Pair Name | Beta-Elemene, Cetuximab | ||
Phytochemical Name | Beta-Elemene (PubChem CID: 6918391 ) | ||
Anticancer drug Name | Cetuximab (PubChem CID: / ) | ||
Structure of Phytochemical |
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MOL
3D
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Structure of Anticancer Drug |
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2D
MOL
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MOL
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Pair Name | Beta-Elemene, Cetuximab | |||
Disease Info | [ICD-11: 2B91] | Colorectal cancer | Investigative | |
Biological Phenomena | Induction-->Ferroptosis | |||
Gene Regulation | Up-regulation | Expression | CDH1 | hsa999 |
Down-regulation | Expression | CDH2 | hsa1000 | |
Down-regulation | Expression | FTH1 | hsa2495 | |
Down-regulation | Expression | GLS | hsa2744 | |
Down-regulation | Expression | GPX4 | hsa2879 | |
Up-regulation | Expression | HMOX1 | hsa3162 | |
Down-regulation | Expression | MMP9 | hsa4318 | |
Down-regulation | Expression | SLC40A1 | KEGG ID N.A. | |
Down-regulation | Expression | SLC7A11 | hsa23657 | |
Down-regulation | Expression | SNAI1 | hsa6615 | |
Down-regulation | Expression | SNAI2 | hsa6591 | |
Up-regulation | Expression | TF | KEGG ID N.A. | |
Down-regulation | Expression | VIM | hsa7431 | |
In Vitro Model | HCT 116 | Colon carcinoma | Homo sapiens (Human) | CVCL_0291 |
LoVo | Colon adenocarcinoma | Homo sapiens (Human) | CVCL_0399 | |
In Vivo Model | HCT116-luc cells were digested and washed by cold PBS for three times, and the final concentration was 2.5×10⁶/ml in cold PBS. A volume of 100 μl cell suspension was injected subcutaneously into right dorsal flank of mice. | |||
Result | natural product β-elemene is a new ferroptosis inducer and combinative treatment of β-elemene and cetuximab is sensitive to KRAS mutant CRC cells by inducing ferroptosis and inhibiting EMT, which will hopefully provide a prospective strategy for CRC patients with RAS mutations. |
No. | Title | Href |
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1 | Combinative treatment of β-elemene and cetuximab is sensitive to KRAS mutant colorectal cancer cells by inducing ferroptosis and inhibiting epithelial-mesenchymal transformation. Theranostics. 2020;10(11):5107-5119. Published 2020 Apr 6. doi:10.7150/thno.44705 | Click |