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Study · Animal study (in vivo) · mouse · 2017

15 results

The anti-diabetic drug exenatide, a glucagon-like peptide-1 receptor agonist, counteracts hepatocarcinogenesis through cAMP-PKA-EGFR-STAT3 axis.

Zhou M, Mok MT, Sun H, Chan AW, Huang Y, Cheng AS, Xu G

Oncogene20 Mar 2017Cited by 51 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study15

15 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In obese DEN-treated mice, Ex-4 improved obesity-induced hyperglycemia.

    In plain wordsIn obese DEN-treated mice, Ex-4 improved high blood glucose.

    Outcome
    DecreaseHyperglycemia
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Administration of Ex-4 significantly improved obesity-induced hyperglycemia and hyperlipidemia and reduced HCC multiplicity in obese DEN-treated mice, in which suppressed proliferation and induced apoptosis were confined to tumor cells.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In obese DEN-treated mice, Ex-4 improved obesity-induced hyperlipidemia.

    In plain wordsIn obese DEN-treated mice, Ex-4 improved high blood lipid levels.

    Outcome
    DecreaseHyperlipidemia
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Lipids · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Administration of Ex-4 significantly improved obesity-induced hyperglycemia and hyperlipidemia and reduced HCC multiplicity in obese DEN-treated mice, in which suppressed proliferation and induced apoptosis were confined to tumor cells.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In obese DEN-treated mice, Ex-4 reduced hepatocellular carcinoma multiplicity.

    In plain wordsIn obese DEN-treated mice, Ex-4 reduced liver tumor multiplicity.

    Outcome
    DecreaseHepatocellular carcinoma multiplicity
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Administration of Ex-4 significantly improved obesity-induced hyperglycemia and hyperlipidemia and reduced HCC multiplicity in obese DEN-treated mice, in which suppressed proliferation and induced apoptosis were confined to tumor cells.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In obese DEN-treated mice, Ex-4 suppressed proliferation confined to tumor cells.

    In plain wordsIn obese DEN-treated mice, Ex-4 suppressed tumor cell multiplication.

    Outcome
    DecreaseTumor cell proliferation
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Administration of Ex-4 significantly improved obesity-induced hyperglycemia and hyperlipidemia and reduced HCC multiplicity in obese DEN-treated mice, in which suppressed proliferation and induced apoptosis were confined to tumor cells.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In obese DEN-treated mice, Ex-4 induced apoptosis confined to tumor cells.

    In plain wordsIn obese DEN-treated mice, Ex-4 induced tumor cell death.

    Outcome
    IncreaseTumor cell apoptosis
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Administration of Ex-4 significantly improved obesity-induced hyperglycemia and hyperlipidemia and reduced HCC multiplicity in obese DEN-treated mice, in which suppressed proliferation and induced apoptosis were confined to tumor cells.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In obese DEN-treated mice, Ex-4 tumor suppression was associated with high GLP-1R expression.

    In plain wordsIn obese DEN-treated mice, Ex-4 tumor suppression was linked to high GLP-1 receptor expression.

    Outcome
    Not applicableGLP-1R expression association
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The tumor suppression effects of Ex-4 were associated with high expression of GLP-1R and activation of cyclic AMP (cAMP) and protein kinase A (PKA).
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In obese DEN-treated mice, Ex-4 tumor suppression was associated with cAMP activation.

    In plain wordsIn obese DEN-treated mice, Ex-4 tumor suppression was linked to cAMP activation.

    Outcome
    IncreasecAMP activation
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The tumor suppression effects of Ex-4 were associated with high expression of GLP-1R and activation of cyclic AMP (cAMP) and protein kinase A (PKA).
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  8. 08AnimalAnimal study (in vivo)Mechanism

    In obese DEN-treated mice, Ex-4 tumor suppression was associated with PKA activation.

    In plain wordsIn obese DEN-treated mice, Ex-4 tumor suppression was linked to PKA activation.

    Outcome
    IncreasePKA activation
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The tumor suppression effects of Ex-4 were associated with high expression of GLP-1R and activation of cyclic AMP (cAMP) and protein kinase A (PKA).
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  9. 09AnimalAnimal study (in vivo)Mechanism

    In the hepatocarcinogenesis study, Ex-4 downregulated EGFR.

    In plain wordsIn mice, Ex-4 reduced EGFR in the liver cancer study.

