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Study · In vitro (cells) · 2022

13 results

Carnosine suppresses human colorectal cancer cell proliferation by inducing necroptosis and autophagy and reducing angiogenesis.

Hsieh SL, Li JH, Dong CD, Chen CW, Wu CC

Oncology letters9 Dec 2021Cited by 17 (Europe PMC)

Summary

Carnosine (β-alanyl-L-histidine) is found in beef and fish. The present study aimed to investigate the effects of carnosine on the cell proliferation of human colorectal cancer cells. After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study. Treatment of HCT-116 cells with 5, 10 or 15 mM carnosine for 72 or 96 h significantly decreased cell viability (P<0.05). The mRNA expression of β-catenin and transcription factor 4 (Tcf-4) was significantly reduced by 15-23% and 11-80%, respectively (P<0.05). When HCT-116 cells were treated with 15 mM carnosine, the mRNA levels of 1A/1B-light chain 3 and phosphatidylinositol 3-kinase were significantly increased by 235% and 249%, respectively (P<0.05). The mRNA level of Beclin-1 and autophagy levels were significantly increased by 137-141% in HCT-116 cells treated with 5, 10 or 15 mM carnosine (P<0.05). Carnosine (15 mM) also increased reactive oxygen species levels and mixed lineage kinase domain-like protein mRNA expression and depleted ATP levels (P<0.05). The angiogenesis-regulating molecules vascular endothelial growth factor, epidermal growth factor receptor and hypoxia-inducible factor 1-α were all significantly decreased by 10 or 15 mM carnosine treatment. These results showed that carnosine could suppress human colorectal cell proliferation by reducing β-catenin/Tcf-4 signaling, inducing autophagy and necroptosis and inhibiting angiogenesis. It was demonstrated that carnosine is a potential compound from dietary food for the future clinical treatment and/or prevention of colorectal cancer.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study13

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

  1. 01LabIn vitro (cells)Activity measurement

    In HCT-116 cells, carnosine significantly decreased viability at 5, 10 or 15 mM for 72 or 96 h.

    In plain wordsIn cells, carnosine decreased colorectal cancer cell viability.

    Outcome
    DecreaseCell viability
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Tumor growth · Cancer
    Studied dose
    5, 10 or 15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    Treatment of HCT-116 cells with 5, 10 or 15 mM carnosine for 72 or 96 h significantly decreased cell viability (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  2. 02LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly reduced β-catenin mRNA by 15-23%.

    In plain wordsIn cells, carnosine reduced β-catenin gene expression.

    Outcome
    Decreaseβ-catenin mRNA
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The mRNA expression of β-catenin and transcription factor 4 (Tcf-4) was significantly reduced by 15-23% and 11-80%, respectively (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  3. 03LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly reduced Tcf-4 mRNA by 11-80%.

    In plain wordsIn cells, carnosine reduced Tcf-4 gene expression.

    Outcome
    DecreaseTcf-4 mRNA
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The mRNA expression of β-catenin and transcription factor 4 (Tcf-4) was significantly reduced by 15-23% and 11-80%, respectively (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  4. 04LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly increased 1A/1B-light chain 3 mRNA by 235%.

    In plain wordsIn cells, carnosine increased 1A/1B-light chain 3 gene expression.

    Outcome
    Increase1A/1B-light chain 3 mRNA
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    When HCT-116 cells were treated with 15 mM carnosine, the mRNA levels of 1A/1B-light chain 3 and phosphatidylinositol 3-kinase were significantly increased by 235% and 249%, respectively (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  5. 05LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly increased phosphatidylinositol 3-kinase mRNA by 249%.

    In plain wordsIn cells, carnosine increased phosphatidylinositol 3-kinase gene expression.

    Outcome
    IncreasePhosphatidylinositol 3-kinase mRNA
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    When HCT-116 cells were treated with 15 mM carnosine, the mRNA levels of 1A/1B-light chain 3 and phosphatidylinositol 3-kinase were significantly increased by 235% and 249%, respectively (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  6. 06LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly increased Beclin-1 mRNA, with a reported 137-141% increase for Beclin-1 and autophagy.

