Skip to content

Study · In vitro (cells) · 2007

7 results

Actin-sequestering protein, thymosin-beta-4 (TB4), inhibits caspase-3 activation in paclitaxel-induced tumor cell death.

Moon EY, Song JH, Yang KH

Oncology research1 Jan 2007Cited by 19 (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 study7

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

  1. 01LabIn vitro (cells)Mechanism

    In tumor cells treated with paclitaxel, TB4 peptides increased cell survival.

    In plain wordsIn tumor cells, TB4 peptides raised cell survival during paclitaxel treatment.

    Outcome
    IncreaseCell survival with TB4 peptides after paclitaxel
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Cell survival rate was increased and caspase-3 activity was decreased by the treatment with TB4 peptides.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.
  2. 02LabIn vitro (cells)Mechanism

    In tumor cells treated with paclitaxel, TB4 peptides decreased caspase-3 activity.

    In plain wordsIn tumor cells, TB4 peptides lowered caspase-3 activity during paclitaxel treatment.

    Outcome
    DecreaseCaspase-3 activity with TB4 peptides
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Cell survival rate was increased and caspase-3 activity was decreased by the treatment with TB4 peptides.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.
  3. 03LabIn vitro (cells)Mechanism

    In tumor cells, TB4 peptide treatment reduced the population in the G2/M phase.

    In plain wordsIn tumor cells, TB4 peptide treatment reduced the share of cells in the G2/M phase.

    Outcome
    DecreaseG2/M phase cell population with TB4 peptide
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The reduced population in G2/M phase by TB4 peptide treatment was correlated with the decreased expression of cyclin B1.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.
  4. 04LabIn vitro (cells)Mechanism

    In tumor cells, TB4 peptide treatment decreased cyclin B1 expression.

    In plain wordsIn tumor cells, TB4 peptide treatment lowered cyclin B1 levels.

    Outcome
    DecreaseCyclin B1 expression with TB4 peptide
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer
    Studied dose
    Dose not stated

    Source sentences

    Summary
    The reduced population in G2/M phase by TB4 peptide treatment was correlated with the decreased expression of cyclin B1.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.

Studies that did not test the peptide alone3

In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Thymosin beta-4 (human).

  1. 05LabNot a test of Thymosin beta-4 (human) aloneIn vitro (cells)Mechanism

    In tumor cells, siRNA against TB4 inhibited cell viability.

    In plain wordsIn tumor cells, blocking the cells' own TB4 with siRNA lowered cell viability.

    Outcome
    DecreaseCell viability after TB4 siRNA
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer

    Source sentences

    Summary
    In contrast, small interfering RNA (siRNA) of TB4 inhibited cell viability and augmented caspase-3 activity.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  2. 06LabNot a test of Thymosin beta-4 (human) aloneIn vitro (cells)Mechanism

    In tumor cells, siRNA against TB4 augmented caspase-3 activity.

    In plain wordsIn tumor cells, blocking the cells' own TB4 with siRNA raised caspase-3 activity.

    Outcome
    IncreaseCaspase-3 activity after TB4 siRNA
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer

    Source sentences

    Summary
    In contrast, small interfering RNA (siRNA) of TB4 inhibited cell viability and augmented caspase-3 activity.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

  3. 07LabNot a test of Thymosin beta-4 (human) aloneIn vitro (cells)Mechanism

    In HeLa cells, TB4 peptide treatment or TB4 gene overexpression caused significant changes in Bcl-2 phosphorylation.

    In plain wordsIn HeLa cells, Tβ4 peptide or raised Tβ4 gene activity changed Bcl-2 phosphorylation. The direction is not stated.

    Outcome
    Direction not reportedBcl-2 phosphorylation with TB4 peptide or TB4 overexpression
    Study

    humann: not reported in source

    HeLa cells and gastric tumor cell lines with paclitaxel
    Outcome group
    Tumor growth · Cancer

    Source sentences

    Summary
    Significant changes in Bcl-2 phosphorylation were detected by TB4 peptide treatment or by the overexpression of TB4 gene in Hela cells.
    1 context sentence
    Summary · context
    Here we investigated the inhibitory effect of TB4 peptides on tumor cell death by paclitaxel. The effect of TB4 peptides was assayed by the measurement of caspase-3 activity, G2/M arrest, and Bcl-2 phosphorylation.

    In this study, Thymosin beta-4 (human) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Thymosin beta-4 (human).

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

    13 Oct 2026, 01:52 UTC

    Study results updated

  2. Version 1

    12 Oct 2026, 18:17 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.