    Outcome
    DecreaseEGFR downregulation
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Importantly, Ex-4 also downregulated epidermal growth factor receptor (EGFR) and signal transducer and activator of transcription 3 (STAT3), which lie downstream of cAMP-PKA signaling, resulting in suppression of multiple STAT3-targeted genes including c-Myc, cyclin D1, survivin, Bcl-2 and Bcl-xl.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  10. 10AnimalAnimal study (in vivo)Mechanism

    In the hepatocarcinogenesis study, Ex-4 downregulated STAT3.

    In plain wordsIn mice, Ex-4 reduced STAT3 in the liver cancer study.

    Outcome
    DecreaseSTAT3 downregulation
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Importantly, Ex-4 also downregulated epidermal growth factor receptor (EGFR) and signal transducer and activator of transcription 3 (STAT3), which lie downstream of cAMP-PKA signaling, resulting in suppression of multiple STAT3-targeted genes including c-Myc, cyclin D1, survivin, Bcl-2 and Bcl-xl.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  11. 11AnimalAnimal study (in vivo)Mechanism

    In the hepatocarcinogenesis study, Ex-4 suppressed STAT3-targeted genes including c-Myc, cyclin D1, survivin, Bcl-2 and Bcl-xl.

    In plain wordsIn mice, Ex-4 suppressed several STAT3-targeted genes in the liver cancer study.

    Outcome
    DecreaseSTAT3-targeted gene suppression
    Study

    mousen: not reported in source

    Obese DEN-treated mice
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Importantly, Ex-4 also downregulated epidermal growth factor receptor (EGFR) and signal transducer and activator of transcription 3 (STAT3), which lie downstream of cAMP-PKA signaling, resulting in suppression of multiple STAT3-targeted genes including c-Myc, cyclin D1, survivin, Bcl-2 and Bcl-xl.
    1 context sentence
    Summary · context
    Herein we investigated the effect of Ex-4 in diethylnitrosamine (DEN)-treated mice consuming control or high-fat high-carbohydrate diet.
  12. 12AnimalAnimal study (in vivo)Efficacy outcome

    In a xenograft mouse model, Ex-4 inhibited growth, with PKA and EGFR required for its effects.

    In plain wordsIn mice with tumor grafts, Ex-4 inhibited growth, with PKA and EGFR required for its effects.

    Outcome
    DecreaseXenograft growth
    Study

    mousen: not reported in source

    Xenograft mouse model
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The growth inhibitory effects of Ex-4 were consistent in GLP-1R-abundant hepatoma cell lines and xenograft mouse model, wherein both PKA and EGFR had obligatory roles in mediating Ex-4 functions.
  13. 13AnimalAnimal study (in vivo)Efficacy outcome

    In mice fed methionine-choline-deficient diet, Ex-4 suppressed inflammatory phenotypes.

    In plain wordsIn mice fed methionine-choline-deficient diet, Ex-4 suppressed inflammatory changes.

    Outcome
    DecreaseInflammatory phenotype
    Study

    mousen: not reported in source

    Mice fed methionine-choline-deficient diet
    Outcome group
    Inflammation markers · Liver
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In addition, Ex-4 also effectively suppressed inflammatory and fibrotic phenotypes in mice fed with methionine-choline-deficient (MCD) diet and choline-deficient ethionine-supplemented (CDE) diet, respectively.
  14. 14AnimalAnimal study (in vivo)Efficacy outcome

    In mice fed choline-deficient ethionine-supplemented diet, Ex-4 suppressed fibrotic phenotypes.

    In plain wordsIn mice fed choline-deficient ethionine-supplemented diet, Ex-4 suppressed fibrotic changes.

    Outcome
    DecreaseFibrotic phenotype
    Study

    mousen: not reported in source

    Mice fed choline-deficient ethionine-supplemented diet
    Outcome group
    Liver fat and liver function · Liver
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In addition, Ex-4 also effectively suppressed inflammatory and fibrotic phenotypes in mice fed with methionine-choline-deficient (MCD) diet and choline-deficient ethionine-supplemented (CDE) diet, respectively.
  15. 15LabIn vitro (cells)Efficacy outcome

    In GLP-1R-abundant hepatoma cell lines, Ex-4 inhibited growth, with PKA and EGFR required for its effects.

    In plain wordsIn cells, Ex-4 inhibited liver cancer cell growth, with PKA and EGFR required for its effects.

    Outcome
    DecreaseHepatoma cell growth
    Study

    n: not reported in source

    GLP-1R-abundant hepatoma cell lines
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The growth inhibitory effects of Ex-4 were consistent in GLP-1R-abundant hepatoma cell lines and xenograft mouse model, wherein both PKA and EGFR had obligatory roles in mediating Ex-4 functions.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

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