | 0.8214 | - |
pEC50 Note: pEC50 is the negative logarithm of EC50 (half-maximal effective concentration, dosage unit Mol), calculated as pEC50 = -log10(EC50), which quantifies the potency of a drug or compound.
Function score:
source: funscoRNo data.