General Information of the Molecule (ID: Mol01205)
Name
WD repeat domain 7 (WDR7) ,Homo sapiens
Synonyms
WDR7
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Molecule Type
LncRNA
Gene Name
WDR7
Gene ID
23335
Location
chr18:56651343-57029811[+]
Ensembl ID
ENSG00000091157
HGNC ID
HGNC:13490
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Kingdom: Metazoa
Phylum: Chordata
Class: Mammalia
Order: Primates
Family: Hominidae
Genus: Homo
Species: Homo sapiens
Type(s) of Resistant Mechanism of This Molecule
  EADR: Epigenetic Alteration of DNA, RNA or Protein
Drug Resistance Data Categorized by Drug
Clinical Trial Drug(s)
1 drug(s) in total
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Calycosin
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
       Epigenetic Alteration of DNA, RNA or Protein (EADR) Click to Show/Hide
Disease Class: ER negative breast cancer [1]
Resistant Disease ER negative breast cancer [ICD-11: 2C60.7]
Resistant Drug Calycosin
Molecule Alteration Expression
Down-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Cell growth Inhibition hsa05200
WDR7-7/GPR30 signaling pathway Regulation hsa01522
In Vitro Model MCF-7 cells Breast Homo sapiens (Human) CVCL_0031
SkBR3 cells Breast Homo sapiens (Human) CVCL_0033
MDA-MB-231 cells Breast Homo sapiens (Human) CVCL_0062
T47D cells Breast Homo sapiens (Human) CVCL_0553
MDA-MB-468 cells Breast Homo sapiens (Human) CVCL_0419
MCF10A cells Breast Homo sapiens (Human) CVCL_0598
In Vivo Model Nude mouse xenograft model Mus musculus
Experiment for
Molecule Alteration
qPCR
Experiment for
Drug Resistance
CCK8 assay
Mechanism Description Calycosin inhibited the proliferation of breast cancer cells through WDR7-7-GPR30 signaling. WDR7-7 overexpression led to the inhibition of the GPR30-mediated phosphorylation of SRC, EGFR, ERk1/2, and Akt, ultimately resulting in reduced cell growth, which are key regulators of cell proliferation and survival in breast cancer cells, act as downstream effectors of the WDR7-7-GPR30 pathway.
References
Ref 1 Calycosin inhibits the in vitro and in vivo growth of breast cancer cells through WDR7-7-GPR30 Signaling. J Exp Clin Cancer Res. 2017 Nov 2;36(1):153. doi: 10.1186/s13046-017-0625-y.

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