General Information of the Disease (ID: DIS00527)
Name
Gastric cancer
ICD
ICD-11: 2B72
Resistance Map
Type(s) of Resistant Mechanism of This Disease
  MRAP: Metabolic Reprogramming via Altered Pathways
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
Click to Show/Hide the Full List of Drugs
Trastuzumab
Click to Show/Hide
Drug Resistance Data Categorized by Their Corresponding Mechanisms
  Metabolic Reprogramming via Altered Pathways (MRAP) Click to Show/Hide
Key Molecule: Metastasis associated in colon cancer protein 1 (MACC1) [1]
Metabolic Type Glucose metabolism
Resistant Disease HER2-positive advanced gastric cancer [ICD-11: 2B72.1]
Resistant Drug Trastuzumab
Molecule Alteration Expression
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Human papillomavirus infection Activation hsa05165
In Vitro Model BGC823 cells Gastric Homo sapiens (Human) CVCL_3360
NCI-N87 with high HER2 expressions cells Stomach Homo sapiens (Human) CVCL_1603
MkN28 cells Gastric Homo sapiens (Human) CVCL_1416
MKN45 parental cells with high HER2 expressions Stomach Homo sapiens (Human) CVCL_0434
SGC-7901 cells Gastric Homo sapiens (Human) CVCL_0520
Experiment for
Drug Resistance
MTT assay
Mechanism Description Overexpression of MACC1-induced trastuzumab resistance, enhanced the Warburg effect, and activated the PI3K/AKT signaling pathway, while downregulation of MACC1 presented the opposite effects.
Key Molecule: Metastasis associated in colon cancer protein 1 (MACC1) [1]
Metabolic Type Glucose metabolism
Resistant Disease HER2-positive advanced gastric cancer [ICD-11: 2B72.1]
Resistant Drug Trastuzumab
Molecule Alteration Expression
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Human papillomavirus infection Activation hsa05165
In Vivo Model BALB/c nude mouse xenograft model using NCI-N87 MACC1-overexpressing Mice
Experiment for
Drug Resistance
Tumor volume assay
Mechanism Description Overexpression of MACC1-induced trastuzumab resistance, enhanced the Warburg effect, and activated the PI3K/AKT signaling pathway, while downregulation of MACC1 presented the opposite effects.
Drug Sensitivity Data Categorized by Their Corresponding Mechanisms
  Metabolic Reprogramming via Altered Pathways (MRAP) Click to Show/Hide
Key Molecule: Metastasis associated in colon cancer protein 1 (MACC1) [1]
Metabolic Type Glucose metabolism
Sensitive Disease HER2-positive advanced gastric cancer [ICD-11: 2B72.1]
Sensitive Drug Trastuzumab
Molecule Alteration Expression
Down-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Human papillomavirus infection Activation hsa05165
In Vitro Model MKN45 cells Liver Homo sapiens (Human) CVCL_0434
NCI-N87 cells Gastric Homo sapiens (Human) CVCL_1603
Experiment for
Drug Resistance
Cell viability assay
Mechanism Description Overexpression of MACC1-induced trastuzumab resistance, enhanced the Warburg effect, and activated the PI3K/AKT signaling pathway, while downregulation of MACC1 presented the opposite effects.
Key Molecule: Metastasis associated in colon cancer protein 1 (MACC1) [1]
Metabolic Type Glucose metabolism
Sensitive Disease HER2-positive advanced gastric cancer [ICD-11: 2B72.1]
Sensitive Drug Trastuzumab
Molecule Alteration Expression
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Human papillomavirus infection Activation hsa05165
In Vivo Model BALB/c nude mouse xenograft model using NCI-N87 MACC1-silenced Mice
Experiment for
Drug Resistance
Tumor volume assay
Mechanism Description Overexpression of MACC1-induced trastuzumab resistance, enhanced the Warburg effect, and activated the PI3K/AKT signaling pathway, while downregulation of MACC1 presented the opposite effects.
References
Ref 1 A new mechanism of trastuzumab resistance in gastric cancer: MACC1 promotes the Warburg effect via activation of the PI3K/AKT signaling pathway. J Hematol Oncol. 2016 Aug 31;9(1):76.

If you find any error in data or bug in web service, please kindly report it to Dr. Sun and Dr. Yu.