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Study · In vitro (cells) · 2000

4 results

Luteinizing hormone-releasing hormone agonist triptorelin and antagonist cetrorelix inhibit EGF-induced c-fos expression in human gynecological cancers.

Gründker C, Völker P, Schulz KD, Emons G

Gynecologic oncology1 Aug 2000Cited by 56 (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 study4

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

  1. 01LabIn vitro (cells)Mechanism

    In LHRH-receptor-positive cancer cell lines, cetrorelix reduced EGF-induced c-fos mRNA expression dose-dependently versus EGF stimulation alone.

    In plain wordsIn cells expressing LHRH receptors, cetrorelix reduced EGF-induced c-fos gene expression dose-dependently compared with EGF stimulation alone.

    Peptide
    Cetrorelix
    Outcome
    DecreaseEGF-induced c-fos mRNA expression
    Study

    humann: not reported in source

    Human endometrial, ovarian, and breast cancer cell lines
    Comparator
    EGF stimulation without LHRH analog
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In all of the lines expressing LHRH receptor, EGF-induced c-fos mRNA expression as well as c-Fos protein synthesis was dose-dependently reduced by treatment with LHRH agonists and antagonists.
    2 context sentences
    Summary · context
    Human endometrial (Ishikawa, Hec-1A), ovarian (EFO-21, EFO-27, SK-OV-3), and breast cancer cell lines (MCF-7) were rendered quiescent by incubation (72 h) in the absence of fetal calf serum and phenol red.
    Summary · context
    This was followed by a 15-min incubation in the absence or presence of the LHRH agonist triptorelin (100 nM) or the antagonist Cetrorelix (100 nM) before the cells were stimulated for 10 min with EGF (100 nM).
  2. 02LabIn vitro (cells)Mechanism

    In LHRH-receptor-positive cancer cell lines, cetrorelix reduced EGF-induced c-Fos protein synthesis dose-dependently versus EGF stimulation alone.

    In plain wordsIn cells expressing LHRH receptors, cetrorelix reduced EGF-induced c-Fos protein production dose-dependently compared with EGF stimulation alone.

    Peptide
    Cetrorelix
    Outcome
    DecreaseEGF-induced c-Fos protein synthesis
    Study

    humann: not reported in source

    Human endometrial, ovarian, and breast cancer cell lines
    Comparator
    EGF stimulation without LHRH analog
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    In all of the lines expressing LHRH receptor, EGF-induced c-fos mRNA expression as well as c-Fos protein synthesis was dose-dependently reduced by treatment with LHRH agonists and antagonists.
    2 context sentences
    Summary · context
    Human endometrial (Ishikawa, Hec-1A), ovarian (EFO-21, EFO-27, SK-OV-3), and breast cancer cell lines (MCF-7) were rendered quiescent by incubation (72 h) in the absence of fetal calf serum and phenol red.
    Summary · context
    This was followed by a 15-min incubation in the absence or presence of the LHRH agonist triptorelin (100 nM) or the antagonist Cetrorelix (100 nM) before the cells were stimulated for 10 min with EGF (100 nM).
  3. 03LabIn vitro (cells)Mechanism

    In LHRH-receptor-positive cancer cell lines, cetrorelix at 100 nM reduced EGF-induced c-fos expression to baseline levels.

    In plain wordsIn cells expressing LHRH receptors, cetrorelix at 100 nM reduced EGF-induced c-fos expression to baseline compared with EGF stimulation alone.

    Peptide
    Cetrorelix
    Outcome
    Decreasec-fos expression at 100 nM
    Study

    humann: not reported in source

    Human endometrial, ovarian, and breast cancer cell lines
    Comparator
    EGF stimulation without LHRH analog
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    100 nMAs given in this study (human).

    Source sentences

    Summary
    At 100 nM concentrations of the LHRH analogs, c-fos expression was reduced to baseline levels.
    2 context sentences
    Summary · context
    Human endometrial (Ishikawa, Hec-1A), ovarian (EFO-21, EFO-27, SK-OV-3), and breast cancer cell lines (MCF-7) were rendered quiescent by incubation (72 h) in the absence of fetal calf serum and phenol red.
    Summary · context
    This was followed by a 15-min incubation in the absence or presence of the LHRH agonist triptorelin (100 nM) or the antagonist Cetrorelix (100 nM) before the cells were stimulated for 10 min with EGF (100 nM).
  4. 04LabIn vitro (cells)Mechanism

    In LHRH-receptor-negative SK-OV-3 cells, cetrorelix did not affect EGF-induced c-fos expression versus EGF stimulation alone.

    In plain wordsIn SK-OV-3 cells without LHRH receptors, cetrorelix did not affect EGF-induced c-fos expression compared with EGF stimulation alone.

    Peptide
    Cetrorelix
    Outcome
    No significant changeEGF-induced c-fos expression in SK-OV-3
    Study

    humann: not reported in source

    LHRH-receptor-negative SK-OV-3 ovarian cancer cells
    Comparator
    EGF stimulation without LHRH analog
    Outcome group
    Receptor activity and mechanism · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    No effect of LHRH analogs on EGF-induced c-fos expression was observed in the ovarian cancer cell line SK-OV-3, which does not express the LHRH receptor.
    2 context sentences
    Summary · context
    Human endometrial (Ishikawa, Hec-1A), ovarian (EFO-21, EFO-27, SK-OV-3), and breast cancer cell lines (MCF-7) were rendered quiescent by incubation (72 h) in the absence of fetal calf serum and phenol red.
    Summary · context
    This was followed by a 15-min incubation in the absence or presence of the LHRH agonist triptorelin (100 nM) or the antagonist Cetrorelix (100 nM) before the cells were stimulated for 10 min with EGF (100 nM).

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

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:35 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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