    In plain wordsIn cells, carnosine increased Beclin-1 gene expression.

    Outcome
    IncreaseBeclin-1 mRNA
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    5, 10 or 15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The mRNA level of Beclin-1 and autophagy levels were significantly increased by 137-141% in HCT-116 cells treated with 5, 10 or 15 mM carnosine (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  7. 07LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly increased autophagy, with a reported 137-141% increase for Beclin-1 and autophagy.

    In plain wordsIn cells, carnosine increased autophagy.

    Outcome
    IncreaseAutophagy
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    5, 10 or 15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The mRNA level of Beclin-1 and autophagy levels were significantly increased by 137-141% in HCT-116 cells treated with 5, 10 or 15 mM carnosine (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  8. 08LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine increased reactive oxygen species levels.

    In plain wordsIn cells, carnosine increased reactive oxygen species.

    Outcome
    IncreaseReactive oxygen species
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Oxidative stress · Cancer
    Studied dose
    15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    Carnosine (15 mM) also increased reactive oxygen species levels and mixed lineage kinase domain-like protein mRNA expression and depleted ATP levels (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  9. 09LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine increased mixed lineage kinase domain-like protein mRNA expression.

    In plain wordsIn cells, carnosine increased mixed lineage kinase domain-like protein gene expression.

    Outcome
    IncreaseMixed lineage kinase domain-like protein mRNA
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    Carnosine (15 mM) also increased reactive oxygen species levels and mixed lineage kinase domain-like protein mRNA expression and depleted ATP levels (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  10. 10LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine depleted ATP levels.

    In plain wordsIn cells, carnosine reduced ATP levels.

    Outcome
    DecreaseATP levels
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Mitochondrial function · Cancer
    Studied dose
    15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    Carnosine (15 mM) also increased reactive oxygen species levels and mixed lineage kinase domain-like protein mRNA expression and depleted ATP levels (P<0.05).
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  11. 11LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly decreased vascular endothelial growth factor.

    In plain wordsIn cells, carnosine reduced vascular endothelial growth factor.

    Outcome
    DecreaseVascular endothelial growth factor
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    10 or 15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The angiogenesis-regulating molecules vascular endothelial growth factor, epidermal growth factor receptor and hypoxia-inducible factor 1-α were all significantly decreased by 10 or 15 mM carnosine treatment.
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  12. 12LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly decreased epidermal growth factor receptor.

    In plain wordsIn cells, carnosine reduced epidermal growth factor receptor.

    Outcome
    DecreaseEpidermal growth factor receptor
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    10 or 15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The angiogenesis-regulating molecules vascular endothelial growth factor, epidermal growth factor receptor and hypoxia-inducible factor 1-α were all significantly decreased by 10 or 15 mM carnosine treatment.
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.
  13. 13LabIn vitro (cells)Mechanism

    In HCT-116 cells, carnosine significantly decreased hypoxia-inducible factor 1-α.

    In plain wordsIn cells, carnosine reduced hypoxia-inducible factor 1-α.

    Outcome
    DecreaseHypoxia-inducible factor 1-α
    Study

    humann: not reported in source

    HCT-116 colorectal cancer cells
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    10 or 15 mM · 72 or 96 hAs given in this study (human).

    Source sentences

    Summary
    The angiogenesis-regulating molecules vascular endothelial growth factor, epidermal growth factor receptor and hypoxia-inducible factor 1-α were all significantly decreased by 10 or 15 mM carnosine treatment.
    1 context sentence
    Summary · context
    After human colorectal cancer HCT-116 cells were treated carnosine for 72 or 96 h, the cell proliferation, apoptosis, autophagy, necroptosis, angiogenesis and the expression of related regulatory molecules were detected using MTT assays, fluorescence image analysis and RT-qPCR in this study.

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

    27 Oct 2026, 18:20 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:32 UTC

    First added · source update from Europe PMC

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